Yamamoto S, Francis D, Greaves M W
J Invest Dermatol. 1976 Dec;67(6):696-9. doi: 10.1111/1523-1747.ep12598572.
The effects of burimamide, an H2-antihistamine, on the anaphylactic reaction in the skin of ovalbumin-sensitized guinea pigs were studied in vitro. Burimamide enhanced the concentration of histamine in the supernatant fraction of antigen-challenged sensitized guinea-pig skin in a dose-related way, but did not alter the concentration of residual histamine in the skin after antigen challenge. The enhanced histamine concentration in the supernatant was not due to increased histamine synthesis by the target cells during the reaction because the increase was not inhibited by a histidine decarboxylase inhibitor, Brocresine. In further experiments it was shown that guinea-pig skin possesses potent histamine degrading enzyme activity which is inhibited by burimamide. We suggest that inhibition of these degrading enzymes leads to the increase in histamine concentration in the presence of burimamide.
研究了H2抗组胺药布立马胺对卵清蛋白致敏豚鼠皮肤过敏反应的体外作用。布立马胺以剂量相关的方式提高了抗原攻击致敏豚鼠皮肤上清液中组胺的浓度,但不改变抗原攻击后皮肤中残留组胺的浓度。上清液中组胺浓度的升高并非由于反应过程中靶细胞组胺合成增加,因为这种增加不受组氨酸脱羧酶抑制剂溴克辛的抑制。进一步实验表明,豚鼠皮肤具有强大的组胺降解酶活性,该活性受到布立马胺的抑制。我们认为,在布立马胺存在的情况下,这些降解酶的抑制导致组胺浓度升高。