Literature DB >> 23188550

Cyclooxygenase-2 expression in skeletal muscle of knockout mice suffering Duchenne muscular dystrophy.

Flavia de Oliveira1, De Oliveira Flavia, Hananiah Tardivo Quintana, Jeferson André Bortolin, Odair Alfredo Gomes, Edson Aparecido Liberti, Daniel Araki Ribeiro.   

Abstract

The purpose of the present study was to investigate the role of cyclooxygenase-2 (COX-2) expression in fibrotic lesion in mdx mice. A total of six male C57BL/10 mice and six C57BL/10-DMD/mdx were distributed into two groups: control and animals with Duchenne muscular dystrophy (DMD). The medial part of gastrocnemius muscle was evaluated being the specimens stained with hematoxylin and eosin (H&E) and Sirius Red under normal and polarized light to differentiate type I (red and yellow) and III (green) collagen. COX-2 expression was assessed by immunohistochemistry. The results revealed histopathological changes in C57BL/10-DMD/mdx as depicted by regenerating fibers. Sirius Red stain showed a substantial increase in the amount of type I collagen of mdx mice. DMD induced a strong COX-2 immunoexpression in intercellular space. Taken together, our results are consistent with the notion that necrotic and fibrotic lesions are able to increase COX-2 expression in DMD.

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Year:  2012        PMID: 23188550     DOI: 10.1007/s00418-012-1056-7

Source DB:  PubMed          Journal:  Histochem Cell Biol        ISSN: 0948-6143            Impact factor:   4.304


  19 in total

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Authors:  Marco Testa; Bianca Rocca; Lucia Spath; Franco O Ranelletti; Giovanna Petrucci; Giovanni Ciabattoni; Fabio Naro; Stefano Schiaffino; Massimo Volpe; Carlo Reggiani
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Review 5.  Cyclooxygenase in biology and disease.

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Journal:  FASEB J       Date:  1998-09       Impact factor: 5.191

6.  The COX-2 pathway is essential during early stages of skeletal muscle regeneration.

Authors:  Brenda A Bondesen; Stephen T Mills; Kristy M Kegley; Grace K Pavlath
Journal:  Am J Physiol Cell Physiol       Date:  2004-04-14       Impact factor: 4.249

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8.  Cardiomyopathy in the dystrophin/utrophin-deficient mouse model of severe muscular dystrophy is characterized by dysregulation of matrix metalloproteinases.

Authors:  Dawn A Delfín; Kara E Zang; Kevin E Schill; Nikita T Patel; Paul M L Janssen; Subha V Raman; Jill A Rafael-Fortney
Journal:  Neuromuscul Disord       Date:  2012-06-29       Impact factor: 4.296

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Journal:  Brain       Date:  1987-04       Impact factor: 13.501

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Authors:  Brenda A Bondesen; Stephen T Mills; Grace K Pavlath
Journal:  Am J Physiol Cell Physiol       Date:  2006-02-08       Impact factor: 4.249

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Journal:  Histochem Cell Biol       Date:  2021-09-02       Impact factor: 4.304

Review 3.  Autonomic dysfunction in muscular dystrophy: a theoretical framework for muscle reflex involvement.

Authors:  Scott A Smith; Ryan M Downey; Jon W Williamson; Masaki Mizuno
Journal:  Front Physiol       Date:  2014-02-18       Impact factor: 4.566

4.  Dystrophin Deficiency Causes Progressive Depletion of Cardiovascular Progenitor Cells in the Heart.

Authors:  Sarka Jelinkova; Yvonne Sleiman; Petr Fojtík; Franck Aimond; Amanda Finan; Gerald Hugon; Valerie Scheuermann; Deborah Beckerová; Olivier Cazorla; Marie Vincenti; Pascal Amedro; Sylvain Richard; Josef Jaros; Petr Dvorak; Alain Lacampagne; Gilles Carnac; Vladimir Rotrekl; Albano C Meli
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