Diabetes-induced alterations of central nervous system G proteins. ADP-ribosylation, immunoreactivity, and gene-expression studies in rat striatum

Mol Chem Neuropathol. 1992 Dec;17(3):259-72. doi: 10.1007/BF03160015.

Abstract

Previous studies from our laboratory have suggested that diabetes-associated central nervous system abnormalities are characterized by progressive alterations of neurotransmitters and of transductional Gi/Go proteins. In this study, we have further characterized these abnormalities in the striatum of alloxan-diabetic rats by means of adenosine 5'-diphosphate (ADP)-ribosylation, and Western and Northern blotting techniques. Fourteen weeks after diabetes induction, pertussis-toxin (PTX) catalyzed ADP-ribosylation of Gi/Go proteins was markedly reduced in diabetic animals, as shown by a clear decrease of 32P-ADPribose incorporation into G protein alpha subunits. In agreement with our previous pharmacological studies that showed a reduction of Gi-mediated modulation of adenylate cyclase activity only at this stage of diabetes, no changes in PTX-mediated ADP-ribosylation were observed earlier (5-wk diabetes). Immunoblotting studies performed by using antibodies selectively raised against Gi-2, Go, and Gs proteins did not reveal any differences between control and diabetic animals at any stage of diabetes. Similarly, the mRNAs corresponding to the alpha subunits of Gi-2, Go, and Gs proteins did not show any marked changes in chronic diabetic rats with respect to control animals. It is therefore concluded that diabetes is associated with development of a time-related alteration of cerebral Gi/Go proteins and that this defect is not owing to gross changes in either content of G proteins or mRNA level, but probably reflects modifications of G protein's structure or physiological status affecting the coupling with membrane effector systems and the sensitivity to PTX.

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism*
  • Adenylyl Cyclases / metabolism
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Corpus Striatum / metabolism*
  • Diabetes Mellitus, Experimental / metabolism*
  • GTP-Binding Proteins / biosynthesis*
  • GTP-Binding Proteins / immunology
  • Gene Expression Regulation / physiology*
  • Immunohistochemistry
  • In Vitro Techniques
  • RNA, Messenger / biosynthesis
  • Rats

Substances

  • RNA, Messenger
  • Adenosine Diphosphate Ribose
  • GTP-Binding Proteins
  • Adenylyl Cyclases