Mol Pharm. 2019 Sep 3;16(9):4059-4064. doi: 10.1021/acs.molpharmaceut.9b00459. Epub 2019 Aug 19.
Cytochrome P450 (CYP) 3A4 and P-glycoprotein (P-gp) have broad substrate overlap and are involved in the metabolism and transport of nearly 50% of currently prescribed medications. In the intestine, CYP3A4 and P-gp are coexpressed in the enterocytes at the intestinal villous tip and act in a coordinated manner to limit drug and xenobiotic oral bioavailability prior to further metabolism and disposition in the liver. Crohn's disease (CD), a form of inflammatory bowel disease, introduces a transmural intestinal insult that disrupts the intestinal barrier function; it therefore has the potential to affect intestinal drug metabolism and transport. We hypothesized that individuals with CD have reduced intestinal expression of CYP3A4 and P-gp. We obtained intestinal biopsy samples from individuals with and without CD and quantified the expression of CYP3A4 and P-gp. When we carried out Western analysis for protein expression, we observed a significant reduction in ileal (45% decrease) and colonic (78% decrease) CYP3A4 protein expression in subjects with CD compared with those without. Similarly, an 85% reduction in colonic P-gp protein expression was seen in the CD patients. Our data highlight important and novel findings pertaining to CD-associated changes to the intestinal expression of CYP3A4 and P-gp that are of relevance to better predict substrate drug dosing for patients with CD.
细胞色素 P450(CYP)3A4 和 P-糖蛋白(P-gp)具有广泛的底物重叠,参与近 50%的当前处方药物的代谢和转运。在肠道中,CYP3A4 和 P-gp 在肠绒毛尖端的肠上皮细胞中共同表达,并以协调的方式作用,以限制药物和外源性物质在肝脏进一步代谢和处置之前的口服生物利用度。克罗恩病(CD)是一种炎症性肠病,会造成肠壁损伤,破坏肠道屏障功能;因此,它有可能影响肠道药物代谢和转运。我们假设 CD 患者的肠道 CYP3A4 和 P-gp 表达减少。我们从 CD 患者和无 CD 患者中获取肠道活检样本,并定量检测 CYP3A4 和 P-gp 的表达。当我们进行蛋白质表达的 Western 分析时,与无 CD 患者相比,CD 患者的回肠(减少 45%)和结肠(减少 78%)CYP3A4 蛋白表达显著降低。同样,在 CD 患者中也观察到结肠 P-gp 蛋白表达降低 85%。我们的数据突出了与 CD 相关的、对 CYP3A4 和 P-gp 肠道表达的重要和新颖的发现,这与更好地预测 CD 患者的底物药物剂量有关。