Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
Toxicol Sci. 2011 Oct;123(2):359-67. doi: 10.1093/toxsci/kfr177. Epub 2011 Jul 11.
Feeding bile acids (BAs) to rodents has been used to study BA signaling and toxicity in vivo. However, little is known about the effect of feeding BAs on the concentrations of BAs in serum and liver as well as the dose of the fed BAs that causes liver toxicity. The present study was designed to investigate the relative hepatotoxicity of individual BAs by feeding mice cholic acid (CA), chenodeoxycholic acid (CDCA), deoxycholic acid (DCA), lithocholic acid (LCA), or ursodeoxycholic acid (UDCA) at concentrations of 0.01, 0.03, 0.1, 0.3, 1.0, or 3% in their diet for 7 days. The data demonstrate that (1) the ability of the fed BAs to produce hepatotoxicity is UDCA<CA<CDCA<DCA<LCA; (2) the lowest concentration of each BA in the feed that causes hepatotoxicity in mice is CA and CDCA at 0.3%, DCA at 0.1%, and LCA at 0.03%; (3) BA feeding results in a dose-dependent increase in the total serum BA concentrations but had little effect on liver total BA concentrations; (4) hepatotoxicity of the fed BAs does not simply depend on the concentration or hydrophobicity of total BAs in the liver; and (5) liver BA-conjugation enzymes are saturated by feeding UDCA at concentrations higher than 0.3%. In conclusion, the findings of the present study provide guidance for choosing the feeding concentrations of BAs in mice and will aid in interpreting BA hepatotoxicity as well as BA-mediated gene regulation.
给啮齿动物喂食胆酸(BAs)已被用于研究体内 BA 信号转导和毒性。然而,对于喂食 BAs 对血清和肝脏中 BAs 浓度的影响以及引起肝毒性的喂食 BAs 剂量知之甚少。本研究旨在通过在饮食中以 0.01、0.03、0.1、0.3、1.0 或 3%的浓度分别给小鼠喂食胆酸(CA)、鹅去氧胆酸(CDCA)、脱氧胆酸(DCA)、石胆酸(LCA)或熊去氧胆酸(UDCA)来研究单个 BAs 的相对肝毒性,连续喂食 7 天。数据表明:(1)喂食 BAs 产生肝毒性的能力为 UDCA<CA<CDCA<DCA<LCA;(2)引起小鼠肝毒性的每种 BA 饲料中的最低浓度分别为 CA 和 CDCA 为 0.3%,DCA 为 0.1%,LCA 为 0.03%;(3)BA 喂养导致总血清 BA 浓度呈剂量依赖性增加,但对肝脏总 BA 浓度影响不大;(4)喂食 BAs 的肝毒性并不简单取决于肝脏中总 BA 的浓度或疏水性;(5)当 UDCA 的喂食浓度高于 0.3%时,肝 BA 结合酶会饱和。总之,本研究的结果为选择小鼠中 BAs 的喂食浓度提供了指导,并有助于解释 BA 肝毒性以及 BA 介导的基因调控。