Literature DB >> 17957000

Global and targeted gene expression and protein content in skeletal muscle of young men following short-term creatine monohydrate supplementation.

Adeel Safdar1, Nicholas J Yardley, Rodney Snow, Simon Melov, Mark A Tarnopolsky.   

Abstract

Creatine monohydrate (CrM) supplementation has been shown to increase fat-free mass and muscle power output possibly via cell swelling. Little is known about the cellular response to CrM. We investigated the effect of short-term CrM supplementation on global and targeted mRNA expression and protein content in human skeletal muscle. In a randomized, placebo-controlled, crossover, double-blind design, 12 young, healthy, nonobese men were supplemented with either a placebo (PL) or CrM (loading phase, 20 g/day x 3 days; maintenance phase, 5 g/day x 7 days) for 10 days. Following a 28-day washout period, subjects were put on the alternate supplementation for 10 days. Muscle biopsies of the vastus lateralis were obtained and were assessed for mRNA expression (cDNA microarrays + real-time PCR) and protein content (Kinetworks KPKS 1.0 Protein Kinase screen). CrM supplementation significantly increased fat-free mass, total body water, and body weight of the participants (P < 0.05). Also, CrM supplementation significantly upregulated (1.3- to 5.0-fold) the mRNA content of genes and protein content of kinases involved in osmosensing and signal transduction, cytoskeleton remodeling, protein and glycogen synthesis regulation, satellite cell proliferation and differentiation, DNA replication and repair, RNA transcription control, and cell survival. We are the first to report this large-scale gene expression in the skeletal muscle with short-term CrM supplementation, a response that suggests changes in cellular osmolarity.

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Year:  2007        PMID: 17957000     DOI: 10.1152/physiolgenomics.00157.2007

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  32 in total

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Review 3.  "Nutraceuticals" in relation to human skeletal muscle and exercise.

Authors:  Colleen S Deane; Daniel J Wilkinson; Bethan E Phillips; Kenneth Smith; Timothy Etheridge; Philip J Atherton
Journal:  Am J Physiol Endocrinol Metab       Date:  2017-01-31       Impact factor: 4.310

Review 4.  The creatine kinase system and pleiotropic effects of creatine.

Authors:  Theo Wallimann; Malgorzata Tokarska-Schlattner; Uwe Schlattner
Journal:  Amino Acids       Date:  2011-03-30       Impact factor: 3.520

5.  Enhanced mitochondrial biogenesis is associated with the ameliorative action of creatine supplementation in rat soleus and cardiac muscles.

Authors:  Mennatallah A Gowayed; Shimaa A Mahmoud; Yousria El-Sayed; Nehal Abu-Samra; Maher A Kamel
Journal:  Exp Ther Med       Date:  2019-11-07       Impact factor: 2.447

Review 6.  Creatine for treating muscle disorders.

Authors:  Rudolf A Kley; Mark A Tarnopolsky; Matthias Vorgerd
Journal:  Cochrane Database Syst Rev       Date:  2013-06-05

7.  Current nutritional recommendations and novel dietary strategies to manage sarcopenia.

Authors:  Riccardo Calvani; Alfredo Miccheli; Francesco Landi; Maurizio Bossola; Matteo Cesari; Christiaan Leeuwenburgh; Cornel C Sieber; Roberto Bernabei; Emanuele Marzetti
Journal:  J Frailty Aging       Date:  2013

8.  Creatine ( methyl-d3) dilution in urine for estimation of total body skeletal muscle mass: accuracy and variability vs. MRI and DXA.

Authors:  Richard V Clark; Ann C Walker; Ram R Miller; Robin L O'Connor-Semmes; Eric Ravussin; William T Cefalu
Journal:  J Appl Physiol (1985)       Date:  2017-08-31

9.  Aberrant mitochondrial homeostasis in the skeletal muscle of sedentary older adults.

Authors:  Adeel Safdar; Mazen J Hamadeh; Jan J Kaczor; Sandeep Raha; Justin Debeer; Mark A Tarnopolsky
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Review 10.  Can the use of creatine supplementation attenuate muscle loss in cachexia and wasting?

Authors:  Giorgos K Sakkas; Morris Schambelan; Kathleen Mulligan
Journal:  Curr Opin Clin Nutr Metab Care       Date:  2009-11       Impact factor: 4.294

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