Abstract
Kisspeptin neurons in the rostral hypothalamus are hypothesized to initiate preovulatory gonadotropin-releasing hormone (GnRH) surges by causing estradiol-dependent activation of GnRH neuron action potential firing and subsequent GnRH release. To determine if estradiol or ovarian cycle stage modulates functional connectivity in this circuit, we used optogenetics to photostimulate anteroventral-periventricular (AVPV) area kisspeptin neurons while recording electrical activity and/or evoked synaptic currents from preoptic area GnRH neurons in acutely-prepared mouse brain slices. Slices were prepared from mice in multiple hormonal states, including 2-days post ovariectomy (OVX) and OVX plus estradiol during the morning or afternoon, diestrus, proestrus and 1-week post OVX, and 6-weeks post OVX with or without 1 week of estradiol replacement. Photostimulation induced a sustained, frequency-dependent increase in GnRH neuron firing rate. This neuromodulatory-typical response was not different in diestrous vs proestrous mice but was blunted in 1-week OVX mice, suggesting ovarian steroids amplify this response. Neuromodulatory responses were infrequent in 6-week OVX mice even with 1-week of estradiol treatment. A minority of GnRH neurons exhibited a substantial and near-immediate increase in firing rate typical of fast synaptic transmission. Monosynaptic connectivity was low and stable across the hormone states tested and mediated by GABA. Interestingly, evidence of a monosynaptic connection was not a requirement for GnRH neurons to exhibit a sustained increase in firing rate, suggesting non-synaptic or volume transmission occurs in this system. Synaptic connectivity did, however, amplify the increase in firing rate observed in GnRH neurons from proestrous mice, indicating proestrous hormonal conditions can amplify this response. Significance statement Ovulation is initiated by central positive feedback effects of estradiol stimulating a surge of gonadotropin-releasing hormone (GnRH) release. Estradiol feedback is conveyed to GnRH neurons by afferents expressing estrogen receptor alpha, including kisspeptin-expressing neurons in the anteroventral periventricular (AVPV) area. To determine if endocrine milieu modulates functional interactions between AVPV kisspeptin and GnRH neurons, optogenetics was used to stimulate AVPV kisspeptin neurons while recording GnRH neuron spiking activity or synaptic currents in brain slices from ovariectomized, estradiol-treated, and ovary-intact mice. Stimulation (20Hz) increased GnRH neuron firing rate in all hormone conditions. This effect was stronger during proestrus and was further increased in GnRH neurons receiving fast-synaptic transmission. A synaptic connection was not required, however, suggesting volume transmission occurs.
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Abstract
Kisspeptin neurons in the rostral hypothalamus are hypothesized to initiate preovulatory gonadotropin-releasing hormone (GnRH) surges by causing estradiol-dependent activation of GnRH neuron action potential firing and subsequent GnRH release. To determine if estradiol or ovarian cycle stage modulates functional connectivity in this circuit, we used optogenetics to photostimulate anteroventral-periventricular (AVPV) area kisspeptin neurons while recording electrical activity and/or evoked synaptic currents from preoptic area GnRH neurons in acutely-prepared mouse brain slices. Slices were prepared from mice in multiple hormonal states, including 2-days post ovariectomy (OVX) and OVX plus estradiol during the morning or afternoon, diestrus, proestrus and 1-week post OVX, and 6-weeks post OVX with or without 1 week of estradiol replacement. Photostimulation induced a sustained, frequency-dependent increase in GnRH neuron firing rate. This neuromodulatory-typical response was not different in diestrous vs proestrous mice but was blunted in 1-week OVX mice, suggesting ovarian steroids amplify this response. Neuromodulatory responses were infrequent in 6-week OVX mice even with 1-week of estradiol treatment. A minority of GnRH neurons exhibited a substantial and near-immediate increase in firing rate typical of fast synaptic transmission. Monosynaptic connectivity was low and stable across the hormone states tested and mediated by GABA. Interestingly, evidence of a monosynaptic connection was not a requirement for GnRH neurons to exhibit a sustained increase in firing rate, suggesting non-synaptic or volume transmission occurs in this system. Synaptic connectivity did, however, amplify the increase in firing rate observed in GnRH neurons from proestrous mice, indicating proestrous hormonal conditions can amplify this response.
Significance statement Ovulation is initiated by central positive feedback effects of estradiol stimulating a surge of gonadotropin-releasing hormone (GnRH) release. Estradiol feedback is conveyed to GnRH neurons by afferents expressing estrogen receptor alpha, including kisspeptin-expressing neurons in the anteroventral periventricular (AVPV) area. To determine if endocrine milieu modulates functional interactions between AVPV kisspeptin and GnRH neurons, optogenetics was used to stimulate AVPV kisspeptin neurons while recording GnRH neuron spiking activity or synaptic currents in brain slices from ovariectomized, estradiol-treated, and ovary-intact mice. Stimulation (20Hz) increased GnRH neuron firing rate in all hormone conditions. This effect was stronger during proestrus and was further increased in GnRH neurons receiving fast-synaptic transmission. A synaptic connection was not required, however, suggesting volume transmission occurs.
Competing Interest Statement
The authors have declared no competing interest.
Abbreviations
- GnRH
- gonadotropin-releasing hormone
- LH
- luteinizing hormone
- ERα
- estrogen receptor alpha
- AVPV
- anteroventral periventricular area
- POA
- preoptic area
- GFP
- green fluorescent protein
- Cre
- Cre recombinase
- AAV
- adeno-associated virus
- OVX
- ovariectomized
- OVX+E
- ovariectomized plus estradiol implant
- E
- estradiol
- kiss
- kisspeptin
- LED
- light-emitting diode
- FWHM
- full width at half maximum
- ACSF
- artificial cerebrospinal fluid
- TTX
- tetrodotoxin
- 4-AP
- 4-aminopyridine
- CNQX
- 6-cyano-7-nitroquinoxaline-2,3-dione
- PSC
- postsynaptic current
- ZT
- Zeitgeber time
- ePSC
- evoked post-synaptic current
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