Fibroblast Growth Factor 21 and Autophagy Modulation Ameliorates Amyloid β-Induced Alzheimer Disease Pathology in Rats

dc.contributor.authorTaliyan, Rajeev
dc.date.accessioned2023-12-14T04:01:44Z
dc.date.available2023-12-14T04:01:44Z
dc.date.issued2021-12
dc.description.abstractAlzheimer's disease (AD) is a multifactorial neurodegenerative condition and the most common cause of its initiation is accumulation of oligomeric amyloid beta1-42 (Aβ1-42). In recent past, several studies have shown autophagy deficits in AD may resulted accumulation of misfolded protein, Aβ1-42 and phosphorylated tau (ptau). Fibroblast growth factor 21 (FGF21), a metabolic hormone, has shown strong neuroprotective efficacy via increasing autophagic flux in AD. Therefore, this study was designed to investigate the synergistic neuroprotective efficacy of lentiviral FGF21 gene (LV-FGF21) delivery and rapamycin-autophagy modulator in Aβ1-42 induced AD in rats.en_US
dc.identifier.urihttps://alz-journals.onlinelibrary.wiley.com/doi/abs/10.1002/alz.058695
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13413
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectPharmacyen_US
dc.subjectAlzheimer's disease (AD)en_US
dc.subjectNeurodegenerative conditionen_US
dc.titleFibroblast Growth Factor 21 and Autophagy Modulation Ameliorates Amyloid β-Induced Alzheimer Disease Pathology in Ratsen_US
dc.typeArticleen_US

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