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反式棕榈油酸可内源性产生于膳食中的瘤胃脂酸。

trans Palmitoleic acid arises endogenously from dietary vaccenic acid.

机构信息

Department of Physiology and Biochemistry of Nutrition, Max Rubner-Institut, Federal Research Institute of Nutrition and Food, Karlsruhe, Germany (AJ, MP, and AR), and the Department of Nutritional Physiology, Institute of Nutrition, Friedrich Schiller University of Jena, Jena, Germany (RK, GJ, and KK).

出版信息

Am J Clin Nutr. 2014 Mar;99(3):431-5. doi: 10.3945/ajcn.113.076117. Epub 2014 Jan 15.

Abstract

BACKGROUND

trans Palmitoleic acid (t-16:1n-7, or 16:1 t9 in the δ nomenclature usually applied to trans fatty acids and used herein) arouses great scientific interest because it has been suggested to serve as a biomarker for lower risks of type 2 diabetes and coronary artery disease.

OBJECTIVE

Although 16:1 t9 has been assumed to derive from dietary sources, we examined the hypothesis that 16:1 t9 might also be endogenously produced from its metabolic precursor vaccenic acid (t-18:1n-7 or 18:1 t11).

DESIGN

We reevaluated fatty acid data obtained from one human intervention study and one cellular model in both of which 18:1 t11 was supplemented. Both studies have already been published, but to our knowledge, 16:1 t9 has not yet been considered. This reanalysis of the datasets was reasonable because a new methodology for identifying 16:1 cis and trans isomers allowed us to address the subject presented in this article.

RESULTS

Data showed that the systemic or intracellular increase in 16:1 t9 was strongly correlated with the increase in 18:1 t11 after the dietary intake or cellular uptake of 18:1 t11. The conversion rate in humans was, on average, 17%.

CONCLUSION

Our findings suggest that endogenous 16:1 t9 is not, as has been assumed, exclusively diet derived but may also be produced by the partial β oxidation of dietary 18:1 t11.

摘要

背景

反式棕榈油酸(t-16:1n-7,或在通常应用于反式脂肪酸的δ命名法中为 16:1 t9,本文中使用)引起了极大的科学兴趣,因为它被认为是 2 型糖尿病和冠心病风险降低的生物标志物。

目的

尽管 16:1 t9 被假定来自饮食来源,但我们检验了这样一种假设,即 16:1 t9 也可能源自其代谢前体油酸(t-18:1n-7 或 18:1 t11)的内源性产生。

设计

我们重新评估了从一项人体干预研究和一项细胞模型中获得的脂肪酸数据,在这两项研究中都补充了 18:1 t11。这两项研究都已经发表,但据我们所知,16:1 t9 尚未被考虑。对这些数据集进行重新分析是合理的,因为一种新的方法学用于识别 16:1 顺式和反式异构体,使我们能够解决本文提出的问题。

结果

数据显示,在摄入或摄取 18:1 t11 后,16:1 t9 的系统或细胞内增加与 18:1 t11 的增加强烈相关。人体的转化率平均为 17%。

结论

我们的研究结果表明,内源性 16:1 t9 并非如之前假设的那样,完全来自饮食,它也可能是由饮食中的 18:1 t11 的部分β氧化产生的。

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