Literature DB >> 6602877

A reclassification of B and C neurones in the ninth and tenth paravertebral sympathetic ganglia of the bullfrog.

J Dodd, J P Horn.   

Abstract

1. The cellular organization of the ninth and tenth paravertebral sympathetic ganglia in the bullfrog was studied with intracellular and extracellular recording methods. An isolated preparation was used in which anatomical details of individual cells could be resolved while making physiological measurements. This permitted the characterization of neurones in terms of their size, the segmental origin of their cholinergic innervation, and their orthodromic and antidromic conduction velocities. With these criteria, three classes of sympathetic neurones were identified. 2. As in previous studies, C cells were distinguished from B cells by the origin of their innervation. C cells are innervated by slowly conducting axons (0.4 m/sec) from spinal nerves 7 and 8 and B cells are innervated by rapidly conducting axons (2.4 m/sec) from the sympathetic chain above ganglion 7. 3. In earlier work it has been suggested that the conduction velocity of a preganglionic axon generally matches that of its target neurone. In this study we have characterized a large group of B cells for which this is not true. The axons of B cells fall into a rapidly conducting group (2.0 m/sec) and a slowly conducting group (0.6 m/sec). In contrast, C neurones, like their preganglionic inputs, have only slowly conducting axons (0.3 m/sec). Consequently, neurones have been classified as C type, fast B type, and slow B type. Fifty-nine percent of the B cells that we studied were slow B cells. These findings were corroborated by measurements of compound extracellular responses in post-ganglionic nerves. 4. Some neurones can be identified also by the size of their cell bodies. C cells are about 30 microns in diameter while B cells are about 50 microns in diameter. In our sample, 96% of the cells with radius less than 16 microns were C cells and 94% of the cells with radius greater than 21 microns were B cells. However, fast B cells could not be distinguished from slow B cells by size.

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Year:  1983        PMID: 6602877      PMCID: PMC1197313          DOI: 10.1113/jphysiol.1983.sp014493

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


  21 in total

1.  Identification of small intensely fluorescent (SIF) cells as chromaffin cells in bullfrog sympathetic ganglia.

Authors:  F F Weight; H A Weitsen
Journal:  Brain Res       Date:  1977-06-10       Impact factor: 3.252

2.  Synaptic innervation of sympathetic ganglion cells in the bullfrog.

Authors:  H A Weitsen; F F Weight
Journal:  Brain Res       Date:  1977-06-10       Impact factor: 3.252

3.  Acetylcholine and slow synaptic inhibition in frog sympathetic ganglion cells.

Authors:  F F Weight; A Padjen
Journal:  Brain Res       Date:  1973-05-30       Impact factor: 3.252

4.  On the presynaptic acetylcholine receptors in sympathetic ganglia of the frog.

Authors:  B L Ginsborg
Journal:  J Physiol       Date:  1971-07       Impact factor: 5.182

5.  Slow synaptic responses and excitability in sympathetic ganglia of the bullfrog.

Authors:  B Libet; S Chichibu; T Tosaka
Journal:  J Neurophysiol       Date:  1968-05       Impact factor: 2.714

6.  Intracellular analysis of slow inhibitors and excitatory postsynaptic potentials in sympathetic ganglia of the frog.

Authors:  T Tosaka; S Chichibu; B Libet
Journal:  J Neurophysiol       Date:  1968-05       Impact factor: 2.714

7.  Slow synaptic inhibition: evidence for synaptic inactivation of sodium conductance in sympathetic ganglion cells.

Authors:  F F Weight; A Padjen
Journal:  Brain Res       Date:  1973-05-30       Impact factor: 3.252

8.  Functional differentiation in sB and sC neurons of toad sympathetic ganglia.

Authors:  S Honma
Journal:  Jpn J Physiol       Date:  1970-06-15

9.  Studies on sympathetic B and C neurons and patterns of pregnaglionic innervation.

Authors:  S Nishi; H Soeda; K Koketsu
Journal:  J Cell Physiol       Date:  1965-08       Impact factor: 6.384

10.  Analysis of the slow excitatory postsynaptic potential in bullfrog sympathetic ganglion cells.

Authors:  K Kuba; K Koketsu
Journal:  Jpn J Physiol       Date:  1976
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  23 in total

1.  A four-compartment model for Ca2+ dynamics: an interpretation of Ca2+ decay after repetitive firing of intact nerve terminals.

Authors:  Y Y Peng; K S Wang
Journal:  J Comput Neurosci       Date:  2000 May-Jun       Impact factor: 1.621

2.  Secondary nicotinic synapses on sympathetic B neurons and their putative role in ganglionic amplification of activity.

Authors:  P Karila; J P Horn
Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

3.  Calcium current modulation in frog sympathetic neurones: multiple neurotransmitters and G proteins.

Authors:  K S Elmslie
Journal:  J Physiol       Date:  1992       Impact factor: 5.182

4.  Dynamic Clamp Analysis of Synaptic Integration in Sympathetic Ganglia.

Authors:  J P Horn; P H M Kullmann
Journal:  Neirofiziologiia       Date:  2007-11-01

5.  Changes in sodium and calcium channel activity following axotomy of B-cells in bullfrog sympathetic ganglion.

Authors:  B S Jassar; P S Pennefather; P A Smith
Journal:  J Physiol       Date:  1993-12       Impact factor: 5.182

6.  Role of ganglionic cotransmission in sympathetic control of the isolated bullfrog aorta.

Authors:  R Thorne; J P Horn
Journal:  J Physiol       Date:  1997-01-01       Impact factor: 5.182

7.  Potassium currents evoked by brief depolarizations in bull-frog sympathetic ganglion cells.

Authors:  B Lancaster; P Pennefather
Journal:  J Physiol       Date:  1987-06       Impact factor: 5.182

8.  Muscarinic regulation of two ionic currents in the bullfrog sympathetic neurone.

Authors:  S Tsuji; K Kuba
Journal:  Pflugers Arch       Date:  1988-04       Impact factor: 3.657

9.  In vitro relation between preganglionic sympathetic stimulation and activity of cutaneous glands in the bullfrog.

Authors:  P Jobling; J P Horn
Journal:  J Physiol       Date:  1996-07-01       Impact factor: 5.182

10.  Ryanodine-sensitive component of calcium transients evoked by nerve firing at presynaptic nerve terminals.

Authors:  Y Peng
Journal:  J Neurosci       Date:  1996-11-01       Impact factor: 6.167

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