Warpman U, Alafuzoff I, Nordberg A
Department of Pharmacology, Uppsala University, Sweden.
Neurosci Lett. 1993 Feb 5;150(1):39-43. doi: 10.1016/0304-3940(93)90103-r.
The coupling of muscarinic agonist receptors to guanine nucleotide-binding (G) proteins was investigated in the frontal, temporal cortices and thalamus of control and Alzheimer brains by using carbachol in competition experiments with [3H]QNB. In the presence of GppNHp, the carbachol/[3H]QNB competition binding data showed a 6-fold increase in the high-affinity muscarinic agonist coefficient (Ki high) in the thalami of control brains and a significantly increased proportion of low-affinity agonist binding sites (Bmax low) in the temporal cortices of control brains, while no significant effect of GppNHp was observed in Alzheimer brains. The results suggest a disturbance of the muscarinic receptor-G protein coupling in Alzheimer's disease.
通过在与[3H]QNB的竞争实验中使用卡巴胆碱,研究了对照和阿尔茨海默病大脑的额叶、颞叶皮质及丘脑中毒蕈碱激动剂受体与鸟嘌呤核苷酸结合(G)蛋白的偶联情况。在GppNHp存在的情况下,卡巴胆碱/[3H]QNB竞争结合数据显示,对照大脑丘脑的高亲和力毒蕈碱激动剂系数(Ki高)增加了6倍,对照大脑颞叶皮质中低亲和力激动剂结合位点(Bmax低)的比例显著增加,而在阿尔茨海默病大脑中未观察到GppNHp的显著影响。结果表明,阿尔茨海默病中毒蕈碱受体-G蛋白偶联存在紊乱。