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通过耐洗脱的占诺美林结合对M3毒蕈碱受体进行调节的机制

Mechanisms of M3 muscarinic receptor regulation by wash-resistant xanomeline binding.

作者信息

Noetzel Meredith J, Grant Marianne K O, El-Fakahany Esam E

机构信息

Division of Neuroscience Research in Psychiatry, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

出版信息

Pharmacology. 2009;83(5):301-17. doi: 10.1159/000214843. Epub 2009 Apr 28.

Abstract

BACKGROUND/AIMS: Xanomeline has been shown to bind in a unique manner at M1 and M3 muscarinic receptors, with interactions at both the orthosteric site and an allosteric site. We have previously shown that brief exposure of Chinese hamster ovary cells that express the M3 receptor to xanomeline followed by removal of free agonist results in a delayed decrease in radioligand binding and receptor response to agonists. In the current study, we were interested in determining the mechanisms of this effect.

METHODS

Cells were treated with carbachol, pilocarpine or xanomeline for 1 h followed by washing and either used immediately or after waiting for 23 h. Control groups included cells that were not exposed to agonists and cells that were treated with agonists for 24 h. Radioligand binding and functional assays were conducted to determine the effects of agonist treatments.

RESULTS

The above treatment protocol with xanomeline resulted in similar effects of the binding of [(3)H]NMS and [(3)H]QNB. When receptor function is blocked using a variety of methods, the long-term effects of xanomeline binding were absent.

CONCLUSION

Our data indicate that xanomeline wash-resistant binding at the receptor allosteric site leads to receptor downregulation and that receptor activation is necessary for these effects.

摘要

背景/目的:已证明占诺美林以独特方式与M1和M3毒蕈碱受体结合,在正构位点和变构位点均有相互作用。我们之前已表明,短暂暴露表达M3受体的中国仓鼠卵巢细胞于占诺美林,随后去除游离激动剂,会导致放射性配体结合和受体对激动剂的反应延迟降低。在本研究中,我们感兴趣于确定这种效应的机制。

方法

用卡巴胆碱、毛果芸香碱或占诺美林处理细胞1小时,随后洗涤,立即使用或等待23小时后使用。对照组包括未暴露于激动剂的细胞和用激动剂处理24小时的细胞。进行放射性配体结合和功能测定以确定激动剂处理的效果。

结果

上述占诺美林处理方案对[(3)H]NMS和[(3)H]QNB的结合产生类似影响。当使用多种方法阻断受体功能时,占诺美林结合的长期效应不存在。

结论

我们的数据表明,占诺美林在受体变构位点的耐洗脱结合导致受体下调,且这些效应需要受体激活。

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Allosteric binding sites on muscarinic acetylcholine receptors.毒蕈碱型乙酰胆碱受体上的变构结合位点。
Mol Pharmacol. 2005 Dec;68(6):1506-9. doi: 10.1124/mol.105.019141. Epub 2005 Sep 23.
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Muscarinic receptor subtype pharmacology and physiology.毒蕈碱受体亚型药理学与生理学
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