Literature DB >> 14530991

Longitudinal pathologic study of the gastrocnemius muscle group in mdx mice.

Manuel Roig1, Josep Roma, Arnau Fargas, Francina Munell.   

Abstract

Muscle necrosis in mdx mice is rare before the 2nd week of life, but becomes pronounced from weeks 2 to 6. There is no agreement on what happens after this age. Using sequential microscopic histology, immunohistochemistry and histomorphometry, we studied the evolution of muscle pathology throughout the mdx life span. Between 2 weeks and 3 months, multiple necrotic groups involving variable numbers of fibres were observed in the same section. During this period, most necrotic groups comprised more than 15 fibres. From 3 to 6 months, necrosis diminished progressively, involving isolated fibres or groups of two to five fibres, and most fibres had a centrally located nucleus. From 6 months onward there was progressive variation of fibre size and deposition of fibrillary collagens. Mast cell counts increased progressively until 6 months of age. Diminishing necrosis rather than increasing regeneration may explain the differences in muscle pathology observed between human DMD and mouse mdx. Mast cells play a secondary role in pathogenesis.

Entities:  

Mesh:

Year:  2003        PMID: 14530991     DOI: 10.1007/s00401-003-0773-3

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  13 in total

1.  Markers of degeneration and regeneration in Duchenne muscular dystrophy.

Authors:  E Abdel-Salam; I Abdel-Meguid; S S Korraa
Journal:  Acta Myol       Date:  2009-12

Review 2.  Immunobiology of Inherited Muscular Dystrophies.

Authors:  James G Tidball; Steven S Welc; Michelle Wehling-Henricks
Journal:  Compr Physiol       Date:  2018-09-14       Impact factor: 9.090

3.  Plantarflexion contracture in the mdx mouse.

Authors:  Michael W Garlich; Kristen A Baltgalvis; Jarrod A Call; Lisa L Dorsey; Dawn A Lowe
Journal:  Am J Phys Med Rehabil       Date:  2010-12       Impact factor: 2.159

4.  The chondrogenic response to exercise in the proximal femur of normal and mdx mice.

Authors:  David J Nye; Jeffrey M Costas; Jessica B Henley; Jin-Kwang Kim; Jeffrey H Plochocki
Journal:  BMC Musculoskelet Disord       Date:  2010-09-03       Impact factor: 2.362

5.  Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation.

Authors:  Deborah Merrick; Lukas Kurt Josef Stadler; Dean Larner; Janet Smith
Journal:  Dis Model Mech       Date:  2009-06-17       Impact factor: 5.758

6.  The pro-fibrotic connective tissue growth factor (CTGF/CCN2) correlates with the number of necrotic-regenerative foci in dystrophic muscle.

Authors:  María Gabriela Morales; María José Acuña; Daniel Cabrera; Roel Goldschmeding; Enrique Brandan
Journal:  J Cell Commun Signal       Date:  2017-09-08       Impact factor: 5.782

7.  Upregulation of the creatine synthetic pathway in skeletal muscles of mature mdx mice.

Authors:  Warren C McClure; Rick E Rabon; Hirofumi Ogawa; Brian S Tseng
Journal:  Neuromuscul Disord       Date:  2007-06-27       Impact factor: 4.296

8.  The effects of glucocorticoid and voluntary exercise treatment on the development of thoracolumbar kyphosis in dystrophin-deficient mice.

Authors:  Daniel Brereton; Jeffrey Plochocki; Daniel An; Jeffrey Costas; Erin Simons
Journal:  PLoS Curr       Date:  2012-10-10

9.  Voluntary wheel running in dystrophin-deficient (mdx) mice: Relationships between exercise parameters and exacerbation of the dystrophic phenotype.

Authors:  Gayle M Smythe; Jason D White
Journal:  PLoS Curr       Date:  2011-12-18

10.  Catalpol counteracts the pathology in a mouse model of Duchenne muscular dystrophy by inhibiting the TGF-β1/TAK1 signaling pathway.

Authors:  Deng-Qiu Xu; Lei Zhao; Si-Jia Li; Xiao-Fei Huang; Chun-Jie Li; Li-Xin Sun; Xi-Hua Li; Lu-Yong Zhang; Zhen-Zhou Jiang
Journal:  Acta Pharmacol Sin       Date:  2020-09-16       Impact factor: 7.169

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.