Hishinuma Shigeru, Shoji Masaru
Department of Pharmacodynamics, Meiji Pharmaceutical University, Japan.
Yakugaku Zasshi. 2010 Mar;130(3):451-5. doi: 10.1248/yakushi.130.451.
Histamine regulates a variety of physiological or pathophysiological processes via the activation of G(q/11) protein-coupled and Ca(2+)-mobilizing histamine H(1) receptors, including smooth muscle contraction. We have found that histamine induces progression from heterologous to homologous desensitization of contraction under normal physiological conditions in smooth muscle of guinea pig taenia caeci. In this study, we characterized the development of histamine-induced desensitization under Ca(2+)-free conditions and we found that histamine developed only a homologous phase of desensitization to histamine with an increase in EC(50) values for histamine and basal tone. In contrast, histamine treatment reduced EC(50) values for a muscarinic agonist, carbachol, and depolarizing high K(+). These results suggest that the failure of excess histamine to induce a normal Ca(2+) response under Ca(2+)-free conditions may lead to homologous desensitization to histamine with apparent hyper-reactivity of smooth muscles to cholinergic and depolarizing stimuli. We estimate that this characteristic of histamine to change smooth muscle contractility may be potentially involved in its physiological and pathophysiological aspects, including histamine-induced allergic conditions, depending on cellular circumstances.
组胺通过激活G(q/11)蛋白偶联和钙动员的组胺H(1)受体来调节多种生理或病理生理过程,包括平滑肌收缩。我们发现,在正常生理条件下,组胺可诱导豚鼠盲肠带平滑肌收缩从异源脱敏发展为同源脱敏。在本研究中,我们对无钙条件下组胺诱导的脱敏发展进行了表征,发现组胺仅产生了对组胺的同源脱敏阶段,组胺的半数有效浓度(EC50)值和基础张力增加。相反,组胺处理降低了毒蕈碱激动剂卡巴胆碱和去极化高钾的EC50值。这些结果表明,在无钙条件下,过量组胺未能诱导正常的钙反应,可能导致对组胺的同源脱敏,同时平滑肌对胆碱能和去极化刺激出现明显的高反应性。我们估计,组胺改变平滑肌收缩力的这一特性可能在其生理和病理生理方面发挥潜在作用,包括组胺诱导的过敏情况,这取决于细胞环境。