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Assignment of muscarinic receptor subtypes mediating G-protein modulation of Ca2+ channels by using knockout mice

机译:通过使用敲除小鼠介导G蛋白调节Ca2 +通道的毒蕈碱受体亚型的分配

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摘要

There are five known subtypes of muscarinic receptors (M1–M5). We have used knockout mice lacking the M1, M2, or M4 receptors to determine which subtypes mediate modulation of voltage-gated Ca2+ channels in mouse sympathetic neurons. Muscarinic agonists modulate N- and L-type Ca2+ channels in these neurons through two distinct G-protein-mediated mechanisms. One pathway is fast and membrane-delimited and inhibits N- and P/Q-type channels by shifting their activation to more depolarized potentials. The other is slow and voltage-independent and uses a diffusible cytoplasmic messenger to inhibit both Ca2+ channel types. Using patch-clamp methods on acutely dissociated sympathetic neurons, we isolated each pathway by pharmacological and kinetic means and found that each one is nearly absent in a particular knockout mouse. The fast and voltage-dependent pathway is lacking in the M2 receptor knockout mice; the slow and voltage-independent pathway is absent from the M1 receptor knockout mice; and neither pathway is affected in the M4 receptor knockout mice. The knockout effects are clean and are apparently not accompanied by compensatory changes in other muscarinic receptors.
机译:毒蕈碱受体(M1-M5)有五种已知的亚型。我们已经使用缺乏M1,M2或M4受体的基因敲除小鼠来确定哪些亚型介导小鼠交感神经元中电压门控的Ca 2 + 通道的调节。毒蕈碱激动剂通过两种不同的G蛋白介导的机制调节这些神经元中的N型和L型Ca 2 + 通道。一种途径是快速的且膜定界的,并且通过将N和P / Q型通道的活化转移到更多的去极化电位来抑制它们。另一个是缓慢且不依赖电压的,并且使用可扩散的胞质信使来抑制两种Ca 2 + 通道类型。在急性分离的交感神经元上使用膜片钳方法,我们通过药理学和动力学方法分离了每种途径,发现在特定的基因敲除小鼠中几乎没有每种途径。 M2受体基因敲除小鼠缺乏快速和电压依赖性途径。 M1受体基因敲除小鼠缺少慢速且不依赖电压的途径。 M4受体基因敲除小鼠中这两种途径均不受影响。敲除作用是干净的,并且显然不伴随其他毒蕈碱受体的代偿性变化。

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