Daidzein improves neuronal health and alleviates inflammation and apoptosis through BDNF and estrogen receptors in the hippocampus of ovariectomized rats

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 169

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شناسه ملی سند علمی:

JR_IJBMS-28-7_008

تاریخ نمایه سازی: 16 اردیبهشت 1404

چکیده مقاله:

Objective(s): Isoflavone Daidzein (DDZ) has emerged as a promising alternative to hormone replacement therapy (HRT) for ameliorating estrogen deficiency (ED). However, the stereological and molecular mechanism of its effects in the OVX-hippocampus are unclear. We studied the impact of DDZ on stereological changes, estrogen receptor (ERs) expression, BDNF, GSK-۳β, and inflammatory and apoptosis-related genes in the hippocampus of ovariectomized rats, compared to ۱۷β-estradiol (E۲).Materials and Methods: OVX rats were treated with DDZ or E۲. The stereological analysis assessed the total volume and number of pyramidal and granular neurons in the hippocampus CA۱ and DG subregions. Expression of proinflammatory cytokines, apoptotic-related genes, ERs, and BDNF genes was evaluated using Real-Time PCR, and the GSK-۳β phosphorylation level was measured by western blot analysis.Results: DDZ has effectively increased the volume and total number of pyramidal neurons in the CA۱ region, the expression of ERα, ERβ, BDNF, and Bcl-۲ genes, and the phosphorylation rate of GSK-۳β protein. However, the effect of DDZ on the DG region, ERα, and BDNF genes was not significant in comparison with E۲; DDZ significantly suppressed the expression of TNF-α, IL-۶, and the Bax/Bcl۲ ratio compared with OVX rats.Conclusion: DDZ effectively reversed the stereological changes in the CA۱ region by stimulating BDNF gene expression, increasing the phosphorylation ratio of the GSK-۳β protein, and modulating inflammatory and apoptotic pathways. Although its effects on the DG region, BDNF, and ERα molecules were less significant than E۲, DDZ could still be a promising candidate for ameliorating ED.

نویسندگان

Asma Neisy

Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Zahra Khoshdel

Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Farhad Koohpeyma

Research committee, endocrine and metabolism research center, Shiraz University of Medical Sciences, Shiraz, Iran

atefeh Seghatoleslam

Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Zohreh Mostafavi-Pour

Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Sanaz Alaee

Reproductive Biology Department, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran

Fatemeh Keshavarzi

Autophagy Research Center, Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Saeed Shokri

School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia

Fatemeh Zal

Infertility Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran

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