Literature DB >> 20725872

Effects of β-hydroxy-β-methylbutyrate treatment in different types of skeletal muscle of intact and septic rats.

Miroslav Kovarik1, Tomas Muthny, Ludek Sispera, Milan Holecek.   

Abstract

β-Hydroxy-β-methylbutyrate (HMB) is a leucine metabolite that may have a positive effect in protein catabolic conditions. Therefore, we hypothesized that HMB treatment could attenuate the sepsis-induced protein catabolic state. The aims of our study were to elucidate the effect of HMB in healthy and septic animals and to evaluate the differences in the action of HMB in different muscle types. Intact and septic (5 mg endotoxin/kg i.p.) rats were administered with HMB (0.5 g/kg/day) or saline. After 24 h, extensor digitorum longus (EDL) and soleus (SOL) muscles were isolated and used for determination of total and myofibrillar proteolysis, protein synthesis, leucine oxidation, activity of cathepsins B and L, chymotrypsin-like activity, and expression of α-subunits of proteasome. Our results indicate that the catabolic state induced by the endotoxin treatment was caused both by increase in protein breakdown (due to activation of proteasome system) and by attenuation of protein synthesis. The EDL (muscle composed of white, fast-twitch fibers) was more susceptible to these changes than the SOL (muscle composed of red, slow-twitch fibers). The HMB treatment had no effect in healthy animals but counteracted the changes in septic animals. The action of HMB was mediated by attenuation of proteasome activity and protein breakdown, not by stimulation of protein synthesis. More pronounced effect of the HMB treatment on myofibrillar proteolysis was observed in the SOL.

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Year:  2010        PMID: 20725872     DOI: 10.1007/s13105-010-0037-3

Source DB:  PubMed          Journal:  J Physiol Biochem        ISSN: 1138-7548            Impact factor:   4.158


  41 in total

1.  Sepsis-induced muscle proteolysis is prevented by a proteasome inhibitor in vivo.

Authors:  D Fischer; G Gang; T Pritts; P O Hasselgren
Journal:  Biochem Biophys Res Commun       Date:  2000-04-02       Impact factor: 3.575

2.  Nutritional treatment for acquired immunodeficiency virus-associated wasting using beta-hydroxy beta-methylbutyrate, glutamine, and arginine: a randomized, double-blind, placebo-controlled study.

Authors:  R H Clark; G Feleke; M Din; T Yasmin; G Singh; F A Khan; J A Rathmacher
Journal:  JPEN J Parenter Enteral Nutr       Date:  2000 May-Jun       Impact factor: 4.016

3.  Evidence that the intracellular pool of tyrosine serves as precursor for protein synthesis in muscle.

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4.  Attenuation of proteasome-induced proteolysis in skeletal muscle by {beta}-hydroxy-{beta}-methylbutyrate in cancer-induced muscle loss.

Authors:  Helen J Smith; Pradip Mukerji; Michael J Tisdale
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6.  Increased expression of proteasome subunits in skeletal muscle of cancer patients with weight loss.

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Journal:  Am J Physiol Endocrinol Metab       Date:  2007-07-03       Impact factor: 4.310

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  34 in total

1.  Metabolic and functional effects of beta-hydroxy-beta-methylbutyrate (HMB) supplementation in skeletal muscle.

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2.  The dose-dependent effects of endotoxin on protein metabolism in two types of rat skeletal muscle.

Authors:  Miroslav Kovarik; Tomas Muthny; Ludek Sispera; Milan Holecek
Journal:  J Physiol Biochem       Date:  2012-02-07       Impact factor: 4.158

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Journal:  J Physiol Sci       Date:  2017-01-12       Impact factor: 2.781

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Journal:  Am J Physiol Endocrinol Metab       Date:  2016-05-03       Impact factor: 4.310

6.  β-Hydroxy-β-methylbutyrate (HMB) prevents dexamethasone-induced myotube atrophy.

Authors:  Zaira Aversa; Nima Alamdari; Estibaliz Castillero; Maurizio Muscaritoli; Filippo Rossi Fanelli; Per-Olof Hasselgren
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9.  Metabolomics as a novel approach for early diagnosis of pediatric septic shock and its mortality.

Authors:  Beata Mickiewicz; Hans J Vogel; Hector R Wong; Brent W Winston
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10.  Protein synthesis in skeletal muscle of neonatal pigs is enhanced by administration of β-hydroxy-β-methylbutyrate.

Authors:  Scott M Wheatley; Samer W El-Kadi; Agus Suryawan; Claire Boutry; Renán A Orellana; Hanh V Nguyen; Steven R Davis; Teresa A Davis
Journal:  Am J Physiol Endocrinol Metab       Date:  2013-11-05       Impact factor: 4.310

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