Ainz L F, Casis E, de Gandarias J M, Gil-Rodrigo C E, Goiriena de Gandarias J J
Br J Pharmacol. 1983 Jun;79(2):373-8. doi: 10.1111/j.1476-5381.1983.tb11009.x.
A water-soluble splenic factor, which produces a contractile response of the guinea-pig ileum, that is resistant to cholinoceptor and adrenoceptor antagonists is described. The ileal contractions elicited by the splenic extract showed some significant differences from those elicited by 5-hydroxytryptamine. The responses to splenic extract were not affected by the D-tryptamine-receptor antagonist, methysergide. The effect of the splenic extract on the guinea-pig ileum was similar to that of histamine. The H1-histamine antagonists, (+)-chloropheniramine and diphenhydramine, caused a parallel shift to the right of the splenic extract dose-response curve without suppression of the maximum response. A pA2 value of 8.97 +/- 0.03 for (+)-chloropheniramine and 7.55 +/- 0.1 for diphenhydramine was calculated. Significant histamine levels, as determined by fluorometric methods, could not be detected in the splenic extract. Likewise, the splenic factor did not release histamine from the intestinal preparation. These results support the view that: (i) the splenic factor acts through H1-histamine receptors; (ii) it is not histamine; (iii) it does not have any histamine releasing effect on the ileal smooth muscle.
本文描述了一种水溶性脾因子,它能引起豚鼠回肠的收缩反应,且对胆碱能受体和肾上腺素能受体拮抗剂具有抗性。脾提取物引起的回肠收缩与5-羟色胺引起的收缩有一些显著差异。脾提取物的反应不受D-色胺受体拮抗剂美西麦角的影响。脾提取物对豚鼠回肠的作用与组胺相似。H1组胺拮抗剂(+)-氯苯那敏和苯海拉明使脾提取物剂量反应曲线平行右移,而不抑制最大反应。计算出(+)-氯苯那敏的pA2值为8.97±0.03,苯海拉明的pA2值为7.55±0.1。通过荧光法测定,在脾提取物中未检测到显著的组胺水平。同样,脾因子也不会从肠道制剂中释放组胺。这些结果支持以下观点:(i)脾因子通过H1组胺受体起作用;(ii)它不是组胺;(iii)它对回肠平滑肌没有任何组胺释放作用。