Gatti S, Coutts A, Francis D, Greaves M W
Br J Dermatol. 1980 Dec;103(6):671-7. doi: 10.1111/j.1365-2133.1980.tb01691.x.
The antagonistic activity of oxatomide, and its effects on evoked histamine release and histamine-N-methyl transferase activity in skin, have been studied. Oxatomide antagonizes H1 activity in a dose-dependent but non-competitive manner. It also shows some atropine-like activity. Oxatomide did not cause detectable inhibition of antigen-stimulated histamine release from skin slices of sensitized guinea-pigs although the possibility that oxatomide may cause weak inhibition could not be excluded. In the presence of low concentrations of histamine, oxatomide suppressed human skin histamine-N-methyl transferase, but in the presence of higher substrate concentrations it enhanced activity of this enzyme. These observations, which were limited by the poor solubility of oxatomide in aqueous media, should encourage further in vivo studies of oxatomide's histamine-suppressing properties in the human subjects.
已对奥沙米特的拮抗活性及其对皮肤中组胺释放和组胺 - N - 甲基转移酶活性的影响进行了研究。奥沙米特以剂量依赖性但非竞争性方式拮抗H1活性。它还表现出一些阿托品样活性。尽管不能排除奥沙米特可能产生微弱抑制作用的可能性,但它并未对致敏豚鼠皮肤切片中抗原刺激的组胺释放产生可检测到的抑制作用。在低浓度组胺存在下,奥沙米特抑制人皮肤组胺 - N - 甲基转移酶,但在较高底物浓度存在下,它增强了该酶的活性。这些观察结果受奥沙米特在水性介质中溶解度差的限制,应鼓励对奥沙米特在人体中的组胺抑制特性进行进一步的体内研究。