Literature DB >> 16542837

First evaluation of the potential effectiveness in muscular dystrophy of a novel chimeric compound, BN 82270, acting as calpain-inhibitor and anti-oxidant.

Rosa Burdi1, Maria Paola Didonna, Bernadette Pignol, Beatrice Nico, Domenica Mangieri, Jean-François Rolland, Claudia Camerino, Alberta Zallone, Paolo Ferro, Francesca Andreetta, Paolo Confalonieri, Annamaria De Luca.   

Abstract

BN 82270 is a membrane-permeable prodrug of a chimeric compound (BN 82204) dually acting as calpain inhibitor and anti-oxidant. Acute in vivo injection of dystrophic mdx mice (30 mg/kg, s.c.) fully counteracted calpain overactivity in diaphragm. A chronic 4-6 weeks administration significantly prevented in vivo the fore limb force drop occurring in mdx mice exercised on treadmill. Ex vivo electrophysiological recordings showed that BN 82270 treatment contrasted the decrease in chloride channel function (gCl) in diaphragm, an index of spontaneous degeneration, while it was less effective on both exercise-impaired gCl and calcium-dependent mechanical threshold of the hind limb extensor digitorum longus (EDL) muscle fibres. The BN 82270 treated mdx mice showed a marked reduction of plasma creatine kinase and of the pro-fibrotic cytokine TGF-beta1 in both hind limb muscles and diaphragm; however, the histopathological profile of gastrocnemious muscle was poorly ameliorated. In hind limb muscles of treated mice, the active form was detected by HPLC in the low therapeutic concentration range. In vitro exposure to 100 microM BN 82270 led to higher active form in diaphragm than in EDL muscle. This is the first demonstration that this class of chimeric compounds, dually targeting pathology-related events, exerts beneficial effects in muscular dystrophy. The drug/prodrug system may require posology adjustment to produce wider beneficial effects on all muscle types.

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Year:  2006        PMID: 16542837     DOI: 10.1016/j.nmd.2006.01.013

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  17 in total

1.  Overexpression of SERCA1a in the mdx diaphragm reduces susceptibility to contraction-induced damage.

Authors:  Kevin J Morine; Meg M Sleeper; Elisabeth R Barton; H Lee Sweeney
Journal:  Hum Gene Ther       Date:  2010-12       Impact factor: 5.695

2.  Regulation of the calpain and ubiquitin-proteasome systems in a canine model of muscular dystrophy.

Authors:  Kristine M Wadosky; Luge Li; Jessica E Rodríguez; Jin-Na Min; Dan Bogan; Jason Gonzalez; Cam Patterson; Joe N Kornegay; Monte Willis
Journal:  Muscle Nerve       Date:  2011-08-08       Impact factor: 3.217

3.  Long-term wheel running compromises diaphragm function but improves cardiac and plantarflexor function in the mdx mouse.

Authors:  Joshua T Selsby; Pedro Acosta; Meg M Sleeper; Elisabeth R Barton; H Lee Sweeney
Journal:  J Appl Physiol (1985)       Date:  2013-07-03

4.  Leupeptin-based inhibitors do not improve the mdx phenotype.

Authors:  Joshua Selsby; Klara Pendrak; Monica Zadel; Zuozhen Tian; Jennifer Pham; Ted Carver; Pedro Acosta; Elisabeth Barton; H Lee Sweeney
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-09-15       Impact factor: 3.619

Review 5.  Gene therapy in large animal models of muscular dystrophy.

Authors:  Zejing Wang; Jeffrey S Chamberlain; Stephen J Tapscott; Rainer Storb
Journal:  ILAR J       Date:  2009

6.  Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures.

Authors:  Christopher F Spurney; Heather Gordish-Dressman; Alfredo D Guerron; Arpana Sali; Gouri S Pandey; Rashmi Rawat; Jack H Van Der Meulen; Hee-Jae Cha; Emidio E Pistilli; Terence A Partridge; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  Muscle Nerve       Date:  2009-05       Impact factor: 3.217

Review 7.  Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy.

Authors:  Miranda D Grounds; Hannah G Radley; Gordon S Lynch; Kanneboyina Nagaraju; Annamaria De Luca
Journal:  Neurobiol Dis       Date:  2008-04-09       Impact factor: 5.996

8.  In situ measurements of calpain activity in isolated muscle fibres from normal and dystrophin-lacking mdx mice.

Authors:  P Gailly; F De Backer; M Van Schoor; J M Gillis
Journal:  J Physiol       Date:  2007-05-17       Impact factor: 5.182

9.  Subcutaneous injection, from birth, of epigallocatechin-3-gallate, a component of green tea, limits the onset of muscular dystrophy in mdx mice: a quantitative histological, immunohistochemical and electrophysiological study.

Authors:  Yoshiko Nakae; Katsuya Hirasaka; Junpei Goto; Takeshi Nikawa; Masayuki Shono; Mizuko Yoshida; Peter J Stoward
Journal:  Histochem Cell Biol       Date:  2008-02-09       Impact factor: 4.304

Review 10.  Pre-clinical drug tests in the mdx mouse as a model of dystrophinopathies: an overview.

Authors:  Annamaria De Luca
Journal:  Acta Myol       Date:  2012-05
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