Leurs R, Smit M J, Bast A, Timmerman H
Department of Pharmacochemistry, Faculty of Chemistry, Vrije Universiteit, Amsterdam, The Netherlands.
Eur J Pharmacol. 1991 Apr 24;196(3):319-22. doi: 10.1016/0014-2999(91)90446-w.
Prolonged exposure of the guinea-pig intestinal longitudinal smooth muscle to histamine caused homologous desensitization of the H1 receptor, which led to reduced H1 receptor-mediated production of [3H]inositol phosphates as well as to reduced H1 agonist-induced contractions. [3H]Mepyramine binding studies showed that desensitization affected neither the agonist affinity nor the number of H1 receptors. Combining the data from the binding studies and the contraction measurements it was found that desensitization results in a selective reduction of agonist efficacy.
豚鼠肠道纵行平滑肌长时间暴露于组胺会导致H1受体的同源脱敏,这会导致H1受体介导的[3H]肌醇磷酸生成减少以及H1激动剂诱导的收缩减弱。[3H]美吡拉敏结合研究表明,脱敏既不影响激动剂亲和力,也不影响H1受体的数量。结合结合研究和收缩测量的数据发现,脱敏导致激动剂效能选择性降低。