Reddy J K, Azarnoff D L, Sirtori C R
Arch Int Pharmacodyn Ther. 1978 Jul;234(1):4-14.
Administration of BR-931, an ethanolamine derivative of Wy-14,643 [4-chloro-6-(2,3-xylidino)-2-pyrimidinythio]acetic acid, at a dietary concentration of 0.125% for 3 weeks 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 All these hepatic effects were reversible when the drugs were withdrawn from the diet.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.
以0.125%的膳食浓度给雄性F-344大鼠喂食BR-931(Wy-14,643 [4-氯-6-(2,3-二甲基苯胺基)-2-嘧啶硫基]乙酸的乙醇胺衍生物)3周,导致肝脏显著肿大。肝肿大似乎是由于肝细胞增生和肥大,部分原因是过氧化物酶体和平滑内质网增殖。肝过氧化氢酶和肉碱乙酰转移酶活性与过氧化物酶体增殖相关显著增加。BR-931诱导的肝肿大和过氧化物酶体增殖程度与喂食等量Wy-14,643所导致的相当。当从饮食中撤去药物时,所有这些肝脏效应都是可逆的。鉴于肝脏过氧化物酶体增殖与低脂血症之间经常存在关联,筛选新化合物的肝脏过氧化物酶体增殖情况以及过氧化物酶体相关酶的增加情况,可能被证明是评估它们作为降血脂药物效力的一种辅助手段。