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大鼠肝细胞中长链多不饱和脂肪酸的甘油三酯生成减少。

Reduced triglyceride formation from long-chain polyenoic fatty acids in rat hepatocytes.

作者信息

Wong S, Reardon M, Nestel P

出版信息

Metabolism. 1985 Oct;34(10):900-5. doi: 10.1016/0026-0495(85)90135-0.

Abstract

The mechanism for the marked reduction in hepatic triglyceride secretion when rats are fed fish oils was explored in studies with isolated rat hepatocytes. Hepatocytes obtained from Sprague-Dawley rats fed either chow or fish oil or safflower oil were incubated in the presence of [3H]-glycerol to estimate triglyceride formation. In some experiments, various fatty acids, complexed to albumin, were added to the incubations. Similar experiments were carried out with hepatocytes from a genetic strain of hypertriglyceridemic, obese rats. In the absence of added fatty acid, hepatocytes from fish oil-fed rats produced and secreted substantially less triglyceride than cells from safflower oil-fed rats. However, the addition of 2 mmol/L Na oleate stimulated triglyceride formation similarly in both types of hepatocytes. When hepatocytes from chow fed rats were incubated with fatty acids of increasing chain length and unsaturation (oleate, linolenate, arachidonate, eicosapentaenoate, and docosahexaenoate), the latter two, which characterize the fish oil used, almost totally suppressed triglyceride formation. Coincubation with oleate partly reversed this effect. Hepatocytes from the hypertriglyceridemic rats synthesized significantly more triglyceride than hepatocytes from normal rats; however triglyceride formation was markedly reduced also in this strain of rat by feeding fish oil or by adding docosahexaenoate to hepatocytes in vitro. These studies confirm previous conclusions with perfused livers from fish oil-fed rats that showed diminished triglyceride production and secretion. These findings suggest that diversion of polyenoic acids from pathways of esterification is a major factor in the triglyceride lowering effect of fish oils.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在对分离的大鼠肝细胞进行的研究中,探索了给大鼠喂食鱼油后肝脏甘油三酯分泌显著减少的机制。从喂食普通饲料、鱼油或红花油的Sprague-Dawley大鼠中获取肝细胞,在[3H]-甘油存在的情况下进行孵育,以估计甘油三酯的形成。在一些实验中,将与白蛋白结合的各种脂肪酸添加到孵育体系中。对来自遗传性高甘油三酯血症肥胖大鼠品系的肝细胞进行了类似实验。在不添加脂肪酸的情况下,来自喂食鱼油大鼠的肝细胞产生和分泌的甘油三酯比来自喂食红花油大鼠的细胞少得多。然而,添加2 mmol/L油酸钠可使两种类型的肝细胞中甘油三酯的形成受到类似刺激。当将喂食普通饲料大鼠的肝细胞与链长和不饱和度不断增加的脂肪酸(油酸盐、亚麻酸盐、花生四烯酸盐、二十碳五烯酸盐和二十二碳六烯酸盐)一起孵育时,后两种脂肪酸(这是所用鱼油的特征性成分)几乎完全抑制了甘油三酯的形成。与油酸盐共同孵育可部分逆转这种作用。高甘油三酯血症大鼠的肝细胞合成的甘油三酯明显多于正常大鼠的肝细胞;然而,通过喂食鱼油或在体外向肝细胞中添加二十二碳六烯酸盐,该品系大鼠的甘油三酯形成也显著减少。这些研究证实了先前对喂食鱼油大鼠的灌注肝脏所做研究得出的结论,即甘油三酯的产生和分泌减少。这些发现表明,多不饱和脂肪酸从酯化途径的转移是鱼油降低甘油三酯作用的主要因素。(摘要截选至250词)

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