4.4 Article

Acorus calamus extract and its component α-asarone attenuate murine hippocampal neuronal cell death induced by l-glutamate and tunicamycin

Journal

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Volume 85, Issue 3, Pages 493-501

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bbb/zbaa071

Keywords

Acorus calamus; alpha-asarone; HT22; oxidative stress; endoplasmic reticulum stress

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Acorus calamus extract and alpha-asarone demonstrate protective effects against oxidative stress and ER stress in hippocampal cells by reducing ROS production and inhibiting PERK signaling. Alpha-asarone shows potential as a therapeutic candidate for neurodegenerative diseases, including Alzheimer's disease.
The Asian traditional medicinal plant Acorus calamus and its component alpha-asarone exhibited various biological activities, such as antiinflammation and antioxidant effects. In the present study, we investigated the in vitro effects of A. calamus extract and alpha-asarone on oxidative stress- and endoplasmic reticulum (ER) stress-induced cell death in hippocampal HT22 cells. A. calamus extract and alpha-asarone both significantly suppressed cell death induced by the oxidative stress inducer l-glutamate and ER stress inducer tunicamycin. A. calamus extract and alpha-asarone also significantly reduced reactive oxygen species (ROS) production induced by l-glutamate. Moreover, A. calamus extract and alpha-asarone suppressed the phosphorylation of protein kinase RNA-like ER kinase (PERK) induced by tunicamycin. These results suggest that A. calamus extract and alpha-asarone protect hippocampal cells from oxidative stress and ER stress by decreasing ROS production and suppressing PERK signaling, respectively. alpha-Asarone has potential as a potent therapeutic candidate for neurodegenerative diseases, including Alzheimer's disease.

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