Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice

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Standard

Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice. / Lauritzen, Hans Peter M. Mortensen; Galbo, Henrik; Toyoda, Taro; Goodyear, Laurie J.

I: Diabetes, Bind 59, Nr. 9, 01.09.2010, s. 2134-44.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Lauritzen, HPMM, Galbo, H, Toyoda, T & Goodyear, LJ 2010, 'Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice', Diabetes, bind 59, nr. 9, s. 2134-44. https://doi.org/10.2337/db10-0233

APA

Lauritzen, H. P. M. M., Galbo, H., Toyoda, T., & Goodyear, L. J. (2010). Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice. Diabetes, 59(9), 2134-44. https://doi.org/10.2337/db10-0233

Vancouver

Lauritzen HPMM, Galbo H, Toyoda T, Goodyear LJ. Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice. Diabetes. 2010 sep. 1;59(9):2134-44. https://doi.org/10.2337/db10-0233

Author

Lauritzen, Hans Peter M. Mortensen ; Galbo, Henrik ; Toyoda, Taro ; Goodyear, Laurie J. / Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice. I: Diabetes. 2010 ; Bind 59, Nr. 9. s. 2134-44.

Bibtex

@article{726cc76efda040e59e6f26c470ebc247,
title = "Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice",
abstract = "Exercise is an important strategy for the treatment of type 2 diabetes. This is due in part to an increase in glucose transport that occurs in the working skeletal muscles. Glucose transport is regulated by GLUT4 translocation in muscle, but the molecular machinery mediating this process is poorly understood. The purpose of this study was to 1) use a novel imaging system to elucidate the kinetics of contraction-induced GLUT4 translocation in skeletal muscle and 2) determine the function of AMP-activated protein kinase alpha2 (AMPKalpha2) in this process.",
author = "Lauritzen, {Hans Peter M. Mortensen} and Henrik Galbo and Taro Toyoda and Goodyear, {Laurie J}",
year = "2010",
month = sep,
day = "1",
doi = "http://dx.doi.org/10.2337/db10-0233",
language = "English",
volume = "59",
pages = "2134--44",
journal = "Diabetes",
issn = "0012-1797",
publisher = "American Diabetes Association",
number = "9",

}

RIS

TY - JOUR

T1 - Kinetics of contraction-induced GLUT4 translocation in skeletal muscle fibers from living mice

AU - Lauritzen, Hans Peter M. Mortensen

AU - Galbo, Henrik

AU - Toyoda, Taro

AU - Goodyear, Laurie J

PY - 2010/9/1

Y1 - 2010/9/1

N2 - Exercise is an important strategy for the treatment of type 2 diabetes. This is due in part to an increase in glucose transport that occurs in the working skeletal muscles. Glucose transport is regulated by GLUT4 translocation in muscle, but the molecular machinery mediating this process is poorly understood. The purpose of this study was to 1) use a novel imaging system to elucidate the kinetics of contraction-induced GLUT4 translocation in skeletal muscle and 2) determine the function of AMP-activated protein kinase alpha2 (AMPKalpha2) in this process.

AB - Exercise is an important strategy for the treatment of type 2 diabetes. This is due in part to an increase in glucose transport that occurs in the working skeletal muscles. Glucose transport is regulated by GLUT4 translocation in muscle, but the molecular machinery mediating this process is poorly understood. The purpose of this study was to 1) use a novel imaging system to elucidate the kinetics of contraction-induced GLUT4 translocation in skeletal muscle and 2) determine the function of AMP-activated protein kinase alpha2 (AMPKalpha2) in this process.

U2 - http://dx.doi.org/10.2337/db10-0233

DO - http://dx.doi.org/10.2337/db10-0233

M3 - Journal article

VL - 59

SP - 2134

EP - 2144

JO - Diabetes

JF - Diabetes

SN - 0012-1797

IS - 9

ER -

ID: 34109514