42
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Female reproduction requires the precise temporal organization of interacting, estradiol-sensitive neural circuits that converge to optimally drive hypothalamo-pituitary–gonadal (HPG) axis functioning. In mammals, the master circadian pacemaker in the suprachiasmatic nucleus (SCN) of the anterior hypothalamus coordinates reproductively relevant neuroendocrine events necessary to maximize reproductive success. Likewise, in species where periods of fertility are brief, circadian oversight of reproductive function ensures that estradiol-dependent increases in sexual motivation coincide with ovulation. Across species, including humans, disruptions to circadian timing (e.g., through rotating shift work, night shift work, poor sleep hygiene) lead to pronounced deficits in ovulation and fecundity. Despite the well-established roles for the circadian system in female reproductive functioning, the specific neural circuits and neurochemical mediators underlying these interactions are not fully understood. Most work to date has focused on the direct and indirect communication from the SCN to the gonadotropin-releasing hormone (GnRH) system in control of the preovulatory luteinizing hormone (LH) surge. However, the same clock genes underlying circadian rhythms at the cellular level in SCN cells are also common to target cell populations of the SCN, including the GnRH neuronal network. Exploring the means by which the master clock synergizes with subordinate clocks in GnRH cells and its upstream modulatory systems represents an exciting opportunity to further understand the role of endogenous timing systems in female reproduction. Herein we provide an overview of the state of knowledge regarding interactions between the circadian timing system and estradiol-sensitive neural circuits driving GnRH secretion and the preovulatory LH surge.

          Related collections

          Most cited references169

          • Record: found
          • Abstract: not found
          • Article: not found

          Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Circadian rhythms in drinking behavior and locomotor activity of rats are eliminated by hypothalamic lesions.

            Bilateral electrolytic lesions in the suprachiasmatic nuclei permanently eliminated nocturnal and circadian rhythms in drinking behavior and locomotor activity of albino rats. The generation of 24-hr behavioral rhythms and the entrainment of these rhythms to the light-dark cycle of environmental illumination may be coordinated by neurons in the suprachiasmatic region of the rat brain. Destruction of the medial preoptic area had no effect on 24-hr drinking rhythms.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              System-level identification of transcriptional circuits underlying mammalian circadian clocks.

              Mammalian circadian clocks consist of complexly integrated regulatory loops, making it difficult to elucidate them without both the accurate measurement of system dynamics and the comprehensive identification of network circuits. Toward a system-level understanding of this transcriptional circuitry, we identified clock-controlled elements on 16 clock and clock-controlled genes in a comprehensive surveillance of evolutionarily conserved cis elements and measurement of their transcriptional dynamics. Here we report the roles of E/E' boxes, DBP/E4BP4 binding elements and RevErbA/ROR binding elements in nine, seven and six genes, respectively. Our results indicate that circadian transcriptional circuits are governed by two design principles: regulation of E/E' boxes and RevErbA/ROR binding elements follows a repressor-precedes-activator pattern, resulting in delayed transcriptional activity, whereas regulation of DBP/E4BP4 binding elements follows a repressor-antiphasic-to-activator mechanism, which generates high-amplitude transcriptional activity. Our analysis further suggests that regulation of E/E' boxes is a topological vulnerability in mammalian circadian clocks, a concept that has been functionally verified using in vitro phenotype assay systems.
                Bookmark

                Author and article information

                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrin.
                Frontiers in Endocrinology
                Frontiers Research Foundation
                1664-2392
                21 May 2012
                2012
                : 3
                : 60
                Affiliations
                [1] 1simpleDepartment of Psychology, Helen Wills Neuroscience Institute, University of California Berkeley, CA, USA
                Author notes

                Edited by: Henryk Urbanski, Oregon National Primate Research Center, USA

                Reviewed by: Patrick Chappell, Oregon State University, USA; Xavier Bonnefont, CNRS, France; Tomoshige Kino, Eunice Kennedy Shirver National Institute of Child Health and Human Development, USA

                *Correspondence: Lance J. Kriegsfeld, Neurobiology Laboratory, Department of Psychology, Helen Wills Neuroscience Institute, University of California, 3210 Tolman Hall, #1650, Berkeley, CA 94720-1650, USA. e-mail: kriegsfeld@ 123456berkeley.edu

                This article was submitted to Frontiers in Genomic Endocrinology, a specialty of Frontiers in Endocrinology.

                Article
                10.3389/fendo.2012.00060
                3356853
                22661968
                81cf01e1-d24a-40b3-b2b6-73e558b6f606
                Copyright © 2012 Williamsn III and Kriegsfeld.

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

                History
                : 10 December 2011
                : 13 April 2012
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 182, Pages: 14, Words: 14192
                Categories
                Endocrinology
                Review Article

                Endocrinology & Diabetes
                vip,ovulation,kisspeptin,rfrp-3,gnih,suprachiasmatic,avp
                Endocrinology & Diabetes
                vip, ovulation, kisspeptin, rfrp-3, gnih, suprachiasmatic, avp

                Comments

                Comment on this article