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Influence of progestational stress on BDNF and NMDARs in the hippocampus of male offspring and amelioration by Chaihu Shugan San - 03/03/21

Doi : 10.1016/j.biopha.2020.111204 
Ya-hui Xu a, b, 1, Xin-xing Wang a, 1, Ming-jing Wang a, 1, Yue-yun Liu b, Zhe Xue b, Jia-xu Chen b, c,
a School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou, 450046, Henan, China 
b School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China 
c Formula-Pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, Guangdong, China 

Corresponding author at: School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China. Formula-Pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, Guangdong, ChinaSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China. Formula-Pattern Research Center, School of Traditional Chinese Medicine,Jinan UniversityGuangzhouGuangdong510632China

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Highlights

Progestational stress maybe the risk factor for the neural development of offspring.
CSS maybe act as a promising therapeutic herb for offspring’s neural damage by progestational stress.
CSS act the anti-anxiety effect and improved the levels of ERα, ERβ and PR in maternal rats.
CSS ameliorates the decrease of BDNF, NR2A and NR2B in offspring’s hippocampus damage by maternal progestational stress.

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Abstract

Background

Progestational stress has been proven to be a risk for the neural development of offspring, especially in the hippocampus. However, whether Chaihu Shugan San (CSS) can ameliorate hippocampal neural development via the regulation of brain-derived neurotrophic factor (BDNF), and N-methyl-D-aspartate receptors (NMDAR) 2A (NR2A) and 2B (NR2B), and the mechanism of such action remains unclear.

Methods

Thirty-six female rats were randomly allocated into control, chronic immobilization stress (CIS) and CSS groups according to the random number table, respectively. The male offspring were fed for 21 days after birth then randomly divided into the same three groups (6 rats/group) as the female rats. Female rats, except for the control group, underwent 21-day CIS to established a progestational stress anxiety-like model which was evaluated by body weight, the elevated plus-maze (EPM) test and serum dopamine (DA) measured using an enzyme-linked immunosorbent assay (ELISA). The expression levels of estrogen receptors (ERα/ERβ) and progesterone receptor (PR) in female rat ovaries were quantified by real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) and Western blot analysis. The hippocampal tissue in the 21-day offspring was observed by hematoxylin-eosin (HE) staining. The concentration of BDNF, NR2A, and NR2B were measured by RT-qPCR and immunohistochemistry in the CA3 and dentate gyrus (DG) regions of offsprings’ hippocampus.

Results

Compared with the female control group, significant differences in body weight, EPM test and DA concentration were observed in the CIS group, meanwhile, the concentration of ERα (P < 0.05), PR (P < 0.05) and ERβ in the ovaries were decreased. In the offsprings’ hippocampus of the CIS group, the chromatin of the nucleus was edge set and with condensed and irregular morphology nucleus, and the cytoplasm was unevenly stained with spaces around the cells, moreover, the expression levels of BDNF, NR2A, and NR2B were also declined (P < 0.05). However, Chaihu Shugan San reversed these changes, especially the BDNF in the DG region (P < 0.05), and NR2A and NR2B in the CA3 and DG region (P < 0.05).

Conclusions

CSS could ameliorate the neural development of the hippocampus in offspring damaged by anxiety-like progestational stress in female rats via regulating the expression levels of ERα, ERβ, and PR in female rat ovaries and BDNF, NR2A, and NR2B in the hippocampus of their offspring.

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Keywords : Chaihu Shugan San (CSS), Progestational stress, Brain-derived neurotrophic factor (BDNF), N-methyl-D-aspartate receptors (NMDARs), Estrogen receptor, Progesterone receptor


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