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Crohn's Disease Is Associated with Decreased CYP3A4 and P-Glycoprotein Protein Expression. | LitMetric

AI Article Synopsis

  • - CYP3A4 and P-glycoprotein (P-gp) are key proteins that help metabolize and transport about 50% of medications and work together in the intestines to limit the absorption of drugs.
  • - Crohn's disease (CD) damages the intestinal barrier, potentially affecting how drugs are metabolized and transported in patients with the condition.
  • - A study showed that individuals with CD had significantly lower levels of CYP3A4 and P-gp in their intestines, which could influence drug dosing and effectiveness for these patients.

Article Abstract

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.

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Source
http://dx.doi.org/10.1021/acs.molpharmaceut.9b00459DOI Listing

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