Elegbe R A, Oyebola D D
Biochem Exp Biol. 1979;15(1):57-60.
This study reports the quantitative effect of the H1--and H2--receptor antagonists on dextran-induced anaphylactoid oedema in rats. The findings indicate that mepyramine, promethazine and chlorpromazine which are H1--receptor antagonists significantly inhibited this anaphylactoid oedema. While on the other hand burimamide an H2--receptor antagonist at doses below 500 micrograms/kg inhibit dextran-induced oedema but at higher doses enhances oedema formation in the test rats. E.D50 values obtained for mepyramine, chlorpromazine and promethazine are 5.01 mg/kg, 0.36 mg/kg, 1.78 mg/kg respectively. The dual effects of burimamide on dextran-induced oedema merits further investigation and confirmation with the aid of other H1--and/or H2--receptor systems. A modification of the plethysmometric method of Buttle et. al. (1957) is also described.
本研究报告了H1和H2受体拮抗剂对右旋糖酐诱导的大鼠类过敏水肿的定量影响。研究结果表明,作为H1受体拮抗剂的美吡拉敏、异丙嗪和氯丙嗪显著抑制了这种类过敏水肿。另一方面,H2受体拮抗剂布立马胺在剂量低于500微克/千克时抑制右旋糖酐诱导的水肿,但在较高剂量时会增强受试大鼠的水肿形成。美吡拉敏、氯丙嗪和异丙嗪的半数有效剂量(E.D50)值分别为5.01毫克/千克、0.36毫克/千克、1.78毫克/千克。布立马胺对右旋糖酐诱导水肿的双重作用值得借助其他H1和/或H2受体系统作进一步研究和确认。本文还描述了对Buttle等人(1957年)体积描记法的改进。