Blocking endogenous IL-6 impairs mobilization of free fatty acids during rest and exercise in lean and obese men

被引:25
作者
Trinh, Beckey [1 ]
Peletier, Merel [1 ]
Simonsen, Casper [1 ]
Plomgaard, Peter [1 ,2 ,3 ]
Karstoft, Kristian [1 ,4 ]
Pedersen, Bente Klarlund [1 ]
van Hall, Gerrit [2 ,5 ,6 ]
Ellingsgaard, Helga [1 ]
机构
[1] Univ Copenhagen, Rigshosp, Ctr Phys Act Res, Copenhagen, Denmark
[2] Univ Copenhagen, Rigshosp, Dept Clin Biochem, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[4] Univ Copenhagen, Bispebjerg Frederiksberg Hosp, Dept Clin Pharmacol, Copenhagen, Denmark
[5] Rigshosp, Clin Metabol Core Facil, Copenhagen, Denmark
[6] Univ Copenhagen, Dept Biomed Sci, Copenhagen, Denmark
基金
瑞士国家科学基金会;
关键词
HUMAN SKELETAL-MUSCLE; RECOMBINANT HUMAN INTERLEUKIN-6; ANTI-IL-6 RECEPTOR ANTIBODY; ADIPOSE-TISSUE; WHOLE-BODY; SUBSTRATE OXIDATION; CYTOKINE RESPONSE; METABOLISM; GLUCOSE; CARBOHYDRATE;
D O I
10.1016/j.xcrm.2021.100396
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lack of interleukin-6 (IL-6) leads to expansion of adipose tissue mass in rodents and humans. The exact underlying mechanisms have not been identified. In this placebo-controlled, non-randomized, participant-blinded crossover study, we use the IL-6 receptor antibody tocilizumab to investigate the role of endogenous IL-6 in regulating systemic energy metabolism at rest and during exercise and recovery in lean and obese men using tracer dilution methodology. Tocilizumab reduces fatty acid appearance in the circulation under all conditions in lean and obese individuals, whereas lipolysis (the rate of glycerol appearance into the circulation) is mostly unaffected. The fact that fatty acid oxidation is unaffected by IL-6 receptor blockade suggests increased re-esterification of fatty acids. Glucose kinetics are unaffected. We find that blocking endogenous IL-6 signaling with tocilizumab impairs fat mobilization, which may contribute to expansion of adipose tissue mass and, thus, affect the health of individuals undergoing anti-IL-6 therapy
引用
收藏
页数:16
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