Literature DB >> 6128407

Altered developmental changes of neuromuscular junction in hypo- and hyperthyroid rats.

K Kawa, K Obata.   

Abstract

1. Effects of thyroid hormone on the development of neuromuscular junctions (n.m.j.s.) were investigated electrophysiologically in the diaphragms (sternal region) of normal, hypo- and hyperthyroid rats from the age of birth (day 0) to day 35.2. Hypothyroidism in new-born rats was induced either by daily administration of propylthiouracil to mothers or by subcutaneous injection of 150 muCi (131)I on day 1. Hyperthyroidism was induced by daily injection of thyroxine.3. In normal rats up to day 10, muscle fibres were innervated polyneuronally. By day 20, multiple innervation was eliminated and muscle fibres received only a single input. In hypothyroid rats elimination of polyneuronal innervation was retarded by 5-8 days, while in hyperthyroid rats the elimination was accelerated by 2-3 days.4. The frequency of miniature end-plate potentials (m.e.p.p.s) in normal rats increased from one per 40 sec on days 0-5 to 1/sec on days 25-35. The m.e.p.p. frequency in hypothyroid rats was 25-65% of that in normal rats of the same age. In hyperthyroid rats the m.e.p.p. frequency was normal up to day 18 but subnormal afterwards. The duration of m.e.p.p. measured on day 22-23 was slower in hypothyroid rats and faster in hyperthyroid rats, relative to m.e.p.ps in normal rats.5. The sensitivity to acetylcholine (ACh) at extrajunctional regions in normal rats was about 100 mV/nC at birth and declined to 1 mV/nC by day 26. In hypothyroid rats, the ACh sensitivity was as high as 30 mV/nC on day 26; in hyperthyroid rats, ACh sensitivity on day 26 was undetectable.6. With pairs of nerve stimuli (applied at a 50 msec interval), the second end-plate potential was facilitated until day 10 and depressed after day 16 in normal rats. This shift from facilitation to depression during development was not altered in either hypo-or hyperthyroid rats.7. It is concluded that the lack and excess of thyroid hormone retards and facilitates the development of n.m.j.s. respectively. Possible mechanisms for this altered development are discussed.

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Year:  1982        PMID: 6128407      PMCID: PMC1224772          DOI: 10.1113/jphysiol.1982.sp014295

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  53 in total

1.  Correlation between nerve terminal size and transmitter release at the neuromuscular junction of the frog.

Authors:  M Kuno; S A Turkanis; J N Weakly
Journal:  J Physiol       Date:  1971-03       Impact factor: 5.182

2.  Effect of thyroid deficiency on the synaptic organization of the rat cerebellar cortex.

Authors:  F Hajós; A J Patel; R Balázs
Journal:  Brain Res       Date:  1973-02-28       Impact factor: 3.252

3.  An automatic DC-level compensation circuit for electrophysiology.

Authors:  G I Allen; K Toyama
Journal:  IEEE Trans Biomed Eng       Date:  1973-01       Impact factor: 4.538

4.  The effects of early hypo- and hyperthyroidism on the development of rat cerebellar cortex. I. Cell proliferation and differentiation.

Authors:  J L Nicholson; J Altman
Journal:  Brain Res       Date:  1972-09-15       Impact factor: 3.252

5.  Effects of thyroid hormone at the neuromuscular junction.

Authors:  W W Hofmann; E H Denys
Journal:  Am J Physiol       Date:  1972-08

6.  Some physiological, biochemical, and behavioral consequences of neonatal hormone administration: cortisol and thyroxine.

Authors:  S Schapiro
Journal:  Gen Comp Endocrinol       Date:  1968-04       Impact factor: 2.822

7.  Thyroid function during postnatal development in the rat.

Authors:  M Samel
Journal:  Gen Comp Endocrinol       Date:  1968-04       Impact factor: 2.822

8.  Influence of neonatal hypothyroidism and of thyroxine on the acetylcholinesterase and cholinesterase activities in the developing central nervous system of the rat.

Authors:  S E Geel; P S Timiras
Journal:  Endocrinology       Date:  1967-06       Impact factor: 4.736

9.  Neuromuscular transmission in new-born rats.

Authors:  P A Redfern
Journal:  J Physiol       Date:  1970-08       Impact factor: 5.182

10.  Control of ACh sensitivity by muscle activity in the rat.

Authors:  T Lomo; J Rosenthal
Journal:  J Physiol       Date:  1972-03       Impact factor: 5.182

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  2 in total

1.  On the two subdivisions and intrinsic synaptic connexions in the submandibular ganglion of the rat.

Authors:  K Kawa; S Roper
Journal:  J Physiol       Date:  1984-01       Impact factor: 5.182

2.  The open duration of fetal ACh receptor-channel changes during mouse muscle development.

Authors:  F Grassi; O Epifano; A M Mileo; B Barabino; F Eusebi
Journal:  J Physiol       Date:  1998-04-15       Impact factor: 5.182

  2 in total

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