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5-羟色胺对大鼠阴茎勃起功能的抑制作用。

Inhibitory effect of 5-hydroxytryptamine on penile erectile function in the rat.

作者信息

Finberg J P, Vardi Y

机构信息

Rappaport Family Institute for Research in the Medical Sciences, Technion, Haifa, Israel.

出版信息

Br J Pharmacol. 1990 Nov;101(3):698-702. doi: 10.1111/j.1476-5381.1990.tb14143.x.

Abstract
  1. An increase in corporal pressure was elicited in pithed rats by stimulation of the sacral part of the spinal cord. This response was inhibited by intravenous injection of 5-hydroxytryptamine (5-HT) (ED50 = 28.5 +/- 2.2 micrograms kg-1). 2. The inhibitory effect of 5-HT was blocked by methysergide and methiothepin (each 1 mg kg-1), but not by ketanserin (0.02 mg kg-1), MDL 72222 (1 mg kg-1) or prazosin (0.1 mg kg-1). 3. An inhibitory effect on the corporal pressure response to spinal stimulation was also produced by 5-carboxyamidotryptamine (ED50 = 5.6 +/- 2.8 micrograms kg-1), but not by m-chlorophenylpiperazine (mCPP), RU 24969, 8-hydroxy-2-[di-n-propyl-amino]-tetralin (8-OH-DPAT) or fenfluramine (doses up to 1-2 mg kg-1). 4. Neither methiothepin (1 mg kg-1) nor clomipramine (1 mg kg-1) had any effect on the frequency-response curve for increase in corporal pressure by spinal stimulation. 5. The results indicate that 5-HT exerts an inhibitory action on penile erection by a peripheral mechanism. This effect may be mediated by vasoconstriction in cavernosal vessels, or inhibition of release of a vasodilator neurotransmitter. From the spectrum of agonist and antagonist responses, the receptor involved may be of the 5-HT1D subtype.
摘要
  1. 通过刺激脊髓骶部在去大脑大鼠中引发体压升高。静脉注射5-羟色胺(5-HT)(半数有效量=28.5±2.2微克/千克)可抑制此反应。2. 5-HT的抑制作用被麦角新碱和甲硫噻嗪(各1毫克/千克)阻断,但未被酮色林(0.02毫克/千克)、MDL 72222(1毫克/千克)或哌唑嗪(0.1毫克/千克)阻断。3. 5-羧酰胺色胺(半数有效量=5.6±2.8微克/千克)也对脊髓刺激引起的体压反应产生抑制作用,但间氯苯哌嗪(mCPP)、RU 24969、8-羟基-2-[二正丙基氨基]-四氢萘(8-OH-DPAT)或芬氟拉明(剂量高达1-2毫克/千克)则无此作用。4. 甲硫噻嗪(1毫克/千克)和氯米帕明(1毫克/千克)对脊髓刺激引起的体压升高的频率-反应曲线均无影响。5. 结果表明,5-HT通过外周机制对阴茎勃起发挥抑制作用。此效应可能由海绵体血管收缩或抑制血管舒张性神经递质释放介导。从激动剂和拮抗剂反应谱来看,所涉及的受体可能是5-HT1D亚型。

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