Literature DB >> 1375639

Effects of alcohols on responses evoked by inositol trisphosphate in Xenopus oocytes.

V Ilyin1, I Parker.   

Abstract

1. The effects of ethanol and other alcohols on inositol 1,4,5-trisphosphate (InsP3) signalling were studied in Xenopus oocytes by the use of flash photolysis of caged InsP3. Calcium liberation induced by InsP3 was monitored by voltage-clamp recording of Ca(2+)-activated membrane currents, and by fluorescence of the Ca2+ indicator Fluo-3. 2. Membrane current and fluorescence Ca2+ signals evoked by light flashes giving small responses were initially potentiated by bath application of ethanol (80-400 mM). However, the responses subsequently declined while ethanol was present and were strongly reduced or suppressed when it was removed. 3. These effects did not arise artifactually from changes in photolysis of caged InsP3, as similar results were seen with responses evoked by intracellular injections of InsP3. Also, the effects on the membrane current did not arise primarily through actions on the Ca(2+)-dependent Cl- channels, since currents evoked by intracellular injections of Ca2+ were little changed by ethanol. 4. Ethanol reduced the threshold level of InsP3 required to cause Ca2+ liberation. Thus, potentiation was most prominent with small responses evoked by brief light flashes, whereas the predominant effect on larger responses was inhibitory. 5. The facilitatory and inhibitory actions of ethanol persisted after removing extracellular Ca2+. 6. Intracellular injections of ethanol produced an initial inhibition of InsP3 responses, followed, in some oocytes, by a potentiation. 7. Methanol had little effect on InsP3 responses, whereas butanol and other long-chain alcohols produced strong inhibition, but little or no potentiation. 8. We conclude that extracellular application of ethanol produces a rapid potentiation of InsP3-mediated Ca2+ liberation, and a more slowly developing inhibition. The potentiation may arise through stimulation of InsP3 formation at the plasma membrane, whereas the inhibition occurs more deeply in the cell. Both actions were evident at relatively low concentrations (a few tens of millimoles per litre), and might thus be important in the behavioural effects of ethanol intoxication.

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Year:  1992        PMID: 1375639      PMCID: PMC1176203          DOI: 10.1113/jphysiol.1992.sp019045

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


  26 in total

Review 1.  Properties and uses of photoreactive caged compounds.

Authors:  J A McCray; D R Trentham
Journal:  Annu Rev Biophys Biophys Chem       Date:  1989

2.  Nonlinearity and facilitation in phosphoinositide signaling studied by the use of caged inositol trisphosphate in Xenopus oocytes.

Authors:  I Parker; R Miledi
Journal:  J Neurosci       Date:  1989-11       Impact factor: 6.167

Review 3.  Inositol phosphates and cell signalling.

Authors:  M J Berridge; R F Irvine
Journal:  Nature       Date:  1989-09-21       Impact factor: 49.962

4.  Inositol 1,4,5-trisphosphate mimics muscarinic response in Xenopus oocytes.

Authors:  Y Oron; N Dascal; E Nadler; M Lupu
Journal:  Nature       Date:  1985 Jan 10-18       Impact factor: 49.962

5.  Fluorescent indicators for cytosolic calcium based on rhodamine and fluorescein chromophores.

Authors:  A Minta; J P Kao; R Y Tsien
Journal:  J Biol Chem       Date:  1989-05-15       Impact factor: 5.157

6.  Ethanol-induced mobilization of calcium by activation of phosphoinositide-specific phospholipase C in intact hepatocytes.

Authors:  J B Hoek; A P Thomas; R Rubin; E Rubin
Journal:  J Biol Chem       Date:  1987-01-15       Impact factor: 5.157

7.  Inositol 1,4,5-trisphosphate receptor binding: autoradiographic localization in rat brain.

Authors:  P F Worley; J M Baraban; S H Snyder
Journal:  J Neurosci       Date:  1989-01       Impact factor: 6.167

8.  Ethanol and inositol 1,4,5-trisphosphate mobilize calcium from rat brain microsomes.

Authors:  T Machu; J J Woodward; S W Leslie
Journal:  Alcohol       Date:  1989 Nov-Dec       Impact factor: 2.405

Review 9.  Ethanol and the benzodiazepine-GABA receptor-ionophore complex.

Authors:  M K Ticku
Journal:  Experientia       Date:  1989-05-15

10.  Calcium-dependent chloride currents elicited by injection of ethanol into Xenopus oocytes.

Authors:  K A Wafford; T V Dunwiddie; R A Harris
Journal:  Brain Res       Date:  1989-12-29       Impact factor: 3.252

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  6 in total

Review 1.  Effects of ethanol on calcium homeostasis in the nervous system: implications for astrocytes.

Authors:  M C Catlin; M Guizzetti; L G Costa
Journal:  Mol Neurobiol       Date:  1999-02       Impact factor: 5.590

2.  Inhibition of the cerebellar inositol 1,4,5-trisphosphate-sensitive Ca2+ channel by ethanol and other aliphatic alcohols.

Authors:  M Mezna; T Patchick; S Tovey; F Michelangeli
Journal:  Biochem J       Date:  1996-02-15       Impact factor: 3.857

3.  Acetylcholine induces Ca2+ oscillations via m3/m4 muscarinic receptors in the mouse oocyte.

Authors:  Dawon Kang; Jae-Yong Park; Jaehee Han; In-Ha Bae; Sook-Young Yoon; Sang Soo Kang; Wan Sung Choi; Seong-Geun Hong
Journal:  Pflugers Arch       Date:  2003-10-14       Impact factor: 3.657

4.  Actions of long chain alcohols on GABAA and glutamate receptors: relation to in vivo effects.

Authors:  J E Dildy-Mayfield; S J Mihic; Y Liu; R A Deitrich; R A Harris
Journal:  Br J Pharmacol       Date:  1996-05       Impact factor: 8.739

Review 5.  Pharmacological modulation of intracellular Ca(2+) channels at the single-channel level.

Authors:  P Koulen; E C Thrower
Journal:  Mol Neurobiol       Date:  2001 Aug-Dec       Impact factor: 5.682

6.  Analysis of cat oocyte activation methods for the generation of feline disease models by nuclear transfer.

Authors:  Chunmin Wang; William F Swanson; Jason R Herrick; Kiho Lee; Zoltan Machaty
Journal:  Reprod Biol Endocrinol       Date:  2009-12-11       Impact factor: 5.211

  6 in total

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