Chu D, Kovacs B A
Arch Int Pharmacodyn Ther. 1975 Mar;214(1):155-64.
The effects of the newly isolated antihistamine (KC-18) from the Hungarian oak gall extracts on some actions of histamine have been investigated. Intraperitoneally administered KC-18 into guinea pigs and cats in doses of 2.5-16 mg/kg exerted a significant dose-related inhibition of histamine-induced bronchoconstriction, increase in capillary permeability and hypotension. In guinea pigs, actively sensitized with ovalbumin, 4 mg/kg KC-18 administered intraperitoneally prevented the development of anaphylactic shock following antigenic challenge. Histamine-induced gastric acid secretion in the rat was also dose-relatedly reduced by the intravenous administraton of 72 and 120 mg/kg KC-18. However, KC-18 in doses up to 100 mug/ml did not modify the histamine-induced contraction of the isolated guinea pig ileum.
对从匈牙利橡木瘿提取物中新分离出的抗组胺药(KC - 18)对组胺某些作用的影响进行了研究。以2.5 - 16毫克/千克的剂量腹腔注射KC - 18给豚鼠和猫,对组胺诱导的支气管收缩、毛细血管通透性增加和低血压产生了显著的剂量相关抑制作用。在经卵清蛋白主动致敏的豚鼠中,腹腔注射4毫克/千克的KC - 18可预防抗原攻击后过敏性休克的发生。静脉注射72和120毫克/千克的KC - 18也可剂量相关地减少大鼠组胺诱导的胃酸分泌。然而,高达100微克/毫升剂量的KC - 18并未改变组胺诱导的离体豚鼠回肠收缩。