Literature DB >> 21917907

Effects of weight loss and leptin on skeletal muscle in human subjects.

Kenneth M Baldwin1, Denis R Joanisse, Fadia Haddad, Rochelle L Goldsmith, Dympna Gallagher, Katherine H Pavlovich, Elisabeth L Shamoon, Rudolph L Leibel, Michael Rosenbaum.   

Abstract

Maintenance of a 10% or greater reduced body weight results in decreases in the energy cost of low levels of physical activity beyond those attributable to the altered body weight. These changes in nonresting energy expenditure are due mainly to increased skeletal muscle work efficiency following weight loss and are reversed by the administration of the adipocyte-derived hormone leptin. We have also shown previously that the maintenance of a reduced weight is accompanied by a decrease in ratio of glycolytic (phosphofructokinase) to oxidative (cytochrome c oxidase) activity in vastus lateralis muscle that would suggest an increase in the relative expression of the myosin heavy chain I (MHC I) isoform. We performed analyses of vastus lateralis muscle needle biopsy samples to determine whether maintenance of an altered body weight was associated with changes in skeletal muscle metabolic properties as well as mRNA expression of different isoforms of the MHC and sarcoplasmic endoplasmic reticular Ca(2+)-dependent ATPase (SERCA) in subjects studied before weight loss and then again after losing 10% of their initial weight and receiving twice daily injections of either placebo or replacement leptin in a single blind crossover design. We found that the maintenance of a reduced body weight was associated with significant increases in the relative gene expression of MHC I mRNA that was reversed by the administration of leptin as well as an increase in the expression of SERCA2 that was not significantly affected by leptin. Leptin administration also resulted in a significant increase in the expression of the less MHC IIx isoform compared with subjects receiving placebo. These findings are consistent with the leptin-reversible increase in skeletal muscle chemomechanical work efficiency and decrease in the ratio of glycolytic/oxidative enzyme activities observed in subjects following dietary weight loss.

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Year:  2011        PMID: 21917907      PMCID: PMC3213951          DOI: 10.1152/ajpregu.00397.2011

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  59 in total

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Authors:  K M Baldwin; F Haddad
Journal:  J Appl Physiol (1985)       Date:  2001-01

Review 2.  Mechanism of thyroid-hormone regulated expression of the SERCA genes in skeletal muscle: implications for thermogenesis.

Authors:  W S Simonides; M H Thelen; C G van der Linden; A Muller; C van Hardeveld
Journal:  Biosci Rep       Date:  2001-04       Impact factor: 3.840

3.  Effects of changes in body weight on carbohydrate metabolism, catecholamine excretion, and thyroid function.

Authors:  M Rosenbaum; J Hirsch; E Murphy; R L Leibel
Journal:  Am J Clin Nutr       Date:  2000-06       Impact factor: 7.045

4.  Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples.

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Journal:  Anal Biochem       Date:  2000-03-01       Impact factor: 3.365

5.  Recombinant leptin for weight loss in obese and lean adults: a randomized, controlled, dose-escalation trial.

Authors:  S B Heymsfield; A S Greenberg; K Fujioka; R M Dixon; R Kushner; T Hunt; J A Lubina; J Patane; B Self; P Hunt; M McCamish
Journal:  JAMA       Date:  1999-10-27       Impact factor: 56.272

Review 6.  Invited Review: plasticity and energetic demands of contraction in skeletal and cardiac muscle.

Authors:  G C Sieck; M Regnier
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7.  Leptin directly stimulates thermogenesis in skeletal muscle.

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8.  Thyroid hormone influences beta myosin heavy chain (beta MHC) expression.

Authors:  J G Edwards; J J Bahl; I L Flink; S Y Cheng; E Morkin
Journal:  Biochem Biophys Res Commun       Date:  1994-03-30       Impact factor: 3.575

Review 9.  The response of skeletal muscle to leptin.

Authors:  R B Ceddia; W N William; R Curi
Journal:  Front Biosci       Date:  2001-01-01

Review 10.  Human skeletal muscle fibres: molecular and functional diversity.

Authors:  R Bottinelli; C Reggiani
Journal:  Prog Biophys Mol Biol       Date:  2000       Impact factor: 3.667

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  20 in total

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Review 2.  20 years of leptin: role of leptin in energy homeostasis in humans.

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Review 3.  Counterregulation of insulin by leptin as key component of autonomic regulation of body weight.

Authors:  Katarina T Borer
Journal:  World J Diabetes       Date:  2014-10-15

4.  Effects of dietary composition on energy expenditure during weight-loss maintenance.

Authors:  Cara B Ebbeling; Janis F Swain; Henry A Feldman; William W Wong; David L Hachey; Erica Garcia-Lago; David S Ludwig
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5.  A randomized study of dietary composition during weight-loss maintenance: Rationale, study design, intervention, and assessment.

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Journal:  Contemp Clin Trials       Date:  2017-12-09       Impact factor: 2.226

6.  Triiodothyronine and leptin repletion in humans similarly reverse weight-loss-induced changes in skeletal muscle.

Authors:  Michael Rosenbaum; Rochelle L Goldsmith; Fadia Haddad; Kenneth M Baldwin; Richard Smiley; Dympna Gallagher; Rudolph L Leibel
Journal:  Am J Physiol Endocrinol Metab       Date:  2018-06-19       Impact factor: 4.310

7.  Aerobic capacity modulates adaptive thermogenesis: Contribution of non-resting energy expenditure.

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8.  Effects of weight gain induced by controlled overfeeding on physical activity.

Authors:  John W Apolzan; George A Bray; Steven R Smith; Lilian de Jonge; Jennifer Rood; Hongmei Han; Leanne M Redman; Corby K Martin
Journal:  Am J Physiol Endocrinol Metab       Date:  2014-10-07       Impact factor: 4.310

9.  Models of energy homeostasis in response to maintenance of reduced body weight.

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Journal:  Obesity (Silver Spring)       Date:  2016-08       Impact factor: 5.002

Review 10.  The gut microbiota in human energy homeostasis and obesity.

Authors:  Michael Rosenbaum; Rob Knight; Rudolph L Leibel
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