Gushchin I S, Kaminka M E, Deriugin I L
Biull Eksp Biol Med. 1978 Oct;86(10):471-4.
Phenothiazines (chlorpromazine and promethazine) and antihistaminic quinuclidine derivatives [phencarol, quinuclidyl-3-di-(o-tolyl) carbinol, hydrochloride quinuclidyl-3-di-(o-methoxyphenyl) carbinol--HQMC] at concentrations preceding the histamine-releasing ones inhibited the compound 48/80-induced histamine release from the isolated rat mast cells. HQMC inhibited histamine release induced by selective liberators (compound 48/80, MCD-peptide, specific antigen), but potentiated histamine release induced by nonselective liberators (chlorpromazine, tryton X-100). The inhibition by HQMC of histamine release induced by compound 48/80 increased during 1 min and was reversible. The inhibitory effect of all the compounds tested was partially counteracted by glucose.
吩噻嗪类药物(氯丙嗪和异丙嗪)以及抗组胺奎宁环衍生物[苯卡醇、奎宁环基-3-二(邻甲苯基)甲醇、奎宁环基-3-二(邻甲氧基苯基)甲醇盐酸盐——HQMC]在释放组胺的浓度之前,可抑制化合物48/80诱导的组胺从离体大鼠肥大细胞中释放。HQMC抑制由选择性释放剂(化合物48/80、MCD肽、特异性抗原)诱导的组胺释放,但增强由非选择性释放剂(氯丙嗪、曲通X-100)诱导的组胺释放。HQMC对化合物48/80诱导的组胺释放的抑制作用在1分钟内增强且是可逆的。所测试的所有化合物的抑制作用均被葡萄糖部分抵消。