Nishimura Naomichi, Umeda Chie, Oda Hiroaki, Yokogoshi Hidehiko
School of Food and Nutritional Sciences, The University of Shizuoka, 52-1 Yada, Shizuoka 422-8526, Japan.
J Nutr Sci Vitaminol (Tokyo). 2003 Feb;49(1):21-6. doi: 10.3177/jnsv.49.21.
The effects of taurine on serum cholesterol levels and hepatic cholesterol 7alpha-hydroxylase activity (CYP7A1) were studied in rats fed cholestyramine or high amounts of sodium cholate in order to alter the intestinal pool of bile acids. Rats were fed a diet supplemented with 1% cholesterol and 0.25% sodium cholate (high cholesterol, control; C), and C supplemented with 4% cholestyramine (CH) or 0.75% sodium cholate (BA) for 14 d. Taurine groups were fed the diet supplemented with 3% taurine (CT, CHT and BAT). Compared to rats fed C and BA diets, serum cholesterol levels were significantly reduced in rats fed CT and BAT diets, but a significant reduction of serum cholesterol by taurine feeding was not observed in the CHT group as compared to the CH group. An increase in hepatic CYP7A1 activity due to taurine intake was observed in the CT and BAT groups. However, the simultaneous administration of cholestyramine and taurine (CHT group) did not increase hepatic CYP7A1 activity compared the intake of cholestyramine only (CH group). A significant increase in fecal bile acid excretion due to taurine intake was found only in rats fed the CT diet. In conclusion, it is suggested that taurine facilitates hepatic CYP7A1 activity regardless of the enlarged intestinal pool of bile acids due to increased intake of exogenous bile acid, and then reduces the serum cholesterol concentration.
为改变胆汁酸的肠道池,研究了牛磺酸对喂食消胆胺或大量胆酸钠的大鼠血清胆固醇水平和肝脏胆固醇7α-羟化酶活性(CYP7A1)的影响。大鼠喂食补充1%胆固醇和0.25%胆酸钠的饲料(高胆固醇,对照;C),并将C组分别补充4%消胆胺(CH)或0.75%胆酸钠(BA),持续14天。牛磺酸组喂食补充3%牛磺酸的饲料(CT、CHT和BAT)。与喂食C和BA饲料的大鼠相比,喂食CT和BAT饲料的大鼠血清胆固醇水平显著降低,但与CH组相比,CHT组未观察到牛磺酸喂食导致血清胆固醇显著降低。在CT和BAT组中观察到由于摄入牛磺酸导致肝脏CYP7A1活性增加。然而,与仅摄入消胆胺的组(CH组)相比,同时给予消胆胺和牛磺酸(CHT组)并未增加肝脏CYP7A1活性。仅在喂食CT饲料的大鼠中发现由于摄入牛磺酸导致粪便胆汁酸排泄显著增加。总之,提示牛磺酸无论因外源性胆汁酸摄入增加导致胆汁酸肠道池扩大与否均能促进肝脏CYP7A1活性,进而降低血清胆固醇浓度。