Cortijo J, Esplugues J, Morales-Olivas F J, Rubio E
Eur J Pharmacol. 1984 Jan 13;97(1-2):7-12. doi: 10.1016/0014-2999(84)90506-5.
The experiments concerned the effects of histamine and its analogs 4-methylhistamine and 2-pyridyl-ethylamine on the spontaneous activity of the estrogenized rat uterus in vivo. These agonists given intravenously inhibited uterine activity. Histamine and 4-methylhistamine, but not 2-pyridyl ethylamine, produced this effect in a dose-dependent manner. The ability of histamine to reduce uterine activity was lowered by pretreatment with reserpine, adrenalectomy or 6-hydroxydopamine. The effect of 4-methylhistamine also was reduced by reserpine or adrenalectomy. The inhibitory effect of 2-(2-pyridyl) ethylamine was completely abolished by reserpine or adrenalectomy. Cimetidine attenuated the residual inhibitory effect of histamine in reserpinized rats. These results suggest that the uterine inhibitory action of histamine and 4-methylhistamine is mediated through catecholamine release and direct stimulation of the H2-receptors. The effect of 2-(2-pyridyl) ethylamine is only mediated by release catecholamine.
这些实验研究了组胺及其类似物4-甲基组胺和2-吡啶乙胺对体内雌激素化大鼠子宫自发活动的影响。静脉注射这些激动剂会抑制子宫活动。组胺和4-甲基组胺,但不是2-吡啶乙胺,以剂量依赖的方式产生这种作用。用利血平、肾上腺切除术或6-羟基多巴胺预处理会降低组胺降低子宫活动的能力。利血平或肾上腺切除术也会降低4-甲基组胺的作用。利血平或肾上腺切除术可完全消除2-(2-吡啶基)乙胺的抑制作用。西咪替丁减弱了组胺在利血平化大鼠中的残余抑制作用。这些结果表明,组胺和4-甲基组胺对子宫的抑制作用是通过儿茶酚胺释放和对H2受体的直接刺激介导的。2-(2-吡啶基)乙胺的作用仅由儿茶酚胺释放介导。