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Potassium-stimulated release of GABA, glycine, and taurine from the chick retina

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Abstract

The effect of depolarizing potassium concentration on the release of [14C]glycine, [3H]GABA, and [35S]taurine was investigated in the whole chick retina and in a synaptosomal fraction prepared from the chick retina. In the whole retina, increasing potassium concentration above 40 mM resulted in an increased release of the three amino acids. The release of glycine was the most stimulated and that of taurine, the least. The potassium-evoked release of glycine and GABA was calcium dependent. In the synaptosomal fraction, 68.5 mM potassium significantly stimulated the efflux of GABA and glycine by a calcium-dependent mechanism. The release of taurine from this fraction was unaffected by high potassium.

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References

  1. Krnjevic, K. 1974. Chemical nature of synaptic transmission in vertebrates. Physiol. Rev. 54:418–540.

    Google Scholar 

  2. Curtis, D. R., andJohnston, G. A. R. 1974. Amino acid transmitters in the mammalian central nervous system. Ergebn. Physiol. 69:97–188.

    Google Scholar 

  3. Aprison, M. H., Daly, E. C., Shank, R. P., andMcBride, W. J. 1975. Neurochemical evidence for glycine as a transmitter and a model for its intrasynaptosomal compartmentation. Pages 37–63,in Berl, S., Clarke, D. D. andSchneider, D. (eds.), Metabolic Compartmentation and Neurotransmission. Relation to Brain Structure and Function. Plenum Press, New York.

    Google Scholar 

  4. Neal, M. J. 1976. Amino acid transmitter substances in the vertebrate retina. Gen. Pharmacol. 7:321–332.

    Google Scholar 

  5. Bruun, A., andEhinger, B. 1972. Uptake of the putative neurotransmitter glycine into the rabbit retina. Invest. Ophthalmol. 11:191–198.

    Google Scholar 

  6. Cohen, A. I., McDaniel, M., andOrr, H. 1973. Absolute levels of some free amino acids in normal and biologically fractionated retinas. Invest. Ophthalmol 12:686–693.

    Google Scholar 

  7. Ehinger, B., andLindberg, B. 1976. Light-evoked release of glycine from cat and rabbit retina. Brain Res. 113:535–549.

    Google Scholar 

  8. Macaione, S. 1972. Localization of GABA system in rat retina J. Neurochem. 19:1397–1400.

    Google Scholar 

  9. Graham, L. T. 1972. Intraretinal distribution of GABA content and GAD activity. Brain Res. 36:476–479.

    Google Scholar 

  10. Lam, D. M. K. 1972. The biosynthesis and content of gamma-aminobutyric acid in the goldfish retina. J. Cell Biol. 54:215–231.

    Google Scholar 

  11. Pasantes-Morales, H., Klethi, J., Ledig, M., andMandel, P. 1972. Free amino acids of chicken and rat retina. Brain Res. 41:494–497.

    Google Scholar 

  12. Mandel, P., Pasantes-Morales, H., andUrban, P. F. 1976. Taurine, a putative transmitter in retina. Pages 89–108,in Bonting, S. L. (ed.), Transmitters in the Visual Process. Pergamon Press, New York.

    Google Scholar 

  13. Orr, H. T., Cohen, A. I., andLowry, O. H. 1976. The distribution of taurine in the vertebrate retina.J. Neurochem. 26:609–611.

    Google Scholar 

  14. De Robertis, E., Pellegrino De Iraldi A., Rodriguez De Lores Arnaiz, G., andSalganicoff, L. 1962. Cholinergic and non-cholinergic nerve endings in rat brain. I. Isolation and subcellular distribution of acetylcholine and acetyl cholin esterase. J. Neurochem. 9:23–35.

    Google Scholar 

  15. Schmid, R., Sieghart, W., andKarobath, M. 1975. taurine uptake in synaptosomal fractions of rat cerebral cortex. J. Neurochem. 25:5–9.

    Google Scholar 

  16. Bray, G. A. 1960. A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counter. Anal Biochem. 1:279–285.

    Google Scholar 

  17. Hopkin, J., andNeal, M. J. 1971. Effect of electrical stimulation and high potassium concentrations on the efflux of [14C]glycine from slices of spinal cord. Br. J. Pharmacol. 42:215–223.

    Google Scholar 

  18. Lopez-Colome, A. M., Erlij D., andPasantes-Morales, H. 1976. Different effects of calcium flux-blocking agents on light and potassium stimulated release of taurine from retina. Brain Res. 113:527–534.

    Google Scholar 

  19. Neal, M. J., andAtterwill, C. K. 1974. Isolation of photoreceptor and conventional nerve terminals by subcellular fractionation of rabbit retina. Nature 251:331–333.

    Google Scholar 

  20. Macaione, S., Tucci, G., De Luca, G., andDi Giorgio, R. M. 1976. Subcellular distribution of taurine and cysteine sulphinate decarboxylase activity in ox retina. J. Neurochem. 27:1411–1415.

    Google Scholar 

  21. Dowling, J. E. 1970. Organization of vertebrate retinas. Invest. Ophthalmol. 9:655–680.

    Google Scholar 

  22. Pasantes-Morales, H., Klethi, J., Urban, P. F., andMandel, P. 1974. The effect of electrical stimulation, light and amino acids on the efflux of35S-taurine from the retina of the domestic fowl. Exp. Brain Res. 19:131–142.

    Google Scholar 

  23. Salceda, R., andPasantes-Morales, H. 1975. A calcium coupled release of taurine from retina. Brain Res. 96:206–211.

    Google Scholar 

  24. Hagins, W. A., andYoshikami, S. 1974. A role for Ca2+ in excitation of retinal rods and cones. Exp. Eye Res. 18:299–305.

    Google Scholar 

  25. Marshall, J., andVoaden, J. J. 1974. An autoradiographic study of the cells accumulating3H-γ-aminobutyric acid in the isolated retinas of pigeons and chickens. Invest. Ophthalmol. 13:602–607.

    Google Scholar 

  26. Ehinger, B., andFalck, B. 1971. Autoradiography of some suspected neurotransmitter substances: GABA, glycine, glutamic acid, aspartic acid, histamine, dopamine andl-dopa. Brain Res. 33:157–172.

    Google Scholar 

  27. Bennett, J. P., Logan, W. J., andSnyder, S. H. 1973. Amino acids as a central nervous transmitters: the influence of ions, amino acid analogues, and ontogeny on transport systems forl-glutamic andl-aspartic acids and glycine into central nervous synaptosomes of the rat. J. Neurochem. 21:1533–1550.

    Google Scholar 

  28. Clark, R. M., andCollins, G. G. S. 1976. The release of endogenous amino acids from the rat visual cortex. J. Physiol. 262:383–400.

    Google Scholar 

  29. Sieghart, W., andHeckl, K. 1976. Potassium-evoked release of taurine from synaptosomal fractions of rat cerebral cortex. Brain Res. 116:538–543.

    Google Scholar 

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López-Colomé, A.M., Salceda, R. & Pasantes-Morales, H. Potassium-stimulated release of GABA, glycine, and taurine from the chick retina. Neurochem Res 3, 431–441 (1978). https://doi.org/10.1007/BF00966325

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