Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle. / Pataky, Mark W; Van Acker, Sydney L; Dhingra, Rhea; Freeburg, Marina M; Arias, Edward B; Oki, Kentaro; Wang, Haiyan; Treebak, Jonas T.; Cartee, Gregory D.

In: American Journal of Physiology: Endocrinology and Metabolism, Vol. 317, No. 6, 2019, p. E984-E998.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pataky, MW, Van Acker, SL, Dhingra, R, Freeburg, MM, Arias, EB, Oki, K, Wang, H, Treebak, JT & Cartee, GD 2019, 'Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle', American Journal of Physiology: Endocrinology and Metabolism, vol. 317, no. 6, pp. E984-E998. https://doi.org/10.1152/ajpendo.00304.2019

APA

Pataky, M. W., Van Acker, S. L., Dhingra, R., Freeburg, M. M., Arias, E. B., Oki, K., Wang, H., Treebak, J. T., & Cartee, G. D. (2019). Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle. American Journal of Physiology: Endocrinology and Metabolism, 317(6), E984-E998. https://doi.org/10.1152/ajpendo.00304.2019

Vancouver

Pataky MW, Van Acker SL, Dhingra R, Freeburg MM, Arias EB, Oki K et al. Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle. American Journal of Physiology: Endocrinology and Metabolism. 2019;317(6):E984-E998. https://doi.org/10.1152/ajpendo.00304.2019

Author

Pataky, Mark W ; Van Acker, Sydney L ; Dhingra, Rhea ; Freeburg, Marina M ; Arias, Edward B ; Oki, Kentaro ; Wang, Haiyan ; Treebak, Jonas T. ; Cartee, Gregory D. / Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle. In: American Journal of Physiology: Endocrinology and Metabolism. 2019 ; Vol. 317, No. 6. pp. E984-E998.

Bibtex

@article{3163075a2d3844e7a90bf484edcacc66,
title = "Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle",
abstract = "Muscle is a heterogeneous tissue composed of multiple fiber types. Earlier research revealed fiber type-selective postexercise effects on insulin-stimulated glucose uptake (ISGU) from insulin-resistant rats (increased for type IIA, IIB, IIBX, and IIX, but not type I). In whole muscle from insulin-resistant rats, the exercise increase in ISGU is accompanied by an exercise increase in insulin-stimulated AS160 phosphorylation (pAS160), an ISGU-regulating protein. We hypothesized that, in insulin-resistant muscle, the fiber type-selective exercise effects on ISGU would correspond to the fiber type-selective exercise effects on pAS160. Rats were fed a 2-wk high-fat diet (HFD) and remained sedentary (SED) or exercised before epitrochlearis muscles were dissected either immediately postexercise (IPEX) or at 3 h postexercise (3hPEX) using an exercise protocol that previously revealed fiber type-selective effects on ISGU. 3hPEX muscles and SED controls were incubated ± 100µU/mL insulin. Individual myofibers were isolated and pooled on the basis of myosin heavy chain (MHC) expression, and key phosphoproteins were measured. Myofiber glycogen and MHC expression were evaluated in muscles from other SED, IPEX, and 3hPEX rats. Insulin-stimulated pAktSer473 and pAktThr308 were unaltered by exercise in all fiber types. Insulin-stimulated pAS160 was greater for 3hPEX vs. SED on at least one phosphosite (Ser588, Thr642, and/or Ser704) in type IIA, IIBX, and IIB fibers, but not in type I or IIX fibers. Both IPEX and 3hPEX glycogen were decreased versus SED in all fiber types. These results provided evidence that fiber type-specific pAS160 in insulin-resistant muscle may play a role in the previously reported fiber type-specific elevation in ISGU in some, but not all, fiber types.",
author = "Pataky, {Mark W} and {Van Acker}, {Sydney L} and Rhea Dhingra and Freeburg, {Marina M} and Arias, {Edward B} and Kentaro Oki and Haiyan Wang and Treebak, {Jonas T.} and Cartee, {Gregory D}",
year = "2019",
doi = "10.1152/ajpendo.00304.2019",
language = "English",
volume = "317",
pages = "E984--E998",
journal = "American Journal of Physiology - Endocrinology and Metabolism",
issn = "0193-1849",
publisher = "American Physiological Society",
number = "6",

}

RIS

TY - JOUR

T1 - Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle

AU - Pataky, Mark W

AU - Van Acker, Sydney L

AU - Dhingra, Rhea

AU - Freeburg, Marina M

AU - Arias, Edward B

AU - Oki, Kentaro

AU - Wang, Haiyan

AU - Treebak, Jonas T.

AU - Cartee, Gregory D

PY - 2019

Y1 - 2019

N2 - Muscle is a heterogeneous tissue composed of multiple fiber types. Earlier research revealed fiber type-selective postexercise effects on insulin-stimulated glucose uptake (ISGU) from insulin-resistant rats (increased for type IIA, IIB, IIBX, and IIX, but not type I). In whole muscle from insulin-resistant rats, the exercise increase in ISGU is accompanied by an exercise increase in insulin-stimulated AS160 phosphorylation (pAS160), an ISGU-regulating protein. We hypothesized that, in insulin-resistant muscle, the fiber type-selective exercise effects on ISGU would correspond to the fiber type-selective exercise effects on pAS160. Rats were fed a 2-wk high-fat diet (HFD) and remained sedentary (SED) or exercised before epitrochlearis muscles were dissected either immediately postexercise (IPEX) or at 3 h postexercise (3hPEX) using an exercise protocol that previously revealed fiber type-selective effects on ISGU. 3hPEX muscles and SED controls were incubated ± 100µU/mL insulin. Individual myofibers were isolated and pooled on the basis of myosin heavy chain (MHC) expression, and key phosphoproteins were measured. Myofiber glycogen and MHC expression were evaluated in muscles from other SED, IPEX, and 3hPEX rats. Insulin-stimulated pAktSer473 and pAktThr308 were unaltered by exercise in all fiber types. Insulin-stimulated pAS160 was greater for 3hPEX vs. SED on at least one phosphosite (Ser588, Thr642, and/or Ser704) in type IIA, IIBX, and IIB fibers, but not in type I or IIX fibers. Both IPEX and 3hPEX glycogen were decreased versus SED in all fiber types. These results provided evidence that fiber type-specific pAS160 in insulin-resistant muscle may play a role in the previously reported fiber type-specific elevation in ISGU in some, but not all, fiber types.

AB - Muscle is a heterogeneous tissue composed of multiple fiber types. Earlier research revealed fiber type-selective postexercise effects on insulin-stimulated glucose uptake (ISGU) from insulin-resistant rats (increased for type IIA, IIB, IIBX, and IIX, but not type I). In whole muscle from insulin-resistant rats, the exercise increase in ISGU is accompanied by an exercise increase in insulin-stimulated AS160 phosphorylation (pAS160), an ISGU-regulating protein. We hypothesized that, in insulin-resistant muscle, the fiber type-selective exercise effects on ISGU would correspond to the fiber type-selective exercise effects on pAS160. Rats were fed a 2-wk high-fat diet (HFD) and remained sedentary (SED) or exercised before epitrochlearis muscles were dissected either immediately postexercise (IPEX) or at 3 h postexercise (3hPEX) using an exercise protocol that previously revealed fiber type-selective effects on ISGU. 3hPEX muscles and SED controls were incubated ± 100µU/mL insulin. Individual myofibers were isolated and pooled on the basis of myosin heavy chain (MHC) expression, and key phosphoproteins were measured. Myofiber glycogen and MHC expression were evaluated in muscles from other SED, IPEX, and 3hPEX rats. Insulin-stimulated pAktSer473 and pAktThr308 were unaltered by exercise in all fiber types. Insulin-stimulated pAS160 was greater for 3hPEX vs. SED on at least one phosphosite (Ser588, Thr642, and/or Ser704) in type IIA, IIBX, and IIB fibers, but not in type I or IIX fibers. Both IPEX and 3hPEX glycogen were decreased versus SED in all fiber types. These results provided evidence that fiber type-specific pAS160 in insulin-resistant muscle may play a role in the previously reported fiber type-specific elevation in ISGU in some, but not all, fiber types.

U2 - 10.1152/ajpendo.00304.2019

DO - 10.1152/ajpendo.00304.2019

M3 - Journal article

C2 - 31573845

VL - 317

SP - E984-E998

JO - American Journal of Physiology - Endocrinology and Metabolism

JF - American Journal of Physiology - Endocrinology and Metabolism

SN - 0193-1849

IS - 6

ER -

ID: 231301221