Literature DB >> 6630028

Postnatal growth and differentiation of muscle fibres in the mouse. II. A histochemical and morphometrical investigation of dystrophic muscle.

P Wirtz, H M Loermans, P G Peer, A G Reintjes.   

Abstract

Postnatal development of three hind legs muscles, the soleus, plantaris, and gastrocnemius, of dystrophic mice (ReJ 129) was investigated with histochemical and morphometric methods. The results were compared with normal postnatal development. Especially during the second week postnatally, there was severe fibre necrosis with no apparent preference for any particular fibre type. This period of necrosis was shortly followed by a wave or regeneration during the third week that could not, however, compensate for the loss of fibres. In dystrophic animals of 4-5 months of age, the number of fibres was reduced by 40-70%. Cross sectional areas of dystrophic muscles rarely, if ever, exceeded values for normal animals 14 days of age, while body weights were also drastically reduced. Growth and differentiation of the nonaffected fibres proceeded almost normally during the first month. During the second month, the "slow' fibres in the soleus muscle, and the "fast-oxidative-glycolytic' fibres in the plantaris muscle were hypertrophied, while, incidentally, some "fast-glycolytic' fibres showed hypertrophy; but in this case the average size of the fibre type was not increased. After two months, a general fibre atrophy was observed. The fate of the regenerated fibres was difficult to trace, especially in muscles older than one month. It is assumed that a number of them were capable of developing into "adult' fibre types histochemically. During the course of the disease the percentage of "intermediate' fibres increased markedly, whereas nearly all "fast-glycolytic' fibres disappeared. Because of these shifts in fibre profiles, the plantaris and the gastrocnemius muscles obtained a rather "juvenile' and "oxidative' aspect. Changes in the histochemical character of the soleus muscle were less spectacular. In dystrophic muscles, no new fibre types were found, compared with normal muscles. Rather, fibre types were present at the wrong moment, or occurred in quantities unusual for the age concerned.

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Year:  1983        PMID: 6630028      PMCID: PMC1171797     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  14 in total

1.  Investigation of cranial and other nerves in the mouse with muscular dystrophy.

Authors:  T J Biscoe; K W Caddy; D J Pallot; U M Pehrson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-04       Impact factor: 10.154

2.  Histochemical and structural analyses of the phenotypic expression of the dystrophic gene in the 129/ReJ dy/dy and the C57BL/6J dy2J/dy2J mice.

Authors:  J Butler; E Cosmos
Journal:  Exp Neurol       Date:  1977-12       Impact factor: 5.330

3.  Abnormalities of peripheral nerves in murine muscular dystrophy.

Authors:  W G Bradley; M Jenkison
Journal:  J Neurol Sci       Date:  1973-02       Impact factor: 3.181

4.  Histochemical observations in preclinical mouse muscular dystrophy.

Authors:  H Meier
Journal:  Am J Pathol       Date:  1967-04       Impact factor: 4.307

5.  Muscle fibre growth in five different muscles in both sexes of mice. II. Dystrophic mice.

Authors:  R W Rowe; G Goldspink
Journal:  J Anat       Date:  1969-05       Impact factor: 2.610

6.  Development of the amyelinated lesion in the ventral root of the dystrophic mouse. Ultrastructural, quantitative and autoradiographic study.

Authors:  E Jaros; W G Bradley
Journal:  J Neurol Sci       Date:  1978-05       Impact factor: 3.181

7.  Further observations on myelinated axon numbers in normal and dystrophic mice.

Authors:  A Montgomery; L Swenarchuk
Journal:  J Neurol Sci       Date:  1978-08       Impact factor: 3.181

8.  [Development, destruction and regeneration of sceletal muscular fibers].

Authors:  H Schmalbruch
Journal:  Dtsch Med Wochenschr       Date:  1980-04-25       Impact factor: 0.628

9.  Relative resistance to dystrophy of slow skeletal muscle of the mouse.

Authors:  M Brust
Journal:  Am J Physiol       Date:  1966-03

10.  Ultrastructural evidence of "abortive" regeneration in murine muscular dystrophy.

Authors:  P J Summers; R Parsons
Journal:  J Neurol Sci       Date:  1978-12       Impact factor: 3.181

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  4 in total

1.  Chronic electromyograms in treadmill running SOD1 mice reveal early changes in muscle activation.

Authors:  Katharina A Quinlan; Elma Kajtaz; Jody D Ciolino; Rebecca D Imhoff-Manuel; Matthew C Tresch; Charles J Heckman; Vicki M Tysseling
Journal:  J Physiol       Date:  2017-07-05       Impact factor: 5.182

2.  Postnatal growth and differentiation in three hindlimb muscles of the rat. Characterization with biochemical and enzyme-histochemical methods.

Authors:  J G Zuurveld; P Wirtz; H M Loermans; J H Veerkamp
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

3.  Long term functional improvement of dystrophic mouse leg muscles upon early immobilization.

Authors:  P Wirtz; H Loermans; W Wallinga-de Jonge
Journal:  Br J Exp Pathol       Date:  1986-04

4.  Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse.

Authors:  Y Tanabe; K Esaki; T Nomura
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

  4 in total

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