| Texto completo | |
| Autor(es): |
Guido, Anderson Neri
[1]
;
Rocha Campos, Gerson Eduardo
[1]
;
Santo Neto, Humberto
[1]
;
Marques, Maria Julia
[1]
;
Minatel, Elaine
[1]
Número total de Autores: 5
|
| Afiliação do(s) autor(es): | [1] Univ Estadual Campinas UNICAMP, Inst Biol, Dept Anat Biol Celular Fisiol & Biofis, BR-13083970 Sao Paulo - Brazil
Número total de Afiliações: 1
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology; v. 293, n. 10, p. 1722-1728, OCT 2010. |
| Citações Web of Science: | 9 |
| Resumo | |
The muscle fiber phenotype is mainly determined by motoneuron innervation and changes in neuromuscular interaction alter the muscle fiber type. In dystrophin-deficient mdx mice, changes in the molecular assembly of the neuromuscular junction and in nerve terminal sprouting occur in the sternomastoid (STN) muscle during early stages of the disease. In this study, we were interested to see whether early changes in neuromuscular assembly are correlated with alterations in fiber type in dystrophic STN at 2 months of age. A predominance of hybrid fast myo-fibers (about 52% type IIDB) was observed in control (C57B1/10) STN. In mdx muscle, the lack of dystrophin did not change this profile (about 54% hybrid type IIDB). Pure fast type HD fibers predominated in normal and dystrophic diaphragm (DIA; about 39% in control and 30% in mdx muscle) and a population of slow Type I fibers was also present (about 10% in control and 13% in mdx muscle). In conclusion, early changes in neuromuscular assembly do not affect the fiber type composition of dystrophic STN. In contrast to the pure fast fibers of the more affected DIA, the hybrid phenotype of the STN may permit dynamic adaptations during progression of the disease. Anat Rec, 293:1722-1728, 2010. (C) 2010 Wiley-Liss, Inc. (AU) | |
| Processo FAPESP: | 07/50189-1 - Influencia do acido ascorbico no processo de degeneracao muscular em camundongos distroficos. |
| Beneficiário: | Elaine Minatel |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 08/50731-3 - Tratamento in vivo e in vitro com N-acetilcisteína (NAC) em camundongos distróficos |
| Beneficiário: | Elaine Minatel |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 08/58491-1 - Mecanismos de proteção da distrofia muscular: estudo proteômico e terapia farmacológica |
| Beneficiário: | Maria Julia Marques |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 04/15526-9 - Proteínas reguladoras do cálcio e proteção à mionecrose na distrofia muscular de Duchenne |
| Beneficiário: | Maria Julia Marques |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |