Ogawa H, Nishikawa T, Fukushima S, Sasagawa S
Nihon Eiseigaku Zasshi. 1989 Jun;44(2):648-58. doi: 10.1265/jjh.44.648.
It is well known that taurine, a final metabolite of sulfur-containing amino acids, plays an important role in bile acid metabolism and that it also has a moderately hypotensive effect. Moreover, it has recently been revealed that taurine shows a hypocholesterolemic effect in animals with experimentally induced hypercholesterolemia. However, the hypocholesterolemic mechanism remains unresolved. Stroke-prone spontaneously hypertensive rats (SHRSP) easily develop hypercholesterolemia when fed a high-fat and high-cholesterol diet (HFC diet). In our previous paper, we reported changes in the concentrations and distributions of serum lipoproteins and apolipoproteins in hypercholesterolemic SHRSP and Kyo: Wistar rats (WKY) induced by HFC feeding. In this paper, to elucidate the mechanism of the hypocholesterolemic effect of taurine, we investigated the effects of taurine on concentrations and distributions of serum lipoproteins and apolipoproteins in hypercholesterolemic SHRSP and WKY induced by HFC feeding. The results obtained were as follows: 1) The hypocholesterolemic effect of taurine in hypercholesterolemic SHRSP was remarkable in comparison with that in hypercholesterolemic WKY. 2) The hypocholesterolemic effect of taurine was mainly due to a marked suppression of extreme elevations of cholesterol contents in the VLDL and IDL fractions of both strains. This was associated with a decrease in the elevated contents of apo B and apo E which are major components of VLDL and IDL. This suppressive effect was more obvious in SHRSP than in WKY, which explains the greater hypocholesterolemic effect of taurine in SHRSP. It could be that, as a result of taurine administration, the catabolism of cholesterol to bile acid in the liver is accelerated, followed by a decrease of the hepatic cholesterol pool, resulting in a suppression of the synthesis and/or secretion of VLDL (beta-VLDL) in the liver. 3) The hypocholesterolemic effect of taurine was also observed in the LDL fractions of both strains, but the effect was not as strong as that observed in the VLDL and IDL fractions. This effect might be attributable to suppression of the synthesis and/or secretion of LDL in the liver and a decrease in the elevated content of apo E HDL (HDLc) which spans two density fractions (the LDL and HDL fractions). 4) In HDL fractions of both strains, the decreased content of apo E HDL (HDL1 and HDLc) was even lower, whereas the decreased apo A-I content in the HDL fraction of SHRSP was significantly restored and the cholesterol level was slightly elevated.(ABSTRACT TRUNCATED AT 400 WORDS)
众所周知,牛磺酸是含硫氨基酸的终末代谢产物,在胆汁酸代谢中起重要作用,并且还具有一定的降压作用。此外,最近发现牛磺酸对实验性诱导的高胆固醇血症动物具有降胆固醇作用。然而,其降胆固醇机制仍未明确。易患中风的自发性高血压大鼠(SHRSP)在喂食高脂高胆固醇饮食(HFC饮食)时容易发生高胆固醇血症。在我们之前的论文中,我们报道了HFC喂养诱导的高胆固醇血症SHRSP和京都:Wistar大鼠(WKY)血清脂蛋白和载脂蛋白的浓度及分布变化。在本文中,为阐明牛磺酸降胆固醇作用的机制,我们研究了牛磺酸对HFC喂养诱导的高胆固醇血症SHRSP和WKY血清脂蛋白和载脂蛋白浓度及分布的影响。得到的结果如下:1)与高胆固醇血症WKY相比,牛磺酸对高胆固醇血症SHRSP的降胆固醇作用显著。2)牛磺酸的降胆固醇作用主要是由于显著抑制了两品系极低密度脂蛋白(VLDL)和中间密度脂蛋白(IDL)组分中胆固醇含量的极度升高。这与VLDL和IDL的主要成分载脂蛋白B和载脂蛋白E升高的含量降低有关。这种抑制作用在SHRSP中比在WKY中更明显,这解释了牛磺酸在SHRSP中具有更大的降胆固醇作用。可能是由于给予牛磺酸后,肝脏中胆固醇向胆汁酸的分解代谢加速,随后肝脏胆固醇池减少,导致肝脏中VLDL(β-VLDL)的合成和/或分泌受到抑制。3)在两品系的低密度脂蛋白(LDL)组分中也观察到牛磺酸的降胆固醇作用,但该作用不如在VLDL和IDL组分中观察到的强。这种作用可能归因于肝脏中LDL的合成和/或分泌受到抑制以及跨越两个密度组分(LDL和高密度脂蛋白(HDL)组分)的载脂蛋白E HDL(HDLc)升高的含量降低。4)在两品系的HDL组分中,载脂蛋白E HDL(HDL1和HDLc)降低的含量更低,而SHRSP的HDL组分中载脂蛋白A-I降低的含量显著恢复,胆固醇水平略有升高。(摘要截短至400字)