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Effects of nociceptin and endomorphin 1 on the electrically stimulated human vas deferens.

机译:伤害感受肽和内啡肽1对电刺激的人输精管的作用。

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摘要

AIMS: To examine the effects of nociceptin (NC) and endomorphin 1 (EM1) on electrical field stimulation (EFS)-induced contractions of the human vas deferens (hVD). METHODS: Concentration-response curves to NC and EM1 were constructed in the absence and in presence of peptidase inhibitors (PI). In some experiments a NC receptor antagonist, [Phe1psi(CH2-NH)Gly2]NC(1-13)NH2 [F/G], 10 microM) or naloxone (1 microM) were included. RESULTS: All data are mean(95%CI). In the presence of PI, NC inhibited twitches (Emax = 67(44,90)%; pEC50 = 7.28(6.95,7.61)). NC inhibition was sensitive to [F/G]. EM1 also inhibited twitches both in the absence (Emax = 82(73,91)% pEC50 = 7.07(6.92,7.22)) and presence (Emax = 83(76,90)%; pEC50 = 7.00(6.91, 7.09)) of PI. EM1 inhibition was sensitive to naloxone. CONCLUSIONS: These data suggest that hVD express NC and opioid receptors that inhibit neurogenic contractions.
机译:目的:研究伤害感受素(NC)和内啡肽1(EM1)对电场刺激(EFS)诱导的人输精管(hVD)收缩的影响。方法:在不存在和存在肽酶抑制剂(PI)的情况下,建立了对NC和EM1的浓度-响应曲线。在某些实验中,还包括NC受体拮抗剂[Phe1psi(CH2-NH)Gly2] NC(1-13)NH2 [F / G],10 microM)或纳洛酮(1 microM)。结果:所有数据均为均值(95%CI)。在存在PI的情况下,NC抑制抽搐(Emax = 67(44,90)%; pEC50 = 7.28(6.95,7.61))。 NC抑制对[F / G]敏感。 EM1还可以在不存在(Emax = 82(73,91)%pEC50 = 7.07(6.92,7.22))和存在(Emax = 83(76,90)%; pEC50 = 7.00(6.91,7.09))的情况下抑制抽搐。 PI。 EM1抑制对纳洛酮敏感。结论:这些数据表明hVD表达抑制神经源性收缩的NC和阿片样物质受体。

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