Reduced skeletal muscle protein turnover and thyroid hormone metabolism in adaptive thermogenesis that facilitates body fat recovery during weight regain
Open accessAbstract
Objective: The recovery of body composition after weight loss is characterized by an accelerated rate of fat recovery (preferential catch-up fat) resulting partly from an adaptive suppression of thermogenesis. Although the skeletal muscle has been implicated as an effector site for such thrifty (energy conservation) metabolism driving catch-up fat, the underlying mechanisms remain to be elucidated. We test here the hypothesis that this thrifty metabolism driving catch-up fat could reside in a reduced rate of protein turnover (an energetically costly ‘futile’ cycle) and in altered local thyroid hormone metabolism in skeletal muscle. Methods: Using a validated rat model of semistarvation-refeeding in which catch-up fat is driven solely by suppressed thermogenesis, we measured after 1 week of refeeding in refed and control animals the following: (i) in-vivo rates of protein synthesis in hindlimb skeletal muscles using the flooding dose technique of 13C-labeled valine incorporation in muscle protein, (ii) ex-vivo muscle assay of net formation of thyroid hormone tri-iodothyronine (T3) from precursor hormone thyroxine (T4), and (iii) protein expression of skeletal muscle deiodinases (type 1, 2 and 3). Results: We show that after 1 week of calorie-controlled refeeding, the fractional protein synthesis rate was lower in skeletal muscles of refed animals than in controls (by 30-35%, p<0.01) despite no between-group differences in the rate of skeletal muscle growth or whole-body protein deposition - thereby underscoring concomitant reductions in both protein synthesis and protein degradation rates in skeletal muscles of refed animals compared to controls. These differences in skeletal muscle protein turnover during catch-up fat were found to be independent of muscle type and fiber composition, and were associated with a slower net formation of muscle T3 from precursor hormone T4, together with increases in muscle protein expression of deiodinases which convert T4 and T3 to inactive forms. Conclusions: These results suggest that diminished skeletal muscle protein turnover, together with altered local muscle metabolism of thyroid hormones leading to diminished intracellular T3 availability, are features of the thrifty metabolism that drives the rapid restoration of the fat reserves during weight regain after caloric restriction.
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Weight cycling and body composition trajectory may cause repeated fat-free mass loss that is not fully recovered during weight regain, due to post-restriction metabolic and hormonal changes during refeeding.
“weight cycling and body composition trajectory [113] as it may induce repeated FFM loss which is not completely recovered during weight regain in relation to post-restriction metabolic and hormonal alterations during refeeding [114].”
From Critical appraisal of definitions and diagnostic criteria for sarcopenic obesity based on a systematic review (2020) · cites this paper as [114]
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Cites
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works
Cellular energy utilization and molecular origin of standard metabolic rate in mammals
Rolfe, D. F., & Brown, G. C. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.3.731 · Cited by 2,021 · see citing works
Thyroid hormones and skeletal muscle—new insights and potential implications
Salvatore, D., Simonides, W. S., Dentice, M., Zavacki, A. M., & Larsen, P. R. (2013) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2013.238 · Cited by 389 · see citing works
Skeletal-muscle growth and protein turnover
Millward, D. J., Garlick, P. J., Stewart, R. J. C., Nnanyelugo, D. O., & Waterlow, J. C. (1975) · Biochemical Journal · doi:10.1042/bj1500235 · Cited by 364 · see citing works
Iodothyronine Metabolism in Rat Liver Homogenates
Kaplan, M. M., & Utiger, R. D. (1978) · Journal of Clinical Investigation · doi:10.1172/jci108957 · Cited by 312 · see citing works
PROTEIN TURNOVER WITH SPECIAL REFERENCE TO MAN
Waterlow, J. C. (1984) · Quarterly Journal of Experimental Physiology · doi:10.1113/expphysiol.1984.sp002829 · Cited by 301 · see citing works
Young, V. R., & Marchini, J. S. (1990) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/51.2.270 · Cited by 231 · see citing works
Dulloo, A. G., Jacquet, J., Seydoux, J., & Montani, J.-P. (2006) · International Journal of Obesity · doi:10.1038/sj.ijo.0803516 · Cited by 225 · see citing works
Self-citationJepson, M. M., Pell, J. M., BATES, P. C., & Millward, D. J. (1986) · Biochemical Journal · doi:10.1042/bj2350329 · Cited by 206 · see citing works
The classic pathways of thyroid hormone metabolism
van der Spek, A. H., Fliers, E., & Boelen, A. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.01.025 · Cited by 194 · see citing works
Protein Turnover, Ureagenesis and Gluconeogenesis
Schütz, Y. (2011) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831/a000064 · Cited by 178 · see citing works
Guillet, C., Delcourt, I., Rance, M., Giraudet, C., Walrand, S., Bedu, M., Duché, P., & Boirie, Y. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-2216 · Cited by 175 · see citing works
Self-citationThyroid Hormone as a Determinant of Metabolic and Contractile Phenotype of Skeletal Muscle
Simonides, W. S., & van Hardeveld, C. (2008) · Thyroid · doi:10.1089/thy.2007.0256 · Cited by 169 · see citing works
Uncoupling proteins: their roles in adaptive thermogenesis and substrate metabolism reconsidered
Dulloo, A. G., & Samec, S. (2001) · British Journal Of Nutrition · doi:10.1079/bjn2001412 · Cited by 166 · see citing works
Self-citationEnhanced metabolic efficiency contributes to weight regain after weight loss in obesity-prone rats
MacLean, P. S., HIGGINS, J. A., Johnson, G. C., Fleming‐Elder, B. K., Donahoo, W. T., Melanson, E. L., & Hill, J. O. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00463.2004 · Cited by 162 · see citing works
Redistribution of Glucose From Skeletal Muscle to Adipose Tissue During Catch-Up Fat
Cettour-Rose, P., Samec, S., Russell, A. P., Summermatter, S., Mainieri, D., Theander-Carrillo, C., Montani, J., Seydoux, J., Rohner‐Jeanrenaud, F., & Dulloo, A. G. (2005) · Diabetes · doi:10.2337/diabetes.54.3.751 · Cited by 157 · see citing works
Self-citationTissue-specific regulation of mitochondrial and cytoplasmic protein synthesis rates by insulin
Boirie, Y., Short, K. R., Ahlman, B., Charlton, M., & Nair, K. S. (2001) · Diabetes · doi:10.2337/diabetes.50.12.2652 · Cited by 137 · see citing works
Self-citation[55] General procedures for separating lipid components of tissue
Entenman, C. (1957) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(57)03395-9 · Cited by 130 · see citing works
Dulloo, A. G., & Girardier, L. (1990) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/52.3.415 · Cited by 130 · see citing works
Self-citationImpaired protein metabolism: interlinks between obesity, insulin resistance and inflammation
Guillet, C., Masgrau, A., Walrand, S., & Boirie, Y. (2012) · Obesity Reviews · doi:10.1111/j.1467-789x.2012.01037.x · Cited by 118 · see citing works
Self-citationA Role for Suppressed Thermogenesis Favoring Catch-Up Fat in the Pathophysiology of Catch-Up Growth
Crescenzo, R., Samec, S., Antic, V., Rohner‐Jeanrenaud, F., Seydoux, J., Montani, J., & Dulloo, A. G. (2003) · Diabetes · doi:10.2337/diabetes.52.5.1090 · Cited by 111 · see citing works
Self-citationIncreased efficiency of food utilization following weight loss
Boyle, P. C., Storlien, L. H., & Keesey, R. E. (1978) · Physiology & Behavior · doi:10.1016/0031-9384(78)90050-1 · Cited by 107 · see citing works
Dorchies, O. M., Reutenauer, J., Dahmane, E., Ismail, H. M., Petermann, O., Patthey-Vuadens, O., Comyn, S. A., Gayi, E., Piacenza, T., Handa, R. J., et al. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.10.018 · Cited by 107 · see citing works
Reawakened interest in type III iodothyronine deiodinase in critical illness and injury
Huang, S. A., & Bianco, A. C. (2008) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0727 · Cited by 95 · see citing works
Time‐course changes of muscle protein synthesis associated with obesity‐induced lipotoxicity
Masgrau, A., Mishellany‐Dutour, A., Murakami, H., Beaufrére, A. M., Walrand, S., Giraudet, C., Migné, C., Gerbaix, M., Metz, L., Courteix, D., et al. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.238576 · Cited by 93 · see citing works
Self-citationAn adipose-specific control of thermogenesis in body weight regulation
Dulloo, A. G., & Jacquet, J. (2001) · International Journal of Obesity · doi:10.1038/sj.ijo.0801907 · Cited by 92 · see citing works
Self-citationHuman Uncoupling Protein‐3 and Obesity: An Update
Hesselink, M. K. C., Mensink, M., & Schrauwen, P. (2003) · Obesity Research · doi:10.1038/oby.2003.192 · Cited by 85 · see citing works
Crescenzo, R., Lionetti, L., Mollica, M. P., Ferraro, M., D’Andrea, E., Mainieri, D., Dulloo, A. G., Liverini, G., & Iossa, S. (2006) · Diabetes · doi:10.2337/db06-0312 · Cited by 72 · see citing works
Self-citationEffects of fasting and restricted refeeding on utilization of ingested energy in rats
Hill, J. O., Fried, S. K., & DiGirolamo, M. (1984) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1984.247.2.r318 · Cited by 71 · see citing works
The effects of severe zinc deficiency on protein turnover in muscle and thymus
Giugliano, R., & Millward, D. J. (1987) · British Journal Of Nutrition · doi:10.1079/bjn19870017 · Cited by 68 · see citing works
Summermatter, S., Mainieri, D., Russell, A. P., Seydoux, J., Montani, J. P., Buchala, A. J., Solinas, G., & Dulloo, A. G. (2007) · The FASEB Journal · doi:10.1096/fj.07-8972com · Cited by 57 · see citing works
Self-citationA Role for Adipose Tissue De Novo Lipogenesis in Glucose Homeostasis During Catch-up Growth
Marcelino, H., Veyrat‐Durebex, C., Summermatter, S., Sarafian, D., Miles-Chan, J. L., Arsenijevic, D., Zani, F., Montani, J., Seydoux, J., Solinas, G., et al. (2012) · Diabetes · doi:10.2337/db12-0255 · Cited by 54 · see citing works
Self-citationEvans, S. A., Messina, M. M., Knight, W. D., Parsons, A. D., & Overton, J. M. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00602.2004 · Cited by 51 · see citing works
Insulin resistance syndrome blunts the mitochondrial anabolic response following resistance exercise
Nilsson, M. I., Greene, N. P., Dobson, J. P., Wiggs, M. P., Gasier, H. G., Macias, B. R., Shimkus, K. L., & Fluckey, J. D. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00118.2010 · Cited by 50 · see citing works
The hormonal control of protein turnover
Millward, D. J. (1990) · Clinical Nutrition · doi:10.1016/0261-5614(90)90042-q · Cited by 48 · see citing works
Dulloo, A. G., & Schütz, Y. (2015) · Current Obesity Reports · doi:10.1007/s13679-015-0156-9 · Cited by 46 · see citing works
Self-citationCharacteristics of skeletal muscle growth and protein turnover in a fast-growing rat strain
BATES, P. C., & Millward, D. J. (1981) · British Journal Of Nutrition · doi:10.1079/bjn19810004 · Cited by 46 · see citing works
Andrade, P. B. M. D., Neff, L. A., Štrosová, M., Arsenijevic, D., Patthey-Vuadens, O., Scapozza, L., Montani, J., Rüegg, U. T., Dulloo, A. G., & Dorchies, O. M. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00254 · Cited by 46 · see citing works
Self-citationReutenauer-Patte, J., Boittin, F., Patthey-Vuadens, O., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.10.038 · Cited by 41 · see citing works
Higher skeletal muscle protein synthesis and lower breakdown after chemotherapy in cachectic mice
Samuels, S. E., Knowles, A. L., TILIGNAC, T., et al. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.281.1.r133 · Cited by 40 · see citing works
Chanséaume, E., Giraudet, C., Gryson, C., Walrand, S., Rousset, P., Boirie, Y., & Morio, B. (2007) · Obesity · doi:10.1038/oby.2007.582 · Cited by 37 · see citing works
Self-citationA role for skeletal muscle stearoyl‐CoA desaturase 1 in control of thermogenesis
Mainieri, D., Summermatter, S., Seydoux, J., Montani, J., Rusconi, S., Russell, A. P., Boss, O., Buchala, A. J., & Dulloo, A. G. (2006) · The FASEB Journal · doi:10.1096/fj.06-5934fje · Cited by 36 · see citing works
Self-citationSamuels, S. E., Thompson, J. R., & Christopherson, R. J. (1996) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1996.270.6.r1231 · Cited by 15 · see citing works
Skeletal and cardiac muscle protein turnover during cold acclimation in young rats
McAllister, T. A., Thompson, J. R., & Samuels, S. E. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.3.r705 · Cited by 15 · see citing works
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Research works printed but not linked: 1
- [31]Waterlow JC Garlick PJ Millward DJ Protein Turnover in Mammalian Tissues and in the Whole Body, Chapter 17, 18. North-Holland Amsterdam: Elsevier, (1978).
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Donini, L. M., Busetto, L., Bauer, J. M., Bischoff, S., Boirie, Y., Cederholm, T., Cruz-Jentoft, A. J., Dicker, D., Frühbeck, G., Giustina, A., et al. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2019.11.024 · Cited by 326 · see citing works
Self-citationLi, M., Wang, S., Li, Y., Zhao, M., Kuang, J., Liang, D., Wang, J., Wei, M., Rajani, C., Ma, X., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29589-7 · Cited by 175 · see citing works
Calonne, J., Arsenijevic, D., Scerri, I., Miles-Chan, J. L., Montani, J.-P., & Dulloo, A. G. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00092.2019 · Cited by 15 · see citing works
Self-citation
- Authors
- Calonne, J., Isacco, L., Miles-Chan, J., Arsenijevic, D., Montani, J.-P., Guillet, C., Boirie, Y., & Dulloo, A. G.
- Affiliations
- University of Fribourg (CH)
- Université Clermont Auvergne (FR)
- Corresponding author
- Dulloo, Abdul G.
- Venue
- Frontiers in Endocrinology
- Publisher
- Frontiers Media SA
- Published
- 2019-02-28
- Volume
- 10
- Pages
- 119-119
- ISSN
- 1664-2392 (ISSN-L)
- PMC
- PMC6403129
- OpenAlex
- W2920001649
- Cited by
- 29
- References
- 44
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 2 · 2023: 6 · 2022: 4 · 2021: 5 · 2020: 2 · 2019: 5
- FWCI
- 2.12
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Endocrinology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- reroDoc Digital Library (submittedVersion)
- HAL (submittedVersion, cc-by)
- HAL (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (310030_152870)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- weight regain, skeletal muscle protein turnover, thyroid hormone metabolism, triiodothyronine, deiodinases, adaptive thermogenesis, muscle protein synthesis, muscle protein degradation, caloric restriction
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