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肝脏过氧化物酶体增殖:由两种结构上与氯贝丁酯无关的新型化合物诱导产生。

Hepatic peroxisome proliferation: induction by two novel compounds structurally unrelated to clofibrate.

作者信息

Reddy J K, Krishnakantha T P

出版信息

Science. 1975 Nov 21;190(4216):787-9. doi: 10.1126/science.1198095.

Abstract

Two hypolipidemic compounds [ 4-chloro-6(2,3-xylidino)-2-pyrimidinyl-thio] acetic acid, and 2-chloro-5(3,5-dimethylpiperidinosufony)benzoic acid (tibric acid) greatly increased the number of peroxisomes (microbodies) in liver cells of rats and mice. This augmented peroxisome population was accompanied by significant elevation of liver catalase activity. These two hypolipidemic peroxisome proliferators are structurally different from ethyl a-p-chlorophenozyisobutyrate (clofibrate) and other hypolipidemic, arylocyisobutyrate derivatives which cause hepatic peroxisome proliferation. Induction of peroxisome proliferation by these structurally unrelated hypolipidemic compounds suggests a possible relation between hepatic peroxisome proliferation and hypolipidemia.

摘要

两种降血脂化合物,即[4-氯-6(2,3-二甲苯胺基)-2-嘧啶基硫代]乙酸和2-氯-5(3,5-二甲基哌啶磺酰基)苯甲酸(吉非贝齐),可显著增加大鼠和小鼠肝细胞中过氧化物酶体(微体)的数量。过氧化物酶体数量的增加伴随着肝脏过氧化氢酶活性的显著升高。这两种降血脂的过氧化物酶体增殖剂在结构上与α-对氯苯氧异丁酸乙酯(氯贝丁酯)及其他引起肝脏过氧化物酶体增殖的降血脂芳基异丁酸衍生物不同。这些结构不相关的降血脂化合物诱导过氧化物酶体增殖,提示肝脏过氧化物酶体增殖与降血脂之间可能存在关联。

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