Literature DB >> 8242258

Ionomycin-induced acetylcholine release and its inhibition by adenosine at frog motor nerve endings.

J M Hunt1, E M Silinsky.   

Abstract

1. Acetylcholine (ACh) evoked secretion by the calcium ionophore, ionomycin, was studied at frog motor nerve endings. 2. Bath application of ionomycin stimulated an irreversible increase in the rate of spontaneous, quantal ACh release in the presence of extracellular Ca2+. In contrast, local application of ionomycin stimulated a rapid, reversible acceleration of spontaneous ACh release. 3. The magnitude of the secretory response to ionomycin was dependent both upon the concentration of ionophore and the concentration of extracellular Ca2+. 4. Adenosine or 2-chloroadenosine inhibited ionomycin-stimulated ACh release with the same potency and efficacy observed previously for these adenosine analogues as inhibitors of ACh secretion evoked by nerve impulses. 5. These results support the conclusion that adenosine receptor activation inhibits quantal ACh secretion at a site distal to that of Ca2+ entry at frog motor nerve endings.

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Year:  1993        PMID: 8242258      PMCID: PMC2175912          DOI: 10.1111/j.1476-5381.1993.tb13887.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  31 in total

1.  Inhibition of evoked acetylcholine release: two different mechanisms in the Torpedo electric organ.

Authors:  D Muller; F Loctin; Y Dunant
Journal:  Eur J Pharmacol       Date:  1987-01-13       Impact factor: 4.432

Review 2.  Adenosine receptors and calcium: basis for proposing a third (A3) adenosine receptor.

Authors:  J A Ribeiro; A M Sebastião
Journal:  Prog Neurobiol       Date:  1986       Impact factor: 11.685

3.  Blocking and isolation of a calcium channel from neurons in mammals and cephalopods utilizing a toxin fraction (FTX) from funnel-web spider poison.

Authors:  R Llinás; M Sugimori; J W Lin; B Cherksey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

4.  Omega-conotoxin does not block the verapamil-sensitive calcium channels at mouse motor nerve terminals.

Authors:  A J Anderson; A L Harvey
Journal:  Neurosci Lett       Date:  1987-11-23       Impact factor: 3.046

5.  Potentiation of synaptic transmission in the hippocampus by phorbol esters.

Authors:  R C Malenka; D V Madison; R A Nicoll
Journal:  Nature       Date:  1986 May 8-14       Impact factor: 49.962

6.  Inhibition of quantal transmitter release in the absence of calcium influx by a G protein-linked adenosine receptor at hippocampal synapses.

Authors:  K P Scholz; R J Miller
Journal:  Neuron       Date:  1992-06       Impact factor: 17.173

7.  Calcium currents at motor nerve endings: absence of effects of adenosine receptor agonists in the frog.

Authors:  E M Silinsky; C S Solsona
Journal:  J Physiol       Date:  1992-11       Impact factor: 5.182

8.  Strontium, barium, and manganese metabolism in isolated presynaptic nerve terminals.

Authors:  H Rasgado-Flores; S Sanchez-Armass; M P Blaustein; D A Nachshen
Journal:  Am J Physiol       Date:  1987-06

9.  Autoreceptor-mediated purinergic and cholinergic inhibition of motor nerve terminal calcium currents in the rat.

Authors:  B R Hamilton; D O Smith
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

10.  Phorbol ester-induced synaptic facilitation is different than long-term potentiation.

Authors:  D Muller; J Turnbull; M Baudry; G Lynch
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

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  3 in total

1.  Adenosine decreases both presynaptic calcium currents and neurotransmitter release at the mouse neuromuscular junction.

Authors:  Eugene M Silinsky
Journal:  J Physiol       Date:  2004-05-14       Impact factor: 5.182

2.  Reduction by intracellular calcium chelation of acetylcholine secretion without occluding the effects of adenosine at frog motor nerve endings.

Authors:  J M Hunt; R S Redman; E M Silinsky
Journal:  Br J Pharmacol       Date:  1994-03       Impact factor: 8.739

3.  LY 294002 inhibits adenosine receptor activation by a mechanism independent of effects on PI-3 kinase or casein kinase II.

Authors:  T J Searl; E M Silinsky
Journal:  Purinergic Signal       Date:  2005-12-03       Impact factor: 3.765

  3 in total

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