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血浆 MOTS-c 水平与瘦人而非肥胖人群的胰岛素敏感性相关。

Plasma MOTS-c levels are associated with insulin sensitivity in lean but not in obese individuals.

机构信息

Departamento de Nutrición, Diabetes y Metabolismo, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

Carrera de Nutrición y Dietética, Departamento de Ciencias de la Salud, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

J Investig Med. 2018 Aug;66(6):1019-1022. doi: 10.1136/jim-2017-000681. Epub 2018 Mar 27.

Abstract

Mitochondrial open reading frame of the 12S rRNA-c (MOTS-c) is a mitochondrial-derived peptide that attenuates weight gain and hyperinsulinemia when administered to high fat-fed mice. MOTS-c is therefore a potential regulator of metabolic homeostasis under conditions of high-energy supply. However, the effect of insulin resistance and obesity on plasma MOTS-c concentration in humans is unknown. To gain insight into MOTS-c regulation, we measured plasma MOTS-c concentration and analyzed its relationship with insulin sensitivity surrogates, in lean and obese humans (n=10 per group). Obese individuals had impaired insulin sensitivity as indicated by low Matsuda and high Homeostatic Model Assessment (HOMA) indexes. Although plasma MOTS-c concentration was similar in lean and obese individuals (0.48±0.16 and 0.52±0.15 ng/mL; p=0.60), it was correlated with HOMA (r=0.53; p<0.05) and Matsuda index (r=-0.46; p<0.05). Notably, when the groups were analyzed separately, the associations remained only in lean individuals. We conclude that plasma MOTS-c concentration is unaltered in human obesity. However, MOTS-c associates positively with insulin resistance mostly in lean individuals, indicating that plasma MOTS-c concentration depends on the metabolic status in this population. Such dependence seems altered when obesity settles. The implications of plasma MOTS-c for human metabolic homeostasis deserve future examination.

摘要

线粒体 12S rRNA-c(MOTS-c)的开放阅读框是一种线粒体衍生肽,当给高脂肪喂养的小鼠给药时,可减轻体重增加和高胰岛素血症。因此,MOTS-c 是高能供应条件下代谢稳态的潜在调节剂。然而,胰岛素抵抗和肥胖对人类血浆 MOTS-c 浓度的影响尚不清楚。为了深入了解 MOTS-c 的调节作用,我们测量了血浆 MOTS-c 浓度,并分析了其与胰岛素敏感性替代物的关系,在瘦人和肥胖人群(每组 10 人)中进行了分析。肥胖个体的胰岛素敏感性受损,表现为 Matsuda 和 Homeostatic Model Assessment (HOMA) 指数降低。尽管瘦人和肥胖个体的血浆 MOTS-c 浓度相似(0.48±0.16 和 0.52±0.15ng/mL;p=0.60),但它与 HOMA(r=0.53;p<0.05)和 Matsuda 指数(r=-0.46;p<0.05)相关。值得注意的是,当分别对两组进行分析时,这种关联仅在瘦人群体中存在。我们的结论是,人类肥胖症患者的血浆 MOTS-c 浓度没有改变。然而,MOTS-c 与胰岛素抵抗呈正相关,主要发生在瘦人群体中,这表明在该人群中,血浆 MOTS-c 浓度取决于代谢状态。当肥胖发生时,这种依赖性似乎发生了变化。血浆 MOTS-c 对人类代谢稳态的影响值得未来进一步研究。

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