Chloride dependence of the K+-stimulated release of taurine from synaptosomes

[1]  R. Huxtable.  Taurine in the central nervous system and the mammalian actions of taurine , 1989, Progress in Neurobiology.

[2]  H. Pasantes‐Morales,et al.  A volume‐dependent, chloride—sensitive component of taurine release stimulated by potassium from retina , 1989, Journal of neuroscience research.

[3]  L. Cubeddu,et al.  Effects of low extracellular chloride on dopamine release and the dopamine transporter. , 1989, The Journal of pharmacology and experimental therapeutics.

[4]  J. Montenegro,et al.  A chloride-dependent component of the release of labeled GABA and taurine from the chick retina , 1988, Brain Research.

[5]  J. Lombardini,et al.  Is taurine a hypothalamic neurotransmitter?: a model of the differential uptake and compartmentalization of taurine by neuronal and glial cell particles from the rat hypothalamus , 1987, Brain Research Reviews.

[6]  W. Walz.  Swelling and potassium uptake in cultured astrocytes. , 1987, Canadian journal of physiology and pharmacology.

[7]  R. Boakes,et al.  Efflux of Putative Transmitters from Superfused Rat Brain Slices Induced by Low Chloride Ion Concentrations , 1987, Journal of neurochemistry.

[8]  F. Fonnum,et al.  Differences in Anionic Dependence of the Synaptic Efflux of d‐Aspartic Acid and γ‐Aminobutyric Acid , 1986, Journal of neurochemistry.

[9]  P. Lelkes,et al.  Membrane Potential and Catecholamine Secretion by Bovine Adrenal Chromaffin Cells: Use of Tetraphenylphosphonium Distribution and Carbocyanine Dye Fluorescence , 1985, Journal of neurochemistry.

[10]  J. Hardy,et al.  Release of Aspartate and Glutamate Caused by Chloride Reduction in Synaptosomal Incubation Media , 1984, Journal of neurochemistry.

[11]  W. Sieghart,et al.  Properties of [3H]taurine release from crude synaptosomal fractions of rat cerebral cortex , 1979, Neurochemical Research.

[12]  P. Kontro.  Components of taurine efflux in rat brain synaptosomes , 1979, Neuroscience.

[13]  A. Loud,et al.  Quantitative stereological evaluation of KCl-induced ultrastructural changes in frog brain , 1977, Neuroscience.

[14]  H. Kimelberg,et al.  THE EFFECT OF HCO3− ON THE SWELLING AND ION UPTAKE OF MONKEY CEREBRAL CORTEX UNDER CONDITIONS OF RAISED EXTRACELLULAR POTASSIUM , 1975, Journal of neurochemistry.

[15]  F. Hajós.  An improved method for the preparation of synaptosomal fractions in high purity , 1975, Brain Research.

[16]  K. Kamino,et al.  Potassium ion-induced swelling of nerve-ending particles by light-scattering measurement. , 1973, Biochimica et biophysica acta.

[17]  P. Lipton,et al.  Effects of membrane depolarization on light scattering by cerebral cortical slices , 1973, The Journal of physiology.

[18]  P. Keen,et al.  A LIGHT‐SCATTERING TECHNIQUE FOR THE STUDY OF THE PERMEABILITY OF RAT BRAIN SYNAPTOSOMES IN VITRO , 1970, Journal of neurochemistry.

[19]  A. van Harreveld,et al.  Changes in cortical extracellular space during spreading depression investigated with the electron microscope. , 1967, Journal of neurophysiology.

[20]  D. B. Tower,et al.  FLUID COMPARTMENTATION AND ELECTROLYTES OF CAT CEREBRAL CORTEX IN VITRO–I SWELLING AND SOLUTE DISTRIBUTION IN MATURE CEREBRAL CORTEX * , 1966, Journal of neurochemistry.

[21]  A. Hodgkin,et al.  Potassium contractures in single muscle fibres , 1960, The Journal of physiology.

[22]  R. A. Naumann,et al.  Studies of the production and subsequent reduction of swelling in primate cerebral cortex under isosmotic conditionsin vivo , 2006, Experimental Brain Research.

[23]  Y. Olsson,et al.  Pathogenesis of brain lesions caused by experimental epilepsy , 2004, Acta Neuropathologica.

[24]  R. S. Bourke.  Studies of the development and subsequent reduction of swelling of mammalian cerebral cortex under isosmotic conditions in vitro , 2004, Experimental Brain Research.

[25]  A. Schousboe,et al.  Release of taurine from astrocytes during potassium‐evoked swelling , 1989, Glia.

[26]  S. Oja,et al.  Cation effects on taurine release from brain slices: Comparison to GABA , 1987, Journal of neuroscience research.

[27]  O. Petersen,et al.  Pancreatic acinar cells: ionic dependence of acetylcholine‐induced membrane potential and resistance change. , 1975, The Journal of physiology.