Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training

Research output: Contribution to journalJournal articleResearchpeer-review

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Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. / Alsted, Thomas J; Schweiger, Martina; Nybo, Lars; Fledelius, Christian; Jacobsen, Poul; Zimmermann, Robert; Zechner, Rudolf; Kiens, Bente.

In: American Journal of Physiology: Endocrinology and Metabolism, Vol. 296, No. 3, 2009, p. E445-E453.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Alsted, TJ, Schweiger, M, Nybo, L, Fledelius, C, Jacobsen, P, Zimmermann, R, Zechner, R & Kiens, B 2009, 'Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training', American Journal of Physiology: Endocrinology and Metabolism, vol. 296, no. 3, pp. E445-E453. https://doi.org/10.1152/ajpendo.90912.2008

APA

Alsted, T. J., Schweiger, M., Nybo, L., Fledelius, C., Jacobsen, P., Zimmermann, R., Zechner, R., & Kiens, B. (2009). Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. American Journal of Physiology: Endocrinology and Metabolism, 296(3), E445-E453. https://doi.org/10.1152/ajpendo.90912.2008

Vancouver

Alsted TJ, Schweiger M, Nybo L, Fledelius C, Jacobsen P, Zimmermann R et al. Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. American Journal of Physiology: Endocrinology and Metabolism. 2009;296(3):E445-E453. https://doi.org/10.1152/ajpendo.90912.2008

Author

Alsted, Thomas J ; Schweiger, Martina ; Nybo, Lars ; Fledelius, Christian ; Jacobsen, Poul ; Zimmermann, Robert ; Zechner, Rudolf ; Kiens, Bente. / Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. In: American Journal of Physiology: Endocrinology and Metabolism. 2009 ; Vol. 296, No. 3. pp. E445-E453.

Bibtex

@article{98d87f901d0911deb43e000ea68e967b,
title = "Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training",
abstract = "Mobilization of fatty acids from stored triacylglycerol (TG) in adipose tissue and skeletal muscle [intramyocellular triacylglycerol (IMTG)] requires activity of lipases. Although exercise training increases the lipolytic capacity of skeletal muscle, the expression of hormone-sensitive lipase (HSL) is not changed. Recently, adipose triglyceride lipase (ATGL) was identified as a TG-specific lipase in various rodent tissues. To investigate whether human skeletal muscle ATGL protein is regulated by endurance exercise training, 10 healthy young men completed 8 wk of supervised endurance exercise training. Western blotting analysis on lysates of skeletal muscle biopsy samples revealed that exercise training induced a twofold increase in skeletal muscle ATGL protein content. In contrast to ATGL, expression of comparative gene identification 58 (CGI-58), the activating protein of ATGL, and HSL protein was not significantly changed after the training period. The IMTG concentration was significantly decreased by 28% at termination of the training program compared with before. HSL-phoshorylation at Ser(660) was increased, HSL-Ser(659) phosporylation was unchanged, and HSL-phoshorylation at Ser(565) was decreased altogether, indicating an enhanced basal activity of this lipase. No change was found in the expression of diacylglycerol acyl transferase 1 (DGAT1) after training. Inhibition of HSL with a monospecific, small molecule inhibitor (76-0079) and stimulation of ATGL with CGI-58 revealed that significant ATGL activity is present in human skeletal muscle. These results suggest that ATGL in addition to HSL may be important for human skeletal muscle lipolysis.",
author = "Alsted, {Thomas J} and Martina Schweiger and Lars Nybo and Christian Fledelius and Poul Jacobsen and Robert Zimmermann and Rudolf Zechner and Bente Kiens",
note = "CURIS 2009 5200 014",
year = "2009",
doi = "10.1152/ajpendo.90912.2008",
language = "English",
volume = "296",
pages = "E445--E453",
journal = "American Journal of Physiology - Endocrinology and Metabolism",
issn = "0193-1849",
publisher = "American Physiological Society",
number = "3",

}

RIS

TY - JOUR

T1 - Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training

AU - Alsted, Thomas J

AU - Schweiger, Martina

AU - Nybo, Lars

AU - Fledelius, Christian

AU - Jacobsen, Poul

AU - Zimmermann, Robert

AU - Zechner, Rudolf

AU - Kiens, Bente

N1 - CURIS 2009 5200 014

PY - 2009

Y1 - 2009

N2 - Mobilization of fatty acids from stored triacylglycerol (TG) in adipose tissue and skeletal muscle [intramyocellular triacylglycerol (IMTG)] requires activity of lipases. Although exercise training increases the lipolytic capacity of skeletal muscle, the expression of hormone-sensitive lipase (HSL) is not changed. Recently, adipose triglyceride lipase (ATGL) was identified as a TG-specific lipase in various rodent tissues. To investigate whether human skeletal muscle ATGL protein is regulated by endurance exercise training, 10 healthy young men completed 8 wk of supervised endurance exercise training. Western blotting analysis on lysates of skeletal muscle biopsy samples revealed that exercise training induced a twofold increase in skeletal muscle ATGL protein content. In contrast to ATGL, expression of comparative gene identification 58 (CGI-58), the activating protein of ATGL, and HSL protein was not significantly changed after the training period. The IMTG concentration was significantly decreased by 28% at termination of the training program compared with before. HSL-phoshorylation at Ser(660) was increased, HSL-Ser(659) phosporylation was unchanged, and HSL-phoshorylation at Ser(565) was decreased altogether, indicating an enhanced basal activity of this lipase. No change was found in the expression of diacylglycerol acyl transferase 1 (DGAT1) after training. Inhibition of HSL with a monospecific, small molecule inhibitor (76-0079) and stimulation of ATGL with CGI-58 revealed that significant ATGL activity is present in human skeletal muscle. These results suggest that ATGL in addition to HSL may be important for human skeletal muscle lipolysis.

AB - Mobilization of fatty acids from stored triacylglycerol (TG) in adipose tissue and skeletal muscle [intramyocellular triacylglycerol (IMTG)] requires activity of lipases. Although exercise training increases the lipolytic capacity of skeletal muscle, the expression of hormone-sensitive lipase (HSL) is not changed. Recently, adipose triglyceride lipase (ATGL) was identified as a TG-specific lipase in various rodent tissues. To investigate whether human skeletal muscle ATGL protein is regulated by endurance exercise training, 10 healthy young men completed 8 wk of supervised endurance exercise training. Western blotting analysis on lysates of skeletal muscle biopsy samples revealed that exercise training induced a twofold increase in skeletal muscle ATGL protein content. In contrast to ATGL, expression of comparative gene identification 58 (CGI-58), the activating protein of ATGL, and HSL protein was not significantly changed after the training period. The IMTG concentration was significantly decreased by 28% at termination of the training program compared with before. HSL-phoshorylation at Ser(660) was increased, HSL-Ser(659) phosporylation was unchanged, and HSL-phoshorylation at Ser(565) was decreased altogether, indicating an enhanced basal activity of this lipase. No change was found in the expression of diacylglycerol acyl transferase 1 (DGAT1) after training. Inhibition of HSL with a monospecific, small molecule inhibitor (76-0079) and stimulation of ATGL with CGI-58 revealed that significant ATGL activity is present in human skeletal muscle. These results suggest that ATGL in addition to HSL may be important for human skeletal muscle lipolysis.

U2 - 10.1152/ajpendo.90912.2008

DO - 10.1152/ajpendo.90912.2008

M3 - Journal article

C2 - 19106247

VL - 296

SP - E445-E453

JO - American Journal of Physiology - Endocrinology and Metabolism

JF - American Journal of Physiology - Endocrinology and Metabolism

SN - 0193-1849

IS - 3

ER -

ID: 11638958