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Biochem Biophys Res Commun. 2017 Dec 16;494(3-4):615-620. doi: 10.1016/j.bbrc.2017.09.154. Epub 2017 Oct 5.

Regulatory effects of the AMPKα-SIRT1 molecular pathway on insulin resistance in PCOS mice: An in vitro and in vivo study.

Author information

1
Center for Reproductive Medicine, The Third Affiliated Hospital, Sun-Yet Sen University, People's Republic of China. Electronic address: doctort@163.com.
2
Center for Reproductive Medicine, The Third Affiliated Hospital, Sun-Yet Sen University, People's Republic of China.
3
Department of Infertility and Sexual Medicine, The Third Affiliated Hospital, Sun-Yet Sen University, People's Republic of China.

Abstract

In order to preliminarily explore the correlation between the AMPKα-SIRT1 pathway and insulin resistance and reproductive function in PCOS mice and find the pathogenesis molecular mechanism and potential therapeutic target of PCOS, we carried out in vitro study of human granulosa KGN cells and in vivo study of PCOS mouse model which was constructed with DHEA, and AICAR and Compound C were applied. We have found that SIRT1 and AMPKα expression in KGN cells gradually decreased as DHEA concentration increased; Mice of the PCOS model were in an obvious status of IR (P < 0.05). Granulosa cells in their ovarian were present in fewer numbers and were disorderly arranged, their numbers of immature follicles were significantly increased, and their AMPKα-SIRT1 pathways were down-regulated. The AMPKα-SIRT1 pathway could be up-regulated after AICAR treatment, resulting in improved IR status (P < 0.0001); however, the abovementioned effect was blocked by Compound C. Thus we concluded that the AMPKα-SIRT1 molecular pathway may be a molecular mechanism of IR in PCOS and may serve as a therapeutic target for the development of potential treatments for improving metabolic and reproductive function in PCOS.

KEYWORDS:

AMPKα-SIRT1 molecular pathway; Insulin resistance; Mice; PCOS

PMID:
28988114
DOI:
10.1016/j.bbrc.2017.09.154
[Indexed for MEDLINE]

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