Literature DB >> 22214335

Glucocorticoid analogues: potential therapeutic alternatives for treating inflammatory muscle diseases.

Erica K M Reeves1, Sree Rayavarapu, Jesse M Damsker, Kanneboyina Nagaraju.   

Abstract

Glucocorticoids (GCs) have been prescribed to treat a variety of diseases, including inflammatory myopathies and Duchenne muscular dystrophy for over 50 years. However, their prescription remains controversial due to the significant side effects associated with the chronic treatment. It is a common belief that the clinical efficacy of GCs is due to their transrepression of pro-inflammatory genes through inhibition of inflammatory transcription factors (i.e. NF-κB, AP-1) whereas the adverse side effects are attributed to the glucocorticoid receptor (GR)-mediated transcription of target genes (transactivation). The past decade has seen an increased interest in the development of GR modulators that maintain the effective anti-inflammatory properties but lack the GR-dependent transcriptional response as a safe alternative to traditional GCs. Many of these analogues or "dissociative" compounds show potential promise in in vitro studies but fail to reach human clinical trials. In this review, we discuss molecular effects of currently prescribed GCs on skeletal muscle and also discuss the current state of development of GC analogues as alternative therapeutics for inflammatory muscle diseases.

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Year:  2012        PMID: 22214335     DOI: 10.2174/187153012799279045

Source DB:  PubMed          Journal:  Endocr Metab Immune Disord Drug Targets        ISSN: 1871-5303            Impact factor:   2.895


  7 in total

1.  VBP15: preclinical characterization of a novel anti-inflammatory delta 9,11 steroid.

Authors:  Erica K M Reeves; Eric P Hoffman; Kanneboyina Nagaraju; Jesse M Damsker; John M McCall
Journal:  Bioorg Med Chem       Date:  2013-02-18       Impact factor: 3.641

2.  Forward subtractive libraries containing genes transactivated by dexamethasone in ataxia-telangiectasia lymphoblastoid cells.

Authors:  Sara Biagiotti; Michele Menotta; Elisa Giacomini; Lucia Radici; Marzia Bianchi; Cristina Bozzao; Luciana Chessa; Mauro Magnani
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3.  Friedreich Ataxia and nephrotic syndrome: a series of two patients.

Authors:  Julianna E Shinnick; Charles J Isaacs; Sharon Vivaldi; Kimberly Schadt; David R Lynch
Journal:  BMC Neurol       Date:  2016-01-12       Impact factor: 2.474

4.  Skeletal muscle secretome in Duchenne muscular dystrophy: a pivotal anti-inflammatory role of adiponectin.

Authors:  S Lecompte; M Abou-Samra; R Boursereau; L Noel; S M Brichard
Journal:  Cell Mol Life Sci       Date:  2017-02-10       Impact factor: 9.261

5.  Preliminary Evidences of Safety and Efficacy of Flavonoids- and Omega 3-Based Compound for Muscular Dystrophies Treatment: A Randomized Double-Blind Placebo Controlled Pilot Clinical Trial.

Authors:  Clementina Sitzia; Mirella Meregalli; Marzia Belicchi; Andrea Farini; Maddalena Arosio; Denise Bestetti; Chiara Villa; Luca Valenti; Paolo Brambilla; Yvan Torrente
Journal:  Front Neurol       Date:  2019-07-23       Impact factor: 4.003

6.  Downregulation of the NLRP3 inflammasome by adiponectin rescues Duchenne muscular dystrophy.

Authors:  Raphaël Boursereau; Michel Abou-Samra; Sophie Lecompte; Laurence Noel; Sonia M Brichard
Journal:  BMC Biol       Date:  2018-03-20       Impact factor: 7.431

7.  UBE2E1 Is Preferentially Expressed in the Cytoplasm of Slow-Twitch Fibers and Protects Skeletal Muscles from Exacerbated Atrophy upon Dexamethasone Treatment.

Authors:  Polge Cécile; Aniort Julien; Armani Andrea; Claustre Agnès; Coudy-Gandilhon Cécile; Tournebize Clara; Deval Christiane; Combaret Lydie; Béchet Daniel; Sandri Marco; Attaix Didier; Taillandier Daniel
Journal:  Cells       Date:  2018-11-16       Impact factor: 6.600

  7 in total

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