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膀胱中突触前毒蕈碱受体的功能、信号转导机制及可塑性

Function, signal transduction mechanisms and plasticity of presynaptic muscarinic receptors in the urinary bladder.

作者信息

Somogyi G T, de Groat W C

机构信息

Department of Pharmacology, University of Pittsburgh, PA 15261, USA. somo+@pitt.edu

出版信息

Life Sci. 1999;64(6-7):411-8. doi: 10.1016/s0024-3205(98)00580-3.

Abstract

Presynaptic M1 muscarinic receptors on parasympathetic nerve terminals in rat urinary bladder strips are involved in an autofacilitatory mechanism that markedly enhances acetylcholine release during continuous electrical field stimulation. The facilitatory muscarinic mechanism is dependent upon a PKC mediated second messenger pathway and influx of extracellular Ca2+ into the parasympathetic nerve terminals via L and N-type Ca2+ channels. Prejunctional muscarinic facilitation has also been detected in human bladders. The muscarinic facilitatory mechanism is upregulated in hyperactive bladders from chronic spinal cord transected rats; and the facilitation in these preparations is primarily mediated by M3 muscarinic receptors. Presynaptic muscarinic receptors represent a new target for pharmacological treatment of bladder hyperactivity. If presynaptic facilitation is restricted to the bladder and not present in other tissues then drugs acting at this site might be expected to exhibit uroselectivity.

摘要

大鼠膀胱条副交感神经末梢上的突触前M1毒蕈碱受体参与一种自身易化机制,该机制在连续电场刺激期间可显著增强乙酰胆碱的释放。易化性毒蕈碱机制依赖于蛋白激酶C介导的第二信使途径以及细胞外Ca2+通过L型和N型Ca2+通道流入副交感神经末梢。在人膀胱中也检测到了突触前毒蕈碱易化作用。慢性脊髓横断大鼠的活动亢进膀胱中,毒蕈碱易化机制上调;并且这些标本中的易化作用主要由M3毒蕈碱受体介导。突触前毒蕈碱受体是膀胱活动亢进药物治疗的新靶点。如果突触前易化作用仅限于膀胱而不存在于其他组织中,那么作用于该位点的药物可能具有尿选择性。

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