1983
DOI: 10.1016/0197-0186(83)90030-x
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Neurotransmitter-related features of the retinal pigment epithelium

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Cited by 20 publications
(3 citation statements)
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“…Light-induced changes in retinal dopamine release and subsequent changes in cAMP levels of the RPE may have a role in mediating aspects of RPE physiology other than pigment movement. In addition to our results suggesting that teleost RPE cells possess D2 dopaminergic receptors, other studies have reported highaffinity binding of [3H]spiperone, a D2 antagonist, to isolated RPE of cow and cat (Bondy et al, 1983;Bruinink et al, 1986). These latter species do not exhibit significant RPE pigment movement.…”
Section: Discussionsupporting
confidence: 77%
“…Light-induced changes in retinal dopamine release and subsequent changes in cAMP levels of the RPE may have a role in mediating aspects of RPE physiology other than pigment movement. In addition to our results suggesting that teleost RPE cells possess D2 dopaminergic receptors, other studies have reported highaffinity binding of [3H]spiperone, a D2 antagonist, to isolated RPE of cow and cat (Bondy et al, 1983;Bruinink et al, 1986). These latter species do not exhibit significant RPE pigment movement.…”
Section: Discussionsupporting
confidence: 77%
“…In addition, we have shown that dopamine and epinephrine inhibited forskolin-induced pigment aggregation in isolated RPE-retinas, suggesting that stimulation of either dopaminergic or a-adrenergic receptors acts to inhibit forskolin-stimulated adenylate cyclase activity in RPE (Dearry and Burnside, 1985). Other investigators have demonstrated that D2 dopaminergic and a2-adrenergic receptors can be coupled to adenylate cyclase in an inhibitory manner (see re- views by Creese et al, 1982;Limbird, 1983) and that both dopaminergic and a-adrenergic binding sites are present on RPE (Bondy et al, 1983;Bruinink et al, 1986). Together, these results suggest that dopamine and clonidine produce light-adaptive pigment dispersion by respectively binding to D2 dopaminergic and a2-adrenergic receptors on RPE, thereby inhibiting RPE adenylate cyclase activity.…”
Section: Discussionmentioning
confidence: 81%
“…However, it was necessary to establish the basic binding characteristics of the ligands used. Thus saturability, specificity, and reversibility of different binding sites were delineated (Ali, Slikker, Newport, & Goad, 1986; Bondy et al, 1983).…”
Section: Methodsmentioning
confidence: 99%