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Chemical Communication Between Vagal Afferent Somata in Nodose Ganglia of the Rat and the Guinea Pig In Vitro
Author(s) -
Eun Joo Oh,
Daniel Weinreich
Publication year - 2002
Publication title -
journal of neurophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.302
H-Index - 245
eISSN - 1522-1598
pISSN - 0022-3077
DOI - 10.1152/jn.2002.87.6.2801
Subject(s) - nodose ganglion , depolarization , vagus nerve , neuroscience , chemistry , dorsal root ganglion , membrane potential , stimulation , electrophysiology , biophysics , anatomy , biology , sensory system
The cell bodies of spinal afferents, dorsal root ganglion neurons, are depolarized several millivolts, and their probability of spiking increased when axons of neighboring somata in the same ganglion are electrically stimulated repetitively. This form of neural communication has been designated cross-depolarization (CD) and cross-excitation (CE). The existence of CD and CE between somata of vagal afferents (nodose ganglion neurons, NGNs) of rats and guinea pigs was investigated by electrically stimulating the vagus nerve while recording the electrical activity of NGNs in intact nodose ganglia with sharp intracellular microelectrodes. CD and CE in NGNs were manifested by a membrane depolarization (approximately 4 mV), the presence of spontaneous action potentials, and a decreased spike threshold. CD was dependent on the frequency and intensity of vagal nerve stimulation. Two distinct types of CD were observed: 1) in NGNs with large input resistances (R(in)), CD was dependent on [Ca2+]o, associated with increased membrane conductance, and had an extrapolated reversal potential (E(rev)) value of about -25 mV; and 2) in NGNs with low R(in), CD was independent of [Ca2+]o, not accompanied by a membrane conductance change, or a measurable E(rev) value. These data reveal the existence of a chemical communication pathway between vagal afferent somata and suggest the possibility that communication between different visceral organs may occur at the level of the primary vagal afferent neuron.

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