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Genetically acquired diabetes: adipocyte guanine nucleotide regulatory protein expression and adenylate cyclase regulation.

作者信息

Strassheim D, Palmer T, Houslay M D

机构信息

Department of Biochemistry, University of Glasgow, U.K.

出版信息

Biochim Biophys Acta. 1991 Feb 22;1096(2):121-6. doi: 10.1016/0925-4439(91)90049-f.

DOI:10.1016/0925-4439(91)90049-f
PMID:1848112
Abstract

Adipocyte membranes from diabetic (db/db) animals showed marked elevations in the levels of alpha-subunits for Gi-1 which were almost twice those found in membranes from their normal, lean littermates. In contrast, no apparent differences were noted for levels of the alpha-subunits of Gi-2 and Gi-3, the 42 and 45 kDa forms of Gs and for G-protein beta-subunits. Adenylate cyclase specific activity was similar in membranes from both normal and diabetic animals under basal conditions and also when stimulated by optimal concentrations of either NaF or forskolin. In contrast, the ability of isoprenaline, glucagon and secretin to stimulate adenylate cyclase activity was greater in membranes from normal animals compared with membranes from diabetic animals. Receptor-mediated inhibition of adenylate cyclase, as assessed using PGE1 and nicotinate, was similar using membranes from both sources, but PIA (phenylisopropyladenosine) was a slightly more effective inhibitor in membranes from diabetic animals. A doubling in the expression of Gi-1 thus appears to have little discernible effect upon the inhibitory regulation of adenylate cyclase.

摘要

相似文献

1
Genetically acquired diabetes: adipocyte guanine nucleotide regulatory protein expression and adenylate cyclase regulation.
Biochim Biophys Acta. 1991 Feb 22;1096(2):121-6. doi: 10.1016/0925-4439(91)90049-f.
2
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Alterations in G-protein expression and the hormonal regulation of adenylate cyclase in the adipocytes of obese (fa/fa) Zucker rats.肥胖(fa/fa) Zucker大鼠脂肪细胞中G蛋白表达的改变及腺苷酸环化酶的激素调节
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Multiple defects occur in the guanine nucleotide regulatory protein system in liver plasma membranes of obese (fa/fa) but not lean (Fa/Fa) Zucker rats: loss of functional Gi and abnormal Gs function.肥胖(fa/fa)而非瘦型(Fa/Fa) Zucker大鼠肝细胞膜鸟嘌呤核苷酸调节蛋白系统存在多种缺陷:功能性Gi丧失和Gs功能异常。
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