Christenson W R, Reddy V R, Piper W N
Life Sci. 1986 May 5;38(18):1679-84. doi: 10.1016/0024-3205(86)90412-1.
The ability of rat hepatic uroporphyrinogen cosynthase to direct formation of uroporphyrinogen III and the synthesis of uroporphyrinogen in vitro was impaired by sulfamerazine. Inhibition was reversed by the addition of folic acid. Administration of a single, oral dose (1 g/kg) of sulfamerazine to rats was associated with elevated levels of hepatic uroporphyrin I isomer. These results suggest that sulfonamides may interfere with the biosynthesis of uroporphyrinogen III.
磺胺甲基嘧啶损害了大鼠肝脏尿卟啉原合酶在体外指导尿卟啉原III形成及尿卟啉原合成的能力。添加叶酸可逆转这种抑制作用。给大鼠单次口服剂量为1克/千克的磺胺甲基嘧啶后,肝脏尿卟啉I异构体水平升高。这些结果表明,磺胺类药物可能会干扰尿卟啉原III的生物合成。