Developmental appearance and age related changes in specific 2-[125I]iodomelatonin binding sites in the suprachiasmatic nuclei of female Syrian hamsters

Marilyn J. Duncan, Frederick C. Davis

Producción científica: Articlerevisión exhaustiva

42 Citas (Scopus)

Resumen

In Syrian hamsters, the circadian timing system is sensitive to melatonin during gestation but is not responsive in the adult. In order to further understand this developmental change in melatonin responsiveness, in vitro autoradiography was used to assess the presence of specific 2-[125I]iodomelatonin binding sites in the suprachiasmatic nuclei of female hamsters of selected embryonic (E) and postnatal (PN) ages (e.g. E13, E14, E15, PN1, PN2, PN12, PN25, PN112-133). Specific 2-[125I]iodomelatonin binding sites were seen in the suprachiasmatic nuclei of some of the E14 hamsters and all the perinatal hamsters (E15, PN1 and PN2) but not in older hamsters. In contrast, specific 2-[125I]iodomelatonin binding sites were seen in the pars tuberalis of all hamsters (with the exception of one), regardless of age. The transient expression of specific 2-[125I]iodomelatonin binding sites in the suprachiasmatic nuclei suggests that melatonin may have some special functions restricted to early development. The specific 2-[125I]iodomelatonin binding sites in the embryonic suprachiasmatic nuclei may represent the substrate for maternal melatonin to set the phase of the developing circadian timing system.

Idioma originalEnglish
Páginas (desde-hasta)205-212
Número de páginas8
PublicaciónDevelopmental Brain Research
Volumen73
N.º2
DOI
EstadoPublished - jun 8 1993

Nota bibliográfica

Funding Information:
Acknowledgements. The authors thank Lih Sia Mann, Karen Heller and Kathrin Jaeck for technical assistance with experiments and Dr. Willis K. Paull for assistance with identification of fetal ueu-roanatomical structures. We are grateful to Dr. Bruce Maley and Mary Gail Engle for photography. This work was supported by USPHS Grants DK-42056 (to MJ.D.) and HD-18686 (to F.C.D.) and by an award from the University of Missouri Medical School Research Council (to M.J.D.). Portions of this work were previously presented in abstract form: Soc. Neurosci. Abstr., 16 (19901 773 and Soc. Neurosci. Abstr., 17 (1991) 674.

Financiación

Acknowledgements. The authors thank Lih Sia Mann, Karen Heller and Kathrin Jaeck for technical assistance with experiments and Dr. Willis K. Paull for assistance with identification of fetal ueu-roanatomical structures. We are grateful to Dr. Bruce Maley and Mary Gail Engle for photography. This work was supported by USPHS Grants DK-42056 (to MJ.D.) and HD-18686 (to F.C.D.) and by an award from the University of Missouri Medical School Research Council (to M.J.D.). Portions of this work were previously presented in abstract form: Soc. Neurosci. Abstr., 16 (19901 773 and Soc. Neurosci. Abstr., 17 (1991) 674.

FinanciadoresNúmero del financiador
University of Missouri Medical School Research Council
U.S. Public Health ServiceDK-42056
U.S. Public Health Service
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentR01HD018686
Eunice Kennedy Shriver National Institute of Child Health and Human Development

    ASJC Scopus subject areas

    • Developmental Neuroscience
    • Developmental Biology

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