Titlebook: Neurobiology of the Inner Retina; Reto Weiler,Neville N. Osborne Conference proceedings 1989 Springer-Verlag Berlin Heidelberg 1989 cells.

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The Release of Acetylcholine and Gaba by Neurons of the Rabbit Retina, it was thought that they were separate groups of cells. However, several laboratories have now reported that the cholinergic neurons also contain GABA (Vaney & Young, 1988; Kosaka et al, 1988; Brecha et al, 1988; see also Agardh & Ehinger, 1983). If these cells release both an excitatory and an inh

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Studies on the Localization of Serotonergic Neurones and the Types of Serotonin Receptors in the Maina. There is now strong support for the idea that serotonin is a transmitter substance in non-mammalian species, i. e. that serotonin is present in significant amounts in these retinas and can be localized in specific populations of amacrine cells by the Falck and Hillarp method or with immunohisto

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The Function of Multiple Subclasses of GABA Receptors in Rabbit Retina,ey, 1987). In most instances markers for GABAergic properties, such as high affinity uptake systems, endogenous stores of GABA and the presence of its synthetic enzyme, glutamic acid decarboxylase (GAD) are routinely observed within specific populations of amacrine cells. Labeling in the outer retin

Peak-Bone-Mass

The Anatomy of Multiple Gabaergic and Glycinergic Pathways in the Inner Plexiform Layer of The Goldtwo such transmitters necessary? One compelling explanation is that a greater range of additivity of inhibitory currents is achieved by having two different pre-synaptic systems converge on the same kind of post-synaptic mechanism, as demonstrated by Gold and Martin (1984) for Muller cells in the la

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Distribution and Spatial Organization of Dopaminergic Interplexiform Cells in the Rat Retina,n established for DA (see Ehinger, 1983, for review). The best documented at the level of cellular and molecular biology is unquestionably the uncoupling action of DA on horizontal cell gap junctions via a D. receptor mechanism. The DA released by light stimulation (flashes or light adaptation from

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Neuronal and Glial Release of GABA from the Rat Retina,t vertebrate retinas GABA is an inhibitory transmitter in about one third of amacrine cells. However, in contrast to horizontal cells, from which the release of GABA has been convincingly demonstrated (Schwartz, 1982; Yazulla & Kleinschmidt, 1983; Yazulla, 1983; Ayoub & Lam, 1985; Cunningham & N

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Efferent Projections to the Goldfish Retina, demonstrated in a variety of other species, including several species of fish (Witkovsky, 1971; Ebbesson and Meyer, 1981; Munz and Claas, 1981; Munz et al, 1982; Gerwerzhagen et al, 1982; Crapon de Caprona and Fritzsch, 1983; Meyer et al, 1983; Springer, 1983). Retrograde tracing methods have shown

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Correlation Between Electrophysiological Responses and Morphological Classes of Turtle Retinal Amacic physiological types of amacrine cell responses (ON, OFF, slow ON-OFF and fast ON- OFF; e. g. Teranishi et al. 1987) have been described in turtle retina which can be correlated to some of the morphological types (Marchiafava and Weiler 1982; Weiler and Marchiafava 1981; Jensen and DeVoe 1982; Amm

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