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Genetically acquired diabetes: adipocyte guanine nucleotide regulatory protein expression and adenylate cyclase regulation
Authors:Derek Strasshein  Timothy Palmer  Miles D Houslay
Institution:1. Molecular Pharmacology Group, Department of Biochemistry, University of Glasgow, Glasgow, U.K.
Abstract:Adipocyte membranes from diabetic (db/db) animals showed marked elevations in the levels of α-subunits for Gi-1 which were almost twice those in membranes from their normal, lean littermates. In contrast, no apparent differences were noted for levels of the α-subunits of Gi-2 and Gi-3, and 42 and 45 kDa forms of Gs and for G-protein β-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 forsckolin. 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 G1-1 thus appears to have little discernible effect upon the inhibitory regulation of adenylate cyclase.
Keywords:G protein  Adenylase cyclase  Diabetes  Protein expression  (Rat membrane)  G-protein  guanine nucleotide regulatory/binding protein  p[NH]ppG  guanylyl 5′-imidodiphosphate  stimulatory receptors coupled to adenylate cyclase  inhibitory receptors coupled to adenylate cyclase  TSH  thyroid stimulating hormones  PIA  phenylisopropyladenosine  concentration at which 50% of maximum effect occurs
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