Literature DB >> 5500776

Electrical interaction between antidromically stimulated frog motoneurones and dorsal root afferents: enhancement by gallamine and TEA.

A D Grinnell.   

Abstract

1. Electrical interactions have been studied in the isolated frog spinal cord preparation. It is found that gallamine and tetraethylammonium chloride (TEA) markedly enhance all non-cholinergic synaptic interactions, including the electrical interaction between motoneurones (VR-VRP). In addition, in the presence of either of these drugs, a short-latency interaction is seen to exist between antidromically stimulated motoneurones and dorsal root afferents (early VR-DRP). The early VR-DRP is rarely seen in the absence of gallamine or TEA.2. The early VR-DRP is of the same short latency as the VR-VRP and fulfils the same criteria for electrical interaction: it increases in amplitude with cooling from 17-10 degrees C, it is not blocked by a wide variety of pharmacological blocking agents, and it is suppressed by both Mg(2+) and Ca(2+), with no antagonism of action between the two.3. The early VR-DRP appears as a cluster of unitary events: all-or-none spikes conducted out the dorsal root fibres. No initial graded slow potentials are seen. Often there are two peaks in the response.4. The early VR-DRP is facilitated by a dorsal root volley, with a time course normally intermediate between that of the orthodromic ventral root potential (DR-VRP) and the dorsal root potential (DR-DRP). This orthodromic facilitation apparently is achieved by increasing invasion of motoneurone dendritic trees and depolarization of dorsal root afferents toward threshold.5. If the same ventral root is stimulated twice, or adjacent roots stimulated at different intervals, the second early VR-DRP, like the VR-VRP, is seen to be occluded for 10-20 msec, then facilitated to supranormal amplitudes. It is concluded that motoneurone dendrites are presynaptic to both interactions.6. Evidence is presented that gallamine and TEA act by increasing the duration of activity both in axon terminals and in antidromically invaded motoneurones. Often second or multiple spikes result. The increased duration of depolarization can increase transmitter release at terminals and increase coupling at electrical junctions.7. Possible morphological correlates for the two electrical interactions are discussed. It is speculated that the motoneurone interaction arises at numerous areas of close apposition between dendrites in dendritic ;thickets', and that the early VR-DRP is mediated by fewer, lower-resistance, electrical junctions between dendrites and afferent nerve terminals.

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Year:  1970        PMID: 5500776      PMCID: PMC1395640          DOI: 10.1113/jphysiol.1970.sp009194

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


  22 in total

1.  RECURRENT FACILITATION OF FROG MOTONEURONS.

Authors:  K KUBOTA; J M BROOKHART
Journal:  J Neurophysiol       Date:  1963-11       Impact factor: 2.714

2.  A STUDY OF SPONTANEOUS MINIATURE POTENTIALS IN SPINAL MOTONEURONES.

Authors:  B KATZ; R MILEDI
Journal:  J Physiol       Date:  1963-09       Impact factor: 5.182

3.  Potential field initiated during monosynaptic activation of frog motoneurones.

Authors:  J M BROOKHART; E FADIGA
Journal:  J Physiol       Date:  1960-03       Impact factor: 5.182

4.  Ultrastructural aspects of electrotonic junctions in the spinal cord of the frog.

Authors:  C Sotelo; J Taxi
Journal:  Brain Res       Date:  1970-01-06       Impact factor: 3.252

5.  Patterns of firing in cuneate neurones and some effects of Flaxedil.

Authors:  A Galindo; K Krnjević; S Schwartz
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

6.  Facilitatory and excitatory interaction between motoneurons of adjacent segments in the spinal cord of the frog.

Authors:  H S Meij; K C Holemans; B J Meyer
Journal:  Exp Neurol       Date:  1968-04       Impact factor: 5.330

7.  Inhibitory interaction between motoneurons of adjacent segments in the frog spinal cord.

Authors:  H S Meij; K C Holemans
Journal:  Exp Neurol       Date:  1969-02       Impact factor: 5.330

8.  Actions of gallamine and tetraethylammonium at the frog neuromuscular junction.

Authors:  B W Payton; D G Shand
Journal:  Br J Pharmacol Chemother       Date:  1966-10

9.  Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.

Authors:  R K Orkand; J G Nicholls; S W Kuffler
Journal:  J Neurophysiol       Date:  1966-07       Impact factor: 2.714

10.  Comparative electron microscopy of synapses in the vertebrate spinal cord.

Authors:  B T Charlton; E G Gray
Journal:  J Cell Sci       Date:  1966-03       Impact factor: 5.285

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  15 in total

1.  Bulbospinal inhibition of PAD elicited by stimulation of afferent and motor axons in the isolated frog spinal cord and brainstem.

Authors:  H González; I Jiménez; P Rudomin
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

2.  Studies on convulsants in the isolated frog spinal cord. II. Effects on root potentials.

Authors:  J L Barker; R A Nicoll; A Padjen
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

3.  Mixed synapses discovered and mapped throughout mammalian spinal cord.

Authors:  J E Rash; R K Dillman; B L Bilhartz; H S Duffy; L R Whalen; T Yasumura
Journal:  Proc Natl Acad Sci U S A       Date:  1996-04-30       Impact factor: 11.205

4.  The ultrastructure of the nucleus of the oculomotor nerve (somatic efferent portion) of the cat.

Authors:  G Tredici; G Pizzini; S Milanesi
Journal:  Anat Embryol (Berl)       Date:  1976-09-30

5.  Electron microscopic identification of postsynaptic dorsal root terminals: a possible substrate of dorsal root potentials in the frog spinal cord.

Authors:  G Székely; B Kosaras
Journal:  Exp Brain Res       Date:  1977-09-28       Impact factor: 1.972

6.  Electrical coupling between primary afferents and amphibian motoneurons.

Authors:  A I Shapovalov; B I Shiriaev
Journal:  Exp Brain Res       Date:  1978-11-15       Impact factor: 1.972

7.  The organization of primary afferent depolarization in the isolated spinal cord of the frog.

Authors:  D O Carpenter; P Rudomin
Journal:  J Physiol       Date:  1973-03       Impact factor: 5.182

8.  Electronic coupling between neurons in the rat lateral vestibular nucleus.

Authors:  H Korn; C Sotelo; F Crepel
Journal:  Exp Brain Res       Date:  1973-01-29       Impact factor: 1.972

9.  Hyperpolarization of frog primary afferent fibres caused by activation of a sodium pump.

Authors:  R A Davidoff; J C Hackman
Journal:  J Physiol       Date:  1980-05       Impact factor: 5.182

10.  Facilitation of noradrenaline release by gallamine in the rat salivary gland.

Authors:  R K Malhotra; T D Wakade; A R Wakade
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1985-11       Impact factor: 3.000

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