Administration of BR 931, an ethanolamine derivative of Wy 14,643 [4-chloro-6-(2,3 xylidino)-2-pyrimidinylthio]acetic acid, at a dietary concentration of 0.125% for 3 wk to male F 344 rats, resulted in a significant enlargement of the liver. The hepatomegaly appeared to be due to liver cell hyperplasia and hypertrophy resulting, in part, from peroxisome and smooth endoplasmic reticulum proliferation. The hepatic catalase and carnitine acetyltransferase activities increased significantly in association with peroxisome proliferation. The hepatomegaly and peroxisome proliferation induced by BR 931 were comparable in degree to those resulting from feeding of an equivalent dose of Wy 14,643. All these hepatic effects were reversible when the drugs were withdrawn from the diet. Screening of new compounds for hepatic peroxisome proliferation and for increases in peroxisome associated enzymes may prove to be an adjunct to evaluating their potency as hypolipidemic agents, in view of frequent association between hepatic peroxisome proliferation and hypolipidemia.

Hepatic peroxisome proliferation: induction by BR-931, a hypolipidemic analog of WY-14,643 / J. Reddy, D.L. Azarnoff, C.R. Sirtori. - In: ARCHIVES INTERNATIONALES DE PHARMACODYNAMIE ET DE THERAPIE. - ISSN 0003-9780. - 234:1(1978), pp. 4-14.

Hepatic peroxisome proliferation: induction by BR-931, a hypolipidemic analog of WY-14,643

C.R. Sirtori
Ultimo
1978

Abstract

Administration of BR 931, an ethanolamine derivative of Wy 14,643 [4-chloro-6-(2,3 xylidino)-2-pyrimidinylthio]acetic acid, at a dietary concentration of 0.125% for 3 wk to male F 344 rats, resulted in a significant enlargement of the liver. The hepatomegaly appeared to be due to liver cell hyperplasia and hypertrophy resulting, in part, from peroxisome and smooth endoplasmic reticulum proliferation. The hepatic catalase and carnitine acetyltransferase activities increased significantly in association with peroxisome proliferation. The hepatomegaly and peroxisome proliferation induced by BR 931 were comparable in degree to those resulting from feeding of an equivalent dose of Wy 14,643. All these hepatic effects were reversible when the drugs were withdrawn from the diet. Screening of new compounds for hepatic peroxisome proliferation and for increases in peroxisome associated enzymes may prove to be an adjunct to evaluating their potency as hypolipidemic agents, in view of frequent association between hepatic peroxisome proliferation and hypolipidemia.
Settore BIO/14 - Farmacologia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/203778
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