Literature DB >> 3612563

Activation patterns of embryonic chick hind-limb muscles following blockade of activity and motoneurone cell death.

L T Landmesser, M Szente.   

Abstract

Motoneurone cell death and spontaneous embryonic motility were blocked in chick embryos by daily in ovo injections of d-tubocurarine from stage 28-36 (E5-10). Isolated spinal cord-hind-limb preparations were prepared from these embryos and movement sequences in response to electrical stimulation of the thoracic cord were assessed, after drug wash-out, by electromyogram (e.m.g.) or muscle-nerve recordings. In embryos in which complete blockade of lumbar motoneurone cell death was later confirmed histologically, flexor and extensor motoneurone pools were found to be activated in alternating bursts as occurs in control embryos. Thus the development of the basic cord circuits responsible for these patterns of motoneurone activation does not require motoneurone cell death. Partial blockade of motoneurone cell death by guanosine 3',5'-phosphate (cyclic GMP) was also without effect on muscle activation patterns. In ovo injection of d-tubocurarine or alpha-bungarotoxin in doses sufficient to block embryonic motility was found to have a direct effect on the spinal cord, preventing the patterned activation of motoneurone pools in alternating bursts. Cords removed from treated embryos behaved similarly to cords in which these drugs were applied acutely in the bath. Minor changes in muscle activation patterns that occurred with chronic drug treatment were also observed in acutely treated cords and appear to be a direct and persistent effect of the drugs on cord circuits. It is possible to conclude that cholinergic circuits within the chick lumbar cord play a role in the normal patterned activation of flexor and extensor motoneurone pools. Systemically applied drugs can have access to these circuits, indicating a need for caution when interpreting the results of drugs applied in this manner to developing embryos. We also conclude that neither the activation of motoneurones in patterned bursts, nor the afferent feed-back from the movements that result, are required to form the basic spinal cord circuits responsible for the activation of extensor and flexor motoneurone pools in alternating bursts.

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Year:  1986        PMID: 3612563      PMCID: PMC1182930          DOI: 10.1113/jphysiol.1986.sp016278

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


  36 in total

1.  The development of functional innervation in the hind limb of the chick embryo.

Authors:  L Landmesser; D G Morris
Journal:  J Physiol       Date:  1975-07       Impact factor: 5.182

2.  Cell death in the development of the lateral motor column of the chick embryo.

Authors:  V Hamburger
Journal:  J Comp Neurol       Date:  1975-04-15       Impact factor: 3.215

3.  Consequences of tenotomy on the evolution of multiinnervation in developing rat soleus muscle.

Authors:  P Benoit; J P Changeux
Journal:  Brain Res       Date:  1975-12-05       Impact factor: 3.252

4.  The projection patterns of the ventral horn to the hind limb during development.

Authors:  A H Lamb
Journal:  Dev Biol       Date:  1976-11       Impact factor: 3.582

5.  The role of supraspinal input in embryonic motility: a re-examination in the chick.

Authors:  R W Oppenheim
Journal:  J Comp Neurol       Date:  1975-03-01       Impact factor: 3.215

6.  Discrimination between nicotinic receptors in vertebrate ganglia and skeletal muscle by alpha-bungarotoxin and cobra venoms.

Authors:  S Bursztajn; M D Gershon
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

7.  Ontogeny of leg motor output in the chick embryo: a neural analysis.

Authors:  A Bekoff
Journal:  Brain Res       Date:  1976-04-23       Impact factor: 3.252

8.  Polyneuronal innervation of skeletal muscle in new-born rats and its elimination during maturation.

Authors:  M C Brown; J K Jansen; D Van Essen
Journal:  J Physiol       Date:  1976-10       Impact factor: 5.182

9.  Specificity of early motoneuron growth cone outgrowth in the chick embryo.

Authors:  K W Tosney; L T Landmesser
Journal:  J Neurosci       Date:  1985-09       Impact factor: 6.167

10.  Periodic motility of normal and spinal chick embryos between 8 and 17 days of incubation.

Authors:  V Hamburger; M Balaban; R Oppenheim; E Wenger
Journal:  J Exp Zool       Date:  1965-06
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  7 in total

1.  Cholinergic and GABAergic inputs drive patterned spontaneous motoneuron activity before target contact.

Authors:  L D Milner; L T Landmesser
Journal:  J Neurosci       Date:  1999-04-15       Impact factor: 6.167

2.  Reduction of neuromuscular activity is required for the rescue of motoneurons from naturally occurring cell death by nicotinic-blocking agents.

Authors:  R W Oppenheim; D Prevette; A D'Costa; S Wang; L J Houenou; J M McIntosh
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

3.  Selective innervation of fast and slow muscle regions during early chick neuromuscular development.

Authors:  V F Rafuse; L D Milner; L T Landmesser
Journal:  J Neurosci       Date:  1996-11-01       Impact factor: 6.167

4.  Neuromuscular activity blockade induced by muscimol and d-tubocurarine differentially affects the survival of embryonic chick motoneurons.

Authors:  M F Usiak; L T Landmesser
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

5.  Inhibition of electrical activity by retroviral infection with Kir2.1 transgenes disrupts electrical differentiation of motoneurons.

Authors:  Yone Jung Yoon; Hisashi Kominami; Thomas Trimarchi; Miguel Martin-Caraballo
Journal:  PLoS One       Date:  2008-08-13       Impact factor: 3.240

6.  Emergence of motor circuit activity.

Authors:  Chris Law; Michel Paquet; Artur Kania
Journal:  PLoS One       Date:  2014-04-10       Impact factor: 3.240

7.  GABA and Gap Junctions in the Development of Synchronized Activity in Human Pluripotent Stem Cell-Derived Neural Networks.

Authors:  Meeri Eeva-Liisa Mäkinen; Laura Ylä-Outinen; Susanna Narkilahti
Journal:  Front Cell Neurosci       Date:  2018-03-06       Impact factor: 5.505

  7 in total

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