Table 2.
HN/HN Analogue | Disorder/Pathological Symptom Simulated | In Vitro Cellular Model/In Vitro Beneficial Effects | In Vivo Animal Model/In Vivo Beneficial Effects/Main Route of Administration | Ref. |
---|---|---|---|---|
HN | Parkinson’s disease (PD) | SH-SY5Y human neuroblastoma and PC12 rat pheochromocytoma cell lines/ Neuroprotection through mitochondrial biogenesis |
Mouse models of PD/Neuroprotection and behavioral recovery/ i.n. administration |
[50] |
HNSS | Alzheimer’s disease (AD) | HT22 neuronal cells overexpressing FGFR1/Inhibition of experimentally induced intracellular and mitochondrial ROS production |
3xTg-AD mice/ Mitochondrial rescue, inhibition of Aβ deposition and tau hyperphosphorylation, amelioration of memory defect and neuronal damage/ i.v. administration through a specially developed delivery system |
[36] |
HN | ICH | Rat primary cerebral cortical astrocyte and microglia cultures/ Promotion of a “reparative” microglia phenotype characterized by enhanced phagocytosis and reduced proinflammatory responses |
C57BL/6J mouse model of ICH induced by intrastriatal injection of autologous blood/ Reduction of neurological deficits, and improvement of hematoma clearance/ i.p. or i.n. administration |
[51] |
HN | Intracerebral hemorrhage (ICH) | ICH-like cellular model induced in primary rodent neuron cultures/ HN upregulated phosphorylation of STAT3 and increased Mn-SOD expression in neurons under ICH-like injury and prevented ROS-overexpression |
C57BL6/J mouse and Sprague Dawley rat models of ICH/ Systemic transplantation of astrocytic mitochondria (which contain HN) in ICH promotes antioxidative protection and assists in functional recovery by enhancing Mn-SOD-mediated neuronal antioxidant defense and neuroplasticity in the brain |
[52] |
HN | Mild traumatic brain injury (mTBI) | - | Mouse model of mTBI/Reversal of cognitive impairment through restoration of metabolic pathways within astrocytes/ i.p. administration |
[53] |
HNG | Impairment of object memory | PC12 rat pheochromocytoma cells/ Enhancement of regulated neuronal exocytosis |
Normal mice/ Improvement of object memory/ i.p. administration |
[54] |
HN | Neuronal cell death | Cortical neuron neurotoxicity model induced by calyculin A (CA)/ HN preincubation preserved cell viability, alleviated oxidative stress, blocked tau overphosphorylation, and protected neurons against CA-induced insults |
- | [55] |
HUJInin and c(D-Ser14-HN) | Stroke | Ischemia–reperfusion injury cellular model induced in PC12 cell cultures using ischemia-like oxygen–glycose-deprivation–reoxygenation insult and SH-SY5Y neuronal cell cultures exposed to pathological H2O2 oxidative stress/ Cell neuroprotection |
- | [35] |
HN | Neuronal cell death | SH-SY5Y human neuroblastoma cell line/Neuroprotection against neurotoxicity induced by silver nanoparticles | - | [56] |
CL | Stroke | - | C57BL/6 middle cerebral artery occlusion (MCAO) mouse model/ Decrease in the neurological deficits, improvement of motor and cognitive functions, improvement of infarct lesion/ i.p. administration |
[57] |
HNG | AD | - | APP/PS1 mice/ Improvement of cognitive function/ i.p. administration |
[58] |
HNG | Age-related cognitive decline | SH-SY5Y cells/ Neuroprotective effect against Aβ mitochondrial toxicity |
C57Bl/6N mice/ Improvement of cognitive ability of old-age mice/ i.p. administration |
[59] |
HNG | Stroke | Mouse brain endothelial cells bEnd.3/ Cytoprotection under oxygen–glucose deprivation (OGD) conditions |
Mouse MCAO stroke model/ Amelioration of cerebral infarction and suppression of various inflammatory cytokines/ i.p. administration |
[60] |