Yoshitomi I, Oishi R, Itoh Y, Saeki K, Senoo Y, Teramoto S
Department of Pharmacology, Okayama University Medical School, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 1989 May;339(5):528-32. doi: 10.1007/BF00167256.
alpha-Fluoromethylhistidine (alpha-FMH; 65 mg/kg, i.p.), a specific inhibitor of histidine decarboxylase, significantly decreased the histamine content of the rat right atrium in a time-dependent manner; the maximal decrease of 22.2% was observed 4 h after injection. However, alpha-FMH had no significant effect on the histamine content of the left atrium or the ventricles. The alpha-FMH-induced decrease in the right atrial histamine content was not observed in rats pretreated with 6-hydroxydopamine (25 mg/kg, i.p.). Two i.p. injections of 10 and 5 mg/kg of propranolol and the cardioselective beta 1-adrenoceptor antagonist metoprolol almost completely inhibited the alpha-FMH-induced histamine decrease. On the other hand, phentolamine (10 mg/kg, i.p.) had no influence on the histamine-decreasing action of alpha-FMH. These results suggest that in the rat right atrium there is a histamine pool where a rapid turnover of histamine is maintained by normal sympathetic activity.
α-氟甲基组氨酸(α-FMH;65毫克/千克,腹腔注射),一种组氨酸脱羧酶的特异性抑制剂,以时间依赖性方式显著降低大鼠右心房的组胺含量;注射后4小时观察到最大降幅为22.2%。然而,α-FMH对左心房或心室的组胺含量没有显著影响。在用6-羟基多巴胺(25毫克/千克,腹腔注射)预处理的大鼠中未观察到α-FMH引起的右心房组胺含量降低。两次腹腔注射10毫克/千克和5毫克/千克的普萘洛尔以及心脏选择性β1-肾上腺素能受体拮抗剂美托洛尔几乎完全抑制了α-FMH引起的组胺降低。另一方面,酚妥拉明(10毫克/千克,腹腔注射)对α-FMH的组胺降低作用没有影响。这些结果表明,在大鼠右心房中存在一个组胺池,正常的交感神经活动维持着组胺的快速周转。