Literature DB >> 4031986

Properties of visceral primary afferent neurons in the nodose ganglion of the rabbit.

C E Stansfeld, D I Wallis.   

Abstract

The active and passive membrane properties of rabbit nodose ganglion cells and their responsiveness to depolarizing agents have been examined in vitro. Neurons with an axonal conduction velocity of less than 3 m/s were classified as C-cells and the remainder as A-cells. Mean axonal conduction velocities of A- and C-cells were 16.4 m/s and 0.99 m/s, respectively. A-cells had action potentials of brief duration (1.16 ms), high rate of rise (385 V/s), an overshoot of 23 mV, and relatively high spike following frequency (SFF). C-cells typically had action potentials with a "humped" configuration (duration 2.51 ms), lower rate of rise (255 V/s), an overshoot of 28.6 mV, an after potential of longer duration than A-cells, and relatively low SFF. Eight of 15 A-cells whose axons conducted at less than 10 m/s had action potentials of longer duration with a humped configuration; these were termed Ah-cells. They formed about 10% of cells whose axons conducted above 2.5 m/s. The soma action potential of A-cells was blocked by tetrodotoxin (TTX), but that of 6/11 C-cells was unaffected by TTX. Typically, A-cells showed strong delayed (outward) rectification on passage of depolarizing current through the soma membrane and time-dependent (inward) rectification on inward current passage. Input resistance was thus highly sensitive to membrane potential close to rest. In C-cells, delayed rectification was not marked, and slight time-dependent rectification occurred in only 3 of 25 cells; I/V curves were normally linear over the range: resting potential to 40 mV more negative. Data on Ah-cells were incomplete, but in our sample of eight cells time-dependent rectification was absent or mild. C-cells had a higher input resistance and a higher neuronal capacitance than A-cells. In a proportion of A-cells, RN was low at resting potential (5 M omega) but increased as the membrane was hyperpolarized by a few millivolts. A-cells were depolarized by GABA but were normally unaffected by 5-HT or DMPP. C-cells were depolarized by GABA in a similar manner to A-cells but also responded strongly to 5-HT; 53/66 gave a depolarizing response, and 3/66, a hyperpolarizing response. Of C-cells, 75% gave a depolarizing response to DMPP.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 4031986     DOI: 10.1152/jn.1985.54.2.245

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  26 in total

1.  Potassium channels Kv1.1, Kv1.2 and Kv1.6 influence excitability of rat visceral sensory neurons.

Authors:  Patricia A Glazebrook; Angelina N Ramirez; John H Schild; Char-Chang Shieh; Thanh Doan; Barbara A Wible; Diana L Kunze
Journal:  J Physiol       Date:  2002-06-01       Impact factor: 5.182

Review 2.  Xenobiotic pulmonary exposure and systemic cardiovascular response via neurological links.

Authors:  Phoebe A Stapleton; Alaeddin B Abukabda; Steven L Hardy; Timothy R Nurkiewicz
Journal:  Am J Physiol Heart Circ Physiol       Date:  2015-09-18       Impact factor: 4.733

3.  Melanocortin-4 receptor expression in different classes of spinal and vagal primary afferent neurons in the mouse.

Authors:  Laurent Gautron; Charlotte E Lee; Syann Lee; Joel K Elmquist
Journal:  J Comp Neurol       Date:  2012-12-01       Impact factor: 3.215

4.  Electrophysiological and pharmacological validation of vagal afferent fiber type of neurons enzymatically isolated from rat nodose ganglia.

Authors:  Bai-Yan Li; John H Schild
Journal:  J Neurosci Methods       Date:  2007-04-08       Impact factor: 2.390

5.  Expression of transient receptor potential channels and two-pore potassium channels in subtypes of vagal afferent neurons in rat.

Authors:  Huan Zhao; Leslie K Sprunger; Steven M Simasko
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-12-03       Impact factor: 4.052

6.  Kv1.3 channels regulate synaptic transmission in the nucleus of solitary tract.

Authors:  Angelina Ramirez-Navarro; Patricia A Glazebrook; Michelle Kane-Sutton; Caroline Padro; David D Kline; Diana L Kunze
Journal:  J Neurophysiol       Date:  2011-03-23       Impact factor: 2.714

7.  The role of nodose ganglia in the regulation of cardiovascular function following pulmonary exposure to ultrafine titanium dioxide.

Authors:  Hong Kan; Zhongxin Wu; Yen-Chang Lin; Teh-Hsun Chen; Jared L Cumpston; Michael L Kashon; Steve Leonard; Albert E Munson; Vincent Castranova
Journal:  Nanotoxicology       Date:  2013-05-07       Impact factor: 5.913

8.  Tetrodotoxin-resistant sodium current of rat nodose neurones: monovalent cation selectivity and divalent cation block.

Authors:  S R Ikeda; G G Schofield
Journal:  J Physiol       Date:  1987-08       Impact factor: 5.182

9.  Different types of Na+ and A-type K+ currents in dorsal root ganglion neurones innervating the rat urinary bladder.

Authors:  N Yoshimura; G White; F F Weight; W C de Groat
Journal:  J Physiol       Date:  1996-07-01       Impact factor: 5.182

10.  An electrophysiological investigation of the properties of 5-HT3 receptors of rabbit nodose ganglion neurones in culture.

Authors:  J A Peters; H M Malone; J J Lambert
Journal:  Br J Pharmacol       Date:  1993-10       Impact factor: 8.739

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