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

被引:41
|
作者
Rodrigo Cataldo, Luis [1 ]
Fernandez-Verdejo, Rodrigo [2 ]
Luis Santos, Jose [1 ]
Eduardo Galgani, Jose [1 ,2 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Med, Dept Nutr Diabet & Metab, Santiago 8331150, Chile
[2] Pontificia Univ Catolica Chile, Fac Med, Dept Ciencias Salud, Carrera Nutr & Dietet, Santiago, Chile
关键词
METABOLISM; REGULATORS; PEPTIDES;
D O I
10.1136/jim-2017-000681
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1019 / 1022
页数:4
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