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平滑肌中毒蕈碱受体的亚型

Subtypes of the muscarinic receptor in smooth muscle.

作者信息

Ehlert F J, Ostrom R S, Sawyer G W

机构信息

Department of Pharmacology, College of Medicine, University of California, Irvine 92697, USA.

出版信息

Life Sci. 1997;61(18):1729-40. doi: 10.1016/s0024-3205(97)00433-5.

Abstract

Muscarinic receptors are expressed in smooth muscle throughout the body. In most instances, the muscarinic receptor population in smooth muscle is composed of mainly the M2 and M3 subtypes in an 80% to 20% mixture. The M3 subtype mediates phosphoinositide hydrolysis and calcium mobilization, whereas the M2 subtype mediates an inhibition of cAMP accumulation. In addition, a variety of ionic conductances are elicited by muscarinic receptors. Muscarinic agonists stimulate a nonselective cation conductance that is pertussis toxin-sensitive and dependent on calcium. The pertussis toxin-sensitivity of this response suggests that it is mediated by M2 receptors. Following agonist induced depolarization of smooth muscle, voltage dependent calcium channels are activated to enable an influx of calcium. In some instances, muscarinic agonists enhance this conductance through a mechanism involving protein kinase C, whereas in other instances, muscarinic agonists suppress this calcium conductance. Smooth muscle often contains calcium activated potassium channels that tend to repolarize the membrane following calcium influx. Activation of muscarinic receptors suppresses this potassium conductance in some smooth muscles. Under standard conditions, muscarinic agonists elicit pertussis toxin-insensitive contractions through activation of the M3 receptor. When most of the M3 receptors are inactivated, it is possible to measure a pertussis toxin-sensitive contractile response to muscarinic agonists that is most likely mediated through M2 receptors. M2 receptors also cause an indirect contraction by inhibiting the relaxant effects of agents that increase cAMP (e.g., forskolin and isoproterenol).

摘要

毒蕈碱受体在全身平滑肌中均有表达。在大多数情况下,平滑肌中的毒蕈碱受体群体主要由M2和M3亚型组成,其比例为80%至20%的混合。M3亚型介导磷酸肌醇水解和钙动员,而M2亚型介导对环磷酸腺苷(cAMP)积累的抑制。此外,毒蕈碱受体可引发多种离子电导。毒蕈碱激动剂刺激一种对百日咳毒素敏感且依赖钙的非选择性阳离子电导。这种反应对百日咳毒素的敏感性表明它是由M2受体介导的。激动剂诱导平滑肌去极化后,电压依赖性钙通道被激活,使钙内流。在某些情况下,毒蕈碱激动剂通过一种涉及蛋白激酶C的机制增强这种电导,而在其他情况下,毒蕈碱激动剂则抑制这种钙电导。平滑肌通常含有钙激活钾通道,在钙内流后倾向于使膜复极化。在某些平滑肌中,毒蕈碱受体的激活会抑制这种钾电导。在标准条件下,毒蕈碱激动剂通过激活M3受体引发对百日咳毒素不敏感的收缩。当大多数M3受体失活时,有可能测量到对毒蕈碱激动剂的一种对百日咳毒素敏感的收缩反应,这种反应很可能是通过M2受体介导的。M2受体还通过抑制增加cAMP的药物(如福斯可林和异丙肾上腺素)的舒张作用引起间接收缩。

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