FSHR ablation induces depression-like behaviors

Alteration in reproductive hormones profile is associated with the increasing risk of menopausal depression in women. Serum follicle-stimulating hormone (FSH) level is changed during the menopause transition, while the effect of FSH on menopausal depression has remained undefined. In this study we i...

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Veröffentlicht in:Acta pharmacologica Sinica 2020-08, Vol.41 (8), p.1033-1040
Hauptverfasser: Bi, Wen-kai, Shao, Shan-shan, Li, Zhi-wei, Ruan, Yong-wei, Luan, Si-si, Dong, Zhen-hua, Wang, Jing, Wu, Shan-shan, Guo, Tian, Ma, Shi-zhan, Gao, Ling, Zhao, Jia-jun, He, Zhao
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container_issue 8
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container_title Acta pharmacologica Sinica
container_volume 41
creator Bi, Wen-kai
Shao, Shan-shan
Li, Zhi-wei
Ruan, Yong-wei
Luan, Si-si
Dong, Zhen-hua
Wang, Jing
Wu, Shan-shan
Guo, Tian
Ma, Shi-zhan
Gao, Ling
Zhao, Jia-jun
He, Zhao
description Alteration in reproductive hormones profile is associated with the increasing risk of menopausal depression in women. Serum follicle-stimulating hormone (FSH) level is changed during the menopause transition, while the effect of FSH on menopausal depression has remained undefined. In this study we investigated whether or how FSH affected menopausal depression in postmenopausal (ovariectomized) FSHR knockout mice ( Fshr −/ − ). We found that Fshr −/− mice displayed aggravated depression-like behaviors, accompanied by severe oxidative stress in the whole brain, resulted from significantly reduced glutamate cysteine ligase modifier subunit (GCLm) in glutathione synthesis and glucose-6-phosphate dehydrogenase (G6PD) in NADP/NADPH transition. Importantly, administration of ROS scavenger N-acetyl cysteine (NAC, 150 mg · kg −1  · d −1 , i.p. for 12 weeks) attenuated the depression-like behaviors of Fshr −/ − mice. Consistent with these in vivo experiment results, we found that pretreatment with FSH (50, 100 ng/mL) dose-dependently increased protein levels of GCLm and G6PD, and decreased the ROS production in N2a mouse neuroblastoma cells. These findings demonstrate that FSH signaling is involved in pathogenesis of menopausal depression, and likely to maintain the redox-optimized ROS balance in neurons.
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Serum follicle-stimulating hormone (FSH) level is changed during the menopause transition, while the effect of FSH on menopausal depression has remained undefined. In this study we investigated whether or how FSH affected menopausal depression in postmenopausal (ovariectomized) FSHR knockout mice ( Fshr −/ − ). We found that Fshr −/− mice displayed aggravated depression-like behaviors, accompanied by severe oxidative stress in the whole brain, resulted from significantly reduced glutamate cysteine ligase modifier subunit (GCLm) in glutathione synthesis and glucose-6-phosphate dehydrogenase (G6PD) in NADP/NADPH transition. Importantly, administration of ROS scavenger N-acetyl cysteine (NAC, 150 mg · kg −1  · d −1 , i.p. for 12 weeks) attenuated the depression-like behaviors of Fshr −/ − mice. Consistent with these in vivo experiment results, we found that pretreatment with FSH (50, 100 ng/mL) dose-dependently increased protein levels of GCLm and G6PD, and decreased the ROS production in N2a mouse neuroblastoma cells. 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Serum follicle-stimulating hormone (FSH) level is changed during the menopause transition, while the effect of FSH on menopausal depression has remained undefined. In this study we investigated whether or how FSH affected menopausal depression in postmenopausal (ovariectomized) FSHR knockout mice ( Fshr −/ − ). We found that Fshr −/− mice displayed aggravated depression-like behaviors, accompanied by severe oxidative stress in the whole brain, resulted from significantly reduced glutamate cysteine ligase modifier subunit (GCLm) in glutathione synthesis and glucose-6-phosphate dehydrogenase (G6PD) in NADP/NADPH transition. Importantly, administration of ROS scavenger N-acetyl cysteine (NAC, 150 mg · kg −1  · d −1 , i.p. for 12 weeks) attenuated the depression-like behaviors of Fshr −/ − mice. Consistent with these in vivo experiment results, we found that pretreatment with FSH (50, 100 ng/mL) dose-dependently increased protein levels of GCLm and G6PD, and decreased the ROS production in N2a mouse neuroblastoma cells. 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Serum follicle-stimulating hormone (FSH) level is changed during the menopause transition, while the effect of FSH on menopausal depression has remained undefined. In this study we investigated whether or how FSH affected menopausal depression in postmenopausal (ovariectomized) FSHR knockout mice ( Fshr −/ − ). We found that Fshr −/− mice displayed aggravated depression-like behaviors, accompanied by severe oxidative stress in the whole brain, resulted from significantly reduced glutamate cysteine ligase modifier subunit (GCLm) in glutathione synthesis and glucose-6-phosphate dehydrogenase (G6PD) in NADP/NADPH transition. Importantly, administration of ROS scavenger N-acetyl cysteine (NAC, 150 mg · kg −1  · d −1 , i.p. for 12 weeks) attenuated the depression-like behaviors of Fshr −/ − mice. Consistent with these in vivo experiment results, we found that pretreatment with FSH (50, 100 ng/mL) dose-dependently increased protein levels of GCLm and G6PD, and decreased the ROS production in N2a mouse neuroblastoma cells. These findings demonstrate that FSH signaling is involved in pathogenesis of menopausal depression, and likely to maintain the redox-optimized ROS balance in neurons.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>32203083</pmid><doi>10.1038/s41401-020-0384-8</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Ablation
Acetylcysteine
Biomedical and Life Sciences
Biomedicine
Cysteine
Endocrinology
Estrogens
Follicle-stimulating hormone
Glucosephosphate dehydrogenase
Glutathione
Hormones
Immunology
Internal Medicine
Medical Microbiology
Medical research
Menopause
Mental depression
Metabolism
NADP
Neuroblastoma
Neuroblastoma cells
Oophorectomy
Ovariectomy
Oxidative stress
Pathogenesis
Pharmacology/Toxicology
Post-menopause
Reproductive behavior
Sucrose
Vaccine
title FSHR ablation induces depression-like behaviors
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