Literature DB >> 19260102

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

Christopher F Spurney1, 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.   

Abstract

The availability of animal models for Duchenne muscular dystrophy has led to extensive preclinical research on potential therapeutics. Few studies have focused on reliability and sensitivity of endpoints for mdx mouse drug trials. Therefore, we sought to compare a wide variety of reported and novel endpoint measures in exercised mdx and normal control mice at 10, 20, and 40 weeks of age. Statistical analysis as well as power calculations for expected effect sizes in mdx preclinical drug trials across different ages showed that body weight, normalized grip strength, horizontal activity, rest time, cardiac function measurements, blood pressure, total central/peripheral nuclei per fiber, and serum creatine kinase are the most effective measurements for detecting drug-induced changes. These data provide an experimental basis upon which standardization of preclinical drug testing can be developed. Muscle Nerve, 2008.

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Year:  2009        PMID: 19260102      PMCID: PMC4116326          DOI: 10.1002/mus.21211

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  43 in total

1.  Modulation of disease severity in mice with targeted disruption of the acid alpha-glucosidase gene.

Authors:  N Raben; K Nagaraju; E Lee; P Plotz
Journal:  Neuromuscul Disord       Date:  2000-06       Impact factor: 4.296

2.  Pre-clinical screening of drugs using the mdx mouse.

Authors:  J A Granchelli; C Pollina; M S Hudecki
Journal:  Neuromuscul Disord       Date:  2000-06       Impact factor: 4.296

Review 3.  Mdx mouse as therapeutic model system: development and implementation of phenotypic monitoring.

Authors:  M S Hudecki; C M Pollina
Journal:  Adv Exp Med Biol       Date:  1990       Impact factor: 2.622

4.  Dystrophin: the protein product of the Duchenne muscular dystrophy locus.

Authors:  E P Hoffman; R H Brown; L M Kunkel
Journal:  Cell       Date:  1987-12-24       Impact factor: 41.582

5.  Evolution of the mdx mouse cardiomyopathy: physiological and morphological findings.

Authors:  John G Quinlan; Harvey S Hahn; Brenda L Wong; John N Lorenz; Alexandra S Wenisch; Linda S Levin
Journal:  Neuromuscul Disord       Date:  2004-09       Impact factor: 4.296

6.  Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1.

Authors:  Annamaria De Luca; Sabata Pierno; Antonella Liantonio; Michela Cetrone; Claudia Camerino; Bodvael Fraysse; Massimo Mirabella; Serenella Servidei; Urs T Rüegg; Diana Conte Camerino
Journal:  J Pharmacol Exp Ther       Date:  2003-01       Impact factor: 4.030

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.  Functional regeneration in the hindlimb skeletal muscle of the mdx mouse.

Authors:  J E Anderson; B H Bressler; W K Ovalle
Journal:  J Muscle Res Cell Motil       Date:  1988-12       Impact factor: 2.698

9.  Standardization and statistical approaches to therapeutic trials in the R6/2 mouse.

Authors:  Emma Hockly; Benjamin Woodman; Amarbirpal Mahal; Cathryn M Lewis; Gillian Bates
Journal:  Brain Res Bull       Date:  2003-09-30       Impact factor: 4.077

Review 10.  Pre-clinical trials in Duchenne dystrophy: what animal models can tell us about potential drug effectiveness.

Authors:  Annamaria De Luca; Sabata Pierno; Antonella Liantonio; Diana Conte Camerino
Journal:  Neuromuscul Disord       Date:  2002-10       Impact factor: 4.296

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  85 in total

1.  Activation of the ubiquitin proteasome pathway in a mouse model of inflammatory myopathy: a potential therapeutic target.

Authors:  Sree Rayavarapu; William Coley; Jack H Van der Meulen; Erdinc Cakir; Kathyayini Tappeta; Travis B Kinder; Blythe C Dillingham; Kristy J Brown; Yetrib Hathout; Kanneboyina Nagaraju
Journal:  Arthritis Rheum       Date:  2013-12

2.  Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy.

Authors:  Jessica R Terrill; Gavin J Pinniger; Jamie A Graves; Miranda D Grounds; Peter G Arthur
Journal:  J Physiol       Date:  2016-01-18       Impact factor: 5.182

3.  Developing standard procedures for murine and canine efficacy studies of DMD therapeutics: report of two expert workshops on "Pre-clinical testing for Duchenne dystrophy": Washington DC, October 27th-28th 2007 and Zürich, June 30th-July 1st 2008.

Authors:  Kanneboyina Nagaraju; Raffaella Willmann
Journal:  Neuromuscul Disord       Date:  2009-06-26       Impact factor: 4.296

4.  Enhancing translation: guidelines for standard pre-clinical experiments in mdx mice.

Authors:  Raffaella Willmann; Annamaria De Luca; Michael Benatar; Miranda Grounds; Judith Dubach; Jean-Marc Raymackers; Kanneboyina Nagaraju
Journal:  Neuromuscul Disord       Date:  2011-07-06       Impact factor: 4.296

5.  Linking GABA(A) receptor subunits to alcohol-induced conditioned taste aversion and recovery from acute alcohol intoxication.

Authors:  Y A Blednov; J M Benavidez; M Black; D Chandra; G E Homanics; U Rudolph; R A Harris
Journal:  Neuropharmacology       Date:  2012-11-09       Impact factor: 5.250

Review 6.  Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trials.

Authors:  Joe N Kornegay; Christopher F Spurney; Peter P Nghiem; Candice L Brinkmeyer-Langford; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  ILAR J       Date:  2014

7.  Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophy.

Authors:  Kitipong Uaesoontrachoon; James L Quinn; Kathleen S Tatem; Jack H Van Der Meulen; Qing Yu; Aditi Phadke; Brittany K Miller; Heather Gordish-Dressman; Ennio Ongini; Daniela Miglietta; Kanneboyina Nagaraju
Journal:  Hum Mol Genet       Date:  2014-01-23       Impact factor: 6.150

8.  Functional and molecular effects of arginine butyrate and prednisone on muscle and heart in the mdx mouse model of Duchenne Muscular Dystrophy.

Authors:  Alfredo D Guerron; Rashmi Rawat; Arpana Sali; Christopher F Spurney; Emidio Pistilli; Hee-Jae Cha; Gouri S Pandey; Ramkishore Gernapudi; Dwight Francia; Viken Farajian; Diana M Escolar; Laura Bossi; Magali Becker; Patricia Zerr; Sabine de la Porte; Heather Gordish-Dressman; Terence Partridge; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  PLoS One       Date:  2010-06-21       Impact factor: 3.240

9.  Characterization of dysferlin deficient SJL/J mice to assess preclinical drug efficacy: fasudil exacerbates muscle disease phenotype.

Authors:  Sree Rayavarapu; Jack H Van der Meulen; Heather Gordish-Dressman; Eric P Hoffman; Kanneboyina Nagaraju; Susan M Knoblach
Journal:  PLoS One       Date:  2010-09-24       Impact factor: 3.240

10.  Evaluation of skeletal and cardiac muscle function after chronic administration of thymosin beta-4 in the dystrophin deficient mouse.

Authors:  Christopher F Spurney; Hee-Jae Cha; Arpana Sali; Gouri S Pandey; Emidio Pistilli; Alfredo D Guerron; Heather Gordish-Dressman; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  PLoS One       Date:  2010-01-29       Impact factor: 3.240

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