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dc.contributor.authorVoliotis, M
dc.contributor.authorFeng Li, X
dc.contributor.authorDe Burgh, R
dc.contributor.authorLass, G
dc.contributor.authorLightman, SL
dc.contributor.authorO’Byrne, KT
dc.contributor.authorTsaneva-Atanasova, K
dc.date.accessioned2019-10-25T08:34:03Z
dc.date.issued2019-10-23
dc.description.abstractFertility critically depends on the gonadotropin-releasing hormone (GnRH) pulse generator, a neural construct comprised of hypothalamic neurons co-expressing kisspeptin, neurokoinin-B and dynorphin. Here, using mathematical modelling and in-vivo optogenetics we reveal for the first time how this neural construct initiates and sustains the appropriate ultradian frequency essential for reproduction. Prompted by mathematical modelling, we show experimentally using female estrous mice that robust pulsatile release of luteinizing hormone, a proxy for GnRH, emerges abruptly as we increase the basal activity of the neuronal network using continuous low frequency optogenetic stimulation. Further increase in basal activity markedly increases pulse frequency and eventually leads to pulse termination. Additional model predictions that pulsatile dynamics emerge from non-linear positive and negative feedback interactions mediated through neurokinin-B and dynorphin signaling respectively are confirmed neuropharmacologically. Our results shed light on the long-elusive GnRH pulse generator offering new horizons for reproductive health and wellbeing.SIGNIFICANCE STATEMENTThe gonadotropin-releasing hormone (GnRH) pulse generator controls the pulsatile secretion of the gonadotropic hormones LH and FSH and is critical for fertility. The hypothalamic arcuate kisspeptin neurons are thought to represent the GnRH pulse generator, since their oscillatory activity is coincident with LH pulses in the blood; a proxy for GnRH pulses. However, the mechanisms underlying GnRH pulse generation remain elusive. We developed a mathematical model of the kisspeptin neuronal network and confirmed its predictions experimentally, showing how LH secretion is frequency-modulated as we increase the basal activity of the arcuate kisspeptin neurons in-vivo using continuous optogenetic stimulation. Our model provides a quantitative framework for understanding the reproductive neuroendocrine system and opens new horizons for fertility regulation.en_GB
dc.description.sponsorshipEngineering and Physical Sciences Research Council (EPSRC)en_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council (BBSRC)en_GB
dc.identifier.citationPublished online 23 October 2019en_GB
dc.identifier.doi10.1523/JNEUROSCI.0828-19.2019
dc.identifier.grantnumberEP/N014391/1en_GB
dc.identifier.grantnumberMR/N022637/1en_GB
dc.identifier.grantnumberBB/S001255/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/39329
dc.language.isoenen_GB
dc.publisherSociety for Neuroscienceen_GB
dc.rights.embargoreasonUnder embargo until 23 April 2020 in compliance with publisher policyen_GB
dc.rights© 2019 the authorsen_GB
dc.titleThe origin of GnRH pulse generation: An integrative mathematical-experimental approachen_GB
dc.typeArticleen_GB
dc.date.available2019-10-25T08:34:03Z
dc.identifier.issn0270-6474
dc.descriptionThis is the author accepted manuscript. The final version is available from the Society for Neuroscience via the DOI in this recorden_GB
dc.identifier.journalJournal of Neuroscienceen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2019-07-29
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-10-23
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-10-25T07:45:41Z
refterms.versionFCDAM
refterms.panelBen_GB


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