Takehana Y, Kikuchi S, Hara K, Hamano S, Komatsu H, Ujiie A, Okegawa T, Ikeda S
Research Laboratories, Kissei Pharmaceutical Co., Ltd., Matsumoto, Japan.
Nihon Yakurigaku Zasshi. 1990 Mar;95(3):121-30. doi: 10.1254/fpj.95.121.
We studied the effects of OKY-046 on type I allergic reactions. OKY-046 (100 mg/kg) given orally suppressed antigen-induced bronchoconstriction and TXB2 generation in broncho alveolar lavage fluid in rats passively sensitized with anti-DNP-As monoclonal IgE. At the dose of 30 mg/kg given intraduodenally, it also inhibited antigen-induced bronchoconstriction in guinea pigs passively sensitized with anti DNP-As serum and actively sensitized with ovalbumin. However, aspirin (30 mg/kg) didn't suppressed them significantly. Azelastine (10 mg/kg) inhibited bronchoconstriction in passively sensitized rats and actively sensitized guinea pigs. In 48 hour homologous PCA reactions of rats and mice, oral administration of OKY-046 (300 mg/kg) and tranilast (100 mg/kg) suppressed the extravasated dye in the skin. OKY-046 decreased histamine release from passively sensitized rat peritoneal exudate cells. There was no effect of OKY-046 on SRS-A and leukotriene release from actively sensitized guinea pig lungs and passively sensitized rats. In conclusion, we think that OKY-046 should be an useful asthmatic drug or anti-allergic drug by oral administration.
我们研究了OKY-046对I型过敏反应的影响。口服给予OKY-046(100毫克/千克)可抑制用抗DNP-As单克隆IgE被动致敏的大鼠抗原诱导的支气管收缩以及支气管肺泡灌洗液中TXB2的生成。十二指肠内给予30毫克/千克剂量时,它也能抑制用抗DNP-As血清被动致敏并用卵清蛋白主动致敏的豚鼠的抗原诱导支气管收缩。然而,阿司匹林(30毫克/千克)对其抑制作用不显著。氮卓斯汀(10毫克/千克)可抑制被动致敏大鼠和主动致敏豚鼠的支气管收缩。在大鼠和小鼠48小时的同种PCA反应中,口服给予OKY-046(300毫克/千克)和曲尼司特(100毫克/千克)可抑制皮肤中渗出的染料。OKY-046可减少被动致敏大鼠腹腔渗出细胞中组胺的释放。OKY-046对主动致敏豚鼠肺和被动致敏大鼠中SRS-A和白三烯的释放没有影响。总之,我们认为口服OKY-046应该是一种有用的平喘药或抗过敏药。