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The protective effect of Centella asiatica and its constituent, araliadiol on neuronal cell damage and cognitive impairment

Authors :
Masashi Mikami
Honoka Fujimori
Hiroyuki Kojima
Hideaki Hara
Kenichi Ito
Takuya Ohba
Masamitsu Shimazawa
Shinsuke Nakamura
Arunasiri Iddamalgoda
Tatsuji Takahashi
Source :
Journal of Pharmacological Sciences, Vol 148, Iss 1, Pp 162-171 (2022)
Publication Year :
2022
Publisher :
Elsevier, 2022.

Abstract

Alzheimer’s disease (AD) is characterized by progressive cognitive decline, and the number of affected individuals has increased worldwide. However, there are no effective treatments for AD. Therefore, it is important to prevent the onset of dementia. Oxidative stress and endoplasmic reticulum (ER) stress are increased in the brains of AD patients, and are postulated to induce neuronal cell death and cognitive dysfunction. In this study, Centella asiatica, a traditional Indian medicinal herb, were fractionated and compared for their protective effects against glutamate and tunicamycin damage. Araliadiol was identified as a component from the fraction with the highest activity. Further, murine hippocampal cells (HT22) were damaged by glutamate, an oxidative stress inducer. Centella asiatica and araliadiol suppressed cell death and reactive oxygen species production. HT22 cells were also injured by tunicamycin, an ER stress inducer. Centella asiatica and araliadiol prevented cell death by mainly inhibiting PERK phosphorylation; additionally, Centella asiatica also suppressed the expression levels of GRP94 and BiP. In Y-maze test, oral administration of araliadiol (10 mg/kg/day) for 7 days ameliorated the arm alternation ratio in mice with scopolamine-induced cognitive impairment. These results suggest that Centella asiatica and its active component, araliadiol, have neuroprotective effects, which may prevent cognitive dysfunction.

Details

Language :
English
ISSN :
13478613
Volume :
148
Issue :
1
Database :
OpenAIRE
Journal :
Journal of Pharmacological Sciences
Accession number :
edsair.doi.dedup.....a8abb24295f8a10acc6cfad88f7dfbd4