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Antagonizing Effects of Soybean Isoflavones on β-Amyloid Peptide-Induced Oxidative Damage in Neuron Mitochondria of Rats.

Authors :
Feng, Jin-Fang
He, Ling-Ling
Li, Dan
Yuan, Lin-Hong
Yu, Huan-Ling
Ma, Wei-Wei
Yang, Yue
Xi, Yuan-Di
Ding, Juan
Xiao, Yi-Xiu
Xiao, Rong
Source :
Basic & Clinical Pharmacology & Toxicology. Oct2012, Vol. 111 Issue 4, p248-253. 6p. 1 Black and White Photograph, 1 Diagram, 1 Chart, 5 Graphs.
Publication Year :
2012

Abstract

Soybean isoflavone ( SIF) has been demonstrated to have neuroprotective effects induced by β-amyloid peptides ( Aβ) through suppressing oxidative stress; however, the explicit mechanisms still remain uncovered. In the present study, 32 Wistar rats were randomly divided into four groups: an Aβ1-42-treated group, a SIF + Aβ1-42 group, a SIF-treated group and a control group. We measured the protein content of 8-hydroxydeoxyguanosine (8- Ohd G) and m RNA expression of 8-oxoguanine DNA glycosylase ( OGG1). The protein expression of OGG1, Bcl-xl, Bad, beta subunit of ATP synthase ( ATPB) and pyruvate dehydrogenase ( PDH) in brain was also measured. The results showed that the level of 8- OHd G in both SIF groups was significantly decreased compared to the Aβ1-42-treated group ( p < 0.05), while the m RNA and protein expression of OGG1 in the SIF + Aβ1-42 groups were up-regulated compared with the Aβ1-42-treated groups ( p < 0.05). The expression of Bcl-xl was up-regulated in the SIF-treated group compared with the Aβ1-42-treated groups ( p < 0.05), while the expression of Bad was down-regulated in the two SIF-treated groups ( p < 0.05). Aβ1-42 significantly down-regulated the expression of ATPase and PDH proteins compared with the control group ( p < 0.05). SIF reversed the down-regulation effects on the mitochondrial energy metabolic enzymes induced by Aβ1-42 ( p < 0.05) in the rats. These results suggest that SIF alleviate the oxidative stress in neurons and mitochondria of rat brains mediated by Aβ1-42, and these protective effects might be associated with the regulation of OGG1, Bad, Bcl-xl, ATPB and PDH. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17427835
Volume :
111
Issue :
4
Database :
Academic Search Index
Journal :
Basic & Clinical Pharmacology & Toxicology
Publication Type :
Academic Journal
Accession number :
80125974
Full Text :
https://doi.org/10.1111/j.1742-7843.2012.00900.x