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四组大鼠对高胆固醇、高胆酸盐饮食有不同的胆固醇血症反应,研究其胆固醇代谢及酯酶情况。

Cholesterol metabolism and esterases in four strains of rats with differential cholesterolemic responses to a high-cholesterol, high-cholate diet.

作者信息

Beynen A C, Lemmens A G, Katan M B, De Bruijne J J, Van Zutphen L F

出版信息

Comp Biochem Physiol B. 1987;87(1):41-8. doi: 10.1016/0305-0491(87)90468-8.

Abstract

The increase in serum cholesterol after feeding a diet containing 2% (w/w) of cholesterol and 0.5% of cholate for 13 days was 200 and 800% in two hypo- and two hyper-responsive inbred strains of rats, respectively. While remaining on the high-cholesterol, high-cholate diet for longer periods, the level of serum cholesterol dropped in the hyper-responsive strains, and after 8 weeks on the diet one hyper-responsive strain had similar serum cholesterol concentrations as the two hypo-responsive strains. The feeding of a semipurified diet, containing 1% (w/w) of cholesterol and 20% of fat, did not discriminate between the two hypo- and hyper-responsive strains with respect to the response of serum cholesterol. The activities in plasma of the indicators for liver function, aspartate amino transferase and alkaline phosphatase, were significantly increased in all strains after feeding the high-cholesterol, high-cholate diet. Only alkaline phosphatase was increased by the semipurified diet. Evidence is presented that in the four inbred strains of rats the differential cholesterolemic response to the high-cholesterol, high-cholate diet is not related to the baseline serum lipoprotein profile, liver cholesterol accumulation, fecal bile acid excretion, and the total activities and patterns of esterases in serum, liver and small intestine.

摘要

给大鼠喂食含2%(w/w)胆固醇和0.5%胆酸盐的饲料13天后,两个低反应性和两个高反应性近交系大鼠的血清胆固醇分别升高了200%和800%。在高胆固醇、高胆酸盐饲料喂养更长时间后,高反应性品系的血清胆固醇水平下降,且在该饲料喂养8周后,一个高反应性品系的血清胆固醇浓度与两个低反应性品系相似。喂食含1%(w/w)胆固醇和20%脂肪的半纯化饲料时,在血清胆固醇反应方面,并未区分出两个低反应性和高反应性品系。喂食高胆固醇、高胆酸盐饲料后,所有品系大鼠血浆中肝功能指标天冬氨酸氨基转移酶和碱性磷酸酶的活性均显著升高。只有半纯化饲料使碱性磷酸酶升高。有证据表明,在这四个近交系大鼠中,对高胆固醇、高胆酸盐饲料的不同胆固醇血症反应与基线血清脂蛋白谱、肝脏胆固醇积累、粪便胆汁酸排泄以及血清、肝脏和小肠中酯酶的总活性和模式无关。

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