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Tachykinin NK1 and NK2 receptors mediate inhibitory vs excitatory motor responses in human isolated corpus cavernosum and spongiosum

机译:速激肽NK1和NK2受体介导人离体海绵体和海绵体的抑制性运动与兴奋性运动反应

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摘要

Motor effects produced by tachykinins were studied in human isolated corpus spongiosum and cavernosum. In quiescent preparations neurokinin A caused potent contractions (pD2=8.3 – 7.9 respectively) prevented by the NK2 receptor-selective antagonist nepadutant, whereas [Sar9]SP sulfone and senktide (NK1 and NK3 receptor-selective agonists) produced no effect or spare contractions. In KCl-precontracted corpus spongiosum septide (pD2=7.1) and [Sar9]SP sulfone (pD2=7.7) produced tetrodotoxin-resistant relaxations, abolished by the tachykinin NK1 receptor-selective antagonist SR 140333. [Sar9]SP sulfone (1 μM) produced similar relaxations in precontracted corpus cavernosum. Electrical field stimulation (EFS) elicited tetrodotoxin-sensitive relaxations, which were additive to those produced by [Sar9]SP sulfone. Nω-nitro-L-arginine (L-NOARG) totally prevented both [Sar9]SP sulfone- and EFS-induced relaxations. These results show that tachykinin NK1 and NK2 receptors mediate opposite motor effects in human penile tissues, suggesting a possible modulatory role of tachykinins on smooth muscle tone in these organs.
机译:在人类分离的海绵体和海绵体中研究了速激肽产生的运动效应。在静态制剂中,神经激肽A引起的强力收缩(分别为pD2 = 8.3-7.9)被NK2受体选择性拮抗剂nepadutant阻止,而[Sar9] SP砜和senktide(NK1和NK3受体选择性激动剂)没有产生作用或产生了多余的收缩。在KCl预收缩的海绵体肽(pD2 = 7.1)和[Sar9] SP砜(pD2 = 7.7)中,产生了河豚毒素抗性松弛,被速激肽NK1受体选择性拮抗剂SR 140333废除。[Sar9] SP砜(1μm)。在预收缩的海绵体中产生了类似的松弛。电场刺激(EFS)引起河豚毒素敏感的弛豫,这是[Sar9] SP砜产生的弛豫的补充。 Nω-硝基-L-精氨酸(L-NOARG)完全阻止了[Sar9] SP砜和EFS诱导的弛豫。这些结果表明速激肽NK1和NK2受体在人的阴茎组织中介导相反的运动作用,表明速激肽对这些器官的平滑肌张力可能具有调节作用。

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