The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Co-release of acetylcholine and gamma-aminobutyric acid by a retinal neuron
Open accessAbstract
Rabbit retinas were vitally stained with 4',6-diamidino-2-phenylindole (DAPI), a fluorescent compound that selectively accumulates within the cholinergic amacrine cells. The retinas were then incubated in vitro in the presence of radioactive gamma-aminobutyric acid (GABA) and autoradiographed. The cells that accumulated DAPI were found to accumulate GABA, confirming immunohistochemical evidence that the cholinergic amacrine cells contain GABA. Incubation of retinas in the presence of elevated concentrations of K+ caused them to release acetylcholine and GABA, and autoradiography showed depletion of radioactive GABA from the cholinergic amacrine cells. This indicates that the cholinergic amacrine cells can secrete acetylcholine and GABA. Retinas were double-labeled with [14C]GABA and [3H]acetylcholine, allowing simultaneous measurement of their release. The release of [14C]GABA was found to be independent of extracellular Ca2+. Radioactive GABA synthesized endogenously from [14C]glutamate behaved the same way as radioactive GABA accumulated from the medium. In the same experiments the simultaneously measured release of [3H]acetylcholine was strongly Ca2+-dependent, indicating that the releases of acetylcholine and GABA are controlled by different mechanisms. Synaptic vesicles immunologically isolated from double-labeled retinas contained much [3H]acetylcholine and little or no [14C]GABA. These results suggest that the cholinergic amacrine cells release acetylcholine primarily by vesicle exocytosis and release GABA primarily by means of a carrier.
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Cites
Role of Transmitter Uptake Mechanisms in Synaptic Neurotransmission
Iversen, L. L. (1971) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1971.tb07066.x · Cited by 776
Buckley, K. M., & Kelly, R. B. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.4.1284 · Cited by 713
Jung, M. J., Lippert, B. J., Metcalf, B. W., Böhlen, P., & Schechter, P. J. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb10721.x · Cited by 481
Eckenstein, F. P., & Thoenen, H. (1982) · The EMBO Journal · doi:10.1002/j.1460-2075.1982.tb01175.x · Cited by 442
Kosaka, T., Tauchi, M., & Dahl, J. L. (1988) · Experimental Brain Research · doi:10.1007/bf00247609 · Cited by 417
The shape and arrangement of the cholinergic neurons in the rabbit retina
Tauchi, M., & Masland, R. H. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0085 · Cited by 385
Self-citationDepolarization Without Calcium Can Release γ-Aminobutyric Acid from a Retinal Neuron
Schwartz, E. A. (1987) · Science · doi:10.1126/science.2443977 · Cited by 345
Autoradiographic identification of acetylcholine in the rabbit retina.
Masland, R. H., & Mills, J. W. (1979) · The Journal of Cell Biology · doi:10.1083/jcb.83.1.159 · Cited by 286
Self-citationCholinergic amacrine cells in the rat retina
Voigt, T. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902480103 · Cited by 284
Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells
Ariel, M., & Daw, N. W. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014105 · Cited by 282
Responses to acetylcholine of ganglion cells in an isolated mammalian retina
Masland, R. H., & Ames, A. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.6.1220 · Cited by 256
Self-citationCalcium‐independent release of GABA from isolated horizontal cells of the toad retina.
Schwartz, E. A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014069 · Cited by 228
Brecha, N., Johnson, D., Peichl, L., & Wässle, H. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.16.6187 · Cited by 225
GABA-like immunoreactivity in cholinergic amacrine cells of the rabbit retina
Vaney, D. I., & Young, H. M. (1988) · Brain Research · doi:10.1016/0006-8993(88)91366-2 · Cited by 211
The functions of acetylcholine in the rabbit retina
Masland, R. H., Mills, J. W., & Cassidy, C. (1984) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1984.0086 · Cited by 200
Self-citationScreening for neurotransmitters: A rapid radiochemical procedure
Hildebrand, J. G., Barker, D. L. A., Herbert, E., & Kravitz, E. A. (1971) · Journal of Neurobiology · doi:10.1002/neu.480020305 · Cited by 197
‘Coronate’ amacrine cells in the rabbit retina have the ‘starburst’ dendritic morphology
Di, V. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0016 · Cited by 193
Masland, R. H., Mills, J. W., & Hayden, S. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0084 · Cited by 190
Self-citationLowe, A. W., Madeddu, L., & Kelly, R. B. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.1.51 · Cited by 185
Novel inhibitors of gamma-aminobutyric acid (GABA) uptake: anticonvulsant actions in rats and mice.
Yunger, L. M., Fowler, P. J., Zarevics, P., & SETLER, P. E. (1984) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21468-9 · Cited by 181
Carrier-mediated release of GABA from retinal horizontal cells
Yazulla, S., & Kleinschmidt, J. (1983) · Brain Research · doi:10.1016/0006-8993(83)91201-5 · Cited by 176
Glial and neuronal uptake of GABA, glutamic acid, glutamine and glutathione in the rabbit retina
Ehinger, B. (1977) · Experimental Eye Research · doi:10.1016/0014-4835(77)90089-6 · Cited by 135
Iversen, L. L., & Kravitz, E. A. (1968) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1968.tb08960.x · Cited by 106
A tonic gamma-aminobutyric acid-mediated inhibition of cholinergic amacrine cells in rabbit retina
Massey, S., & Redburn, D. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-11-01633.1982 · Cited by 92
Marshall, J. A., & Voaden, M. J. (1975) · Vision Research · doi:10.1016/0042-6989(75)90102-9 · Cited by 82
Radian, R., & Kanner, B. I. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39110-x · Cited by 77
Number and distribution of putative cholinergic neurons in the cat retina
Schmidt, M., Wässle, H., & Humphrey, M. F. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90137-5 · Cited by 77
Famiglietti, E. V. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-02-00562.1985 · Cited by 76
Kanner, B. I., Bendahan, A., & Radian, R. (1983) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(83)90397-8 · Cited by 42
Dopaminergic regulation of GABA release from the intact goldfish retina
O'Brien, D. R., & Dowling, J. E. (1985) · Brain Research · doi:10.1016/0006-8993(85)91218-1 · Cited by 40
Retinal Gaba neuron labelling with [3H]isoguvacine in different species
Agardh, E., & Ehinger, B. (1983) · Experimental Eye Research · doi:10.1016/0014-4835(83)90007-6 · Cited by 30
PHOTIC RELEASE OF RADIOACTIVITY FROM RABBIT RETINA PRELOADED WITH [3H]GABA
Bauer, B. (1978) · Acta Ophthalmologica · doi:10.1111/j.1755-3768.1978.tb01353.x · Cited by 28
The resting release of acetylcholine by a retinal neuron
Masland, R. H., & Cassidy, C. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0071 · Cited by 18
Self-citationBEDWANI, J. R., & Mehta, A. (1987) · Neurochemical Research · doi:10.1007/bf00971363 · Cited by 5
The release of (3H)‐GABA from the rabbit retina
Agardh, E., & Bauer, B. (1984) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1984.tb07485.x · Cited by 4
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Kaufman, D. L., Houser, C. R., & Tobin, A. J. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb08211.x · Cited by 789
Two isoforms of glutamate decarboxylase: why?
Soghomonian, J., & Martin, D. L. (1998) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(98)01270-x · Cited by 643
Direction selectivity in the retina: symmetry and asymmetry in structure and function
Vaney, D. I., Sivyer, B., & Taylor, W. R. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3165 · Cited by 330
Ion channel expression by white matter glia: The O-2A glial progenitor cell
Barres, B. A., Koroshetz, W. J., Swartz, K. J., Chun, L. L. Y., & Corey, D. P. (1990) · Neuron · doi:10.1016/0896-6273(90)90109-s · Cited by 306
Role of ACh-GABA cotransmission in detecting image motion and motion direction
Lee, S., Kim, K., & Zhou, Z. J. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.031 · Cited by 241
Metadata
- Authors
- O'Malley, D. M., & Masland, R. H.
- Affiliations
- Harvard University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1989-05
- Volume
- 86
- Issue
- 9
- Pages
- 3414-3418
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC287143
- OpenAlex
- W2126180763
- Cited by
- 150
- References
- 35
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 9 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 3 · 2019: 3 · 2018: 3 · 2017: 7 · 2016: 2 · 2015: 5 · 2014: 4 · 2013: 5 · 2012: 3
- FWCI
- 3.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ey005747-10, 5r37ey001075-23)
- National Eye Institute (R37 EY01075, R01-EY05747)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Keywords
- acetylcholine release, gamma-aminobutyric acid release, cholinergic amacrine cells, retinal neurons, CO release, calcium-dependent exocytosis, synaptic vesicles, potassium-evoked release, rabbit retina
- MeSH terms
- Acetylcholine, Animals, Autoradiography, Calcium, Carbon Radioisotopes, Choline, Fluorescent Dyes, gamma-Aminobutyric Acid, Glutamates, Indoles, Magnesium, Neurons, Potassium, Rabbits, Retina, Tritium, Glutamic Acid
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