Literature DB >> 3348087

Correlative study of the incidence of opaque, necrotic and regenerative fibers in Duchenne dystrophy.

M Uchino1, S Araki, T Miike.   

Abstract

We studied the incidence of opaque, necrotic, and regenerative muscle fibers (OFs, NFs, RFs) in muscle biopsies from 21 patients, aged 8 months to 24 years, with Duchenne muscular dystrophy (DMD). OFs varied from case to case with an average rate of 8.3%. NFs and RFs were high in younger patients and decreased with age. The incidence of OFs, NFs, and RFs correlated to patient age with these coefficients: r = -0.38, -0.91, and -0.86. Except for OFs, all correlations were significant (p less than 0.001). There was no significant correlation between the incidence of OFs and NFs in each case of DMD. Considering the results of previous biochemical analysis of single OFs, we suggest that OFs may comprise two types of muscle fibers: (1) pathological muscle fibers to be regarded as precursors of NFs, and (2) muscle fibers undergoing artificial changes.

Entities:  

Mesh:

Year:  1988        PMID: 3348087     DOI: 10.1007/bf00690539

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


  10 in total

1.  Stages in fibre breakdown in Duchenne muscular dystrophy. An electron-microscopic study.

Authors:  M J Cullen; J J Fulthorpe
Journal:  J Neurol Sci       Date:  1975-02       Impact factor: 3.181

2.  Hyperreactive (hyaline, opaque, dark) muscle fibers in Duchenne dystrophy. A biopsy study of 16 dystrophy and 205 other neuronmuscular disease cases and controls.

Authors:  K Boxler; F Jerusalem
Journal:  J Neurol       Date:  1978-09-12       Impact factor: 4.849

3.  Ca-activated neutral protease and its inhibitors: in vitro effect on intact myofibrils.

Authors:  H Sugita; S Ishiura; K Suzuki; K Imahori
Journal:  Muscle Nerve       Date:  1980 Jul-Aug       Impact factor: 3.217

4.  Proteolysis of vimentin and desmin by the Ca2+-activated proteinase specific for these intermediate filament proteins.

Authors:  W J Nelson; P Traub
Journal:  Mol Cell Biol       Date:  1983-06       Impact factor: 4.272

5.  Segmental fibre breakdown and defects of the plasmalemma in diseased human muscles.

Authors:  H Schmalbruch
Journal:  Acta Neuropathol       Date:  1975-12-08       Impact factor: 17.088

6.  The significance of type 2C muscle fibers in Duchenne muscular dystrophy.

Authors:  I Nonaka; A Takagi; H Sugita
Journal:  Muscle Nerve       Date:  1981 Jul-Aug       Impact factor: 3.217

7.  Muscle fiber degeneration and necrosis in muscular dystrophy and other muscle diseases: cytochemical and immunocytochemical data.

Authors:  F Cornelio; I Dones
Journal:  Ann Neurol       Date:  1984-12       Impact factor: 10.422

8.  A fluorescent microscopy study of biopsied muscles from infantile neuromuscular disorders.

Authors:  T Miike; H Tamari; Y Ohtani; H Nakamura; I Matsuda; S Miyoshino
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

9.  Structural proteins of the opaque muscle fibers in Duchenne muscular dystrophy.

Authors:  M Uchino; S Araki; O Yoshida; K Uekawa
Journal:  Neurology       Date:  1985-09       Impact factor: 9.910

10.  Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies.

Authors:  J B Bodensteiner; A G Engel
Journal:  Neurology       Date:  1978-05       Impact factor: 9.910

  10 in total
  1 in total

1.  Initial pulmonary respiration causes massive diaphragm damage and hyper-CKemia in Duchenne muscular dystrophy dog.

Authors:  Akinori Nakamura; Masanori Kobayashi; Mutsuki Kuraoka; Katsutoshi Yuasa; Naoko Yugeta; Takashi Okada; Shin'ichi Takeda
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.