Characterization of GnRH Pulse Generator Activity in Male Mice Using GCaMP Fiber Photometry.

Kisspeptin neurons located in the hypothalamic arcuate nucleus are thought to represent the GnRH pulse generator responsible for driving pulsatile LH secretion. The recent development of GCaMP6 fiber photometry technology has made it possible to perform long-term recordings of the population activity of the arcuate nucleus kisspeptin (ARNKISS) neurons in conscious-behaving mice. Using this approach, we show that ARNKISS neurons in intact male mice exhibit episodes of synchronized activity that last ∼2 minutes and have a mean inter-episode interval of 166 minutes, with a very wide range (43 to 347 minutes). Gonadectomy resulted in dramatic changes in the dynamics of ARNKISS neuron behavior with temporally distinct alterations in synchronization episode (SE) amplitude (sevenfold increase), inter-SE frequency (range, 2 to 58 minutes), and duration (up to 28 minutes), including the frequent appearance of seemingly unstable clusters of doublet and triplet SEs. The combination of photometry with repeated blood sampling revealed a perfect correlation between ARNKISS neuron population SEs and LH pulses in intact and short-term gonadectomized (GDX) mice. No differences were detected in SE frequency across 24 hours in either intact or GDX mice. These observations further support a role for ARNKISS neurons as the GnRH pulse generator and show that it operates in a stochastic manner without diurnal variation in both intact and GDX male mice. The removal of gonadal steroids has multiple time-dependent effects upon ARNKISS neuron synchronizations, indicating their critical role in shaping pulse generator behavior.

[1]  R. Piet,et al.  Sex‐ and sub region‐dependent modulation of arcuate kisspeptin neurones by vasopressin and vasoactive intestinal peptide , 2018, Journal of neuroendocrinology.

[2]  A. Herbison The Gonadotropin-Releasing Hormone Pulse Generator. , 2018, Endocrinology.

[3]  R. Palmiter,et al.  Estrogenic-dependent glutamatergic neurotransmission from kisspeptin neurons governs feeding circuits in females , 2018, eLife.

[4]  L. Coolen,et al.  KNDy Cells Revisited. , 2018, Endocrinology.

[5]  S. Han,et al.  Definition of the hypothalamic GnRH pulse generator in mice , 2017, Proceedings of the National Academy of Sciences.

[6]  S. Moenter,et al.  Long‐Term Recordings of Arcuate Nucleus Kisspeptin Neurons Reveal Patterned Activity That Is Modulated by Gonadal Steroids in Male Mice , 2017, Endocrinology.

[7]  M. Alreja,et al.  Tac1 Signaling Is Required for Sexual Maturation and Responsiveness of GnRH Neurons to Kisspeptin in the Male Mouse , 2017, Endocrinology.

[8]  K. Iremonger,et al.  Spike and Neuropeptide-Dependent Mechanisms Control GnRH Neuron Nerve Terminal Ca2+ over Diverse Time Scales , 2017, The Journal of Neuroscience.

[9]  L. Sinnett-Smith,et al.  Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse , 2016, Journal of neuroendocrinology.

[10]  A. Herbison,et al.  Pulse and Surge Profiles of Luteinizing Hormone Secretion in the Mouse. , 2016, Endocrinology.

[11]  R. Palmiter,et al.  High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons , 2016, eLife.

[12]  S. Han,et al.  Selective optogenetic activation of arcuate kisspeptin neurons generates pulsatile luteinizing hormone secretion , 2015, Proceedings of the National Academy of Sciences.

[13]  N. Inoue,et al.  Lack of Pulse and Surge Modes and Glutamatergic Stimulation of Luteinising Hormone Release in Kiss1 Knockout Rats , 2015, Journal of neuroendocrinology.

[14]  Z. Liposits,et al.  Neuropeptide co-expression in hypothalamic kisspeptin neurons of laboratory animals and the human , 2015, Front. Neurosci..

[15]  R. Piet,et al.  Electrical properties of kisspeptin neurons and their regulation of GnRH neurons , 2015, Frontiers in Neuroendocrinology.

[16]  A. Herbison,et al.  Optogenetic activation of GnRH neurons reveals minimal requirements for pulsatile luteinizing hormone secretion , 2014, Proceedings of the National Academy of Sciences.

[17]  J. Veldhuis,et al.  Development of a methodology for and assessment of pulsatile luteinizing hormone secretion in juvenile and adult male mice. , 2013, Endocrinology.

[18]  S. Moenter,et al.  Regulation of arcuate neurons coexpressing kisspeptin, neurokinin B, and dynorphin by modulators of neurokinin 3 and κ-opioid receptors in adult male mice. , 2013, Endocrinology.

[19]  M. Alreja Electrophysiology of kisspeptin neurons. , 2013, Advances in experimental medicine and biology.

[20]  R. Piet,et al.  Spontaneous kisspeptin neuron firing in the adult mouse reveals marked sex and brain region differences but no support for a direct role in negative feedback. , 2012, Endocrinology.

[21]  R. Palmiter,et al.  Regulation of NKB pathways and their roles in the control of Kiss1 neurons in the arcuate nucleus of the male mouse. , 2011, Endocrinology.

[22]  S. Schlatt,et al.  Age-Related Changes in Diurnal Rhythms and Levels of Gonadotropins, Testosterone, and Inhibin B in Male Rhesus Monkeys (Macaca mulatta)1 , 2008, Biology of reproduction.

[23]  A. Evans,et al.  The introduction of rams induces an increase in pulsatile LH secretion in cyclic ewes during the breeding season. , 2007, Theriogenology.

[24]  S. O’Rahilly,et al.  The GPR54 Gene as a Regulator of Puberty , 2003 .

[25]  Suzanne M. Moenter,et al.  Mechanisms underlying episodic gonadotropin-releasing hormone secretion , 2003, Frontiers in Neuroendocrinology.

[26]  A C Camproux,et al.  Stochastic modeling of the hypothalamic pulse generator activity. , 1994, The American journal of physiology.

[27]  David Handelsman,et al.  Effect of undernutrition on pulsatile luteinizing hormone (LH) secretion in castrate and intact male rats using an ultrasensitive immunofluorometric LH assay. , 1994, Endocrinology.

[28]  M. Nishihara,et al.  Hypothalamic electrical activity that relates to the pulsatile release of luteinizing hormone exhibits diurnal variation in ovariectomized rats , 1992, Brain Research.

[29]  J. Thalabard,et al.  Duration of phasic electrical activity of the hypothalamic gonadotropin-releasing hormone pulse generator and dynamics of luteinizing hormone pulses in the rhesus monkey. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[30]  D Rodbard,et al.  Pulsatile secretion of luteinizing hormone in agonadal men before and during testosterone replacement therapy , 1990, Journal of endocrinological investigation.

[31]  J. Butler,et al.  Neuroendocrine-gonadal axis in men: frequent sampling of LH, FSH, and testosterone. , 1988, The American journal of physiology.

[32]  A. Caraty,et al.  Effect of time after castration on secretion of LHRH and LH in the ram. , 1988, Journal of reproduction and fertility.

[33]  J. Butler,et al.  Interpulse interval sequence of LH in normal men essentially constitutes a renewal process. , 1986, The American journal of physiology.

[34]  W. Crowley,et al.  Hypogonadotropic disorders in men and women: diagnosis and therapy with pulsatile gonadotropin-releasing hormone. , 1986, Endocrine reviews.

[35]  G. B. Ellis,et al.  Mapping episodic fluctuations in plasma LH in orchidectomized rats. , 1984, The American journal of physiology.

[36]  R. Steiner,et al.  Regulation of luteinizing hormone pulse frequency and amplitude by testosterone in the adult male rat. , 1982, Endocrinology.

[37]  C. Desjardins,et al.  Luteinizing hormone and testosterone secretion in young and old male mice. , 1982, The American journal of physiology.

[38]  T. Plant,et al.  Effects of orchidectomy and testosterone replacement treatment on pulsatile luteinizing hormone secretion in the adult rhesus monkey (Macaca mulatta). , 1982, Endocrinology.

[39]  T. Plant,et al.  Hypophysial responses to continuous and intermittent delivery of hypopthalamic gonadotropin-releasing hormone , 1978 .