Literature DB >> 26494902

Combinatorial therapeutic activation with heparin and AICAR stimulates additive effects on utrophin A expression in dystrophic muscles.

Christine Péladeau1, Aatika Ahmed1, Adel Amirouche1, Tara E Crawford Parks1, Lucas M Bronicki1, Vladimir Ljubicic1, Jean-Marc Renaud1, Bernard J Jasmin2.   

Abstract

Upregulation of utrophin A is an attractive therapeutic strategy for treating Duchenne muscular dystrophy (DMD). Over the years, several studies revealed that utrophin A is regulated by multiple transcriptional and post-transcriptional mechanisms, and that pharmacological modulation of these pathways stimulates utrophin A expression in dystrophic muscle. In particular, we recently showed that activation of p38 signaling causes an increase in the levels of utrophin A mRNAs and protein by decreasing the functional availability of the destabilizing RNA-binding protein called K-homology splicing regulatory protein, thereby resulting in increases in the stability of existing mRNAs. Here, we treated 6-week-old mdx mice for 4 weeks with the clinically used anticoagulant drug heparin known to activate p38 mitogen-activated protein kinase, and determined the impact of this pharmacological intervention on the dystrophic phenotype. Our results show that heparin treatment of mdx mice caused a significant ∼1.5- to 3-fold increase in utrophin A expression in diaphragm, extensor digitorum longus and tibialis anterior (TA) muscles. In agreement with these findings, heparin-treated diaphragm and TA muscle fibers showed an accumulation of utrophin A and β-dystroglycan along their sarcolemma and displayed improved morphology and structural integrity. Moreover, combinatorial drug treatment using both heparin and 5-amino-4-imidazolecarboxamide riboside (AICAR), the latter targeting 5' adenosine monophosphate-activated protein kinase and the transcriptional activation of utrophin A, caused an additive effect on utrophin A expression in dystrophic muscle. These findings establish that heparin is a relevant therapeutic agent for treating DMD, and illustrate that combinatorial treatment of heparin with AICAR may serve as an effective strategy to further increase utrophin A expression in dystrophic muscle via activation of distinct signaling pathways.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2015        PMID: 26494902      PMCID: PMC4690489          DOI: 10.1093/hmg/ddv444

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  121 in total

1.  Increased expression of utrophin in a slow vs. a fast muscle involves posttranscriptional events.

Authors:  A O Gramolini; G Bélanger; J M Thompson; J V Chakkalakal; B J Jasmin
Journal:  Am J Physiol Cell Physiol       Date:  2001-10       Impact factor: 4.249

2.  Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.

Authors:  Chiara S M Straathof; Dave Van Heusden; Pieternella F Ippel; Jan G Post; Nicol C Voermans; Marianne De Visser; Esther Brusse; Janneke C Van Den Bergen; Anneke J Van Der Kooi; Jan J G M Verschuuren; Hendrika B Ginjaar
Journal:  Muscle Nerve       Date:  2015-06-03       Impact factor: 3.217

3.  Local transcriptional control of utrophin expression at the neuromuscular synapse.

Authors:  A O Gramolini; C L Dennis; J M Tinsley; G S Robertson; J Cartaud; K E Davies; B J Jasmin
Journal:  J Biol Chem       Date:  1997-03-28       Impact factor: 5.157

4.  Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice.

Authors:  J A Rafael; J M Tinsley; A C Potter; A E Deconinck; K E Davies
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

Review 5.  Function and genetics of dystrophin and dystrophin-related proteins in muscle.

Authors:  Derek J Blake; Andrew Weir; Sarah E Newey; Kay E Davies
Journal:  Physiol Rev       Date:  2002-04       Impact factor: 37.312

6.  The in vivo role of p38 MAP kinases in cardiac remodeling and restrictive cardiomyopathy.

Authors:  P Liao; D Georgakopoulos; A Kovacs; M Zheng; D Lerner; H Pu; J Saffitz; K Chien; R P Xiao; D A Kass; Y Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-02       Impact factor: 11.205

7.  Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin.

Authors:  B Yang; D Jung; J A Rafael; J S Chamberlain; K P Campbell
Journal:  J Biol Chem       Date:  1995-03-10       Impact factor: 5.157

Review 8.  PGC-1alpha regulation by exercise training and its influences on muscle function and insulin sensitivity.

Authors:  Vitor A Lira; Carley R Benton; Zhen Yan; Arend Bonen
Journal:  Am J Physiol Endocrinol Metab       Date:  2010-04-06       Impact factor: 4.310

9.  Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1{alpha}, drives utrophin gene expression at the neuromuscular junction.

Authors:  Lindsay M Angus; Joe V Chakkalakal; Alexandre Méjat; Joe K Eibl; Guy Bélanger; Lynn A Megeney; Eva R Chin; Laurent Schaeffer; Robin N Michel; Bernard J Jasmin
Journal:  Am J Physiol Cell Physiol       Date:  2005-06-01       Impact factor: 4.249

10.  The effect of glucocorticoids on the accumulation of utrophin by cultured normal and dystrophic human skeletal muscle satellite cells.

Authors:  F Pasquini; C Guerin; D Blake; K Davies; G Karpati; P Holland
Journal:  Neuromuscul Disord       Date:  1995-03       Impact factor: 4.296

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  9 in total

1.  Poly C Binding Protein 2 dependent nuclear retention of the utrophin-A mRNA in C2C12 cells.

Authors:  Gargi Ghosh; Satyabrata Samui; Santanu Das; Vandana Singh; Doel Pal; Subhanwita Das; Jishu Naskar; Soumya Sinha Roy; Utpal Basu
Journal:  RNA Biol       Date:  2021-12-14       Impact factor: 4.652

Review 2.  Current and Emerging Therapies for Duchenne Muscular Dystrophy.

Authors:  Megan Crone; Jean K Mah
Journal:  Curr Treat Options Neurol       Date:  2018-06-23       Impact factor: 3.598

Review 3.  Targeting IRES-dependent translation as a novel approach for treating Duchenne muscular dystrophy.

Authors:  Christine Péladeau; Bernard J Jasmin
Journal:  RNA Biol       Date:  2020-11-19       Impact factor: 4.652

4.  Long-Term Quercetin Dietary Enrichment Partially Protects Dystrophic Skeletal Muscle.

Authors:  Hannah R Spaulding; Christopher G Ballmann; John C Quindry; Joshua T Selsby
Journal:  PLoS One       Date:  2016-12-15       Impact factor: 3.240

5.  Utrophin haploinsufficiency does not worsen the functional performance, resistance to eccentric contractions and force production of dystrophic mice.

Authors:  Antoine Boulanger Piette; Dounia Hamoudi; Laetitia Marcadet; Frédérique Kyomi Labelle; Rares Ovidiu David; Sabrina Bossé; Anteneh Argaw; Jérôme Frenette
Journal:  PLoS One       Date:  2018-06-07       Impact factor: 3.240

6.  Chronic 5-Aminoimidazole-4-Carboxamide-1-β-d-Ribofuranoside Treatment Induces Phenotypic Changes in Skeletal Muscle, but Does Not Improve Disease Outcomes in the R6/2 Mouse Model of Huntington's Disease.

Authors:  Marie-France Paré; Bernard J Jasmin
Journal:  Front Neurol       Date:  2017-09-27       Impact factor: 4.003

7.  Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD.

Authors:  Simon Guiraud; Benjamin Edwards; Sarah E Squire; Lee Moir; Adam Berg; Arran Babbs; Nesrine Ramadan; Matthew J Wood; Kay E Davies
Journal:  Hum Mol Genet       Date:  2019-01-15       Impact factor: 6.150

8.  Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles.

Authors:  Christine Péladeau; Nadine Adam; Lucas M Bronicki; Adèle Coriati; Mohamed Thabet; Hasanen Al-Rewashdy; Jason Vanstone; Alan Mears; Jean-Marc Renaud; Martin Holcik; Bernard J Jasmin
Journal:  Nat Commun       Date:  2020-04-24       Impact factor: 14.919

9.  Utrophin modulator drugs as potential therapies for Duchenne and Becker muscular dystrophies.

Authors:  Patricia Soblechero-Martín; Andrea López-Martínez; Laura de la Puente-Ovejero; Ainara Vallejo-Illarramendi; Virginia Arechavala-Gomeza
Journal:  Neuropathol Appl Neurobiol       Date:  2021-06-04       Impact factor: 8.090

  9 in total

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