Skeletal muscle adiponectin induction depends on diet, muscle type/activity, and exercise modality in C57BL/6 mice.

Sergio F Martinez-Huenchullan, Babu R Maharjan, Paul F Williams, Charmaine S Tam, Susan V Mclennan, Stephen M Twigg
Author Information
  1. Sergio F Martinez-Huenchullan: Greg Brown Diabetes & Endocrinology Laboratory, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  2. Babu R Maharjan: Greg Brown Diabetes & Endocrinology Laboratory, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  3. Paul F Williams: Greg Brown Diabetes & Endocrinology Laboratory, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  4. Charmaine S Tam: Northern Clinical School and Centre for Translational Data Science, University of Sydney, Sydney, Australia.
  5. Susan V Mclennan: Greg Brown Diabetes & Endocrinology Laboratory, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  6. Stephen M Twigg: Greg Brown Diabetes & Endocrinology Laboratory, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.

Abstract

Changes in skeletal muscle adiponectin induction have been described in obesity and exercise. However, whether changes are consistent across muscle types and with different exercise modalities, remain unclear. This study compared the effects of diet and two isocaloric training programs on adiponectin induction and its regulators in three muscles: quadriceps (exercising/glycolytic-oxidative), gastrocnemius (exercising/glycolytic), and masseter (nonexercising/glycolytic). Ten-week-old male C57BL/6 mice were fed a high-fat diet (HFD) (45% fat) or standard CHOW diet (12% fat) ad libitum and underwent one of two training regimes: (1) constant-moderate training (END), or (2) high intensity interval training (HIIT) for 10 weeks (3 × 40 min sessions/week). Chow and HFD-fed untrained mice were used as control. Compared with Chow, HFD induced an increase in protein levels of low-molecular weight (LMW) adiponectin in gastrocnemius and masseter (~2-fold; P < 0.05), and a decrease of high-molecular weight adiponectin (HMW-most bioactive form) in quadriceps (~0.5-fold; P < 0.05). Only END prevented these changes (P < 0.05). HFD induced a decrease of adiponectin receptor 1 (AdipoR1) protein in exercising muscles of untrained mice (~0.5-0.8-fold; P < 0.05); notably, END also decreased AdipoR1 protein levels in lean and HFD mice. This type of training also normalized HFD-driven mRNA changes found in some adiponectin downstream factors (sirtuin 1, Pgc-1a, and Ucp2) in the three muscles tested. Our results indicate that diet, muscle type/activity, and exercise modality influences muscle adiponectin profile, and some of its mediators. These parameters should be taken into consideration when investigating this endocrine response of the skeletal muscle, particularly in the context of obesity and metabolic disorders.

Keywords

References

  1. Nature. 2010 Apr 29;464(7293):1313-9 [PMID: 20357764]
  2. Best Pract Res Clin Endocrinol Metab. 2014 Jan;28(1):33-41 [PMID: 24417944]
  3. Exp Physiol. 2015 Jul 1;100(7):755-8 [PMID: 26076765]
  4. Int J Obes Relat Metab Disord. 2001 Apr;25(4):449-56 [PMID: 11319645]
  5. Am J Physiol Endocrinol Metab. 2009 Sep;297(3):E657-64 [PMID: 19531641]
  6. Biochem Biophys Res Commun. 2006 Mar 3;341(1):209-17 [PMID: 16414018]
  7. Physiol Rep. 2014 Jun 24;2(6): [PMID: 24963030]
  8. J Hepatol. 2011 Aug;55(2):435-44 [PMID: 21184785]
  9. J Appl Physiol (1985). 2012 Jun;112(11):1839-46 [PMID: 22461440]
  10. Endocrinology. 2010 Oct;151(10):4840-51 [PMID: 20702578]
  11. J Oral Maxillofac Surg. 1990 Oct;48(10):1063-7 [PMID: 1698954]
  12. PLoS One. 2014 Feb 11;9(2):e88653 [PMID: 24523926]
  13. J Mol Endocrinol. 2005 Dec;35(3):465-76 [PMID: 16326833]
  14. Physiol Rep. 2018 Feb;6(4): [PMID: 29446245]
  15. Diabetologia. 2006 Jun;49(6):1311-23 [PMID: 16570160]
  16. Nutr Metab (Lond). 2016 Nov 3;13:75 [PMID: 27822289]
  17. Compr Physiol. 2013 Jul;3(3):1337-62 [PMID: 23897689]
  18. Physiol Rep. 2018 Oct;6(20):e13848 [PMID: 30338665]
  19. Nutr Diabetes. 2015 Dec 14;5:e187 [PMID: 26657013]
  20. J Gerontol A Biol Sci Med Sci. 2013 Feb;68(2):117-28 [PMID: 22562959]
  21. Am J Physiol Cell Physiol. 2008 Jul;295(1):C203-12 [PMID: 18463233]
  22. PLoS One. 2013 Dec 06;8(12):e81929 [PMID: 24324732]
  23. Diabetes Metab. 2008 Feb;34(1):52-61 [PMID: 18222103]
  24. J Anat. 2013 Jul;223(1):46-60 [PMID: 23692055]
  25. Am J Pathol. 2012 Jul;181(1):245-56 [PMID: 22658482]
  26. Diabetes. 2005 Jul;54(7):1926-33 [PMID: 15983191]
  27. Peptides. 2011 May;32(5):1008-12 [PMID: 21291933]
  28. Endocrinology. 2004 Dec;145(12):5589-97 [PMID: 15319349]
  29. Exp Physiol. 2013 Apr;98(4):908-21 [PMID: 23180810]

MeSH Term

Adiponectin
Animals
Diet, High-Fat
Male
Mice
Mice, Inbred C57BL
Muscle, Skeletal
Physical Conditioning, Animal
Receptors, Adiponectin

Chemicals

Adiponectin
Receptors, Adiponectin

Word Cloud

Created with Highcharts 10.0.0muscleadiponectindietexercisetrainingmiceHFDP < 005skeletalinductionchanges1ENDproteinobesitytwothreequadricepsgastrocnemiusmasseterC57BL/6high-fatfatChowuntrainedinducedlevelsweightdecrease~0AdipoR1musclesalsotype/activitymodalityChangesdescribedHoweverwhetherconsistentacrosstypesdifferentmodalitiesremainunclearstudycomparedeffectsisocaloricprogramsregulatorsmuscles:exercising/glycolytic-oxidativeexercising/glycolyticnonexercising/glycolyticTen-week-oldmalefed45%standardCHOW12%ad libitumunderwentoneregimes:constant-moderate2highintensityintervalHIIT10 weeks3 × 40 minsessions/weekHFD-fedusedcontrolComparedincreaselow-molecularLMW~2-foldhigh-molecularHMW-mostbioactiveform5-foldpreventedreceptorexercising5-08-foldnotablydecreasedleantypenormalizedHFD-drivenmRNAfounddownstreamfactorssirtuinPgc-1aUcp2testedresultsindicateinfluencesprofilemediatorsparameterstakenconsiderationinvestigatingendocrineresponseparticularlycontextmetabolicdisordersSkeletaldependsAdiponectin

Similar Articles

Cited By