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阿尔茨海默病患者颞叶皮质中β1-肾上腺素能受体与G蛋白偶联受损。

Disrupted beta 1-adrenoceptor-G protein coupling in the temporal cortex of patients with Alzheimer's disease.

作者信息

Cowburn R F, Vestling M, Fowler C J, Ravid R, Winblad B, O'Neill C

机构信息

Department of Geriatric Medicine, Karolinska Institute, Huddinge University Hospital, Sweden.

出版信息

Neurosci Lett. 1993 Jun 11;155(2):163-6. doi: 10.1016/0304-3940(93)90698-k.

Abstract

The efficacy of beta 1-adrenoceptor-G protein coupling was studied in postmortem temporal cortex synaptic membranes from a series of control and Alzheimer's disease subjects. For the control cases, the non-hydrolysable GTP analogue 5'-guanylylimidodiphosphate (Gpp[NH]p) gave a significant reduction in the affinity of the agonist isoprenaline to displace binding of the radiolabelled antagonist (+/)-4-(3-t-butylamino-2-hydroxypropoxy)[5,7-3H]benzimidazol-2-one ([3H]CGP-12177). This effect was attributed to the conversion of high agonist-affinity sites to a lower-affinity state and was not found for the Alzheimer's disease cases. These data indicate that a disruption of beta 1-adrenoceptor-G protein coupling occurs in the temporal cortex of Alzheimer's disease patients.

摘要

在一系列对照受试者和阿尔茨海默病患者死后的颞叶皮质突触膜中,研究了β1 -肾上腺素能受体与G蛋白偶联的功效。对于对照病例,不可水解的GTP类似物5'-鸟苷酰亚胺二磷酸(Gpp[NH]p)使激动剂异丙肾上腺素取代放射性标记拮抗剂(+/-)-4-(3-叔丁基氨基-2-羟基丙氧基)[5,7-³H]苯并咪唑-2-酮([³H]CGP-12177)结合的亲和力显著降低。这种效应归因于高激动剂亲和力位点向低亲和力状态的转变,而在阿尔茨海默病病例中未发现这种情况。这些数据表明,阿尔茨海默病患者的颞叶皮质中发生了β1 -肾上腺素能受体与G蛋白偶联的破坏。

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