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1.
J Neurochem ; 95(5): 1504-20, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16269010

ABSTRACT

Muscarinic receptors are the predominant cholinergic receptors in the central and peripheral nervous systems. Recently, activation of muscarinic receptors was found to elicit pigment granule dispersion in retinal pigment epithelium isolated from bluegill fish. Pigment granule movement in retinal pigment epithelium is a light-adaptive mechanism in fish. In the present study, we used pharmacological and molecular approaches to identify the muscarinic receptor subtype and the intracellular signaling pathway involved in the pigment granule dispersion in retinal pigment epithelium. Of the muscarinic receptor subtype-specific antagonists used, only antagonists specific for M1 and M3 muscarinic receptors were found to block carbamyl choline (carbachol)-induced pigment granule dispersion. A phospholipase C inhibitor also blocked carbachol-induced pigment granule dispersion, and a similar result was obtained when retinal pigment epithelium was incubated with an inositol trisphosphate receptor inhibitor. We isolated M2 and M5 receptor genes from bluegill and studied their expression. Only M5 was found to be expressed in retinal pigment epithelium. Taken together, pharmacological and molecular evidence suggest that activation of an odd subtype of muscarinic receptor, possibly M5, on fish retinal pigment epithelium induces pigment granule dispersion.


Subject(s)
Acetylcholine/pharmacology , Adaptation, Ocular , Pigment Epithelium of Eye/drug effects , Pigments, Biological/physiology , Receptors, Muscarinic/metabolism , Alkaloids , Animals , Behavior, Animal , Carbachol/pharmacology , Cholinergic Agonists/pharmacology , Cholinesterase Inhibitors/pharmacology , Cloning, Molecular/methods , Colforsin/pharmacology , Dose-Response Relationship, Drug , Drug Interactions , Enzyme Inhibitors/pharmacology , Perciformes , Phylogeny , Pigment Epithelium of Eye/metabolism , Pigment Epithelium of Eye/radiation effects , RNA, Messenger/biosynthesis , Receptors, Muscarinic/classification , Receptors, Muscarinic/genetics , Reverse Transcriptase Polymerase Chain Reaction/methods , Sequence Analysis, DNA/methods , Sequence Analysis, Protein/methods , Sesquiterpenes/pharmacology
2.
BMC Neurosci ; 5: 23, 2004 Jul 13.
Article in English | MEDLINE | ID: mdl-15251036

ABSTRACT

BACKGROUND: In fish, melanin pigment granules in the retinal pigment epithelium disperse into apical projections as part of the suite of responses the eye makes to bright light conditions. This pigment granule dispersion serves to reduce photobleaching and occurs in response to neurochemicals secreted by the retina. Previous work has shown that acetylcholine may be involved in inducing light-adaptive pigment dispersion. Acetylcholine receptors are of two main types, nicotinic and muscarinic. Muscarinic receptors are in the G-protein coupled receptor superfamily, and five different muscarinic receptors have been molecularly cloned in human. These receptors are coupled to adenylyl cyclase, calcium mobilization and ion channel activation. To determine the receptor pathway involved in eliciting pigment granule migration, we isolated retinal pigment epithelium from bluegill and subjected it to a battery of cholinergic agents. RESULTS: The general cholinergic agonist carbachol induces pigment granule dispersion in isolated retinal pigment epithelium. Carbachol-induced pigment granule dispersion is blocked by the muscarinic antagonist atropine, by the M1 antagonist pirenzepine, and by the M3 antagonist 4-DAMP. Pigment granule dispersion was also induced by the M1 agonist 4-[N-(4-chlorophenyl) carbamoyloxy]-4-pent-2-ammonium iodide. In contrast the M2 antagonist AF-DX 116 and the M4 antagonist tropicamide failed to block carbachol-induced dispersion, and the M2 agonist arecaidine but-2-ynyl ester tosylate failed to elicit dispersion. CONCLUSIONS: Our results suggest that carbachol-mediated pigment granule dispersion occurs through the activation of Modd muscarinic receptors, which in other systems couple to phosphoinositide hydrolysis and elevation of intracellular calcium. This conclusion must be corroborated by molecular studies, but suggests Ca2+-dependent pathways may be involved in light-adaptive pigment dispersion.


Subject(s)
Arecoline/analogs & derivatives , Cytoplasmic Granules/physiology , Perciformes/physiology , Pigment Epithelium of Eye/physiology , Pirenzepine/analogs & derivatives , Receptors, Muscarinic/physiology , Retinal Pigments/analysis , Adenylyl Cyclase Inhibitors , Animals , Arecoline/pharmacology , Atropine/pharmacology , Carbachol/pharmacology , Colforsin/pharmacology , Cyclic AMP/physiology , Cytoplasmic Granules/chemistry , Cytoplasmic Granules/drug effects , Light , Muscarinic Agonists/pharmacology , Muscarinic Antagonists/pharmacology , Pigment Epithelium of Eye/drug effects , Pigment Epithelium of Eye/radiation effects , Pigment Epithelium of Eye/ultrastructure , Piperidines/pharmacology , Pirenzepine/pharmacology , Quaternary Ammonium Compounds/pharmacology , Receptor, Muscarinic M1/antagonists & inhibitors , Receptor, Muscarinic M2/antagonists & inhibitors , Receptor, Muscarinic M4/antagonists & inhibitors , Receptors, Muscarinic/drug effects , Second Messenger Systems/drug effects , Tropicamide/pharmacology
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