Department of Neurochemistry, Institute of Physiology Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Physiol Res. 2014;63(Suppl 1):S177-89. doi: 10.33549/physiolres.932675.
Muscarinc receptor-mediated signaling takes part in many physiological functions ranging from complex higher nervous activity to vegetative responses. Specificity of action of the natural muscarinic agonist acetylcholine is effected by action on five muscarinic receptor subtypes with particular tissue and cellular localization, and coupling preference with different G-proteins and their signaling pathways. In addition to physiological roles it is also implicated in pathologic events like promotion of carcinoma cells growth, early pathogenesis of neurodegenerative diseases in the central nervous system like Alzheimer's disease and Parkinson's disease, schizophrenia, intoxications resulting in drug addiction, or overactive bladder in the periphery. All of these disturbances demonstrate involvement of specific muscarinic receptor subtypes and point to the importance to develop selective pharmacotherapeutic interventions. Because of the high homology of the orthosteric binding site of muscarinic receptor subtypes there is virtually no subtype selective agonist that binds to this site. Activation of specific receptor subtypes may be achieved by developing allosteric modulators of acetylcholine binding, since ectopic binding domains on the receptor are less conserved compared to the orthosteric site. Potentiation of the effects of acetylcholine by allosteric modulators would be beneficial in cases where acetylcholine release is reduced due to pathological conditions. When presynaptic function is severely compromised, the utilization of ectopic agonists can be a thinkable solution.
毒蕈碱型乙酰胆碱受体介导的信号转导参与了许多生理功能,从复杂的高级神经活动到植物性反应。天然毒蕈碱激动剂乙酰胆碱的作用特异性是通过作用于具有特定组织和细胞定位的五种毒蕈碱受体亚型来实现的,并且与不同的 G 蛋白及其信号通路偶联偏好。除了生理作用外,它还与病理事件有关,如促进癌细胞生长、中枢神经系统退行性疾病(如阿尔茨海默病和帕金森病)、精神分裂症、导致药物成瘾的中毒或周围性膀胱过度活动等。所有这些紊乱都表明涉及特定的毒蕈碱受体亚型,并指出开发选择性药物治疗干预的重要性。由于毒蕈碱受体亚型的正位结合位点具有高度同源性,因此实际上没有与该位点结合的选择性激动剂。通过开发乙酰胆碱结合的变构调节剂,可以实现特定受体亚型的激活,因为与正位位点相比,受体上的异位结合结构域的保守性较低。变构调节剂增强乙酰胆碱的作用将有益于由于病理条件导致乙酰胆碱释放减少的情况。当突触前功能严重受损时,异位激动剂的利用可能是一个可行的解决方案。