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2-十六碳炔酸甲酯对肝脏脂肪酸代谢的影响。

Effect of methyl 2-hexadecynoate on hepatic fatty acid metabolism.

作者信息

Wood R, Lee T, Gershon H

出版信息

Lipids. 1980 Mar;15(3):141-50. doi: 10.1007/BF02540960.

DOI:10.1007/BF02540960
PMID:7374364
Abstract

Normal and hepatoma bearing rats were fed a low level of methyl 2-hexadecynoate in a low fat diet for one month. The effect of the acetylenic acid on lipid metabolism as derived from mass analysis of lipid classes, fatty acids and positional monoene isomers isolated from the major lipid classes of liver and hepatoma has been assessed. Methyl 2-hexadecynoate caused a 25% decrease in body weight and the appearance of essential fatty acid deficiency symptoms within one week. Non-tumor-bearing animals contained a seven-fold increase in all neutral lipid classes, except cholesterol, while host animals did not contain fatty livers. The apparent protective effect of the host animal by the hepatoma also resulted in only marginal changes in the fatty acid and positional monoene isomers from host liver and hepatoma lipids. In contrast to host liver and hepatoma, methyl 2-hexadecynoate caused a massive accumulation of palmitate and hexadecenoates with a concomitant decrease in stearate and octadecenoates in most of the lipid classes from non-tumor-bearing animals. These changes were accompanied by a shift from the higher molecular weight triglycerides to lower molecular weights corresponding to carbon number 48. The high concentrations of hexadecenoates consisted predominantly of the delta 9 isomer. Despite the high concentrations of cis delta 9 hexadecenoate, precursor of cis delta 11 octadecenoate (vaccenate), total vaccenate levels of the five major lipid classes were lower than control values. All of these data strongly suggest that long-chain 2-ynoic acids inhibit elongation of saturated and monoene fatty acids.

摘要

正常大鼠和荷肝癌大鼠在低脂饮食中摄入低水平的2-十六碳炔酸甲酯,持续一个月。通过对从肝脏和肝癌的主要脂质类别中分离出的脂质类别、脂肪酸和位置单烯异构体进行质量分析,评估了炔酸对脂质代谢的影响。2-十六碳炔酸甲酯在一周内导致体重下降25%,并出现必需脂肪酸缺乏症状。非荷瘤动物体内所有中性脂质类别(胆固醇除外)增加了七倍,而宿主动物没有出现脂肪肝。肝癌对宿主动物的明显保护作用也导致宿主肝脏和肝癌脂质中的脂肪酸和位置单烯异构体仅有微小变化。与宿主肝脏和肝癌相反,2-十六碳炔酸甲酯导致非荷瘤动物大多数脂质类别中棕榈酸和十六碳烯酸大量积累,同时硬脂酸和十八碳烯酸减少。这些变化伴随着从较高分子量的甘油三酯向对应碳数为48的较低分子量甘油三酯的转变。高浓度的十六碳烯酸主要由δ9异构体组成。尽管顺式δ9十六碳烯酸(顺式δ11十八碳烯酸(牛磺酸)的前体)浓度很高,但五种主要脂质类别的总牛磺酸水平低于对照值。所有这些数据都强烈表明,长链2-炔酸抑制饱和脂肪酸和单烯脂肪酸的延长。

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