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饮食中的鱼油可降低瘦鼠的血脂,增加肥胖 LDLR-/- 小鼠的胰岛素敏感性。

Dietary fish oil exerts hypolipidemic effects in lean and insulin sensitizing effects in obese LDLR-/- mice.

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

出版信息

J Nutr. 2009 Dec;139(12):2380-6. doi: 10.3945/jn.109.111567. Epub 2009 Oct 28.

Abstract

Obesity is often associated with dyslipidemia, insulin resistance, and hypertension. Together, these metabolic perturbations greatly increase the risk of developing cardiovascular disease and diabetes. Although fish oil is a well-established hypolipidemic agent, the mechanisms by which it mediates its lipid-lowering effects are not clear. In addition, it has not been established whether dietary fish oil has different effects in lean and obese mice. LDL receptor deficient (LDLR-/-) and leptin deficient mice on a LDLR-/- background (ob/ob;LDLR-/-) were fed a high fat diet (39% total fat) supplemented with 6% olive oil or fish oil for 6 wk. Fish oil supplementation resulted in lower concentrations of plasma total cholesterol (P < 0.01), triglycerides (P < 0.01), and free fatty acids (P < 0.001) in lean LDLR-/- mice, but not in ob/ob;LDLR-/- mice. In contrast, a fish oil diet did not modulate insulin sensitivity in lean LDLR-/- mice, but it improved insulin sensitivity in ob/ob;LDLR-/- mice (P < 0.05) compared with olive oil fed ob/ob;LDLR-/- mice. Interestingly, plasma adiponectin concentrations were significantly higher and hepatic steatosis was reduced in both mouse models upon fish oil feeding. Finally, fish oil fed LDLR-/- mice exhibited higher hepatic AMP activated protein kinase (AMPK) phosphorylation (P < 0.05), whereas AMPK phosphorylation was not elevated by fish oil feeding in ob/ob;LDLR-/- mice. Taken together, our data suggest that fish oil reduces hepatic steatosis in both lean and obese mice, has potent plasma lipid lowering effects in lean mice, and exerts insulin sensitizing effects in obese mice.

摘要

肥胖通常与血脂异常、胰岛素抵抗和高血压有关。这些代谢紊乱极大地增加了患心血管疾病和糖尿病的风险。尽管鱼油是一种成熟的降血脂药物,但它介导降脂作用的机制尚不清楚。此外,尚不清楚饮食中的鱼油在瘦鼠和肥胖鼠中是否有不同的作用。给予 LDL 受体缺陷(LDLR-/-)和瘦素缺陷(ob/ob;LDLR-/-)小鼠高脂饮食(总脂肪 39%),补充 6%橄榄油或鱼油 6 周。鱼油补充可降低瘦型 LDLR-/-小鼠血浆总胆固醇(P < 0.01)、甘油三酯(P < 0.01)和游离脂肪酸(P < 0.001)浓度,但对 ob/ob;LDLR-/-小鼠则无此作用。相反,鱼油饮食并不能调节瘦型 LDLR-/-小鼠的胰岛素敏感性,但可改善 ob/ob;LDLR-/-小鼠的胰岛素敏感性(P < 0.05),与橄榄油喂养的 ob/ob;LDLR-/-小鼠相比。有趣的是,两种小鼠模型中,鱼油喂养均可显著增加血浆脂联素浓度,减少肝脂肪变性。最后,鱼油喂养的 LDLR-/-小鼠肝 AMP 激活蛋白激酶(AMPK)磷酸化水平升高(P < 0.05),而 ob/ob;LDLR-/-小鼠中鱼油喂养并未增加 AMPK 磷酸化。综上所述,我们的数据表明,鱼油可减少瘦鼠和肥胖鼠的肝脂肪变性,对瘦鼠具有很强的血浆降血脂作用,并对肥胖鼠具有胰岛素增敏作用。

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