Abstract
Ethnopharmacological relevance:
Ginsenoside Rg2 is an important ingredient of Panax ginseng which often appears in ancient prescriptions for forgetfulness. Ginsenoside Rg2 exert neuroprotective effects and could be a new potential medicine to treat AD. In our previous study, we reported that ginsenoside Rg2 appears protect PC12 cells against Amyloid β-fragment (25-35) (Aβ25-35)-induced apoptosis via the PI3K/Akt pathway. However, there are no in vivo studies on the protective effects of ginsenoside Rg2 on Aβ-induced neurotoxicity.
Aim of the study:
The present study was performed to investigate the protective effects of ginsenoside Rg2 against Aβ25-35-induced memory impairment, and its underlying mechanisms in rats.
Materials and methods:
An Alzheimer's Disease (AD) rat model was established by injecting the rats with Aβ25-35 (1μg/μl). Cognitive performance was evaluated by the Morris Water Maze test (MWM). The brain sections were processed and neuronal apoptosis in the hippocampus was evaluated by Hematoxylin and Eosin staining (H&E). To explore the anti-neuronal apoptosis mechanism of ginsenoside Rg2, we analyzed the protein expression of Bcl-2/Bax, caspase-3, and phospho-protein kinase B/protein kinase B (p-Akt/Akt) via western blot.
Results:
A significant improvement in cognitive function was observed in administrated ginsenoside Rg2 AD rats.The histological injury in hippocampus CA1 induced by Aβ25-35 was inhibited following administration of the ginsenoside Rg2. Ginsenoside Rg2 increase the Bcl-2/Bax ratio, attenuate the cleavage of caspase-3, and enhance the phosphorylation of Akt.
Conclusions:
These findings suggest that ginsenoside Rg2 could ameliorate Aβ25-35-induced cognitive dysfunction by activating the phosphatidylinositol 3-kinase/protein kinase B (PI3K/Akt) signaling pathway.
Full text
