Literature DB >> 218667

Pharmacological aspects of neuromuscular transmission in the isolated diaphragm of the dystrophic (Rej 129) mouse.

J B Harris, R R Ribchester.   

Abstract

1. Some aspects of the pharmacology of neuromuscular transmission have been studied in the isolated diaphragm of the normal and dystrophic mouse. 2. The effects of (+)-tubocurarine and atropine on the indirectly elicited twitch responses of the dystrophic diaphragm were indistinguishable from normal. 3. Intracellular recording techniques revealed no significant differences between the rise time, time to half decay, frequency and amplitude of miniature endplate potentials (m.e.p.ps) recorded in dystrophic muscle fibres, compared to those recorded in normal muscle fibres. 4. Transmitter null potential, the size of the available store of transmitter, the probability of release of the transmitter, and the characteristics of endplate potentials (e.p.ps) of dystrophic muscle fibres did not differ from normal. 5. The quantum contents of e.p.ps generated in response to nerve stimulation of 0.1 to 100 HZ were consistently larger in dystrophic muscle fibres than in normal muscle fibres, but the differences were not statistically significant under the conditions of the experiment.

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Year:  1979        PMID: 218667      PMCID: PMC1668655          DOI: 10.1111/j.1476-5381.1979.tb07845.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  35 in total

1.  ABNORMAL PHARMACOLOGICAL RESPONSES OF ISOLATED NERVE-MUSCLE PREPARATIONS FROM MUSCULAR DYSTROPHIC MICE.

Authors:  N BAKER; P B SABAWALA
Journal:  J Pharmacol Exp Ther       Date:  1963-08       Impact factor: 4.030

2.  Presynaptic effect of the neuro-muscular transmitter.

Authors:  J A BARSTAD
Journal:  Experientia       Date:  1962-12-15

3.  Histopathology of hereditary, progressive muscular dystrophy in inbred strain 129 mice.

Authors:  W T WEST; E D MURPHY
Journal:  Anat Rec       Date:  1960-07

4.  Supersensitivity to neostigmine and resistance to d-tubocurarine in mice with hereditary myopathy.

Authors:  N BAKER; L WILSON; W OLDENDORF; W H BLAHD
Journal:  Am J Physiol       Date:  1960-05

5.  Presynaptic failure of neuromuscular propagation in rats.

Authors:  K KRNJEVIC; R MILEDI
Journal:  J Physiol       Date:  1959-12       Impact factor: 5.182

6.  A further study of the statistical composition on the end-plate potential.

Authors:  A R MARTIN
Journal:  J Physiol       Date:  1955-10-28       Impact factor: 5.182

7.  Contractility of dystrophic mouse muscle.

Authors:  A SANDOW; M BRUST
Journal:  Am J Physiol       Date:  1958-09

8.  An investigation of spontaneous activity at the neuromuscular junction of the rat.

Authors:  A W LILEY
Journal:  J Physiol       Date:  1956-06-28       Impact factor: 5.182

9.  Quantal components of the end-plate potential.

Authors:  J DEL CASTILLO; B KATZ
Journal:  J Physiol       Date:  1954-06-28       Impact factor: 5.182

10.  Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

Authors:  A M Michelson; E S Russell; P J Harman
Journal:  Proc Natl Acad Sci U S A       Date:  1955-12-15       Impact factor: 11.205

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  2 in total

1.  The origin of (+)-tubocurarine resistance in dystrophic mice.

Authors:  S S Kelly; G P Morgan; J W Smith
Journal:  Br J Pharmacol       Date:  1986-09       Impact factor: 8.739

2.  The relationship between end-plate size and transmitter release in normal and dystrophic muscles of the mouse.

Authors:  J B Harris; R R Ribchester
Journal:  J Physiol       Date:  1979-11       Impact factor: 5.182

  2 in total

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