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DIFFERENCES IN AGONIST POTENCY RATIOS AT HUMAN M1 MUSCARINIC RECEPTORS EXPRESSED IN A9L AND CHO CELLS

机译:在A9L和CHO细胞中表达的人类M1肌肉受体的激动剂强度比率的差异

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摘要

A9L mouse fibroblast and Chinese hamster ovary (CHO) cells appear to differ in their complement of guanine-nucleotide binding proteins (G proteins) and/or isoform of effecters that lead to inositol-monophosphate formation. The influence of these cellular components on receptor activation was examined by comparing agonist-induced inositol monophosphate formation via human muscarinic mi receptors expressed in the two cell lines. The rank order of agonist potencies of five full agonists differed in the two cell lines. In addition, differences in agonist potency ratios for two of the five agonists (carbachol and methacholine) suggest that the agonists differ in their activation of ml receptors and this is reflected in differences in G protein coupling The results provide biological evidence that muscarinic agonists differentially activate mi receptors and that, at least for the systems examined in this study, receptor-effector coupling in a given system may depend on the structure of the agonist. [References: 16]
机译:A9L小鼠成纤维细胞和中国仓鼠卵巢(CHO)细胞的鸟嘌呤核苷酸结合蛋白(G蛋白)和/或导致肌醇一磷酸形成的效应子同工型的补体似乎有所不同。通过比较激动剂诱导的经由在两种细胞系中表达的人毒蕈碱mi受体形成的肌醇单磷酸形成,来检查这些细胞成分对受体激活的影响。在两种细胞系中,五个完全激动剂的激动剂效力的等级顺序不同。另外,五种激动剂中的两种激动剂效力比的差异(咔唑和乙酰甲胆碱)表明,激动剂的ml受体活化不同,这反映在G蛋白偶联的差异上。结果提供了毒蕈碱性激动剂差异活化的生物学证据。 mi受体,至少在本研究中检测的系统中,给定系统中的受体-效应子偶联可能取决于激动剂的结构。 [参考:16]

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