Finco C, Abbracchio M P, Malosio M L, Cattabeni F, Di Giulio A M, Paternieri B, Mantegazza P, Gorio A
Department of Pharmacology, Chemotherapy, and Medical Toxicology, School of Medicine, University of Milano, Italy.
Mol Chem Neuropathol. 1992 Dec;17(3):259-72. doi: 10.1007/BF03160015.
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.
我们实验室之前的研究表明,糖尿病相关的中枢神经系统异常表现为神经递质以及转导性Gi/Go蛋白的渐进性改变。在本研究中,我们通过5'-二磷酸腺苷(ADP)-核糖基化、蛋白质免疫印迹法和Northern印迹法,进一步对四氧嘧啶糖尿病大鼠纹状体中的这些异常进行了表征。糖尿病诱导14周后,百日咳毒素(PTX)催化的Gi/Go蛋白ADP-核糖基化在糖尿病动物中显著降低,这表现为32P-ADP核糖掺入G蛋白α亚基明显减少。与我们之前的药理学研究一致,该研究表明仅在糖尿病的这个阶段Gi介导的腺苷酸环化酶活性调节降低,在早期(糖尿病5周)未观察到PTX介导的ADP-核糖基化有变化。使用针对Gi-2、Go和Gs蛋白选择性产生的抗体进行的免疫印迹研究未发现糖尿病动物与对照动物在糖尿病的任何阶段有任何差异。同样,与Gi-2、Go和Gs蛋白α亚基对应的mRNA在慢性糖尿病大鼠与对照动物相比未显示任何明显变化。因此得出结论,糖尿病与脑Gi/Go蛋白的时间相关改变的发展有关,并且这种缺陷不是由于G蛋白含量或mRNA水平的总体变化,而是可能反映了影响与膜效应系统偶联以及对PTX敏感性的G蛋白结构或生理状态的改变。