Literature DB >> 6663341

Mechanoafferent neurons innervating tail of Aplysia. I. Response properties and synaptic connections.

E T Walters, J H Byrne, T J Carew, E R Kandel.   

Abstract

Mechanical, chemical, or electrical stimulation of the tail elicits a short-latency (less than 1 s) tail-withdrawal reflex that is graded with the intensity of the stimulus. The tail-withdrawal reflex is not elicited by stimulation of parts of the body outside of the tail region. Mechanoafferent neurons innervating the tail are located in a small subcluster within a large, homogeneous group of medium-size (40-80 micron) cells on the ventrocaudal (VC) surface of each pleural ganglion. The tail sensory neurons within this large VC cluster are activated by tactile pressure or by electrical stimulation of discrete regions of the tail. They adapt slowly to maintained stimulation and sometimes respond to stimulus offset as well. Both mechanical and electrical stimuli produce responses that are graded with the intensity of the stimulus. Cells in the VC cluster appear to be primary mechanoreceptors because they have axons in peripheral nerves (including nerves innervating the tail), they exhibit action potentials lacking prepotentials in response to tactile stimulation, and these action potentials are still produced by cutaneous stimulation when peripheral and central chemical synaptic transmission is blocked. Stimulation of fields all over the body surface evokes synaptically mediated hyperpolarizing responses in individual mechanoafferent neurons that may represent afferent inhibition. Hyperpolarizing responses lasting many seconds can be produced by brief cutaneous stimuli. The mechanoafferent neurons innervating the tail region make strong monosynaptic connections to tail motor neurons in the ipsilateral pedal ganglion, and through these connections this subpopulation of the VC neurons appears to make a substantial contribution to the short-latency tail-withdrawal reflex. In addition, the combined excitatory receptive fields of these mechanoafferents match the excitatory receptive field of the tail-withdrawal reflex. Mechanoafferent neurons in the VC cluster that have receptive fields on other parts of the body (outside the excitatory receptive field of the tail-withdrawal reflex) have not been observed to make monosynaptic connections to the tail motor neurons. The neurons innervating the tail are reliably found in a discrete region within the larger VC cluster. In addition to this gross somatotopic organization, there is evidence of a finer level of somatotopic organization between the position of the excitatory receptive field on the tail and the position of the cell soma in the tail subcluster.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1983        PMID: 6663341     DOI: 10.1152/jn.1983.50.6.1522

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


  71 in total

1.  Sites of plasticity in the neural circuit mediating tentacle withdrawal in the snail Helix aspersa: implications for behavioral change and learning kinetics.

Authors:  S A Prescott; R Chase
Journal:  Learn Mem       Date:  1999 Jul-Aug       Impact factor: 2.460

2.  Switching off and on of synaptic sites at aplysia sensorimotor synapses.

Authors:  S Royer; R L Coulson; M Klein
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

3.  Axonal rejoining inhibits injury-induced long-term changes in Aplysia sensory neurons in vitro.

Authors:  S S Bedi; D L Glanzman
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

4.  Changes in D-aspartate ion currents in the Aplysia nervous system with aging.

Authors:  Lynne A Fieber; Stephen L Carlson; Thomas R Capo; Michael C Schmale
Journal:  Brain Res       Date:  2010-05-07       Impact factor: 3.252

5.  Stretch activation of the Aplysia S-channel.

Authors:  D H Vandorpe; C E Morris
Journal:  J Membr Biol       Date:  1992-05       Impact factor: 1.843

6.  Lobster attack induces sensitization in the sea hare, Aplysia californica.

Authors:  Amanda J Watkins; Daniel A Goldstein; Lucy C Lee; Christina J Pepino; Scott L Tillett; Francis E Ross; Elizabeth M Wilder; Virginia A Zachary; William G Wright
Journal:  J Neurosci       Date:  2010-08-18       Impact factor: 6.167

7.  Differential role of inhibition in habituation of two independent afferent pathways to a common motor output.

Authors:  Adam S Bristol; Thomas J Carew
Journal:  Learn Mem       Date:  2005-01-12       Impact factor: 2.460

8.  Latent memory for sensitization in Aplysia.

Authors:  Gary T Philips; Ekaterina I Tzvetkova; Stephane Marinesco; Thomas J Carew
Journal:  Learn Mem       Date:  2006 Mar-Apr       Impact factor: 2.460

9.  Long-lasting hyperexcitability induced by depolarization in the absence of detectable Ca2+ signals.

Authors:  Kumud K Kunjilwar; Harvey M Fishman; Dario J Englot; Roger G O'Neil; Edgar T Walters
Journal:  J Neurophysiol       Date:  2009-01-14       Impact factor: 2.714

10.  MNK-eIF4E signalling is a highly conserved mechanism for sensory neuron axonal plasticity: evidence from Aplysia californica.

Authors:  Sandra M Mihail; Andi Wangzhou; Kumud K Kunjilwar; Jamie K Moy; Gregory Dussor; Edgar T Walters; Theodore J Price
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-09-23       Impact factor: 6.237

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