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海绵体平滑肌中的信号转导

Signal transduction in cavernous smooth muscle.

作者信息

Stief C G, Noack T, Andersson K E

机构信息

Department of Urology, MHH Medical School, Hannover, Germany.

出版信息

World J Urol. 1997;15(1):27-31. doi: 10.1007/BF01275153.

Abstract

Knowledge of intracellular signal propagation in smooth-muscle tone regulation is of major importance to the understanding of both the physiology of erection and the pathophysiology of erectile dysfunction and the development of new and selective pharmacological agents in the treatment of erectile dysfunction. Cavernous smooth-muscle tone depends heavily on the amount of intracellular free Ca2+. In the resting state the sarcoplasmic free Ca2+ amounts to about 120-270 nM, whereas in the extracellular fluid the Ca2+ level is in the range of 1.5-2 mM. Electromechanical and pharmacomechanical coupling induces an increase in the levels of free sarcoplasmic Ca2+ by a factor of 2-3 to 550-700 nM that triggers myosin phosphorylation and subsequent smooth muscle contraction. In this case, modulation of membrane-bound ion channels and regulation of the intracellular second-messenger system are attractive and feasible targets for pharmacological intervention. Besides the amount of free sarcoplasmic Ca2+, smooth-muscle tone is also modulated by the regulation of Ca2+ sensitivity ("Ca-sensitization") and Ca(2+)-independent contraction processes.

摘要

了解细胞内信号传导在平滑肌张力调节中的作用,对于理解勃起生理、勃起功能障碍的病理生理以及开发治疗勃起功能障碍的新型选择性药物具有重要意义。海绵体平滑肌张力在很大程度上取决于细胞内游离Ca2+的量。在静息状态下,肌浆游离Ca2+约为120 - 270 nM,而细胞外液中的Ca2+水平在1.5 - 2 mM范围内。机电耦合和药机耦合可使肌浆游离Ca2+水平增加2 - 3倍,达到550 - 700 nM,从而触发肌球蛋白磷酸化及随后的平滑肌收缩。在这种情况下,调节膜结合离子通道和细胞内第二信使系统是药物干预的有吸引力且可行的靶点。除了肌浆游离Ca2+的量外,平滑肌张力还受到Ca2+敏感性调节(“Ca敏化”)和Ca(2+)非依赖性收缩过程的调节。

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