Literature DB >> 4679731

The physiological role of three acetylcholine receptors in synaptic transmission in Aplysia.

J Kehoe.   

Abstract

1. It is shown that a single presumably cholinergic presynaptic neurone can mediate, monosynaptically, multicomponent responses in a given cell and different responses in different cells.2. Complex responses (whether evoked synaptically or by ACh injection) are shown to be the result of the coexistence on a given post-synaptic neurone of more than one of three cholinergic receptor types previously described. Likewise, different responses in different cells are due to the fact that different post-synaptic neurones bear different combinations of these three receptors.3. Pharmacological analysis shows that the multicomponent nature of many of the responses is not always evident: what appears, under normal conditions, to be a single-component excitatory potential can be shown often to be a complex response consisting of superimposed e.p.s.p.s and rapid i.p.s.p.s which are sometimes, though not always, accompanied by a slow i.p.s.p.4. Although which and how many of the three receptor types is the major factor contributing to the type of response observed, in the case of some of the synaptic potentials certain other factors were found to contribute to the final response form. First, in the large cells of the visceral ganglion, as well as in the left giant cell of the pleural ganglion, there is a marked ;electrical separation' between the region in which the synaptic currents are generated and the point of recording. This ;electrical distance' often altered the inversion potential, and sometimes the form of the responses. Secondly, in some visceral neurones, activation of the cholinergic presynaptic neurone L10 causes (either directly or indirectly) a potential change which cannot be accounted for in terms of the activation of cholinergic receptors. This ;non-cholinergic' response (not imitated by an ionophoretic injection of ACh) is unmasked by the blocking of all three cholinergic receptors. It contributes differentially in different cells to the total response pattern produced by L10 under normal conditions, but its contribution is often characterized by a late hyperpolarizing phase which appears to be impossible to invert. This phase has been shown, however, to be dependent upon the potassium concentration in the extracellular space surrounding the synapse.4. It is tentatively suggested that this residual, non-cholinergic element of the synaptic response in some visceral cells be the result of the activation of an electrical synapse.

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Year:  1972        PMID: 4679731      PMCID: PMC1331097          DOI: 10.1113/jphysiol.1972.sp009932

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


  19 in total

1.  EFFECTS PRODUCED ON INHIBITORY POSTSYNAPTIC POTENTIALS BY THE COUPLED INJECTIONS OF CATIONS AND ANIONS INTO MOTONEURONS.

Authors:  J ECCLES; R M ECCLES; M ITO
Journal:  Proc R Soc Lond B Biol Sci       Date:  1964-05-19

2.  Single presynaptic neurone mediates a two component postsynaptic inhibition.

Authors:  J Kehoe
Journal:  Nature       Date:  1969-03-01       Impact factor: 49.962

3.  Direct and common connections among identified neurons in Aplysia.

Authors:  E R Kandel; W T Frazier; R Waziri; R E Coggeshall
Journal:  J Neurophysiol       Date:  1967-11       Impact factor: 2.714

Review 4.  Ion movements in junctional transmission.

Authors:  B L Ginsborg
Journal:  Pharmacol Rev       Date:  1967-09       Impact factor: 25.468

5.  [Selective suppression by tetraethylammonium ion of a cholinergic inhibition resistant to curare].

Authors:  J S Kehoe
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1969-01-06

6.  Re-evaluation of the synaptic activation of an electrogenic sodium pump.

Authors:  J S Kehoe; P Ascher
Journal:  Nature       Date:  1970-02-28       Impact factor: 49.962

7.  Synaptic activation of an electrogenic sodium pump.

Authors:  H Pinsker; E R Kandel
Journal:  Science       Date:  1969-02-28       Impact factor: 47.728

8.  Anomalous rectification in the metacerebral giant cells and its consequences for synaptic transmission.

Authors:  E R Kandel; L Tauc
Journal:  J Physiol       Date:  1966-03       Impact factor: 5.182

9.  A study of synaptic transmission in the absence of nerve impulses.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1967-09       Impact factor: 5.182

10.  Correlation of transmitter release with membrane properties of the presynaptic fiber of the squid giant synapse.

Authors:  K Kusano; D R Livengood; R Werman
Journal:  J Gen Physiol       Date:  1967-12       Impact factor: 4.086

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  25 in total

1.  Polyphasic synaptic potentials in the ganglion of the mollusc, Navanax.

Authors:  H Levitan; L Tauc
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

2.  The effect of tricyclic antidepressants on cholinergic responses of single cortical neurones.

Authors:  P Bevan; C M Bradshaw; E Szabadi
Journal:  Br J Pharmacol       Date:  1975-01       Impact factor: 8.739

Review 3.  Control of the cardiovascular system of Aplysia by identified neurons.

Authors:  M Skelton; A Alevizos; J Koester
Journal:  Experientia       Date:  1992-09-15

4.  On the acid-induced abolition of reticulo-ruminal motility in sheep [proceedings].

Authors:  B F Leek; J P Ryan; P K Upton
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

5.  Synaptic connexions of two symmetrically placed giant serotonin-containing neurones.

Authors:  G A Cottrell; J B Macon
Journal:  J Physiol       Date:  1974-01       Impact factor: 5.182

6.  Excitatory, inhibitory and biphasic synaptic potentials mediated by an identified dopamine-containing neurone.

Authors:  M S Berry; G A Cottrell
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

7.  Variation in strength of inhibitory synapses in the CA3 region of guinea-pig hippocampus in vitro.

Authors:  R Miles
Journal:  J Physiol       Date:  1990-12       Impact factor: 5.182

8.  Inhibitory and excitatory effects of dopamine on Aplysia neurones.

Authors:  P Ascher
Journal:  J Physiol       Date:  1972-08       Impact factor: 5.182

9.  Ionic mechanisms of a two-component cholinergic inhibition in Aplysia neurones.

Authors:  J Kehoe
Journal:  J Physiol       Date:  1972-08       Impact factor: 5.182

10.  Three acetylcholine receptors in Aplysia neurones.

Authors:  J Kehoe
Journal:  J Physiol       Date:  1972-08       Impact factor: 5.182

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