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Pharmacology and function of melatonin receptors
Abstract
The hormone melatonin is secreted primarily from the pineal gland, with highest levels occurring during the dark period of a circadian cycle. This hormone, through an action in the brain, appears to be involved in the regulation of various neural and endocrine processes that are cued by the daily change in photoperiod. This article reviews the pharmacological characteristics and function of melatonin receptors in the central nervous system, and the role of melatonin in mediating physiological functions in mammals. Melatonin and melatonin agonists, at picomolar concentrations, inhibit the release of dopamine from retina through activation of a site that is pharmacologically different from a serotonin receptor. These inhibitory effects are antagonized by the novel melatonin receptor antagonist luzindole (N‐0774), which suggests that melatonin activates a presynaptic melatonin receptoir. In chicken and rabbit retina, the pharmacological characteristics of the presynaptic melatonin receptor and the site labeled by 2‐[ 125 I]iodomelatonin are identical. It is proposed that 2‐[ 125 I]iodomelatonin binding sites (e.g., chicken brain) that possess the pharmacological characteristics of the retinal melatonin receptor site (order of affinities: 2‐iodomelatonin > 6‐chloromelatonin ≥ melatonin ≥ 6,7‐di‐chloro‐2‐methylmelatonin > 6‐hydroxymelatonin ≥ 6‐methoxymelatonin > N‐acetyltryptamine ≥ luzindole > N‐acetyl‐5‐hydroxytryptamine > 5‐methoxytryptamine >>>> 5‐hydroxytryptamine) be classified as ML‐1 (melatonin 1). The 2‐[ 125 I]iodomelatonin binding site of hamster brain membranes possesses different binding and pharmacological characteristics from the retinal melatonin receptor site and should be classified as ML‐2. In summary, the recent advances in the pharmacological characterization of melatonin receptors in the central nervous system will further stimulate the search for potent and selective melatonin receptor agonists and antagonists, and should aid in our understanding of the mechanism of action of melatonin in mammalian brain.— D ubocovigh , M. L. Pharmacology and function of melatonin receptors. FASEB J. 2: 2765‐2773; 1988.
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Citations
Cited by
Pineal Melatonin: Cell Biology of Its Synthesis and of Its Physiological Interactions*
REITER, R. J. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-151 · Cited by 2,192
Extrapineal melatonin: sources, regulation, and potential functions
Acuña-Castroviejo, D., Escames, G., Venegas, C., Díaz-Casado, M. E., Lima-Cabello, E., López, L. C., Rosales-Corral, S., Tan, D.-X., & Reiter, R. J. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1579-2 · Cited by 1,076
Melatonin receptors: Localization, molecular pharmacology and physiological significance
Morgan, P. J., Barrett, P., Howell, H. E., & Helliwell, R. (1994) · Neurochemistry International · doi:10.1016/0197-0186(94)90100-7 · Cited by 623
Dubocovich, M. L., Delagrange, P., Krause, D. N., Sugden, D., Cardinali, D. P., & Olcese, J. (2010) · Pharmacological Reviews · doi:10.1124/pr.110.002832 · Cited by 621
Self-citationCellular Mechanisms of Melatonin Action
VANECEK, J. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.3.687 · Cited by 578
Metadata
- Authors
- Dubocovich, M. L.
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 1988-09
- Volume
- 2
- Issue
- 12
- Pages
- 2765-2773
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W2055732421
- Cited by
- 294
- References
- 0
- FWCI
- 9.55
- Type
- journal article
- Language
- en
- Open access
- closed
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