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膳食脂肪酸通过RANKL/RANK/OPG系统对破骨细胞生成的急性影响。

Acute effects of dietary fatty acids on osteclastogenesis via RANKL/RANK/OPG system.

作者信息

Naranjo M Carmen, Garcia Indara, Bermudez Beatriz, Lopez Sergio, Cardelo Magdalena P, Abia Rocio, Muriana Francisco J G, Montserrat-de la Paz Sergio

机构信息

Laboratory of Cellular and Molecular Nutrition, Instituto de la Grasa, CSIC, Seville, Spain.

Department of Pharmacology, School of Pharmacy, University of Seville, Seville, Spain.

出版信息

Mol Nutr Food Res. 2016 Nov;60(11):2505-2513. doi: 10.1002/mnfr.201600303. Epub 2016 Jul 27.

Abstract

SCOPE

Postprandial state is directly linked with chronic diseases. We hypothesized that dietary fats may have acute effects on health status by modulating osteoclast differentiation and activation in a fatty acid-dependent manner.

METHODS AND RESULTS

In healthy subjects, a fat-enriched meal increased plasma levels of the RANKL (receptor activator of nuclear factor κB ligand)/OPG (osteoprotegerin) ratio (SFAs > MUFAs = PUFAs) in the postprandial state. Postprandial TRL-SFAs enhanced tartrate-resistant acid phosphatase (TRAP) activity and the expression of osteoclast marker genes (TRAP, OSCAR, RANK, and CATHK) while downregulated the expression of OPG gene in human monocyte-derived osteoclasts. These effects were not observed with monounsaturated fatty acid (MUFA)-enriched postprandial triglyceride-rich lipoproteins (TRLs). Moreover, postprandial TRL-SFAs increased the release of osteoclastogenic cytokines (TNF-α, IL-1β, and IL-6) meanwhile TRL-MUFAs and TRL-PUFAs increased the release of anti-osteoclastogenic cytokines (IL-4 and IL-10) in the medium of human monocyte-derived osteoclasts.

CONCLUSION

For the first time, we show that postprandial TRLs are metabolic entities with osteoclastogenic activity and that this property is related to the type of dietary fatty acid in the meal. The osteoclastogenic potency was as follows: SFAs >>> MUFAs = PUFAs. These exciting findings open opportunities for developing nutritional strategies with olive oil as the principal dietary source of MUFAs, notably oleic acid, to prevent development and progression of osteoclast-related diseases.

摘要

范围

餐后状态与慢性疾病直接相关。我们假设膳食脂肪可能通过以脂肪酸依赖的方式调节破骨细胞的分化和激活,从而对健康状况产生急性影响。

方法与结果

在健康受试者中,富含脂肪的餐食会使餐后状态下血浆中核因子κB受体活化因子配体(RANKL)/骨保护素(OPG)的比值升高(饱和脂肪酸>单不饱和脂肪酸=多不饱和脂肪酸)。餐后富含甘油三酯的脂蛋白(TRL)中的饱和脂肪酸增强了人单核细胞衍生破骨细胞中抗酒石酸酸性磷酸酶(TRAP)的活性以及破骨细胞标记基因(TRAP、OSCAR、RANK和CATHK)的表达,同时下调了OPG基因的表达。而富含单不饱和脂肪酸(MUFA)的餐后TRL则未观察到这些作用。此外,餐后TRL中的饱和脂肪酸增加了破骨细胞生成细胞因子(TNF-α、IL-1β和IL-6)的释放,与此同时,TRL中的单不饱和脂肪酸和多不饱和脂肪酸增加了人单核细胞衍生破骨细胞培养基中抗破骨细胞生成细胞因子(IL-4和IL-10)的释放。

结论

我们首次表明,餐后TRL是具有破骨细胞生成活性的代谢实体,且这种特性与餐食中膳食脂肪酸的类型有关。破骨细胞生成能力如下:饱和脂肪酸>>>单不饱和脂肪酸=多不饱和脂肪酸。这些令人兴奋的发现为开发以橄榄油作为单不饱和脂肪酸(尤其是油酸)的主要膳食来源的营养策略提供了机会,以预防破骨细胞相关疾病的发生和发展。

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