2007
DOI: 10.1016/j.visres.2006.11.004
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Dopaminergic modulation and rod contribution in the generation of oscillatory potentials in the tiger salamander retina

Abstract: The roles of rod and cone input and of dopamine in the generation of oscillatory potentials were studied in tiger salamander retina. Under scotopic conditions, oscillations were elicited with a green, but not a red stimulus. With mesopic background illumination, both stimuli caused oscillations. Addition of quinpirole to a mesopic retina eliminated oscillations while SKF-38393 had no effect. Similarly, addition of sulpiride to a light-adapted retina elicited oscillatory activity, but SCH 22390 had no effect. T… Show more

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Cited by 7 publications
(8 citation statements)
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“…Given that OPs are likely to be generated by the synaptic activity between the bipolar cells, the amacrine cells, and the RGCs (Wachtmeister, ), and that both D1 and D2 receptors are expressed by amacrine cells and RGCs (Mills & Massey, ; Derouiche & Asan, ; Nguyen‐Legros et al ., ; Weber et al ., ; Urschel et al ., ; Mills et al ., ; Kothmann et al ., ; Zhang et al ., ), it is possible that both inactivation of D2 receptors and over‐excitation of D1 receptors could contribute to the changes in OP amplitude of D2 −/− mice. Consistently, activating D2 receptors increases the amplitude of OPs mediated by the rod pathway (Perry & George, ), and blocking of D1 receptors or D1 receptor mutation reduces OP amplitude (Holopigian et al ., ; He et al ., ; Lavoie et al ., ). This possibility is further supported by the results that dark rearing D2 −/− mice, which could potentially block dopamine release from dopaminergic amacrine cells and D1 receptor activation, completely abolishes the effect of D2 receptor mutation on OP amplitude.…”
Section: Discussionmentioning
confidence: 85%
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“…Given that OPs are likely to be generated by the synaptic activity between the bipolar cells, the amacrine cells, and the RGCs (Wachtmeister, ), and that both D1 and D2 receptors are expressed by amacrine cells and RGCs (Mills & Massey, ; Derouiche & Asan, ; Nguyen‐Legros et al ., ; Weber et al ., ; Urschel et al ., ; Mills et al ., ; Kothmann et al ., ; Zhang et al ., ), it is possible that both inactivation of D2 receptors and over‐excitation of D1 receptors could contribute to the changes in OP amplitude of D2 −/− mice. Consistently, activating D2 receptors increases the amplitude of OPs mediated by the rod pathway (Perry & George, ), and blocking of D1 receptors or D1 receptor mutation reduces OP amplitude (Holopigian et al ., ; He et al ., ; Lavoie et al ., ). This possibility is further supported by the results that dark rearing D2 −/− mice, which could potentially block dopamine release from dopaminergic amacrine cells and D1 receptor activation, completely abolishes the effect of D2 receptor mutation on OP amplitude.…”
Section: Discussionmentioning
confidence: 85%
“…Further complicating matters, the D2 antagonist sulpiride enhances the amplitude of the b-wave mediated by rods but diminishes the b-wave mediated by cones in dark-adapted frogs (Popova & Kupenova, 2013). In the inner retina, activating D2 receptors increases the amplitude of OPs mediated by the rod pathway in the tiger salamander (Perry & George, 2007), and blocking of D2 receptors decreases the OP amplitude in the mudpuppy (Wachtmeister & Dowling, 1978;Wachtmeister, 1981Wachtmeister, , 1998.…”
Section: The Effects Of D2 Receptors On the Erg Of Adult Micementioning
confidence: 99%
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“…Dopaminergic inhibitory neurons are likely to underlie the OPs (Wachtmeister & Dowling 1978;Wachtmeister 1981aWachtmeister , 1998Perry & George 2007). The postnatal development and maturation of dopaminergic neurons and receptors in the IPL occur late and dopaminergic neurons are not fully responsive until Day 25 in the rat (Cohen & Neff 1982;Koulen 1999).…”
Section: Discussionmentioning
confidence: 99%
“…Most likely, the oscillatory response represents activity in neuronal inhibitory feed-back circuits initiated by amacrine cells receiving input from both rods and cones (Wachtmeister & Dowling 1978;Heynen et al 1985;Friedburg et al 2004; Lei et al 2006;Lundstr€ om et al 2007;Perry & George 2007). As the OPs respond rapidly to changes of illumination signalling back to distal retina, the OP system offers a good tool to study the neuronal adaptive system.…”
Section: Introductionmentioning
confidence: 99%