Nishimaki-Mogami T, Takahashi A, Toyoda K, Hayashi Y
National Institute of Hygienic Sciences, Tokyo, Japan.
Biochem J. 1993 Oct 1;295 ( Pt 1)(Pt 1):217-20. doi: 10.1042/bj2950217.
The capability of (4R)-4-(2,3,4,6,6a beta,7,8,9,9a alpha,9b beta-decahydro-6a beta-methyl-3-oxo-1H-cyclopental[f]quinolin-7 beta-yl)valeric acid (DCQVA), a catabolite of cholic acid produced by enterobacteria, to induce peroxisome proliferation in vivo and in vitro was studied. Rats given 0.3% DCQVA in the diet for 2 weeks showed marked increases in peroxisomal beta-oxidation, mitochondrial 2,4-dienoyl-CoA reductase and microsomal laurate omega-oxidation activities in the liver compared with control rats given the diet without DCQVA. Cultured rat hepatocytes treated with DCQVA for 72 h also exhibited greatly enhanced beta-oxidation activity. The increased activity was concentration-dependent and the effective concentrations were comparable with those of clofibric acid that produced the same degree of induction in the assay. The results demonstrate that DCQVA is a potent peroxisome proliferator that occurs naturally in rat intestine.
研究了由肠道细菌产生的胆酸分解代谢物(4R)-4-(2,3,4,6,6aβ,7,8,9,9aα,9bβ-十氢-6aβ-甲基-3-氧代-1H-环戊烷并[f]喹啉-7β-基)戊酸(DCQVA)在体内和体外诱导过氧化物酶体增殖的能力。与给予不含DCQVA饮食的对照大鼠相比,给予含0.3%DCQVA饮食2周的大鼠肝脏中过氧化物酶体β-氧化、线粒体2,4-二烯酰辅酶A还原酶和微粒体月桂酸ω-氧化活性显著增加。用DCQVA处理72小时的培养大鼠肝细胞也表现出大大增强的β-氧化活性。活性增加呈浓度依赖性,有效浓度与在该测定中产生相同诱导程度的氯贝酸相当。结果表明,DCQVA是一种在大鼠肠道中天然存在的强效过氧化物酶体增殖剂。