Abstract
Activated in energy depletion conditions, AMP-activated protein kinase (AMPK) acts as a cellular energy sensor and regulator in both central nervous system and peripheral organs. Hypothalamic AMPK restores energy balance by promoting feeding behavior to increase energy intake, increasing glucose production, and reducing thermogenesis to decrease energy output. Besides energy state, many hormones have been shown to act in concert with AMPK to mediate their anorexigenic and orexigenic central effects as well as thermogenic influences. Here we explore the factors that affect hypothalamic AMPK activity and give the underlying mechanisms for the role of central AMPK in energy homeostasis together with the physiological effects of hypothalamic AMPK on energy balance restoration.
1. Introduction
The central nervous system (CNS) plays an important role in energy balance maintenance by regulating energy intake, energy expenditure, and energy storage [1]. The energy obtained from food intake is used for regular physiological activities in the whole body including heat production through metabolism and the excess energy is stored in form of fat, glycogen, and protein [2]. In order to maintain a functional energy homeostasis, it is important to have a balance between energy intake and energy expenditure. Excessive food intake resulting from dysregulated appetite and impaired energy expenditure is among the factors disrupting energy balance [3]. The arcuate nucleus (ARC) of the hypothalamus is composed of neuronal populations responding to orexigenic and anorexigenic neuropeptides and acts as the primary appetite control center [4–6]. In the ARC, activation of the orexigenic neuropeptides, neuropeptide Y (NPY), and agouti-related protein-expressing neurons (AgRP) results in increased food intake while activation of the anorexigenic neuropeptide proopiomelanocortin (POMC) in satiety conditions suppresses food intake [7]. The energy consumed from food is broken down in metabolic processes to make carbon dioxide, water, and heat. Under resting condition, the body releases energy in form of heat and this output of energy is referred to as thermogenesis [8]. When the body is exposed to cold temperature, the sympathetic nervous system is activated via the β-adrenergic receptor resulting in increased thermogenesis [9].
An imbalance in energy consumption and energy expenditure stimulates the CNS and the peripheral metabolic system to initiate metabolic processes in order to restore the energy balance. In case of increased energy intake, the brain suppresses feeding behavior or stimulates storage of the excess energy in other tissues such as glycogen in liver or triglycerides in adipose tissue. On the other hand, increased energy expenditure in comparison to energy intake stimulates appetite and inhibits energy expenditure through various metabolic pathways including fatty acid metabolism and activation of the nutrient sensor AMP-activated protein kinase (AMPK) [10]. AMPK is activated by high ratio of ADP : ATP or AMP : ATP and is regarded as a key player in the peripheral and central energy regulation [11]. Over the past few years many studies have focused on understanding the underlying mechanisms involved in AMPK mediated energy homeostasis regulation.
AMPK, which is a serine threonine kinase comprising α catalytic subunit and two regulatory subunits (β and γ), is a crucial cellular energy sensor in most eukaryotic cells [12]. Energy depletion conditions activate AMPK which promotes ATP production by stimulating catabolic processes and increasing some glycolytic genes such as PFKFB3 and PFKFB4 [13, 14] and inhibits anabolic pathways requiring ATP such as gluconeogenesis, protein synthesis, cholesterol synthesis, and triglycerides synthesis [15–18]. In addition, AMPK receives hormonal and nutritional signals in the hypothalamus and maintains energy homeostasis [19] by regulating feeding behavior [20], circadian rhythms [21], and energy expenditure [22, 23]. This review provides a general concept on conditions that activate and inhibit hypothalamic AMPK activity and the physiological effects resulting from increased AMPK activity.
2. AMP-Activated Protein Kinase: Structure and Regulation
2.1. Structure
AMPK is a heterotrimeric serine/threonine kinase expressed in different tissues including the brain, liver, and skeletal muscle. AMPK consists of a catalytic α subunit, a regulatory β subunit, and an AMP/ATP binding γ subunit [24–26]. α subunit contains an N-terminal kinase domain and a C-terminal regulatory domain required for interaction with β and γ subunits. β subunit associates with α and γ subunits through the C terminus and binds to oligosaccharides through the glycogen-binding domain also known as the carbohydrate-binding module (CBM) [27]. γ subunit isoforms have four tandem repeats called cystathionine-β-synthase (CBS) that bind to AMP or ATP molecules forming an adenine nucleotide-binding region [28]. There are 2 or 3 genes encoding each subunit; as a result, there are 12 possible heterotrimeric combinations, with splice variants further increasing the potential diversity [29].
2.2. Regulation
AMPK activity is determined by the AMP : ATP ratio. It can also be regulated by AMP's direct allosteric activation, reversible phosphorylation, ADP, or degradation by ubiquitination (Figure 1). The allosteric activation of AMPK is specifically affected by AMP and its analogues [30]. AMP can cause more than 10-fold allosteric activation when its concentration is 1-2 times lower than ATP. Besides that, AMP also enhances the activation of AMPK by inhibiting Thr-172 dephosphorylation (10-fold more potent than ADP) and only AMP enhances liver kinase B1- (LKB1-) induced Thr-172 phosphorylation [31]. AMP allosteric control was previously thought to be mediated by both α and γ subunits but one study pointed out that the degree of activation is affected by the nature of γ isoform in the AMPK complex [26]. However, the highest allosteric activation achieved is approximately 5-fold whereas the effect of phosphorylation on AMPK activity can be much higher [32].
Phosphorylation is the primary regulator of AMPK activity. AMPK requires the phosphorylation on a threonine residue (Thr-172) within the catalytic subunit for its activation [33]. Among the kinases involved in the phosphorylation of AMPK, a lot of research has focused on the two upstream kinases, Ca2+/calmodulin-dependent protein kinase kinase β (CaMKKβ) and the tumor suppressor kinase, liver kinase B1 (LKB1) [34–37]. CaMKKβ, activated by calcium and calmodulin, is known to increase the phosphorylation of AMPK at Thr-172 [38] while LKB1 is the major kinase for AMPK's phosphorylation under energy stress conditions [39]. Besides Thr-172, many phosphorylation sites have been identified within α and β subunits of AMPK but, for most of these sites, the direct effects on AMPK activation and physiological relevance are still unclear [32].
Many compounds are known as AMPK activators through an indirect manner: via increasing the intracellular AMP : ATP ratio or via activation or upregulation of upstream kinases. Among these compounds, there are a number of natural compounds involved in the activation of AMPK such as biguanides [40], gallic acid [41], resveratrol [42], berberine [43], baicalein [44], quercetin [45], arctigenin [46], genistein and capsaicin [47], and curcumin [48]. Besides natural compounds, thiazolidinediones, via altering the level of adenine nucleotides, also activate AMPK [49]. Additionally, 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR), a representative AMP analog, is metabolized in cells to 5-aminoimidazole-4-carboxamide-1β-D-ribofuranosyl-5′-monophosphate (ZMP), an AMP mimetic, therefore increasing AMP : ATP ratio and activating AMPK [50].
Although ADP does not allosterically activate the enzyme, ADP can protect AMPK from dephosphorylation [51]. Moreover, ADP and AMP can bind to the three γ subunit complexes preventing AMPK dephosphorylation at Thr-172. ADP and AMP have different binding abilities on the three γ subunits. On γ2 complexes ADP and AMP have the same binding potential, while ADP is less potent than AMP on γ1 and γ3 complexes [52]. ADP can also promote phosphorylation of Thr-172 and, similar to AMP, it requires N-terminal myristoylation of β subunit [53].
Recent studies identified the ubiquitin proteasome system as a factor regulating AMPK activity directly and indirectly [54, 55]. AMPK-related kinases, such as AMPK-related kinase 5 (NUAK1) and microtubule-affinity-regulating kinase 4 (MARK4), are polyubiquitinated in vivo and interact with the deubiquitinating enzyme ubiquitin specific protease-9 (USP9X). The study provides the first evidence that AMPK family kinases are regulated by polyubiquitin chains [56]. Another study described the suppression of AMPK through ubiquitination and degradation by the cancer-specific MAGE-A3/6-TRIM28 ubiquitin ligase [57]. Additionally, CIDEA which is highly expressed in brown adipose tissue (BAT) has been shown to interact with the regulatory β subunit of AMPK resulting in the ubiquitination and degradation of AMPK. Further CIDEA knockout mice showed an increase in stability and activity of AMPK in BAT [58]. Furthermore, malfunction of the ubiquitin/protease system could contribute to energy homeostasis imbalance by increasing inflammation and apoptosis of hypothalamic neurons important for energy homeostasis regulation [59]. In line with this, diet-induced obesity suppresses hypothalamic AMPK activity [60]. These studies indicate the role of ubiquitin/proteasome system in the regulation of AMPK in the hypothalamus.
3. The Activators and Inhibitors of AMPK in the Brain
There are many factors affecting energy intake and energy expenditure via the activation or inhibition of AMPK in the brain, especially in the hypothalamus. They are also variable molecular mechanisms regulating AMPK activity but, in general, these factors affect the activity of AMPK by altering its phosphorylation. In the following, we discuss some factors involved in the activation and inhibition of hypothalamic AMPK activity (Figure 2).
4. The Activators
4.1. Adiponectin
Adiponectin is secreted from white adipose tissue and plays a role in the central and peripheral regulation of energy homeostasis [61–63]. Adiponectin serves as a starvation signal and regulates feeding behavior by stimulating the phosphorylation of AMPK. In fasting condition, adiponectin increases and stimulates the activity of AMPK in the ARC, leading to induction of food intake and reduction of energy expenditure. After refeeding, decrease in adiponectin levels is accompanied by blunted AMPK activity [64–66]. Of the two adiponectin receptors AdipoR1 and AdipoR2 expressed in the ARC, adiponectin increases AMPK activity and stimulates food intake via AdipoR1. The level of adiponectin and expression of AdipoR1 are elevated in the serum and cerebrospinal fluid during fasting and decrease after refeeding [67]. Acute adiponectin ICV injection was shown to increase the phosphorylation of AMPK [68] while adiponectin deficiency and inhibition of AdipoR1 by adeno-AdipoR1 siRNA suppressed phosphorylation of AMPK in the ARC [67, 69]. The adiponectin/AdipoR1/AMPK pathway has also been implicated in the thiazolidinediones (TZDs) induced body weight gain. TZDs are prescribed for glycemic control but induce body weight gain as a side effect [70, 71]. Pioglitazone treatment was reported to increase food intake and decrease energy expenditure by enhancing the adiponectin signaling and increasing the phosphorylation of AMPK via the AdipoR1 in the hypothalamus [72].
4.2. Ghrelin
Ghrelin is a peptide produced mainly by the oxyntic cells of the stomach and released during fasting condition. It is a natural ligand for the hypothalamic growth hormone secretagogue receptor (GHSR) [73]. Ghrelin is the first circulating hormone demonstrated to induce food intake in man [74]. Intracerebroventricular (ICV) and intraperitoneal (IP) administration of ghrelin was shown to stimulate food intake in rats [75]. In the CNS, ghrelin mainly acts on the hypothalamus to regulate appetite and hence energy consumption [76]. ICV administration of ghrelin in rats activates AMPK in both the ventromedial nucleus of the hypothalamus (VMH) [77] and ARC [78] via GHS-R1a [79]. These receptors are mainly expressed in the ARC and the VMH in the hypothalamus [80] and are necessary for ghrelin's effect on hypothalamic AMPK activity. Ghrelin binds to GHSR and activates heterotrimeric G protein containing Gq (also known as G11) leading to increased intracellular Ca2+ release [81]. Ghrelin also stimulates the release of Ca2+ from ryanodine-sensitive internal stores [82, 83]. Increased intracellular Ca2+ activates CaMKKβ pathway and induces AMPK phosphorylation.
4.3. Cannabinoids
Cannabinoids are a class of diverse chemical compounds that act on cannabinoid receptors repressing neurotransmitter release in the brain. Ligands for these receptor proteins include endocannabinoids, phytocannabinoids, and synthetic cannabinoids. Endocannabinoids can stimulate appetite in the hypothalamus via the presynaptic cannabinoid type 1 (CB1) receptor [84]. Cannabinoid receptor antagonists have been reported to suppress the motivation to eat and reduce the consumption of palatable foods. For example, chronic treatment of rimonabant, a CB1 receptor antagonist, resulted in a marked and sustained decrease in body weight and improved metabolic profile [85, 86]. Cannabinoids, just like ghrelin, can stimulate AMPK activity in the hypothalamus leading to increased appetite [87]. Further, androgens such as testosterone induce hyperphagia and potentiate cannabinoid tone at the CB1 receptors by activating AMPK [88]. Endocannabinoids have been shown to be essential for the orexigenic and anorectic effects of ghrelin and leptin, respectively. Acute leptin treatment in normal rats and ob/ob mice reduces endocannabinoids level in the hypothalamus indicating the involvement of endocannabinoids in the leptin induced food intake regulation in the hypothalamus [89]. Ghrelin treatment failed to induce orexigenic effect in CB1 receptor knockout mice. In addition, genetic and pharmacological blockade of CB1 receptor inhibited the effects of ghrelin on AMPK activity indicating that the stimulatory effects of ghrelin need an intact cannabinoids signaling pathway for AMPK activity and food intake [79, 90].
4.4. Glucocorticoids
Glucocorticoids are potent anti-inflammatory agents used in a wide range of inflammatory and immunologically mediated disease processes. Therapeutic doses of glucocorticoids induce obesity by acting directly or indirectly in the central nervous system to regulate appetite and increase energy intake [91]. Glucocorticoids treatment stimulate AMPK activity in rats' hypothalamus directly [92] or via the induction of endocannabinoid synthesis [93]. Additionally, CB1 knockout mice treated with corticosterone showed an increase in hypothalamic AMPK activity accompanied by blunted weight gain indicating the importance of the CB1 receptor in the glucocorticoid induced activation of the hypothalamic AMPK activity [94]. Further, glucocorticoids upregulate gene expression of the orexigenic NPY as well as AgRP via AMPK phosphorylation at Thr-172 in the arcuate nucleus suggesting that glucocorticoids are essential for the hypothalamic AMPK mediated energy homeostasis [95, 96].
4.5. Hypoglycemia
Glucose is the main source of energy source for the body and is particularly essential for normal brain activity. Hypoglycemia, a condition in which the blood glucose drops below normal levels, poses a great danger to the stability and functioning of the brain. The body has therefore developed many mechanisms to prevent glucose insufficiency especially in the brain. Activation of AMPK which senses the nutritional status of the body is among these mechanisms [97]. To demonstrate the role of AMPK as a glucose sensor, ICV administration of glucose reduced hypothalamic AMPK activity while 2-deoxyglucose, an inhibitor of intracellular glucose utilization, induced hypothalamic AMPK activity after 60 minutes of injection [98, 99]. Moreover, selective downregulation of AMPK in the VMH caused impaired response to acute hypoglycemia by glucagon and epinephrine [100] whereas local VMH application of AICAR during hypoglycemia amplified both glucagon and epinephrine levels [101].
5. The Inhibitors
5.1. Estradiol
Estradiol, or 17β-estradiol, is a steroid and estrogen sex hormone. It plays a fundamental role in the reproductive, cardiovascular, skeletal, and central nervous systems. Many studies have shown a correlation between estradiol and metabolic syndromes [102]. In the brain, estradiol receptor (ER) α and/or ERβ are expressed in several hypothalamic nuclei responding to feeding behavior. ERα is mainly expressed in POMC neurons while both ERα and ERβ are present in NPY neurons [103, 104]. A study demonstrates that the central action of estradiol in the ventromedial nucleus of the hypothalamus inhibits the activity of AMPK, leading to decreased food intake and increased energy expenditure through the sympathetic nervous system in a feeding-independent manner [105]. Moreover, ovariectomized rats showed increased phosphorylation of hypothalamic AMPKα and this effect was reversed after administration of estradiol. In addition, treatment with compound C, an AMPKα inhibitor, for 1 week reduced food intake, body weight, plasma leptin, and adiponectin levels [106]. Furthermore, estradiol also regulates AMPK activity in caudal hindbrain A2 noradrenergic neurons [107] and hypothalamic astrocyte pAMPK is augmented by hypoglycemia in the presence of estradiol [108]. In addition, there is a reduction of hypothalamic AMPK depending on estradiol levels in pregnant rats [109].
5.2. Leptin
Leptin is a hormone secreted by adipocytes and is essential for food intake and energy expenditure regulation. In the skeletal muscle, leptin increases AMPK activity directly as well as indirectly through stimulation of the hypothalamosympathetic axis. On the other hand, in the hypothalamus, leptin decreases AMPK activity [110]. In vivo administration of leptin decreases hypothalamic AMPK activity leading to suppressed feeding behavior [111]. In addition, leptin also inhibits AMPK activity in the ARC and PVH exerting its effects on food intake and body weight [20]. To investigate the role of AMPK activity in sympathetic effects of leptin in vivo, siRNA was administered to knock down AMPKα2 in rats. As a result, leptin effects on body weight, food intake, and blood FFA levels were diminished in AMPKα2 siRNA-treated rats [112]. Leptin regulates food intake by selectively activating POMC neurons. Leptin binds to leptin receptor and directly depolarizes the POMC neurons stimulating β-endorphin and α-melanocyte-stimulating hormone (α-MSH) secretion to downregulate elevated synaptic activity [113]. After that, leptin and opioids from POMC can inhibit the activation of AMPK on a positive feedback loop [83].
5.3. Insulin
Insulin is a hormone produced by beta cells in the pancreas. It regulates the metabolism of carbohydrates and fats by promoting the absorption of glucose from the blood. In the central nervous system, insulin acts as a potent anorexigenic hormone [114]. Insulin can reduce the activity of α2-AMPK by 25–40% in all hypothalamic regions but not in the cortex and the effects of insulin are more widespread in the hypothalamus than that of leptin [20]. Furthermore, ICV injection of an acute dose of taurine activating insulin pathway through AKT/FoxO1 reduces food intake and locomotor activity by suppressing AMPK activity via the mTORC1 pathway [115]. Insulin resistance is described as the inability of insulin to regulate blood glucose level and usually leads to hyperglycemia accompanied by metabolic syndrome development including obesity and diabetes. In diabetic rat, hypothalamic AMPK phosphorylation and α2-AMPK activity are higher. Moreover, chronic insulin treatment or suppression of hypothalamic AMPK activity completely prevents diabetes-induced changes in food intake as well as in hypothalamic AMPK activity [116]. In addition, the effect of insulin is significant in the ARC/VMH and paraventricular nucleus (PVN) [117].
5.4. Glucagon-Like Peptide-1 (GLP-1)
GLP-1 is a neuropeptide and an incretin hormone released by L cells in the ileum and colon. In the central nervous system, there are many neuronal populations expressing GLP-1 and GLP-1 receptors (GLP-1R) especially in the hypothalamic nuclei which is important for energy homeostasis [118]. In the hypothalamus, ICV GLP-1 administration inhibits feeding in fasted rats, demonstrating that GLP-1 is a physiological mediator of satiety [119]. In addition, a reduction in the CNS GLP-1 neuronal activity during food deprivation may act to induce feeding behavior and ICV leptin administration prevents a decrease in hypothalamic GLP-1 peptide content [120]. GLP-1 decreases feeding behavior through the inhibition of AMPK activity. GLP-1 treatment can inhibit the activities of AMPK and p70S6K, the downstream target of mTOR signaling, even at the maximal activity of these protein kinases in the ventromedial and lateral hypothalamic areas [121]. GLP-1 and leptin can act together to partly reduce feeding behavior by inhibiting AMPK after binding of the POMC derivative α-MSH to its receptor melanocortin-4-receptor (MC4-R) [122]. Moreover, the GLP-1R agonist, liraglutide, was shown to dephosphorylate and hence inactivate AMPK leading to increased energy expenditure [123]. The GLP-1 receptors in the ventromedial nucleus of the hypothalamus are also essential for thermogenesis in brown adipose tissue and for the browning effect of white adipose tissue to increase energy expenditure and both effects are partly mediated through the inhibition of AMPK activity [124].
6. Physical Exercise and AMPK Activation
AMPK is stimulated by contractile activity in the skeletal muscles and is therefore regarded as an important factor in the regulation of cell metabolism in exercise-induced changes in muscle glucose and fatty acid metabolism. Indeed, high intensity exercise was shown to significantly increase the activity of α2-AMPK but not α1-AMPK in healthy human subjects suggesting that α2-AMPK might play an important role in metabolic responses to exercise in skeletal muscles [125]. Whereas the role of exercise in the central nervous system remains to be clearly elucidated, the effect of exercise in inducing appetite suggests that exercise and physical activities might somehow influence the activity of AMPK in the hypothalamus. However, there was no significant change observed in the hypothalamic AMPK activity after 1 h of strenuous exercise in rats despite an increase in plasma ghrelin [126]. On the contrary, AMPK activity in the hypothalamus was reduced after leptin infusion in both lean and diet-induced obese rats after acute exercise. In addition, exercise was shown to improve insulin and leptin signaling in the cerebral cortex and hypothalamus in diabetic rats treated with high dose of dexamethasone [127]. This indicates that the effects of leptin on AMPK activity, potentiated by acute exercise, may contribute to appetite suppression in the hypothalamus [128].
7. The Physiological Effects of Hypothalamic AMPK
AMPK plays an important role as a nutrient and energy sensor in the central nervous system and maintains energy homeostasis by regulating feeding behavior and energy expenditure (Figure 3).
7.1. Feeding Behavior
Hypothalamic AMPK is considered a key player in the regulation of feeding behavior and energy balance due to its role in sensing and responding to hormonal and nutritional signals from the peripheral. Moreover, studies on knockout mice lacking α2-AMPK in POMC and AgRP neurons indicated that AMPK is essential for energy homeostasis regulation and glucose sensing by POMC and AgRP neurons. Specifically, the α2-AMPK POMC knockout mice developed obesity due to reduced energy expenditure and dysregulated food intake while α2-AMPK AgRP mice showed a lean phenotype. Interestingly, both knockout groups remained sensitive to leptin [129]. Regarded as a possible explanation, a report has suggested that nutrients signals do not regulate the NPY/AgRP or POMC neurons themselves but affect a presynaptic positive feedback loop involving AMPK and create excitatory or inhibitory synaptic input [83]. Although the downstream target(s) of AMPK remain unclear in the presynaptic neurons, AMPK acts as a mediator when activated in fasting state following Ca2+ influx and consequent neurotransmitter release into the NPY/AgRP neurons leading to the activation of these neurons. As a result, there is an increase in appetite and feeding behavior. Furthermore, the activation of orexigenic signals also inhibits anorexigenic signals [130, 131].
In discrete hypothalamic regions, fatty acid metabolism acts as a sensor for nutrient availability [132–134]. Among the many factors involved in fatty acid metabolism, malonyl-CoA is regarded as a potential candidate for food intake regulation. Malonyl-CoA is involved in both fatty acid synthesis and fatty acid β-oxidation. By inhibiting mitochondrial carnitine palmitoyltransferase- (CPT-) 1, malonyl-CoA reduces the number of fatty acid-CoA shuttled into the mitochondria for β-oxidation. Besides that, it is also an important substrate for fatty acid synthesis. The level of hypothalamic malonyl-CoA is low in fasted condition and rapidly increases on refeeding [135]. Moreover, induction of malonyl-CoA and inhibition of hypothalamic CPT-1 leads to decreased food intake whereas reduction in malonyl-CoA increases feeding behavior and weight gain [136–138]. Interestingly, AMPK activation leads to phosphorylation and inactivation of the enzyme acetyl-CoA carboxylase (ACC), which catalyzes the carboxylation of acetyl-CoA to produce malonyl-CoA, resulting in decreased hypothalamic malonyl-CoA and/or long-chain fatty acid-CoA and inducing fatty acid oxidation and feeding behavior. Furthermore, brain-specific CPT-1c knockout mice exhibit decreased food intake and lower body weight compared to wild-type littermates [139] while increased CPT-1c by activation of AMPK leads to the induction of hypothalamic ceramide synthesis in the endoplasmic reticulum [140]. Besides that, activated AMPK also induces CPT-1a in the mitochondria [77] and the induction of both CTP-1 isoforms results in increasing mRNA expression of AgRP and NPY genes by the activation of brain-specific homeobox transcription factor (BSX) together with the forkhead box protein O1 (FoxO1) and the phosphorylated cyclic adenosine monophosphate response-element binding protein (pCREB) [141]. Additionally, AMPK suppresses the synthesis of ACC, fatty acid synthase (FAS), and other enzymes for lipid biogenesis in many tissues, including the hypothalamus, by inhibiting expression of the transcription factor sterol-regulatory-element-binding transcription factor 1 (SREBP1c) [142, 143].
Besides AMPK, the mammalian target of rapamycin (mTOR) is also regarded as a hypothalamic regulator for food intake. mTOR signaling responds to nutrients availability and colocalizes with NPY/AgRP and POMC/cocaine- and amphetamine-regulated transcript (CART) neurons in the arcuate nucleus. Leptin induces hypothalamic mTOR activity in satiety condition and the inhibition of mTOR signaling blunts leptin's anorectic effect [144]. Furthermore, mTOR is inhibited by AMPK-dependent mechanisms in vitro via tuberous sclerosis complex 2 (TSC2) and mammalian vacuolar protein sorting 34 homologue (hVps34) [145, 146]. On the contrary, AMPK is also a substrate for mTOR-p70S6 kinase and is phosphorylated at Ser-491 [147]. Moreover, in a high-protein diet-induced weight loss, both AMPK and mTOR are modulated in the same specific neuronal subsets and regulates hypothalamic neuropeptides, indicating overlapping localization and function [148]. Thus, the overlap in hypothalamic mTOR and AMPK and can lead to a reciprocal interaction in regulating feeding behavior.
7.2. Energy Expenditure
Food is the main source of energy utilized by the body for various physiological functions and excess energy is stored as fat or released from the body in form of heat. Total energy expenditure can be subdivided into three principal components: obligatory energy expenditure; energy expenditure resulting from physical activity and expenditure attributed to adaptive thermogenesis defined as heat production in response to environmental temperature or diet [149]. Changes in the environment or diet condition can be detected and regulated by the brain, especially the hypothalamus. Among the many brain regions involved in thermoregulation, the ventromedial nucleus of the hypothalamus, VMH, was the first to be identified [150]. Electrophysiological stimulation of the VMH enhances interscapular BAT temperature in both lean and obese rats [151]. Additionally, when stimulated, VMH elicits an increase in the rate of norepinephrine turnover in BAT and this effect is abrogated by sympathetic ganglion blockade [152–154]. Furthermore, VMH-specific steroidogenic factor 1 (SF-1) knockout mice display impaired thermogenesis and decreased gene expression of uncoupling protein 1 (UCP1) and peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC1α) [155]. On the other hand, mice lacking forkhead box protein O1 (FoxO1) in SF-1 neurons of the VMH have a lean phenotype due to increased thermogenesis [156]. These studies indicate the role of VMH in thermoregulation. Additionally, sympathetic outflow to tissues involved in thermoregulation and metabolism is regulated by central pathways, including neurons in raphe pallidus (Rpa) and inferior olive (IO) [157–159].
Recent studies have indicated the role of hypothalamic AMPK in sympathetically activated BAT thermogenesis. Constitutively active AMPKα (AMPKα-CA) overexpression is associated with a specific reduction in the expression of BAT thermogenic markers whereas dominant-negative AMPKα (AMPKα-DN) promotes expression of these markers. This indicates that AMPK in the VMH modulates BAT thermogenesis via the sympathetic nervous system [160]. Furthermore, bone morphogenetic proteins (BMPs) knockout mice exhibit thermogenic impairment and display changes in neuropeptide levels and reduced phosphorylation of AMPK. Central BMP8B treatment increases hypothalamic AMPK-dependent sympathetic activation of BAT [161]. Besides BMPs, estradiol and GLP-1 also regulate BAT thermogenesis via hypothalamic AMPK. Estradiol inhibits AMPK activity in the VMH via estrogen receptor alpha, resulting in increased expression of BAT thermogenic markers through a feeding-independent manner [105]. GLP-1R agonist, liraglutide, also stimulates BAT thermogenesis and this central liraglutide-induced thermogenesis is blunted by activation of hypothalamic AMPK [123]. In addition, some compounds like thiazolidinediones and nicotine also modulate hypothalamic AMPK to induce BAT thermogenesis through the sympathetic nervous system [72, 162].
7.3. Glucose Homeostasis
AMPK plays a fundamental role in energy homeostasis as a glucose sensor to protect the CNS from hypoglycemic condition. One of the most important reactions of AMPK towards hypoglycemia is the counterregulatory hormonal responses [99] through glucagon, epinephrine, and corticosterone [100, 101, 117]. Hypothalamic AMPK activation is sufficient and necessary for altering glucose production in vivo. Inhibition of hypothalamic AMPK significantly decreases glucose production with no changes in peripheral glucose uptake during the hyperinsulinemic-euglycemic clamps [163]. Additionally, deletion of LKB1, an important kinase upstream of AMPK, in POMC neurons leads to an impairment in peripheral glucose homeostasis [36]. Furthermore, central administration of olanzapine activates hypothalamic AMPK resulting in induction hepatic glucose production via the sympathetic nervous system [164].
8. Concluding Remarks
AMPK has recently been identified as a key regulator for hypothalamic functions in balancing energy homeostasis. Targeted by nutritional signals and hormones, AMPK activation in hypothalamus, via phosphorylation mainly at Thr-172, leads to changes in both feeding behavior and energy expenditure to protect the body against energy depletion. Recent studies have shown that AMPK, in both central and peripheral region, plays an important role in the activation mechanism of metformin, thiazolidinediones, and statins [72, 165–167]. Moreover, considering the role of hypothalamic AMPK in lipid and glucose metabolism, central AMPK specific drugs can be developed for treatment of metabolic syndrome. Thus, hypothalamic AMPK should be considered as a potential therapeutic target for metabolic diseases.
Although hypothalamic AMPK acts as a regulator for energy status, the role of central AMPK in responding to exercise activities remains unclear and this warrants more studies to investigate its role, if any, and the underlying molecular mechanisms.
Acknowledgments
This work was supported by SMBA (Technological Innovation R&D Program S2178403), Ministry of Oceans and Fisheries (20150071), and National Research Foundation: NRF-2014K1A3A1A19066980 and NRF-2016R1C1B3012748 (to Ki Woo Kim); NRF-2015H1A2A1032009 (to Dong Joo Yang).
Competing Interests
The authors declare that they have no competing interests.
References
- 1.Kennedy G. C. The central nervous regulation of calorie balance. Proceedings of the Nutrition Society. 1961;20:58–64. doi: 10.1079/pns19610014. [DOI] [PubMed] [Google Scholar]
- 2.Bray G. A. Regulation of energy balance: studies on genetic, hypothalamic and dietary obesity. Proceedings of the Nutrition Society. 1982;41(2):95–108. doi: 10.1079/pns19820018. [DOI] [PubMed] [Google Scholar]
- 3.Woods S. C., Seeley R. J., Porte D., Jr., Schwartz M. W. Signals that regulate food intake and energy homeostasis. Science. 1998;280(5368):1378–1383. doi: 10.1126/science.280.5368.1378. [DOI] [PubMed] [Google Scholar]
- 4.Cheung C. C., Clifton D. K., Steiner R. A. Proopiomelanocortin neurons are direct targets for leptin in the hypothalamus. Endocrinology. 1997;138(10):4489–4492. doi: 10.1210/en.138.10.4489. [DOI] [PubMed] [Google Scholar]
- 5.Mercer J. G., Hoggard N., Williams L. M., et al. Coexpression of leptin receptor and preproneuropeptide Y mRNA in arcuate nucleus of mouse hypothalamus. Journal of Neuroendocrinology. 1996;8(10):733–735. doi: 10.1046/j.1365-2826.1996.05161.x. [DOI] [PubMed] [Google Scholar]
- 6.Ollmann M. M., Wilson B. D., Yang Y.-K., et al. Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein. Science. 1997;278(5335):135–138. doi: 10.1126/science.278.5335.135. [DOI] [PubMed] [Google Scholar]
- 7.Aponte Y., Atasoy D., Sternson S. M. AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training. Nature Neuroscience. 2011;14(3):351–355. doi: 10.1038/nn.2739. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Wu N., Zheng B., Shaywitz A., et al. AMPK-dependent degradation of TXNIP upon energy stress leads to enhanced glucose uptake via GLUT1. Molecular Cell. 2013;49(6):1167–1175. doi: 10.1016/j.molcel.2013.01.035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Estler C. J., Ammon H. P. The importance of the adrenergic beta-receptors for thermogenesis and survival of acutely cold-exposed mice. Canadian Journal of Physiology and Pharmacology. 1969;47(5):427–434. doi: 10.1139/y69-077. [DOI] [PubMed] [Google Scholar]
- 10.Hardie D. G., Carling D. The AMP-activated protein kinase—fuel gauge of the mammalian cell? European Journal of Biochemistry. 1997;246(2):259–273. doi: 10.1111/j.1432-1033.1997.00259.x. [DOI] [PubMed] [Google Scholar]
- 11.Moore F., Weekes J., Hardie D. G. Evidence that AMP triggers phosphorylation as well as direct allosteric activation of rat liver AMP-activated protein kinase. A sensitive mechanism to protect the cell against ATP depletion. European Journal of Biochemistry. 1991;199(3):691–697. doi: 10.1111/j.1432-1033.1991.tb16172.x. [DOI] [PubMed] [Google Scholar]
- 12.Hardie D. G. AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy. Nature Reviews Molecular Cell Biology. 2007;8(10):774–785. doi: 10.1038/nrm2249. [DOI] [PubMed] [Google Scholar]
- 13.Marsin A.-S., Bertrand L., Rider M. H., et al. Phosphorylation and activation of heart PFK-2 by AMPK has a role in the stimulation of glycolysis during ischaemia. Current Biology. 2000;10(20):1247–1255. doi: 10.1016/s0960-9822(00)00742-9. [DOI] [PubMed] [Google Scholar]
- 14.Marsin A.-S., Bouzin C., Bertrand L., Hue L. The stimulation of glycolysis by hypoxia in activated monocytes is mediated by AMP-activated protein kinase and inducible 6-phosphofructo-2-kinase. The Journal of Biological Chemistry. 2002;277(34):30778–30783. doi: 10.1074/jbc.m205213200. [DOI] [PubMed] [Google Scholar]
- 15.Berasi S. P., Huard C., Li D., et al. Inhibition of gluconeogenesis through transcriptional activation of EGR1 and DUSP4 by AMP-activated kinase. The Journal of Biological Chemistry. 2006;281(37):27167–27177. doi: 10.1074/jbc.m602416200. [DOI] [PubMed] [Google Scholar]
- 16.Horman S., Browne G. J., Krause U., et al. Activation of AMP-activated protein kinase leads to the phosphorylation of elongation factor 2 and an inhibition of protein synthesis. Current Biology. 2002;12(16):1419–1423. doi: 10.1016/S0960-9822(02)01077-1. [DOI] [PubMed] [Google Scholar]
- 17.Clarke P. R., Hardie D. G. Regulation of HMG-CoA reductase: identification of the site phosphorylated by the AMP-activated protein kinase in vitro and in intact rat liver. The EMBO Journal. 1990;9(8):2439–2446. doi: 10.1002/j.1460-2075.1990.tb07420.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Muoio D. M., Seefeld K., Witters L. A., Coleman R. A. AMP-activated kinase reciprocally regulates triacylglycerol synthesis and fatty acid oxidation in liver and muscle: evidence that sn-glycerol-3-phosphate acyltransferase is a novel target. Biochemical Journal. 1999;338(3):783–791. doi: 10.1042/0264-6021:3380783. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.López M., Nogueiras R., Tena-Sempere M., Diéguez C. Hypothalamic AMPK: a canonical regulator of whole-body energy balance. Nature Reviews Endocrinology. 2016;12(7):421–432. doi: 10.1038/nrendo.2016.67. [DOI] [PubMed] [Google Scholar]
- 20.Minokoshi Y., Alquier T., Furukawa H., et al. AMP-kinase regulates food intake by responding to hormonal and nutrient signals in the hypothalamus. Nature. 2004;428(6982):569–574. doi: 10.1038/nature02440. [DOI] [PubMed] [Google Scholar]
- 21.Bass J., Takahashi J. S. Circadian integration of metabolism and energetics. Science. 2010;330(6009):1349–1354. doi: 10.1126/science.1195027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Landree L. E., Hanlon A. L., Strong D. W., et al. C75, a fatty acid synthase inhibitor, modulates AMP-activated protein kinase to alter neuronal energy Metabolism. The Journal of Biological Chemistry. 2004;279(5):3817–3827. doi: 10.1074/jbc.m310991200. [DOI] [PubMed] [Google Scholar]
- 23.Kim M. S., Lee K. U. Role of hypothalamic 5′-AMP-activated protein kinase in the regulation of food intake and energy homeostasis. Journal of Molecular Medicine. 2005;83(7):514–520. doi: 10.1007/s00109-005-0659-z. [DOI] [PubMed] [Google Scholar]
- 24.Stapleton D., Mitchelhill K. I., Gao G., et al. Mammalian AMP-activated protein kinase subfamily. The Journal of Biological Chemistry. 1996;271(2):611–614. doi: 10.1074/jbc.271.2.611. [DOI] [PubMed] [Google Scholar]
- 25.Stapleton D., Woollatt E., Mitchelhill K. I., et al. AMP-activated protein kinase isoenzyme family: subunit structure and chromosomal location. FEBS Letters. 1997;409(3):452–456. doi: 10.1016/s0014-5793(97)00569-3. [DOI] [PubMed] [Google Scholar]
- 26.Cheung P. C. F., Salt I. P., Davies S. P., Hardie D. G., Carling D. Characterization of AMP-activated protein kinase γ-subunit isoforms and their role in AMP binding. Biochemical Journal. 2000;346(3):659–669. doi: 10.1042/0264-6021:3460659. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Hudson E. R., Pan D. A., James J., et al. A novel domain in AMP-activated protein kinase causes glycogen storage bodies similar to those seen in hereditary cardiac arrhythmias. Current Biology. 2003;13(10):861–866. doi: 10.1016/s0960-9822(03)00249-5. [DOI] [PubMed] [Google Scholar]
- 28.Bateman A. The structure of a domain common to archaebacteria and the homocystinuria disease protein. Trends in Biochemical Sciences. 1997;22(1):12–13. doi: 10.1016/s0968-0004(96)30046-7. [DOI] [PubMed] [Google Scholar]
- 29.Towler M. C., Hardie D. G. AMP-activated protein kinase in metabolic control and insulin signaling. Circulation Research. 2007;100(3):328–341. doi: 10.1161/01.res.0000256090.42690.05. [DOI] [PubMed] [Google Scholar]
- 30.Vogel M., Heinz F. Purification and characterisation of the cyclic amp-dependent protein kinase, the C- and the R-protein from bovine liver. Biochimica et Biophysica Acta (BBA)—Protein Structure. 1981;670(1):47–55. doi: 10.1016/0005-2795(81)90047-7. [DOI] [PubMed] [Google Scholar]
- 31.Gowans G. J., Hawley S. A., Ross F. A., Hardie D. G. AMP is a true physiological regulator of amp-activated protein kinase by both allosteric activation and enhancing net phosphorylation. Cell Metabolism. 2013;18(4):556–566. doi: 10.1016/j.cmet.2013.08.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Carling D., Thornton C., Woods A., Sanders M. J. AMP-activated protein kinase: new regulation, new roles? Biochemical Journal. 2012;445(1):11–27. doi: 10.1042/bj20120546. [DOI] [PubMed] [Google Scholar]
- 33.Hawley S. A., Davison M., Woods A., et al. Characterization of the AMP-activated protein kinase kinase from rat liver and identification of threonine 172 as the major site at which it phosphorylates AMP-activated protein kinase. The Journal of Biological Chemistry. 1996;271(44):27879–27887. doi: 10.1074/jbc.271.44.27879. [DOI] [PubMed] [Google Scholar]
- 34.Woods A., Dickerson K., Heath R., et al. Ca2+/calmodulin-dependent protein kinase kinase-β acts upstream of AMP-activated protein kinase in mammalian cells. Cell Metabolism. 2005;2(1):21–33. doi: 10.1016/j.cmet.2005.06.005. [DOI] [PubMed] [Google Scholar]
- 35.Anderson K. A., Ribar T. J., Lin F., et al. Hypothalamic CaMKK2 contributes to the regulation of energy balance. Cell Metabolism. 2008;7(5):377–388. doi: 10.1016/j.cmet.2008.02.011. [DOI] [PubMed] [Google Scholar]
- 36.Claret M., Smith M. A., Knauf C., et al. Deletion of Lkb1 in pro-opiomelanocortin neurons impairs peripheral glucose homeostasis in mice. Diabetes. 2011;60(3):735–745. doi: 10.2337/db10-1055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Fei-Wang, Tian D.-R., Tso P., Han J.-S. Diet-induced obese rats exhibit impaired LKB1-AMPK signaling in hypothalamus and adipose tissue. Peptides. 2012;35(1):23–30. doi: 10.1016/j.peptides.2012.02.003. [DOI] [PubMed] [Google Scholar]
- 38.Hawley S. A., Pan D. A., Mustard K. J., et al. Calmodulin-dependent protein kinase kinase-β is an alternative upstream kinase for AMP-activated protein kinase. Cell Metabolism. 2005;2(1):9–19. doi: 10.1016/j.cmet.2005.05.009. [DOI] [PubMed] [Google Scholar]
- 39.Carling D., Sanders M. J., Woods A. The regulation of AMP-activated protein kinase by upstream kinases. International Journal of Obesity. 2008;32(supplement 4):S55–S59. doi: 10.1038/ijo.2008.124. [DOI] [PubMed] [Google Scholar]
- 40.Zhou G., Myers R., Li Y., et al. Role of AMP-activated protein kinase in mechanism of metformin action. The Journal of Clinical Investigation. 2001;108(8):1167–1174. doi: 10.1172/jci200113505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Doan K. V., Ko C. M., Kinyua A. W., et al. Gallic acid regulates body weight and glucose homeostasis through AMPK activation. Endocrinology. 2015;156(1):157–168. doi: 10.1210/en.2014-1354. [DOI] [PubMed] [Google Scholar]
- 42.Breen D. M., Sanli T., Giacca A., Tsiani E. Stimulation of muscle cell glucose uptake by resveratrol through sirtuins and AMPK. Biochemical and Biophysical Research Communications. 2008;374(1):117–122. doi: 10.1016/j.bbrc.2008.06.104. [DOI] [PubMed] [Google Scholar]
- 43.Lee Y. S., Kim W. S., Kim K. H., et al. Berberine, a natural plant product, activates AMP-activated protein kinase with beneficial metabolic effects in diabetic and insulin-resistant states. Diabetes. 2006;55(8):2256–2264. doi: 10.2337/db06-0006. [DOI] [PubMed] [Google Scholar]
- 44.Pu P., Wang X.-A., Salim M., et al. Baicalein, a natural product, selectively activating AMPKalpha(2) and ameliorates metabolic disorder in diet-induced mice. Molecular and Cellular Endocrinology. 2012;362(1-2):128–138. doi: 10.1016/j.mce.2012.06.002. [DOI] [PubMed] [Google Scholar]
- 45.Ahn J., Lee H., Kim S., Park J., Ha T. The anti-obesity effect of quercetin is mediated by the AMPK and MAPK signaling pathways. Biochemical and Biophysical Research Communications. 2008;373(4):545–549. doi: 10.1016/j.bbrc.2008.06.077. [DOI] [PubMed] [Google Scholar]
- 46.Huang S.-L., Yu R.-T., Gong J., et al. Arctigenin, a natural compound, activates AMP-activated protein kinase via inhibition of mitochondria complex I and ameliorates metabolic disorders in ob/ob mice. Diabetologia. 2012;55(5):1469–1481. doi: 10.1007/s00125-011-2366-3. [DOI] [PubMed] [Google Scholar]
- 47.Hwang J.-T., Park I.-J., Shin J.-I., et al. Genistein, EGCG, and capsaicin inhibit adipocyte differentiation process via activating AMP-activated protein kinase. Biochemical and Biophysical Research Communications. 2005;338(2):694–699. doi: 10.1016/j.bbrc.2005.09.195. [DOI] [PubMed] [Google Scholar]
- 48.Pan W., Yang H., Cao C., et al. AMPK mediates curcumin-induced cell death in CaOV3 ovarian cancer cells. Oncology Reports. 2008;20(6):1553–1559. doi: 10.3892/or_00000179. [DOI] [PubMed] [Google Scholar]
- 49.LeBrasseur N. K., Kelly M., Tsao T.-S., et al. Thiazolidinediones can rapidly activate AMP-activated protein kinase in mammalian tissues. American Journal of Physiology—Endocrinology and Metabolism. 2006;291(1):E175–E181. doi: 10.1152/ajpendo.00453.2005. [DOI] [PubMed] [Google Scholar]
- 50.Corton J. M., Gillespie J. G., Hawley S. A., Hardie D. G. 5-Aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? European Journal of Biochemistry. 1995;229(2):558–565. doi: 10.1111/j.1432-1033.1995.tb20498.x. [DOI] [PubMed] [Google Scholar]
- 51.Xiao B., Sanders M. J., Underwood E., et al. Structure of mammalian AMPK and its regulation by ADP. Nature. 2011;472(7342):230–233. doi: 10.1038/nature09932. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Ross F. A., Jensen T. E., Hardie D. G. Differential regulation by AMP and ADP of AMPK complexes containing different γ subunit isoforms. Biochemical Journal. 2016;473(2):189–199. doi: 10.1042/bj20150910. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Oakhill J. S., Steel R., Chen Z.-P., et al. AMPK is a direct adenylate charge-regulated protein kinase. Science. 2011;332(6036):1433–1435. doi: 10.1126/science.1200094. [DOI] [PubMed] [Google Scholar]
- 54.Deshmukh R. R., Dou Q. P. Proteasome inhibitors induce AMPK activation via CaMKKβ in human breast cancer cells. Breast Cancer Research and Treatment. 2015;153(1):79–88. doi: 10.1007/s10549-015-3512-2. [DOI] [PubMed] [Google Scholar]
- 55.Xu Y., Gu Y., Liu G., et al. Cidec promotes the differentiation of human adipocytes by degradation of AMPKα through ubiquitin-proteasome pathway. Biochimica et Biophysica Acta (BBA)—General Subjects. 2015;1850(12):2552–2562. doi: 10.1016/j.bbagen.2015.09.008. [DOI] [PubMed] [Google Scholar]
- 56.Al-Hakim A. K., Zagorska A., Chapman L., Deak M., Peggie M., Alessi D. R. Control of AMPK-related kinases by USP9X and atypical Lys29/Lys33-linked polyubiquitin chains. Biochemical Journal. 2008;411(2):249–260. doi: 10.1042/bj20080067. [DOI] [PubMed] [Google Scholar]
- 57.Pineda C. T., Ramanathan S., Fon Tacer K., et al. Degradation of AMPK by a cancer-specific ubiquitin ligase. Cell. 2015;160(4):715–728. doi: 10.1016/j.cell.2015.01.034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Qi J., Gong J., Zhao T., et al. Downregulation of AMP-activated protein kinase by Cidea-mediated ubiquitination and degradation in brown adipose tissue. The EMBO Journal. 2008;27(11):1537–1548. doi: 10.1038/emboj.2008.92. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Ignacio-Souza L. M., Bombassaro B., Pascoal L. B., et al. Defective regulation of the ubiquitin/proteasome system in the hypothalamus of obese male mice. Endocrinology. 2014;155(8):2831–2844. doi: 10.1210/en.2014-1090. [DOI] [PubMed] [Google Scholar]
- 60.Martin T. L., Alquier T., Asakura K., Furukawa N., Preitner F., Kahn B. B. Diet-induced obesity alters AMP kinase activity in hypothalamus and skeletal muscle. The Journal of Biological Chemistry. 2006;281(28):18933–18941. doi: 10.1074/jbc.m512831200. [DOI] [PubMed] [Google Scholar]
- 61.Kadowaki T., Yamauchi T. Adiponectin and adiponectin receptors. Endocrine Reviews. 2005;26(3):439–451. doi: 10.1210/er.2005-0005. [DOI] [PubMed] [Google Scholar]
- 62.Kubota N., Terauchi Y., Yamauchi T., et al. Disruption of adiponectin causes insulin resistance and neointimal formation. Journal of Biological Chemistry. 2002;277(29):25863–25866. doi: 10.1074/jbc.C200251200. [DOI] [PubMed] [Google Scholar]
- 63.Maeda N., Shimomura I., Kishida K., et al. Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nature Medicine. 2002;8(7):731–737. doi: 10.1038/nm724. [DOI] [PubMed] [Google Scholar]
- 64.Lim C. T., Kola B., Korbonits M. AMPK as a mediator of hormonal signalling. Journal of Molecular Endocrinology. 2010;44(2):87–97. doi: 10.1677/JME-09-0063. [DOI] [PubMed] [Google Scholar]
- 65.Klein I., Sanchez-Alavez M., Tabarean I., et al. AdipoR1 and 2 are expressed on warm sensitive neurons of the hypothalamic preoptic area and contribute to central hyperthermic effects of adiponectin. Brain Research. 2011;1423:1–9. doi: 10.1016/j.brainres.2011.09.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Coope A., Milanski M., Araújo E. P., et al. AdipoR1 mediates the anorexigenic and insulin/leptin-like actions of adiponectin in the hypothalamus. FEBS Letters. 2008;582(10):1471–1476. doi: 10.1016/j.febslet.2008.03.037. [DOI] [PubMed] [Google Scholar]
- 67.Kubota N., Yano W., Kubota T., et al. Adiponectin stimulates AMP-activated protein kinase in the hypothalamus and increases food intake. Cell Metabolism. 2007;6(1):55–68. doi: 10.1016/j.cmet.2007.06.003. [DOI] [PubMed] [Google Scholar]
- 68.Guillod-Maximin E., Roy A. F., Vacher C. M., et al. Adiponectin receptors are expressed in hypothalamus and colocalized with proopiomelanocortin and neuropeptide Y in rodent arcuate neurons. Journal of Endocrinology. 2009;200(1):93–105. doi: 10.1677/JOE-08-0348. [DOI] [PubMed] [Google Scholar]
- 69.Kadowaki T., Yamauchi T., Kubota N. The physiological and pathophysiological role of adiponectin and adiponectin receptors in the peripheral tissues and CNS. FEBS Letters. 2008;582(1):74–80. doi: 10.1016/j.febslet.2007.11.070. [DOI] [PubMed] [Google Scholar]
- 70.Shimizu H., Tsuchiya T., Sato N., Shimomura Y., Kobayashi I., Mori M. Troglitazone reduces plasma leptin concentration but increases hunger in NIDDM patients. Diabetes Care. 1998;21(9):1470–1474. doi: 10.2337/diacare.21.9.1470. [DOI] [PubMed] [Google Scholar]
- 71.Lehrke M., Lazar M. A. The many faces of PPARγ . Cell. 2005;123(6):993–999. doi: 10.1016/j.cell.2005.11.026. [DOI] [PubMed] [Google Scholar]
- 72.Quaresma P. G. F., Reencober N., Zanotto T. M., et al. Pioglitazone treatment increases food intake and decreases energy expenditure partially via hypothalamic adiponectin/adipoR1/AMPK pathway. International Journal of Obesity. 2016;40(1):138–146. doi: 10.1038/ijo.2015.134. [DOI] [PubMed] [Google Scholar]
- 73.Kojima M., Hosoda H., Date Y., Nakazato M., Matsuo H., Kangawa K. Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature. 1999;402(6762):656–660. doi: 10.1038/45230. [DOI] [PubMed] [Google Scholar]
- 74.Wren A. M., Seal L. J., Cohen M. A., et al. Ghrelin enhances appetite and increases food intake in humans. Journal of Clinical Endocrinology and Metabolism. 2001;86(12):5992–5995. doi: 10.1210/jc.86.12.5992. [DOI] [PubMed] [Google Scholar]
- 75.Wren A. M., Small C. J., Ward H. L., et al. The novel hypothalamic peptide ghrelin stimulates food intake and growth hormone secretion. Endocrinology. 2000;141(11):4325–4328. doi: 10.1210/endo.141.11.7873. [DOI] [PubMed] [Google Scholar]
- 76.Kirsz K., Zieba D. A. Ghrelin-mediated appetite regulation in the central nervous system. Peptides. 2011;32(11):2256–2264. doi: 10.1016/j.peptides.2011.04.010. [DOI] [PubMed] [Google Scholar]
- 77.Lopez M., Lage R., Saha A. K., et al. Hypothalamic fatty acid metabolism mediates the orexigenic action of ghrelin. Cell Metabolism. 2008;7(5):389–399. doi: 10.1016/j.cmet.2008.03.006. [DOI] [PubMed] [Google Scholar]
- 78.Gao S., Casals N., Keung W., Moran T. H., Lopaschuk G. D. Differential effects of central ghrelin on fatty acid metabolism in hypothalamic ventral medial and arcuate nuclei. Physiology and Behavior. 2013;118:165–170. doi: 10.1016/j.physbeh.2013.03.030. [DOI] [PubMed] [Google Scholar]
- 79.Lim C. T., Kola B., Feltrin D., et al. Ghrelin and cannabinoids require the ghrelin receptor to affect cellular energy metabolism. Molecular and Cellular Endocrinology. 2013;365(2):303–308. doi: 10.1016/j.mce.2012.11.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Bennett P. A., Thomas G. B., Howard A. D., et al. Hypothalamic growth hormone secretagogue-receptor (GHS-R) expression is regulated by growth hormone in the rat. Endocrinology. 1997;138(11):4552–4557. doi: 10.1210/en.138.11.4552. [DOI] [PubMed] [Google Scholar]
- 81.Andrews Z. B. Central mechanisms involved in the orexigenic actions of ghrelin. Peptides. 2011;32(11):2248–2255. doi: 10.1016/j.peptides.2011.05.014. [DOI] [PubMed] [Google Scholar]
- 82.Kohno D., Sone H., Minokoshi Y., Yada T. Ghrelin raises [Ca2+]i via AMPK in hypothalamic arcuate nucleus NPY neurons. Biochemical and Biophysical Research Communications. 2008;366(2):388–392. doi: 10.1016/j.bbrc.2007.11.166. [DOI] [PubMed] [Google Scholar]
- 83.Yang Y., Atasoy D., Su H. H., Sternson S. M. Hunger states switch a flip-flop memory circuit via a synaptic AMPK-dependent positive feedback loop. Cell. 2011;146(6):992–1003. doi: 10.1016/j.cell.2011.07.039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Jamshidi N., Taylor D. A. Anandamide administration into the ventromedial hypothalamus stimulates appetite in rats. British Journal of Pharmacology. 2001;134(6):1151–1154. doi: 10.1038/sj.bjp.0704379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Poirier B., Bidouard J.-P., Cadrouvele C., et al. The anti-obesity effect of rimonabant is associated with an improved serum lipid profile. Diabetes, Obesity and Metabolism. 2005;7(1):65–72. doi: 10.1111/j.1463-1326.2004.00374.x. [DOI] [PubMed] [Google Scholar]
- 86.Kirkham T. C., Williams C. M. Endocannabinoid receptor antagonists: potential for obesity treatment. Treatments in Endocrinology. 2004;3(6):345–360. doi: 10.2165/00024677-200403060-00003. [DOI] [PubMed] [Google Scholar]
- 87.Kola B., Hubina E., Tucci S. A., et al. Cannabinoids and ghrelin have both central and peripheral metabolic and cardiac effects via AMP-activated protein kinase. The Journal of Biological Chemistry. 2005;280(26):25196–25201. doi: 10.1074/jbc.c500175200. [DOI] [PubMed] [Google Scholar]
- 88.Borgquist A., Meza C., Wagner E. J. The role of AMP-activated protein kinase in the androgenic potentiation of cannabinoid-induced changes in energy homeostasis. American Journal of Physiology—Endocrinology and Metabolism. 2015;308(6):E482–E495. doi: 10.1152/ajpendo.00421.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Di Marzo V., Goparaju S. K., Wang L., et al. Leptin-regulated endocannabinoids are involved in maintaining food intake. Nature. 2001;410(6830):822–825. doi: 10.1038/35071088. [DOI] [PubMed] [Google Scholar]
- 90.Kola B., Farkas I., Christ-Crain M., et al. The orexigenic effect of ghrelin is mediated through central activation of the endogenous cannabinoid system. PLoS ONE. 2008;3(3) doi: 10.1371/journal.pone.0001797.e1797 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Tataranni P. A., Larson D. E., Snitker S., Young J. B., Flatt J. P., Ravussin E. Effects of glucocorticoids on energy metabolism and food intake in humans. American Journal of Physiology—Endocrinology and Metabolism. 1996;271(2, part 1):E317–E325. doi: 10.1152/ajpendo.1996.271.2.E317. [DOI] [PubMed] [Google Scholar]
- 92.Christ-Crain M., Kola B., Lolli F., et al. AMP-activated protein kinase mediates glucocorticoid-induced metabolic changes: a novel mechanism in Cushing's syndrome. The FASEB Journal. 2008;22(6):1672–1683. doi: 10.1096/fj.07-094144. [DOI] [PubMed] [Google Scholar]
- 93.Di S., Malcher-Lopes R., Marcheselli V. L., Bazan N. G., Tasker J. G. Rapid glucocorticoid-mediated endocannabinoid release and opposing regulation of glutamate and γ-aminobutyric acid inputs to hypothalamic magnocellular neurons. Endocrinology. 2005;146(10):4292–4301. doi: 10.1210/en.2005-0610. [DOI] [PubMed] [Google Scholar]
- 94.Scerif M., Füzesi T., Thomas J. D., et al. CB1 receptor mediates the effects of glucocorticoids on AMPK activity in the hypothalamus. Journal of Endocrinology. 2013;219(1):79–88. doi: 10.1530/JOE-13-0192. [DOI] [PubMed] [Google Scholar]
- 95.Shimizu H., Arima H., Watanabe M., et al. Glucocorticoids increase neuropeptide Y and agouti-related peptide gene expression via adenosine monophosphate-activated protein kinase signaling in the arcuate nucleus of rats. Endocrinology. 2008;149(9):4544–4553. doi: 10.1210/en.2008-0229. [DOI] [PubMed] [Google Scholar]
- 96.Liu L., Song Z., Jiao H., Lin H. Glucocorticoids increase NPY gene expression via hypothalamic AMPK signaling in broiler chicks. Endocrinology. 2014;155(6):2190–2198. doi: 10.1210/en.2013-1632. [DOI] [PubMed] [Google Scholar]
- 97.McCrimmon R. J., Fan X., Ding Y., Zhu W., Jacob R. J., Sherwin R. S. Potential role for AMP-activated protein kinase in hypoglycemia sensing in the ventromedial hypothalamus. Diabetes. 2004;53(8):1953–1958. doi: 10.2337/diabetes.53.8.1953. [DOI] [PubMed] [Google Scholar]
- 98.Kim M.-S., Park J.-Y., Namkoong C., et al. Anti-obesity effects of α-lipoic acid mediated by suppression of hypothalamic AMP-activated protein kinase. Nature Medicine. 2004;10(7):727–733. doi: 10.1038/nm1061. [DOI] [PubMed] [Google Scholar]
- 99.Alquier T., Kawashima J., Tsuji Y., Kahn B. B. Role of hypothalamic adenosine 5′-monophosphate-activated protein kinase in the impaired counterregulatory response induced by repetitive neuroglucopenia. Endocrinology. 2007;148(3):1367–1375. doi: 10.1210/en.2006-1039. [DOI] [PubMed] [Google Scholar]
- 100.McCrimmon R. J., Shaw M., Fan X., et al. Key Role for AMP-activated protein kinase in the ventromedial hypothalamus in regulating counterregulatory hormone responses to acute hypoglycemia. Diabetes. 2008;57(2):444–450. doi: 10.2337/db07-0837. [DOI] [PubMed] [Google Scholar]
- 101.Fan X., Ding Y., Brown S., et al. Hypothalamic AMP-activated protein kinase activation with AICAR amplifies counterregulatory responses to hypoglycemia in a rodent model of type 1 diabetes. American Journal of Physiology—Regulatory Integrative and Comparative Physiology. 2009;296(6):R1702–R1708. doi: 10.1152/ajpregu.90600.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 102.Salpeter S. R., Walsh J. M. E., Ormiston T. M., Greyber E., Buckley N. S., Salpeter E. E. Meta-analysis: effect of hormone-replacement therapy on components of the metabolic syndrome in postmenopausal women. Diabetes, Obesity and Metabolism. 2006;8(5):538–554. doi: 10.1111/j.1463-1326.2005.00545.x. [DOI] [PubMed] [Google Scholar]
- 103.De Souza F. S. J., Nasif S., López-Leal R., Levi D. H., Low M. J., Rubinsten M. The estrogen receptor α colocalizes with proopiomelanocortin in hypothalamic neurons and binds to a conserved motif present in the neuron-specific enhancer nPE2. European Journal of Pharmacology. 2011;660(1):181–187. doi: 10.1016/j.ejphar.2010.10.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Roepke T. A. Oestrogen modulates hypothalamic control of energy homeostasis through multiple mechanisms. Journal of Neuroendocrinology. 2009;21(2):141–150. doi: 10.1111/j.1365-2826.2008.01814.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105.Martínez de Morentin P. B., González-García I., Martins L., et al. Estradiol regulates brown adipose tissue thermogenesis via hypothalamic AMPK. Cell Metabolism. 2014;20(1):41–53. doi: 10.1016/j.cmet.2014.03.031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106.Tsai Y.-C., Lee Y.-M., Lam K.-K., Wu Y.-C., Yen M.-H., Cheng P.-Y. The role of hypothalamic AMP-activated protein kinase in ovariectomy-induced obesity in rats. Menopause. 2010;17(6):1194–1200. doi: 10.1097/gme.0b013e3181dfca27. [DOI] [PubMed] [Google Scholar]
- 107.Ibrahim B. A., Tamrakar P., Gujar A. D., Cherian A. K., Briski K. P. Caudal fourth ventricular administration of the AMPK activator 5-aminoimidazole-4-carboxamide-riboside regulates glucose and counterregulatory hormone profiles, dorsal vagal complex metabolosensory neuron function, and hypothalamic fos expression. Journal of Neuroscience Research. 2013;91(9):1226–1238. doi: 10.1002/jnr.23230. [DOI] [PubMed] [Google Scholar]
- 108.Tamrakar P., Briski K. P. Estradiol regulation of hypothalamic astrocyte adenosine 5′-monophosphate-activated protein kinase activity: role of hindbrain catecholamine signaling. Brain Research Bulletin. 2015;110:47–53. doi: 10.1016/j.brainresbull.2014.12.002. [DOI] [PubMed] [Google Scholar]
- 109.Martínez de Morentin P. B., Lage R., González-García I., et al. Pregnancy induces resistance to the anorectic effect of hypothalamic malonyl-COA and the thermogenic effect of hypothalamic AMPK inhibition in female rats. Endocrinology. 2015;156(3):947–960. doi: 10.1210/en.2014-1611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Minokoshi Y., Kim Y.-B., Peroni O. D., et al. Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase. Nature. 2002;415(6869):339–343. doi: 10.1038/415339a. [DOI] [PubMed] [Google Scholar]
- 111.Andersson U., Filipsson K., Abbott C. R., et al. AMP-activated protein kinase plays a role in the control of food intake. The Journal of Biological Chemistry. 2004;279(13):12005–12008. doi: 10.1074/jbc.c300557200. [DOI] [PubMed] [Google Scholar]
- 112.Tanida M., Yamamoto N., Shibamoto T., Rahmouni K. Involvement of hypothalamic AMP-activated protein kinase in leptin-induced sympathetic nerve activation. PLoS ONE. 2013;8(2, article e56660) doi: 10.1371/journal.pone.0056660. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 113.Cowley M. A., Smart J. L., Rubinstein M., et al. Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus. Nature. 2001;411(6836):480–484. doi: 10.1038/35078085. [DOI] [PubMed] [Google Scholar]
- 114.Obici S., Zhang B. B., Karkanias G., Rossetti L. Hypothalamic insulin signaling is required for inhibition of glucose production. Nature Medicine. 2002;8(12):1376–1382. doi: 10.1038/nm798. [DOI] [PubMed] [Google Scholar]
- 115.Solon C. S., Franci D., Ignacio-Souza L. M., et al. Taurine enhances the anorexigenic effects of insulin in the hypothalamus of rats. Amino Acids. 2012;42(6):2403–2410. doi: 10.1007/s00726-011-1045-5. [DOI] [PubMed] [Google Scholar]
- 116.Namkoong C., Min S. K., Pil G. J., et al. Enhanced hypothalamic AMP-activated protein kinase activity contributes to hyperphagia in diabetic rats. Diabetes. 2005;54(1):63–68. doi: 10.2337/diabetes.54.1.63. [DOI] [PubMed] [Google Scholar]
- 117.Han S.-M., Namkoong C., Jang P. G., et al. Hypothalamic AMP-activated protein kinase mediates counter-regulatory responses to hypoglycaemia in rats. Diabetologia. 2005;48(10):2170–2178. doi: 10.1007/s00125-005-1913-1. [DOI] [PubMed] [Google Scholar]
- 118.Shimizu I., Hirota M., Ohboshi C., Shima K. Identification and localization of glucagon-like peptide-1 and its receptor in rat brain. Endocrinology. 1987;121(3):1076–1082. doi: 10.1210/endo-121-3-1076. [DOI] [PubMed] [Google Scholar]
- 119.Turton M. D., O'Shea D., Gunn I., et al. A role for glucagon-like peptide-1 in the central regulation of feeding. Nature. 1996;379(6560):69–72. doi: 10.1038/379069a0. [DOI] [PubMed] [Google Scholar]
- 120.Goldstone A. P., Morgan I., Mercer J. G., et al. Effect of leptin on hypothalamic GLP-1 peptide and brain-stem pre-proglucagon mRNA. Biochemical and Biophysical Research Communications. 2000;269(2):331–335. doi: 10.1006/bbrc.2000.2288. [DOI] [PubMed] [Google Scholar]
- 121.Hurtado-Carneiro V., Sanz C., Roncero I., Vazquez P., Blazquez E., Alvarez E. Glucagon-like peptide 1 (GLP-1) can reverse AMP-activated protein kinase (AMPK) and S6 kinase (P70S6K) activities induced by fluctuations in glucose levels in hypothalamic areas involved in feeding behaviour. Molecular Neurobiology. 2012;45(2):348–361. doi: 10.1007/s12035-012-8239-z. [DOI] [PubMed] [Google Scholar]
- 122.Poleni P.-E., Akieda-Asai S., Koda S., et al. Possible involvement of melanocortin-4-receptor and AMP-activated protein kinase in the interaction of glucagon-like peptide-1 and leptin on feeding in rats. Biochemical and Biophysical Research Communications. 2012;420(1):36–41. doi: 10.1016/j.bbrc.2012.02.109. [DOI] [PubMed] [Google Scholar]
- 123.Beiroa D., Imbernon M., Gallego R., et al. GLP-1 agonism stimulates brown adipose tissue thermogenesis and browning through hypothalamic AMPK. Diabetes. 2014;63(10):3346–3358. doi: 10.2337/db14-0302. [DOI] [PubMed] [Google Scholar]
- 124.López M., Diéguez C., Nogueiras R. Hypothalamic GLP-1: the control of BAT thermogenesis and browning of white fat. Adipocyte. 2015;4(2):141–145. doi: 10.4161/21623945.2014.983752. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 125.Fujii N., Hayashi T., Hirshman M. F., et al. Exercise induces isoform-specific increase in 5' AMP-activated protein kinase activity in human skeletal muscle. Biochemical and Biophysical Research Communications. 2000;273(3):1150–1155. doi: 10.1006/bbrc.2000.3073. [DOI] [PubMed] [Google Scholar]
- 126.Andersson U., Treebak J. T., Nielsen J. N., et al. Exercise in rats does not alter hypothalamic AMP-activated protein kinase activity. Biochemical and Biophysical Research Communications. 2005;329(2):719–725. doi: 10.1016/j.bbrc.2005.02.027. [DOI] [PubMed] [Google Scholar]
- 127.Park S., Jin S. J., Dong W. J., Sang M. H. Exercise enhances insulin and leptin signaling in the cerebral cortex and hypothalamus during dexamethasone-induced stress in diabetic rats. Neuroendocrinology. 2006;82(5-6):282–293. doi: 10.1159/000093127. [DOI] [PubMed] [Google Scholar]
- 128.Ropelle E. R., Fernandes M. F. A., Flores M. B. S., et al. Central exercise action increases the AMPK and mTOR response to leptin. PLoS ONE. 2008;3(12) doi: 10.1371/journal.pone.0003856.e3856 [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
- 129.Claret M., Smith M. A., Batterham R. L., et al. AMPK is essential for energy homeostasis regulation and glucose sensing by POMC and AgRP neurons. The Journal of Clinical Investigation. 2007;117(8):2325–2336. doi: 10.1172/jci31516. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130.Hardie D. G., Ross F. A., Hawley S. A. AMPK: a nutrient and energy sensor that maintains energy homeostasis. Nature Reviews Molecular Cell Biology. 2012;13(4):251–262. doi: 10.1038/nrm3311. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 131.Kohno D., Sone H., Tanaka S., Kurita H., Gantulga D., Yada T. AMP-activated protein kinase activates neuropeptide Y neurons in the hypothalamic arcuate nucleus to increase food intake in rats. Neuroscience Letters. 2011;499(3):194–198. doi: 10.1016/j.neulet.2011.05.060. [DOI] [PubMed] [Google Scholar]
- 132.Loftus T. M., Jaworsky D. E., Frehywot C. L., et al. Reduced food intake and body weight in mice treated with fatty acid synthase inhibitors. Science. 2000;288(5475):2379–2381. doi: 10.1126/science.288.5475.2379. [DOI] [PubMed] [Google Scholar]
- 133.Beverly J. L., Martin R. J. Influence of fatty acid oxidation in lateral hypothalamus on food intake and body composition. American Journal of Physiology—Regulatory Integrative and Comparative Physiology. 1991;261(2, part 2):R339–R343. doi: 10.1152/ajpregu.1991.261.2.R339. [DOI] [PubMed] [Google Scholar]
- 134.Kasser T. R., Martin R. J. Induction of ventrolateral hypothalamic fatty acid oxidation in diabetic rats. Physiology and Behavior. 1986;36(2):385–388. doi: 10.1016/0031-9384(86)90033-8. [DOI] [PubMed] [Google Scholar]
- 135.Hu Z., Cha S. H., Chohnan S., Lane M. D. Hypothalamic malonyl-CoA as a mediator of feeding behavior. Proceedings of the National Academy of Sciences of the United States of America. 2003;100(22):12624–12629. doi: 10.1073/pnas.1834402100. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 136.Obici S., Feng Z., Arduini A., Conti R., Rossetti L. Inhibition of hypothalamic carnitine palmitoyltransferase-1 decreases food intake and glucose production. Nature Medicine. 2003;9(6):756–761. doi: 10.1038/nm873. [DOI] [PubMed] [Google Scholar]
- 137.Hu Z., Dai Y., Prentki M., Chohnan S., Lane M. D. A role for hypothalamic malonyl-CoA in the control of food intake. The Journal of Biological Chemistry. 2005;280(48):39681–39683. doi: 10.1074/jbc.c500398200. [DOI] [PubMed] [Google Scholar]
- 138.Wolfgang M. J., Lane M. D. The role of hypothalamic malonyl-CoA in energy homeostasis. Journal of Biological Chemistry. 2006;281(49):37265–37269. doi: 10.1074/jbc.R600016200. [DOI] [PubMed] [Google Scholar]
- 139.Wolfgang M. J., Cha S. H., Millington D. S., et al. Brain-specific carnitine palmitoyl-transferase-1c: role in CNS fatty acid metabolism, food intake, and body weight. Journal of Neurochemistry. 2008;105(4):1550–1559. doi: 10.1111/j.1471-4159.2008.05255.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 140.Ramírez S., Martins L., Jacas J., et al. Hypothalamic ceramide levels regulated by CPT1C mediate the orexigenic effect of ghrelin. Diabetes. 2013;62(7):2329–2337. doi: 10.2337/db12-1451. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 141.Lage R., Vázquez M. J., Varela L., et al. Ghrelin effects on neuropeptides in the rat hypothalamus depend on fatty acid metabolism actions on BSX but not on gender. The FASEB Journal. 2010;24(8):2670–2679. doi: 10.1096/fj.09-150672. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 142.Song Z., Liu L., Yue Y., et al. Fasting alters protein expression of AMP-activated protein kinase in the hypothalamus of broiler chicks (Gallus gallus domesticus) General and Comparative Endocrinology. 2012;178(3):546–555. doi: 10.1016/j.ygcen.2012.06.026. [DOI] [PubMed] [Google Scholar]
- 143.Lei L., Lixian Z. Effect of 24 h fasting on gene expression of AMPK, appetite regulation peptides and lipometabolism related factors in the hypothalamus of broiler chicks. Asian-Australasian Journal of Animal Sciences. 2012;25(9):1300–1308. doi: 10.5713/ajas.2012.12153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 144.Cota D., Proulx K., Blake Smith K. A., et al. Hypothalamic mTOR signaling regulates food intake. Science. 2006;312(5775):927–930. doi: 10.1126/science.1124147. [DOI] [PubMed] [Google Scholar]
- 145.Inoki K., Zhu T., Guan K.-L. TSC2 mediates cellular energy response to control cell growth and survival. Cell. 2003;115(5):577–590. doi: 10.1016/s0092-8674(03)00929-2. [DOI] [PubMed] [Google Scholar]
- 146.Byfield M. P., Murray J. T., Backer J. M. hVps34 is a nutrient-regulated lipid kinase required for activation of p70 S6 kinase. The Journal of Biological Chemistry. 2005;280(38):33076–33082. doi: 10.1074/jbc.m507201200. [DOI] [PubMed] [Google Scholar]
- 147.Dagon Y., Hur E., Zheng B., Wellenstein K., Cantley L. C., Kahn B. B. P70S6 kinase phosphorylates AMPK on serine 491 to mediate leptin's effect on food intake. Cell Metabolism. 2012;16(1):104–112. doi: 10.1016/j.cmet.2012.05.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 148.Ropelle E. R., Pauli J. R., Fernandes M. F. A., et al. A central role for neuronal AMP-activated protein kinase (AMPK) and mammalian target of rapamyein (mTOR) in high-protein diet-induced weight loss. Diabetes. 2008;57(3):594–605. doi: 10.2337/db07-0573. [DOI] [PubMed] [Google Scholar]
- 149.Lowell B. B., Spiegelman B. M. Towards a molecular understanding of adaptive thermogenesis. Nature. 2000;404(6778):652–660. doi: 10.1038/35007527. [DOI] [PubMed] [Google Scholar]
- 150.Perkins M. N., Rothwell N. J., Stock M. J., Stone T. W. Activation of brown adipose tissue thermogenesis by the ventromedial hypothalamus. Nature. 1981;289(5796):401–402. doi: 10.1038/289401a0. [DOI] [PubMed] [Google Scholar]
- 151.Holt S. J., Wheal H. V., York D. A. Hypothalamic control of brown adipose tissue in Zucker lean and obese rats. Effect of electrical stimulation of the ventromedial nucleus and other hypothalamic centres. Brain Research. 1987;405(2):227–233. doi: 10.1016/0006-8993(87)90292-7. [DOI] [PubMed] [Google Scholar]
- 152.Yoshida T., Bray G. A. Catecholamine turnover in rats with ventromedial hypothalamic lesions. American Journal of Physiology. 1984;246(4, part 2):R558–R565. doi: 10.1152/ajpregu.1984.246.4.R558. [DOI] [PubMed] [Google Scholar]
- 153.Saito M., Minokoshi Y., Shimazu T. Ventromedial hypothalamic stimulation accelerates norepinephrine turnover in brown adipose tissue of rats. Life Sciences. 1987;41(2):193–197. doi: 10.1016/0024-3205(87)90493-0. [DOI] [PubMed] [Google Scholar]
- 154.Hugie T., Halvorson I., Thornhill J. Brown adipose tissue temperature responses following electrical stimulation of ventromedial hypothalamic and lateral preoptic areas or after norepinephrine infusion to long evans or sprague-dawley rats. Brain Research. 1992;575(1):57–62. doi: 10.1016/0006-8993(92)90422-6. [DOI] [PubMed] [Google Scholar]
- 155.Kim K. W., Zhao L., Donato J., Jr., et al. Steroidogenic factor 1 directs programs regulating diet-induced thermogenesis and leptin action in the ventral medial hypothalamic nucleus. Proceedings of the National Academy of Sciences of the United States of America. 2011;108(26):10673–10678. doi: 10.1073/pnas.1102364108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 156.Kim K. W., Donato J., Jr., Berglund E. D., et al. FOXO1 in the ventromedial hypothalamus regulates energy balance. The Journal of Clinical Investigation. 2012;122(7):2578–2589. doi: 10.1172/jci62848. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 157.Morrison S. F. RVLM and raphe differentially regulate sympathetic outflows to splanchnic and brown adipose tissue. American Journal of Physiology—Regulatory Integrative and Comparative Physiology. 1999;276(4):R962–R973. doi: 10.1152/ajpregu.1999.276.4.R962. [DOI] [PubMed] [Google Scholar]
- 158.Uno T., Shibata M. Role of inferior olive and thoracic IML neurons in nonshivering thermogenesis in rats. American Journal of Physiology—Regulatory Integrative and Comparative Physiology. 2001;280(2):R536–R546. doi: 10.1152/ajpregu.2001.280.2.R536. [DOI] [PubMed] [Google Scholar]
- 159.Shibata M., Uno T., Hashimoto M. Disinhibition of lower midbrain neurons enhances non-shivering thermogenesis in anesthetized rats. Brain Research. 1999;833(2):242–250. doi: 10.1016/S0006-8993(99)01532-2. [DOI] [PubMed] [Google Scholar]
- 160.López M., Varela L., Vázquez M. J., et al. Hypothalamic AMPK and fatty acid metabolism mediate thyroid regulation of energy balance. Nature Medicine. 2010;16(9):1001–1008. doi: 10.1038/nm.2207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 161.Whittle A. J., Carobbio S., Martins L., et al. BMP8B increases brown adipose tissue thermogenesis through both central and peripheral actions. Cell. 2012;149(4):871–885. doi: 10.1016/j.cell.2012.02.066. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 162.Seoane-Collazo P., Martínez de Morentin P. B., Fernø J., Diéguez C., Nogueiras R., López M. Nicotine improves obesity and hepatic steatosis and ER stress in diet-induced obese male rats. Endocrinology. 2014;155(5):1679–1689. doi: 10.1210/en.2013-1839. [DOI] [PubMed] [Google Scholar]
- 163.Yang C. S., Lam C. K. L., Chari M., et al. Hypothalamic AMP-activated protein kinase regulates glucose production. Diabetes. 2010;59(10):2435–2443. doi: 10.2337/db10-0221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 164.Ikegami M., Ikeda H., Ohashi T., et al. Olanzapine increases hepatic glucose production through the activation of hypothalamic adenosine 5′-monophosphate-activated protein kinase. Diabetes, Obesity and Metabolism. 2013;15(12):1128–1135. doi: 10.1111/dom.12148. [DOI] [PubMed] [Google Scholar]
- 165.Brunmair B., Staniek K., Gras F., et al. Thiazolidinediones, like metformin, inhibit respiratory complex I: a common mechanism contributing to their antidiabetic actions? Diabetes. 2004;53(4):1052–1059. doi: 10.2337/diabetes.53.4.1052. [DOI] [PubMed] [Google Scholar]
- 166.Fryer L. G. D., Parbu-Patel A., Carling D. The anti-diabetic drugs rosiglitazone and metformin stimulate AMP-activated protein kinase through distinct signaling pathways. Journal of Biological Chemistry. 2002;277(28):25226–25232. doi: 10.1074/jbc.M202489200. [DOI] [PubMed] [Google Scholar]
- 167.Sun W., Lee T.-S., Zhu M., et al. Statins activate AMP-activated protein kinase in vitro and in vivo. Circulation. 2006;114(24):2655–2662. doi: 10.1161/CIRCULATIONAHA.106.630194. [DOI] [PubMed] [Google Scholar]