Kolars J C, Lown K S, Schmiedlin-Ren P, Ghosh M, Fang C, Wrighton S A, Merion R M, Watkins P B
Department of Internal Medicine, Veterans Administration Medical Center, Ann Arbor, MI 48109.
Pharmacogenetics. 1994 Oct;4(5):247-59. doi: 10.1097/00008571-199410000-00003.
CYP3A4, a major Phase I xenobiotic metabolizing enzyme present in liver, is also present in human small bowel epithelium where it appears to catalyse significant 'first pass' metabolism of some drugs. To determine whether CYP3A4 or the related enzymes CYP3A3, CYP3A5, and CYP3A7 are present in other regions of the digestive tract, we used CYP3A-specific antibodies to examine histological sections and epithelial microsomes obtained from a human organ donor. CYP3A-related proteins were detected in epithelia throughout the digestive tract and in gastric parietal cells, in pericentral hepatocytes, and in ductular cells of the pancreas. Immunoblot analysis suggested that the major CYP3A protein present in liver, jejunum, colon, and pancreas was CYP3A4 or CYP3A3, whereas CYP3A5 was the major protein present in stomach. Both CYP3A4 and CYP3A5 mRNA were detectable in all regions of the digestive tract using the polymerase chain reaction (PCR); however, only CYP3A4 could be detected by Northern blot analysis. CYP3A7 mRNA was consistently detected only in the liver by PCR and CYP3A3 mRNA was not detected in any of the tissues. We conclude that CYP3A4 and CYP3A5 are present throughout the human digestive tract and that differences in the expression of these enzymes may account for inter-organ differences in the metabolism of CYP3A substrates.
细胞色素P450 3A4(CYP3A4)是肝脏中主要的I相异源生物代谢酶,在人小肠上皮中也有表达,它似乎能催化某些药物显著的“首过”代谢。为了确定CYP3A4或相关酶CYP3A3、CYP3A5和CYP3A7是否存在于消化道的其他区域,我们使用CYP3A特异性抗体检测了取自一名人体器官供体的组织切片和上皮微粒体。在整个消化道上皮、胃壁细胞、中央周围肝细胞和胰腺导管细胞中检测到了CYP3A相关蛋白。免疫印迹分析表明,肝脏、空肠、结肠和胰腺中存在的主要CYP3A蛋白是CYP3A4或CYP3A3,而CYP3A5是胃中存在的主要蛋白。使用聚合酶链反应(PCR)在消化道的所有区域都能检测到CYP3A4和CYP3A5的mRNA;然而通过Northern印迹分析只能检测到CYP3A4。通过PCR仅在肝脏中持续检测到CYP3A7的mRNA,在任何组织中均未检测到CYP3A3的mRNA。我们得出结论,CYP3A4和CYP3A5存在于整个人体消化道中,这些酶表达的差异可能解释了CYP3A底物代谢的器官间差异。