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长期使用全视黄醇受体激动剂十四烷硫代乙酸或鱼油可使大鼠心脏中 n-3 脂肪酸含量增加。

Long-term treatment with the pan-PPAR agonist tetradecylthioacetic acid or fish oil is associated with increased cardiac content of n-3 fatty acids in rat.

机构信息

Institute of Medicine, University of Bergen, Haukeland University Hospital, Laboratory Building 8th floor, 5021 Bergen, Norway.

出版信息

Lipids Health Dis. 2012 Jun 27;11:82. doi: 10.1186/1476-511X-11-82.

Abstract

BACKGROUND

Excess peroxisome proliferator-activated receptor (PPAR) stimulation has been associated with detrimental health effects including impaired myocardial function. Recently, supplementation with n-3 polyunsaturated fatty acids (PUFA) has been associated with improved left ventricular function and functional capacity in patients with dilated cardiomyopathy. We investigated the long-term effects of the pan-PPAR agonist tetradecylthioacetic acid (TTA) and/or high-dose fish oil (FO) on cardiac fatty acid (FA) composition and lipid metabolism. Male Wistar rats were given one out of four different 25% (w/v) fat diets: control diet; TTA diet; FO diet; or diet containing both TTA and FO.

RESULTS

After 50 weeks n-3 PUFA levels were increased by TTA and FO in the heart, whereas liver levels were reduced following TTA administration. TTA was associated with a decrease in arachidonic acid, increased activities of carnitine palmitoyltransferase II, fatty acyl-CoA oxidase, glycerol-3-phosphate acyltransferase, and fatty acid synthase in the heart. Furthermore, cardiac Ucp3 and Cact mRNA was upregulated.

CONCLUSIONS

Long-term treatment with the pan-PPAR agonist TTA or high-dose FO induced marked changes in PUFA composition and enzymatic activity involved in FA metabolism in the heart, different from liver. Changes included increased FA oxidation and a selective increase in cardiac n-3 PUFA.

摘要

背景

过氧化物酶体增殖物激活受体(PPAR)的过度刺激与有害的健康影响有关,包括心肌功能受损。最近,补充 n-3 多不饱和脂肪酸(PUFA)已与扩张型心肌病患者的左心室功能和功能能力改善相关。我们研究了全 PPAR 激动剂十四烷硫代乙酸(TTA)和/或高剂量鱼油(FO)对心脏脂肪酸(FA)组成和脂质代谢的长期影响。雄性 Wistar 大鼠接受了四种不同的 25%(w/v)脂肪饮食中的一种:对照饮食;TTA 饮食;FO 饮食;或含有 TTA 和 FO 的饮食。

结果

50 周后,TTA 和 FO 增加了心脏中的 n-3 PUFA 水平,而 TTA 给药后肝脏中的水平降低。TTA 与心脏中花生四烯酸减少、肉碱棕榈酰转移酶 II、脂肪酸辅酶 A 氧化酶、甘油-3-磷酸酰基转移酶和脂肪酸合酶活性增加有关。此外,心脏 Ucp3 和 Cact mRNA 上调。

结论

全 PPAR 激动剂 TTA 或高剂量 FO 的长期治疗导致心脏中 FA 代谢中 PUFA 组成和酶活性发生明显变化,与肝脏不同。变化包括增加 FA 氧化和心脏中 n-3 PUFA 的选择性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c6/3459737/423474472e45/1476-511X-11-82-1.jpg

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