NORCOCAINE AND N-HYDROXYNORCOCAINE FORMATION IN HUMAN LIVER-MICROSOMES - ROLE OF CYTOCHROME-P-450-3A4

被引:59
作者
LEDUC, BW
SINCLAIR, PR
SHUSTER, L
SINCLAIR, JF
EVANS, JE
GREENBLATT, DJ
机构
[1] TUFTS UNIV,SCH MED,DEPT PHARMACOL & EXPTL THERAPEUT,136 HARRISON AVE,BOSTON,MA 02111
[2] TUFTS UNIV,SCH MED,DEPT BIOCHEM,BOSTON,MA 02111
[3] VET ADM MED CTR,WHITE RIVER JCT,VT
[4] DARTMOUTH COLL,HITCHCOCK MED CTR,DARTMOUTH MED SCH,HANOVER,NH 03756
[5] EUNICE KENNEDY SHRIVER CTR MENTAL RETARDAT INC,WALTHAM,MA
关键词
COCAINE; NORCOCAINE; N-HYDROXYNORCOCAINE; CYTOCHROME-P-450; 3A4; HEPATOTOXICITY;
D O I
10.1159/000139058
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:294 / 300
页数:7
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