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褪黑素受体激动剂Neu-P11对3T3-L1小鼠脂肪细胞蛋白激酶B及其磷酸化的影响

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成果类型:
期刊论文
作者:
Xiu-ping LI;Shi-chang CAI;Wei-dong YIN;Su-jun ZHANG;Rong HU;...
通讯作者:
Cai, S.-C.
作者机构:
[Li X.-P.; Hu R.] Department of Laboratory, Hunan University of Medicine, Huaihua, Hunan 418000, China
[Li X.; Cai S.-C.] Division of Basic Medical Sciences, Hunan University of Medicine, Huaihua, Hunan 418000, China
[Yin W.-D.] Institute of Cardiovascular Disease, University of South China Medical School, Hengyang, Hunan 412000, China
[Zhang S.-J.] Division of Experimental Animal, University of South China, Hengyang, Hunan 412000, China
[Moshe L.] Neurim Pharmaceuticals Ltd., Tel-Aviv, 69710, Israel
通讯机构:
[Cai, S.-C.] D
Division of Basic Medical Sciences, China
语种:
中文
关键词:
褪黑素;胰岛素抵抗;蛋白激酶B
关键词(英文):
Neu-P11;Luzindole
期刊:
海军军医大学学报
ISSN:
2097-1338
年:
2015
卷:
36
期:
7
页码:
802-804
基金类别:
湖南省教育厅科学研究项目(14C0909); 湖南医药学院科学研究项目(2014KY02)~~;
机构署名:
本校为其他机构
院系归属:
医学院
药学与生物科学学院
摘要:
糖尿病(diabetes mellitus,DM)特征性病理生理改变是高血糖、碳水化合物和脂肪代谢紊乱导致的胰岛素抵抗或胰岛素分泌的绝对或相对不足[1-2],以2型糖尿病(type 2 diabetes mellitus,T2DM)为主.T2DM发病原因主要是胰岛素信号转导通路破坏,产生胰岛素抵抗(insulin resistance,IR)[3-4].蛋白激酶B (protein kinase B,PKB)又称Akt,是胰岛素信号转导过程中的关键分子之一[5],磷酸化PKB(p-PKB)是其活性形式[6].
摘要(英文):
Objective: The objective of present study was to examine the changes of melatonin receptor agonist Neu-P11 on expression of PKB and P-PKB in 3T3-L1 adipocytes and to research the variation mechanisms.Methods: 3T3-L1 pre-adipocytes were cultivated and differentiated in adipogenic cocktail by IBMX, DEX and insulin; Confirm the establishment of insulin resistance model. The changes of PKB and P-PKB protein expressions before and after drug action were detected by Western blot; Results: Expression of PKB and P-PKB reduced significantly by compariso...

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