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Circadian Pattern of Melatonin MT1 and MT2 Receptor Localization in the Rat Suprachiasmatic Nucleus
Author(s) -
Nermien E. Waly,
Richard Hallworth
Publication year - 2015
Publication title -
journal of circadian rhythms
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.641
H-Index - 26
ISSN - 1740-3391
DOI - 10.5334/jcr.ab
Subject(s) - melatonin , suprachiasmatic nucleus , circadian rhythm , medicine , endocrinology , melatonin receptor , receptor , biology , dusk , circadian clock , pineal gland , light effects on circadian rhythm , hypothalamus , ecology
The suprachiasmatic nucleus (SCN) is the master circadian pacemaker. The pineal hormone melatonin is involved in the regulation of circadian phase. As a part of the circadian system, its synthesis and secretion is under SCN control. On the other hand, melatonin feeds back on the SCN to regulate its function. Melatonin has two specific windows of time at which it regulates SCN function, namely dusk and dawn. It has been suggested that melatonin exerts its effect on the SCN during that specific window of time via one or both of its specific receptors, MT1 or MT2. The hypothesis that the density of these receptors varies across the circadian cycle was tested. Using immunohistochemistry with receptor-specific antibodies, the localization and distribution of melatonin receptors MT1 and MT2 was studied in the SCN at different Zeitgeber times (ZT): ZT 11–13 (dusk), 23–01 (dawn), 5–7 (mid-day), and 17–19 (midnight). Our results show that MT1 receptor density significantly increased at dusk relative to dawn and midnight (p<0.01 and p<0.001 respectively). Although MT1 receptors were widespread in the SCN and parts of the optic chiasm at dusk, they were restricted to the SCN during the mid-day period. MT2 receptors were not detected in the SCN. Thus, we find that melatonin receptor MT1 density and distribution varies with circadian time. This creates a time window during which melatonin can affect the operation of the SCN. We also find that melatonin regulates SCN function via MT1 receptors with a minimal role for MT2.

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