TY - JOUR TI - Modulation of pulsatile GnRH dynamics across the ovarian cycle via changes in the network excitability and basal activity of the arcuate kisspeptin network AU - Voliotis, Margaritis AU - Li, Xiao Feng AU - De Burgh, Ross Alexander AU - Lass, Geffen AU - Ivanova, Deyana AU - McIntyre, Caitlin AU - O'Byrne, Kevin AU - Tsaneva-Atanasova, Krasimira A2 - McCarthy, Margaret M A2 - Dulac, Catherine A2 - Goodman, Robert A2 - Leng, Gareth VL - 10 PY - 2021 DA - 2021/11/17 SP - e71252 C1 - eLife 2021;10:e71252 DO - 10.7554/eLife.71252 UR - https://doi.org/10.7554/eLife.71252 AB - Pulsatile GnRH release is essential for normal reproductive function. Kisspeptin secreting neurons found in the arcuate nucleus, known as KNDy neurons for co-expressing neurokinin B, and dynorphin, drive pulsatile GnRH release. Furthermore, gonadal steroids regulate GnRH pulsatile dynamics across the ovarian cycle by altering KNDy neurons' signalling properties. However, the precise mechanism of regulation remains mostly unknown. To better understand these mechanisms, we start by perturbing the KNDy system at different stages of the estrous cycle using optogenetics. We find that optogenetic stimulation of KNDy neurons stimulates pulsatile GnRH/LH secretion in estrous mice but inhibits it in diestrous mice. These in vivo results in combination with mathematical modelling suggest that the transition between estrus and diestrus is underpinned by well-orchestrated changes in neuropeptide signalling and in the excitability of the KNDy population controlled via glutamate signalling. Guided by model predictions, we show that blocking glutamate signalling in diestrous animals inhibits LH pulses, and that optic stimulation of the KNDy population mitigates this inhibition. In estrous mice, disruption of glutamate signalling inhibits pulses generated via sustained low-frequency optic stimulation of the KNDy population, supporting the idea that the level of network excitability is critical for pulse generation. Our results reconcile previous puzzling findings regarding the estradiol-dependent effect that several neuromodulators have on the GnRH pulse generator dynamics. Therefore, we anticipate our model to be a cornerstone for a more quantitative understanding of the pathways via which gonadal steroids regulate GnRH pulse generator dynamics. Finally, our results could inform useful repurposing of drugs targeting the glutamate system in reproductive therapy. KW - GnRH pulse generator KW - KNDy KW - mathematical model KW - optogenetics JF - eLife SN - 2050-084X PB - eLife Sciences Publications, Ltd ER -