Malar_2021_J.Biochem.Mol.Toxicol_35_e22632

Reference

Title : Vitexin prevents Abeta proteotoxicity in transgenic Caenorhabditis elegans model of Alzheimer's disease by modulating unfolded protein response - Malar_2021_J.Biochem.Mol.Toxicol_35_e22632
Author(s) : Malar DS , Prasanth MI , Jeyakumar M , Balamurugan K , Devi KP
Ref : J Biochem Mol Toxicol , 35 :e22632 , 2021
Abstract :

Alzheimer's disease (AD) accounts for an estimated 60% to 80% of all dementia cases. The present study is aimed at evaluating the neuroprotective efficacy of vitexin, an apigenin flavone glycoside using transgenic Caenorhabditis elegans strain (CL2006) of AD. The neuroprotective effect of vitexin was determined using physiological assays, quantitative polymerase chain reaction, and Western blotting. The results of survival and paralysis assay indicate that vitexin (200 microM) significantly extended the lifespan of the nematodes. Vitexin-treated nematodes showed a significant reduction in the expression of Abeta, ace-1, and ace-2 genes when compared to control. Further, vitexin significantly upregulated the expression of acr-8 and dnj-14, and increased the lifespan of the nematodes. Vitexin was also found to modulate the unfolded protein response genes (hsp-4, pek-1, ire-1, and xbp-1) and suppress the expression of Abeta. Overall, the results show that vitexin acts as a neuroprotective agent and protects transgenic C. elegans strains from Abeta proteotoxicity.

PubMedSearch : Malar_2021_J.Biochem.Mol.Toxicol_35_e22632
PubMedID: 32926499

Related information

Citations formats

Malar DS, Prasanth MI, Jeyakumar M, Balamurugan K, Devi KP (2021)
Vitexin prevents Abeta proteotoxicity in transgenic Caenorhabditis elegans model of Alzheimer's disease by modulating unfolded protein response
J Biochem Mol Toxicol 35 :e22632

Malar DS, Prasanth MI, Jeyakumar M, Balamurugan K, Devi KP (2021)
J Biochem Mol Toxicol 35 :e22632