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大鼠脑切片培养物中的毒蕈碱受体

Muscarinic receptors in slice cultures of rat brain.

作者信息

Rimvall K, Keller F, Waser P G

出版信息

Neuropharmacology. 1986 Mar;25(3):221-6. doi: 10.1016/0028-3908(86)90243-1.

Abstract

Muscarinic acetylcholine receptors in organotypic slice cultures of hippocampus of the rat, have been examined using the tritiated muscarinic antagonist quinuclidinylbenzilate [( 3H]QNB) as a as a marker. Maximum specific binding of [3H]QNB in mature explants of hippocampus amounted to 316 fmol/mg protein and a dissociation constant (KD) of 185 pM was determined. Scatchard analysis suggested binding to one single binding site. In younger cultures smaller KDs were registered. This decrease in ligand affinity in maturer cultures possibly reflects a decrease in the turnover of acetylcholine. Muscarinic antagonists inhibited the total binding of [3H]QNB significantly, whereas muscarinic agonist, nicotinic antagonists and cholinesterase inhibitors had no influence whatsoever on the total binding of [3H]QNB. The content of muscarinic acetylcholine receptors varied between cultures with explants from different brain areas: hippocampus greater than striatum greater than septum greater than spinal cord greater than cerebellum. These in vitro results are generally in good agreement with results obtained in situ by other investigators and suggest that the binding of [3H]QNB observed in these cultures is indeed correlated to specific muscarinic receptor sites.

摘要

利用放射性标记的毒蕈碱拮抗剂喹核醇基苯甲酸酯[(3H)QNB]作为标记物,对大鼠海马器官型脑片培养物中的毒蕈碱型乙酰胆碱受体进行了检测。海马成熟外植体中[3H]QNB的最大特异性结合量达316 fmol/mg蛋白质,测定的解离常数(KD)为185 pM。Scatchard分析表明其与单一结合位点结合。在较年轻的培养物中记录到较小的KD值。成熟培养物中这种配体亲和力的降低可能反映了乙酰胆碱周转率的下降。毒蕈碱拮抗剂显著抑制[3H]QNB的总结合,而毒蕈碱激动剂、烟碱拮抗剂和胆碱酯酶抑制剂对[3H]QNB的总结合没有任何影响。来自不同脑区的外植体培养物中毒蕈碱型乙酰胆碱受体的含量各不相同:海马>纹状体>隔区>脊髓>小脑。这些体外实验结果与其他研究者原位实验得到的结果总体上吻合良好,表明在这些培养物中观察到的[3H]QNB结合确实与特定的毒蕈碱受体位点相关。

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