Literature DB >> 2965950

Studies on the mechanism by which tryptophan efflux from isolated synaptosomes is stimulated by depolarization.

K J Collard1, L S Wilkinson, D J Lewis.   

Abstract

1. The efflux and influx of tryptophan across the synaptosomal plasma membrane has been studied under a variety of experimental conditions, in order to examine the mechanism by which depolarization enhances the efflux of tryptophan from superfused synaptosomes. 2. Efflux of [3H]-tryptophan from preloaded superfused synaptosomes was found to be enhanced by K+ depolarization in a Ca2+ and dose-dependent manner. In contrast, [3H]-phenylalanine efflux was only poorly stimulated by depolarization and only by very high concentrations of K+. 3. Tryptophan efflux was also enhanced by decreasing the extracellular Na+ concentration, but this effect was not dependent on extracellular Ca2+. 4. Influx of [3H]-tryptophan into synaptosomes was stimulated by extracellular Na+ removal, but the uptake of [3H]-phenylalanine was unaffected by this procedure. 5. Both the induced influx and efflux of tryptophan observed under these experimental conditions was inhibited by immobilizing the plasma membrane carrier with parachlorophenylalanine. This implied that both the enhanced influx and efflux arose as a consequence of the activation of the membrane tryptophan carrier, the direction of the observed effect being dependent upon the manner in which the experiments were conducted. 6. The relationship between depolarization, the activation of the membrane tryptophan carrier and the significance of this to the in vivo situation is discussed.

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Year:  1988        PMID: 2965950      PMCID: PMC1853795          DOI: 10.1111/j.1476-5381.1988.tb11440.x

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


  21 in total

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3.  The regulation of cytosolic calcium in rat brain synaptosomes by sodium-dependent calcium efflux.

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4.  Calcium uptake of rat brain synaptosomes as a function of membrane potential under different depolarizing conditions.

Authors:  V Adam-Vizi; E Ligeti
Journal:  J Physiol       Date:  1986-03       Impact factor: 5.182

5.  Tryptophan hydroxylase inhibition: the mechanism by which p-chlorophenylalanine depletes rat brain serotonin.

Authors:  E Jéquier; W Lovenberg; A Sjoerdsma
Journal:  Mol Pharmacol       Date:  1967-05       Impact factor: 4.436

6.  The stimulus-induced release of unmetabolized 5-hydroxytryptamine from superfused rat brain synaptosomes.

Authors:  K J Collard; D M Cassidy; M A Pye; R M Taylor
Journal:  J Neurosci Methods       Date:  1981-08       Impact factor: 2.390

7.  Opposite effects of extracellular sodium removal on the uptake of tryptophan into rat cortical slices and synaptosomes.

Authors:  L S Wilkinson; K J Collard
Journal:  J Neurochem       Date:  1984-07       Impact factor: 5.372

8.  Uptake and release of tryptophan and serotonin: an HPLC method to study the flux of endogenous 5-hydroxyindoles through synaptosomes.

Authors:  W A Wolf; D M Kuhn
Journal:  J Neurochem       Date:  1986-01       Impact factor: 5.372

9.  Serotonin synthesis with rat brain synaptosomes. Effects of serotonin and monoamineoxidase inhibitors.

Authors:  M Karobath
Journal:  Biochem Pharmacol       Date:  1972-05-01       Impact factor: 5.858

10.  Ca2+ transport by intact synaptosomes: the voltage-dependent Ca2+ channel and a re-evaluation of the role of sodium/calcium exchange.

Authors:  K E Akerman; D G Nicholls
Journal:  Eur J Biochem       Date:  1981-07
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  3 in total

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Journal:  Br J Pharmacol       Date:  1990-12       Impact factor: 8.739

3.  The characteristics of arginine transport by rat cerebellar and cortical synaptosomes.

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