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二十二碳五烯酸(22:5,n-3):代谢及其对内皮细胞中前列环素生成的影响

Docosapentaenoic acid (22:5,n-3): metabolism and effect on prostacyclin production in endothelial cells.

作者信息

Bénistant C, Achard F, Ben Slama S, Lagarde M

机构信息

Université de Montpellier I, Faculté de Pharmacie, Montpellier, France.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 1996 Oct;55(4):287-92. doi: 10.1016/s0952-3278(96)90010-1.

Abstract

Eicosapentaenoic acid (EPA, 20:5,n-3) and docosahexaenoic acid (DHA, 22:6, n-3), the two main fatty acids of fish oil, have been shown to inhibit prostacyclin production and to be actively interconverted, leading to the accumulation of docosapentaenoic acid (DPA, 22:5,n-3) in endothelial cell phospholipids. We have investigated the effect of supplementing endothelial cells with DPA on their capacity to produce prostacyclin. We found that endothelial cells incubated for 22 h with 25 microM DPA bound to albumin (fatty acid/albumin ratio of 1.3) produced two-fold less prostacyclin compared to control cells when stimulated with endogenous arachidonic acid-mobilizing agents such as bradykinin and calcium ionophore A23187. Since the formation of prostacyclin from 0.1-15 microM exogenous arachidonic acid was also reduced, it is suggested that prostacyclin inhibition observed in DPA-treated cells might not proceed from a reduction of arachidonic acid availability only. Such an inhibition was already observed after 1 h incubation of the cells with DPA, and with 2-20 times lower DPA concentrations. The inhibition might depend on EPA which was formed by retroconversion of DPA.

摘要

二十碳五烯酸(EPA,20:5,n-3)和二十二碳六烯酸(DHA,22:6,n-3)是鱼油的两种主要脂肪酸,已被证明可抑制前列环素的产生并能进行活跃的相互转化,导致二十二碳五烯酸(DPA,22:5,n-3)在内皮细胞磷脂中蓄积。我们研究了用DPA补充内皮细胞对其产生前列环素能力的影响。我们发现,与对照细胞相比,用25微摩尔与白蛋白结合的DPA(脂肪酸/白蛋白比率为1.3)孵育22小时的内皮细胞,在用内源性花生四烯酸动员剂如缓激肽和钙离子载体A23187刺激时,产生的前列环素减少了两倍。由于从0.1 - 15微摩尔外源性花生四烯酸形成前列环素的过程也减少了,因此有人提出,在DPA处理的细胞中观察到的前列环素抑制可能不仅仅是由于花生四烯酸可用性的降低。在用DPA孵育细胞1小时后,以及在DPA浓度低2 - 20倍的情况下,就已经观察到了这种抑制作用。这种抑制可能取决于由DPA逆转化形成的EPA。

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