Table 6.
Study | Compound | Model | Increased Level | Decreased Level | References |
---|---|---|---|---|---|
Anti-Parkinson | β-Asarone | 6-OHDA parkinsonian | Bcl-2 expression | GRP78, p-PERK, CHOP, and Beclin-1 expression | [192] |
6-OHDA parkinsonian | - | mRNA levels of GRP78 and CHOP and p-IRE1and XBP1 | [193] | ||
Dopamine in the striatum | TH plasma concentrations | Striatal COMT levels | [194] | ||
6-OHDA parkinsonian | L-DOPA, DA, DOPAC, and HVA levels | P-gp, ZO-1, occludin, actin, and claudin-5 | [195] | ||
Alzheimer’s | Aβ25-35-induced inflammation | Bcl-2 level | TNF-α, IL-1β, IL-6, Beclin-1, and LC3B level | [196] | |
NG108 cells | - | Upregulated SYP and GluR1 expression | [197] | ||
PC12 cells | - | Aβ-induced JNK activation, Bcl-w and Bcl-xL levels, cytochrome c release, and caspase-3 activation | [198] | ||
Aβ-induced cytotoxicity | Cell viability, p-Akt and p-mTOR | NSE levels, Beclin-1 expression | [199] | ||
Neuroprotective | Pb-induced impairments | NR2B protein expression along with Arc/Arg3.1 and Wnt7a mRNA levels | - | [200] | |
β-Asarone, eugenol | Scopolamine-induced | Improvement of neuron organelles and synaptic structure | APP expression | [201] | |
Neotatarine | MTT reduction assay | - | Aβ25-35–induced PC12 cell death | [202] | |
β-asarone, paeonol | MCAo model | Cholecystokinin and NF-κB signaling | TNF-α, IL-1β, IL-6 production | [203] | |
β-Asarone | Cultured rat astrocytes | NGF, BDNF, and GDNF expression | - | [204] | |
SN4741 cells | p62, Bcl-2 expression | JNK, p-JNK and Beclin-1 expressions | [205] | ||
Tatarinolactone | hSERT-HEK293 cell line | - | SERTs activity | [206] | |
β-Asarone | RSC96 Schwann cells | GDNF, BDNF, and CNTF expression | - | [207] | |
Aβ-induced | p-mTOR and p62 expression | AChE and Aβ42 levels, p-Akt, Beclin-1, and LC3B expression, APP mRNA and Beclin-1 mRNA levels | [208] | ||
Aβ1–42-induced injury | - | GFAP, AQP4, IL-1β, and TNF-α expression | [209] | ||
Anti-depression | Chronic unpredictable mild stress | BDNF expression | Blocked ERK1/2-CREB signaling | [210] | |
α-Asarone | Noradrenergic and serotonergic neuromodulators in TST | α1 and α2 adrenoceptors and 5-HT1A receptors | - | [211] | |
Anticonvulsant and sedative | Eudesmin | MES and PTZ | GABA contents, expressions of GAD65, GABAA, and Bcl-2 | Glu contents and ratio of Glu/GABA, caspase-3 | [212] |
Anti-anxiety | α-Asarone | BLA or CFA-induced | Down-regulation of GABAA receptors | Up-regulation of GluR1-containing AMPA, NMDA receptors | [213] |
Anti-epilepsy | Temporal lobe epilepsy | Levels of GABA, GAD67, and GABAAR-mRNA expression | GABA-T | [214] | |
Mitral cells | Down-regulation of GABAA receptors | Na+ channel blockade | [215] | ||
β-Asarone | KA-induced | GABA | Glu | [216] | |
Anti-inflammatory | α-Asarone | Spinal cord injury | IL-4, IL-10, and arginase 1 levels | TNF-α, IL-1β, IL-6, MCP-1, MIP-2, iNOS levels | [217] |
Cytoprotective | β-Asarone | tBHP-induced astrocyte injury | GST, GCLM, GCLC, NQO1, Akt phosphorylation | - | [218] |
Cardioprotective | Cultured neonate rat cardiac myocytes | Viability of cardiac myocytes | Pulse frequency | [219] | |
Arteriosclerosis | ECV304 cell strain | Apoptotic rate of ECV304 cells | Apoptotic rate of MMP, stabilized MMP and VSMC proliferation | [220] | |
Anti-adipogenic | 3T3-L1 preadipocytes | - | C/EBPβ, C/EBPα, and PPARγ expression levels, ERK1/2 phosphorylation | [89] | |
Antioxidant | Cerebral artery occlusion | Antioxidant activity | Focal cerebral ischemic/reperfusion injury | [221] | |
Anti-diabetic | α-Asarone + β-asarone + metformin HCl | STZ-induced | Insulin level | Glucose, glycosylated hemoglobin level, liver dysfunction, and tumor biomarkers | [222] |
Asarone | 3T3-L1 preadipocytes | Hormone-sensitive lipase phosphorylation | Intracellular triglyceride levels, down-regulation of PPARγ and C/EBPα | [223] |
6-OHDA, 6-hydroxydopamine; Ox-LDL, oxidized low-density lipoprotein; BDNF, brain-derived neurotrophic factor; NGF, nerve growth factor; GDNF, glial derived neurotrophic factor; SERTs, serotonin transporters; MCAo, middle cerebral artery occlusion; Aβ, β-amyloid; NSE, neuron specific enolase; AMPA, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid; NMDA, NR2A-containing N-methyl-D-aspartate; GABAA, γ-aminobutyric acid A; BLA, basolateral amygdala; CFA, complete Freund’s adjuvant; CNTF, ciliary neurotrophic factor; COMT, catechol-O-methyltransferase; TH, tyrosine hydroxylase; DA, dopamine; DOPAC, 3,4-dihydroxyphenylacetic acid; HVA, homovanillic acid; P-gp, P-glycoprotein; ZO-1, zonula occludens-1; SYP, synaptophysin; GluR1, glutamatergic receptor 1; GABA-T, GABA transaminase; TST, tail suspension test; KA, kainic acid; MCP-1, monocyte chemoattractant protein 1; MIP-2, macrophage inflammatory protein 2; iNOS, inducible nitric oxide synthase; GST, glutathione S-transferase; GCLM, glutamate-cysteine ligase modulatory subunit; GCLC, glutamate-cysteine ligase catalytic subunit; NQO1, NAD(P)H quinone oxidoreductase; GFAP, glial fibrillary acidic protein; AQP, aquaporin; VSMC, vascular smooth muscle cells; MMP, mitochondrial membrane potential; C/EBP, CCAAT enhancer-binding protein; PPARγ, peroxisome proliferator-activated receptor gamma; ERK1/2, extracellular signal-regulated protein kinase; XBP1, x-box binding protein; IRE1, inositol-requiring enzyme 1; Aβ1-42, amyloid β peptide; mTOR, mammalian target of rapamycin; MTT, 3-(4,5-dimethythiazol-. 2-yl)-2,5-diphenyl tetrazolium bromide; CREB, cAMP response element-binding protein; GABAAR, gamma-aminobutyric acid type-A receptor, tBHP, t-butyl hydroperoxide.