LeDuc B W, Sinclair P R, Shuster L, Sinclair J F, Evans J E, Greenblatt D J
Department of Biochemistry, Tufts University School of Medicine, Boston, MA 02111.
Pharmacology. 1993 May;46(5):294-300. doi: 10.1159/000139058.
Cocaine was metabolized to norcocaine by microsomes prepared from lymphoblastoid cells expressing transfected human P-450 3A4. The specific activities of norcocaine formation by microsomes prepared from three human liver samples correlated with the amount of P-450 3A immunoreactive protein detected by immunoblot. Triacetyloleandomycin, a specific inhibitor of P-450 3A isoforms, inhibited formation of norcocaine from cocaine, but not formation of N-hydroxynorcocaine from norcocaine. The chemical identity of the norcocaine and N-hydroxynorcocaine produced by human liver microsomes was established by combination of gas chromatography and mass spectrometry. Thus, human P-450 3A4 is a cocaine demethylase, and P-450 isoforms of the 3A family are responsible for the majority of norcocaine production by human hepatic microsomes.
可卡因在由表达转染人P - 450 3A4的淋巴母细胞制备的微粒体中代谢为去甲可卡因。从三个人类肝脏样本制备的微粒体形成去甲可卡因的比活性与免疫印迹检测到的P - 450 3A免疫反应性蛋白的量相关。三乙酰竹桃霉素,一种P - 450 3A亚型的特异性抑制剂,抑制可卡因形成去甲可卡因,但不抑制去甲可卡因形成N - 羟基去甲可卡因。通过气相色谱和质谱联用确定了人肝微粒体产生的去甲可卡因和N - 羟基去甲可卡因的化学结构。因此,人P - 450 3A4是一种可卡因脱甲基酶,3A家族的P - 450亚型是人肝微粒体产生大部分去甲可卡因的原因。