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Melatonin receptors in diabetes: A potential new therapeutical target?

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成果类型:
期刊论文
作者:
She, Meihua;Laudon, Moshe;Yin, Weidong*
通讯作者:
Yin, Weidong
作者机构:
[Yin, Weidong; She, Meihua] Univ China South, Inst Cardiovasc Res, Key Lab Arteriosclerol Hunan Prov, Hengyang 421001, Peoples R China.
[Yin, Weidong; She, Meihua] Univ China South, Sch Pharmaceut & Biol Sci, Dept Biochem & Mol Biol, Hengyang 421001, Peoples R China.
[Laudon, Moshe] Neurim Pharmaceut Ltd, Drug Discovery, Tel Aviv, Israel.
通讯机构:
[Yin, Weidong] U
Univ China South, Inst Cardiovasc Res, Key Lab Arteriosclerol Hunan Prov, Hengyang 421001, Peoples R China.
语种:
英文
关键词:
Melatonin;Receptors;Glucose homeostasis;Insulin secretion;Diabetes
期刊:
European Journal of Pharmacology
ISSN:
0014-2999
年:
2014
卷:
744
页码:
220-223
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81200590]; Specialized Research Fund for the Doctoral Program of Higher Education of ChinaSpecialized Research Fund for the Doctoral Program of Higher Education (SRFDP) [20124324120005]
机构署名:
本校为第一且通讯机构
院系归属:
化学化工学院
医学院
药学与生物科学学院
摘要:
Melatonin is synthesized and secreted mainly by the pineal gland in a circadian fashion, and it thus mediates endogenous circadian rhythms and influences other physiological functions. Both the G-protein coupled receptors MT1 (encoded by MTNR1A) and MT2 (encoded by MTNR1B) in mammals mediate the actions of melatonin. Evidence from in vivo and in vitro studies proved a key role of melatonin in the regulation of glucose metabolism and the pathogenesis of diabetes, as further confirmed by the recent studies of human genetic variants of MTNR1B. Remarkably, it was also suggested that genetic variat...

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