Feniuk W, Humphrey P P, Watts A D
Br J Pharmacol. 1979 Oct;67(2):247-54. doi: 10.1111/j.1476-5381.1979.tb08673.x.
1 The effect of 5-hydroxytryptamine on contractile responses to sympathetic nerve stimulation has been studied in the dog isolated saphenous vein.2 Electrical stimulation (0.1 to 10 Hz) of dog saphenous vein strips produced frequency-dependent contractions. Contractions produced by stimulation at 2 Hz were almost completely blocked by tetrodotoxin (3.1 x 10(-8) mol/l) or phentolamine (5.0 x 10(-6) mol/l) but mecamylamine (5.0 x 10(-6) mol/l) had little effect. This suggests that the contractions were mediated predominantly through noradrenaline release from postganglionic noradrenergic nerves.3 Contractions produced by intermittent electrical stimulation at 2 Hz were inhibited by 5-hydroxy-tryptamine (1.0 x 10(-9) to 1.0 x 10(-7) mol/l) in a concentration-dependent manner whilst contractions induced by exogenous noradrenaline were not affected.4 The inhibitory action of 5-hydroxytryptamine was most marked at low frequencies of stimulation and with low pulse numbers.5 High external calcium concentrations (3.9 and 5.2 x 10(-3) mol/l) reduced the inhibitory action of 5-hydroxytryptamine.6 Cyproheptadine (1.0 x 10(-8) mol/l to 1.0 x 10(-6) mol/l) or morphine (1.0 x 10(-7) mol/l to 1.0 x 10(-5) mol/l) did not antagonize the inhibitory action of 5-hydroxytryptamine. Methysergide (1.0 x 10(-7) mol/l) slightly reduced the contractions produced by electrical stimulation and only weakly antagonized the action of 5-hydroxytryptamine.7 It is suggested that a 5-hydroxytryptamine receptor exists presynaptically in the dog isolated saphenous vein strip and that stimulation of this receptor by low concentrations of 5-hydroxytryptamine inhibits the release of noradrenaline from noradrenergic nerves. This receptor type is resistant to blockade by ;classical' 5-hydroxytryptamine antagonists.
已在犬离体隐静脉中研究了5-羟色胺对交感神经刺激所致收缩反应的影响。
对犬隐静脉条进行电刺激(0.1至10赫兹)可产生频率依赖性收缩。2赫兹刺激所产生的收缩几乎完全被河豚毒素(3.1×10⁻⁸摩尔/升)或酚妥拉明(5.0×10⁻⁶摩尔/升)阻断,但美加明(5.0×10⁻⁶摩尔/升)几乎没有作用。这表明收缩主要是通过节后去甲肾上腺素能神经释放去甲肾上腺素介导的。
2赫兹间歇性电刺激所产生的收缩被5-羟色胺(1.0×10⁻⁹至1.0×10⁻⁷摩尔/升)以浓度依赖性方式抑制,而外源性去甲肾上腺素所诱导的收缩则不受影响。
5-羟色胺的抑制作用在低刺激频率和低脉冲数时最为明显。
高细胞外钙浓度(3.9和5.2×10⁻³摩尔/升)可降低5-羟色胺的抑制作用。
赛庚啶(1.0×10⁻⁸至1.0×10⁻⁶摩尔/升)或吗啡(1.0×10⁻⁷至1.0×10⁻⁵摩尔/升)不能拮抗5-羟色胺的抑制作用。麦角新碱(1.0×10⁻⁷摩尔/升)可轻微降低电刺激所产生的收缩,且仅微弱拮抗5-羟色胺的作用。
提示犬离体隐静脉条中存在一种5-羟色胺受体,低浓度的5-羟色胺刺激该受体可抑制去甲肾上腺素能神经释放去甲肾上腺素。这种受体类型对“经典”5-羟色胺拮抗剂的阻断具有抗性。