Chen Z R, Irvine R J, Bochner F, Somogyi A A
Department of Clinical and Experimental Pharmacology, University of Adelaide, Australia.
Life Sci. 1990;46(15):1067-74. doi: 10.1016/0024-3205(90)90415-n.
The O-demethylation of codeine to morphine was demonstrated in rat brain homogenate. Maximal formation occurred at 10 minutes, with a Vmax of 5.93 +/- 0.16 nmol/g brain/h and Km of 37.82 +/- 4.99 microM. The formation was significantly (P less than 0.05) greater in the microvessel-rich brain fraction. Intraperitoneal injection of codeine in the rat resulted in brain concentrations of morphine which could not be solely attributed to transfer of morphine from the blood stream across the blood-brain barrier. Morphine formed in the brain after codeine administration may be an important mechanism for codeine-induced analgesia.
在大鼠脑匀浆中证实了可待因向吗啡的O-去甲基化。最大生成量在10分钟时出现,Vmax为5.93±0.16 nmol/g脑/小时,Km为37.82±4.99 microM。在富含微血管的脑部分中生成量显著更高(P<0.05)。给大鼠腹腔注射可待因后,脑内吗啡浓度不能完全归因于吗啡从血流穿过血脑屏障的转运。可待因给药后在脑内形成的吗啡可能是可待因诱导镇痛的重要机制。