Prevention of atherosclerotic lesion development in mice by taurine

The antiatherosclerotic effects of taurine were evaluated in two murine models. In C57BL/6J mice fed a high-fat diet, 6-month treatment with taurine decreased serum atherogenic low-density lipoprotein (LDL) and very low-density lipoprotein (VLDL) cholesterol by 44%. The same treatment increased antiatherogenic high-density lipoprotein (HDL) cholesterol by 25%. Hepatic cholesterol content was also decreased by taurine. Taurine improved the area of oil red O positive arterial lipid accumulation by 20%. Hepatic cholesterol 7 alpha-hydroxylase activity, a rate-limiting enzyme of bile acid synthesis from cholesterol, was doubled in taurine-treated mice, suggesting stimulation of cholesterol catabolism to bile acid as the cholesterol-lowering mechanism seen with taurine. Thus, taurine prevented the progression of atherosclerotic lesions, and concomitantly improved the serum lipoprotein profile. In another murine model, in apolipoprotein-E-deficient mice fed regular chow, a 3-month treatment with taurine prevented accumulation of arterial lipids by 31%, despite a significant increase in serum LDL and VLDL cholesterol levels. Serum thiobarbituric acid reactive substances (TBARS) in apolipoprotein-E-deficient mice were significantly higher than those in wild type mice and treatment with taurine lowered serum TBARS level by 26%. Thus, taurine prevents the development of atherosclerotic lesions and this antioxidative effect may play an important role in the antiatherosclerotic effect that is unrelated to serum cholesterol levels.