TY - JOUR
T1 - The Origin of GnRH pulse generation
T2 - An integrative mathematical-experimental approach
AU - Voliotis, Margaritis
AU - Li, Xiao Feng
AU - de Burgh, Ross
AU - Lass, Geffen
AU - Lightman, Stafford L.
AU - O’Byrne, Kevin T.
AU - Tsaneva-Atanasova, Krasimira
N1 - Publisher Copyright:
Copyright © 2019 the authors
PY - 2019/12/4
Y1 - 2019/12/4
N2 - Fertility critically depends on the gonadotropin-releasing hormone (GnRH) pulse generator, a neural construct comprised of hypothalamic neurons coexpressing kisspeptin, neurokoinin-B and dynorphin. Here, using mathematical modeling 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 modeling, 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 nonlinear 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.
AB - Fertility critically depends on the gonadotropin-releasing hormone (GnRH) pulse generator, a neural construct comprised of hypothalamic neurons coexpressing kisspeptin, neurokoinin-B and dynorphin. Here, using mathematical modeling 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 modeling, 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 nonlinear 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.
KW - Arcuate nucleus
KW - Fertility
KW - Gonadotrophin-releasing hormone
KW - Kisspeptin neurons
KW - Mathematical model
UR - http://www.scopus.com/inward/record.url?scp=85076124106&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0828-19.2019
DO - 10.1523/JNEUROSCI.0828-19.2019
M3 - Article
C2 - 31645462
AN - SCOPUS:85076124106
SN - 0270-6474
VL - 39
SP - 9738
EP - 9747
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 49
ER -