TY - JOUR
T1 - Hepatic peroxisome proliferation
T2 - Induction by BR 931, a hypolipidemic analog of WY 14,643
AU - Reddy, J. K.
AU - Azarnoff, D. L.
AU - Sirtori, C. R.
PY - 1978
Y1 - 1978
N2 - 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 All these hepatic effects were reversible when the drugs were withdrawn from the diet.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.
AB - 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 All these hepatic effects were reversible when the drugs were withdrawn from the diet.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.
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M3 - Article
C2 - 708142
AN - SCOPUS:0018076262
SN - 0003-9780
VL - 234
SP - 4
EP - 14
JO - Archives internationales de pharmacodynamie et de therapie
JF - Archives internationales de pharmacodynamie et de therapie
IS - 1
ER -