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National Institute of Environmental Health Sciences

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Publication Detail

Title: Drug enterocyte adducts: possible causal factor for diclofenac enteropathy in rats.

Authors: Atchison, C R; West, A B; Balakumaran, A; Hargus, S J; Pohl, L R; Daiker, D H; Aronson, J F; Hoffmann, W E; Shipp, B K; Treinen-Moslen, M

Published In Gastroenterology, (2000 Dec)

Abstract: BACKGROUND & AIMS: Enteropathy is a frequent complication of diclofenac and other nonsteroidal anti-inflammatory drugs, yet little is known about the underlying mechanism. One possibility is that reactive metabolites of diclofenac form adducts with enterocyte macromolecules, as previously shown for liver. We addressed this possibility by using immunohistochemistry to detect diclofenac adducts. METHODS: Rats were treated orally with diclofenac (10-100 mg/kg) and killed after 1-24 hours, and their gastrointestinal (GI) tracts were evaluated for ulcer number and area. Adduct distribution and intensity were assessed by immunohistochemistry by using a technique to simultaneously process and stain multiple intestinal rings. RESULTS: Drug treatment led to dose-dependent formation of both adducts and ulcers only in small intestine and only in animals with intact enterohepatic circulation. Adducts formed within enterocytes by 1 hour, translocated to the brush border, preceded ulceration and vascular protein leakage, and were intense at sites of ulceration. Adducts and ulcers exhibited a parallel distribution within intestinal quintiles: 3rd > 5th >> 1st. CONCLUSIONS: Diclofenac treatment resulted in the formation of drug adducts in enterocytes. Because this molecular change occurred before ulceration, was dose dependent, and exhibited concordant distribution with extent of ulceration, the results suggest a causal role for drug adduct formation in diclofenac enteropathy.

PubMed ID: 11113075 Exiting the NIEHS site

MeSH Terms: Animals; Anti-Inflammatory Agents, Non-Steroidal/adverse effects*; Anti-Inflammatory Agents, Non-Steroidal/metabolism*; Bile/metabolism; Diclofenac/adverse effects*; Diclofenac/metabolism*; Dose-Response Relationship, Drug; Enterocytes/metabolism*; Intestinal Diseases/chemically induced*; Intestinal Diseases/pathology; Male; Rats; Rats, Sprague-Dawley; Time Factors; Tissue Distribution; Ulcer/chemically induced*; Ulcer/pathology

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