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Interleukin-6 is a novel factor mediating glucose homeostasis during skeletal muscle contraction

journal contribution
posted on 2024-11-01, 01:23 authored by Mark Febbraio, Natalie Hiscock, Massimo Sacchetti, Christian P Fischer, Bente Pedersen
The mechanisms that mediate the tightly controlled production and clearance of glucose during muscular work are unclear, and it has been suggested that an unidentified "work factor" exists that influences the contraction-induced increase in endogenous glucose production (EGP). The cytokine interleukin (IL)-6 is released from skeletal muscle during contraction. Here we show that IL-6 contributes to the contraction-induced increase in EGP. Six men performed 2 It of bicycle exercise on three separate occasions, at a relatively high intensity (HI) or at a low intensity with (LO + IL-6) or without (LO) an infusion of recombinant human IL-6 that matched the circulating concentration of IL-6 seen in HI exercise. The stable isotope 6,6 H-2(2) glucose was infused to calculate EGP (rate of glucose appearance [R-a]), whole-body glucose disposal (rate of glucose disappearance [R-d]), and metabolic clearance rate (MCR) of glucose. Glucose R-a, R-d, and MCR were higher (P < 0.05) at HI than at LO. Throughout exercise at LO + IL-6, glucose R-a and R-d, were higher (P < 0.05) than LO, even though the exercise intensity was identical. In addition, MCR was higher (P < 0.05) at LO + IL-6 than at LO at 90 min. Insulin, glucagon, epinephrine, norepinephrine, cortisol, and growth hormone were identical when comparing LO + IL-6 with LO. These data suggest that IL-6 influences glucose homeostasis during exercise. Our results provide potential new insights into factors that mediate glucose production and disposal and implicates IL-6 in the so-called "work factor."

History

Journal

Diabetes

Volume

53

Start page

1643

End page

1648

Total pages

6

Publisher

American Diabetes Association

Place published

USA

Language

English

Copyright

© 2004 by the American Diabetes Association, Inc.

Former Identifier

2004002132

Esploro creation date

2020-06-22

Fedora creation date

2009-02-27

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