Long-Term Recordings of Arcuate Nucleus Kisspeptin Neurons Reveal Patterned Activity That Is Modulated by Gonadal Steroids in Male Mice

Abstract

Pulsatile release of gonadotropin-releasing hormone (GnRH) is key to fertility. Pulse frequency is modulated by gonadal steroids and likely arises subsequent to coordination of GnRH neuron firing activity. The source of rhythm generation and the site of steroid feedback remain critical unanswered questions. Arcuate neurons that synthesize kisspeptin, neurokinin B, and dynorphin (KNDy) may be involved in both of these processes. We tested the hypotheses that action potential firing in KNDy neurons is episodic and that gonadal steroids regulate this pattern. Targeted extracellular recordings were made of green fluorescent protein–identified KNDy neurons in brain slices from adult male mice that were intact, castrated, or castrated and treated with estradiol or dihydrotestosterone (DHT). KNDy neurons exhibited marked peaks and nadirs in action potential firing activity during recordings lasting 1 to 3.5 hours. Peaks, identified by Cluster analysis, occurred more frequently in castrated than intact mice, and either estradiol or DHT in vivo or blocking neurokinin type 3 receptor in vitro restored peak frequency to intact levels. The frequency of peaks in firing rate and estradiol regulation of this frequency is similar to that observed for GnRH neurons, whereas DHT suppressed firing in KNDy but not GnRH neurons. We further examined the patterning of action potentials to identify bursts that may be associated with increased neuromodulator release. Burst frequency and duration are increased in castrated compared with intact and steroid-treated mice. The observation that KNDy neurons fire in an episodic manner that is regulated by steroid feedback is consistent with a role for these neurons in GnRH pulse generation and regulation.

Pulsatile gonadotropin-releasing hormone (GnRH) release is fundamental for the function of the hypothalamic-pituitary-gonadal axis and fertility (1). In adult males, and during most of the adult female reproductive cycle, GnRH secretion occurs in pulses ranging in interval from approximately 30 minutes to several hours and is regulated by sex steroid feedback (2–5). The source of both rhythm generation for pulsatile GnRH release and steroid feedback to regulate frequency remains incompletely understood. In vivo rhythmic volleys of hypothalamic multiunit electrical activity (MUA) that are temporally associated with pulsatile luteinizing hormone (LH) release are observed in the arcuate nucleus of primates, goats, and rats (6–8). These observations suggest that the activity of the GnRH system may arise from coordination of a neuronal population in this region, which is distant from most GnRH neuron somata. Similarly, sex steroid feedback, which regulates the GnRH pulse pattern (9), does not appear to be perceived directly by GnRH neurons because they do not express detectable levels of sex steroid receptors other than estrogen receptor β (10–13). Together these findings suggest the hypothesis that feedback and pulse generation are mediated by neuronal inputs to GnRH neurons (14).

Kisspeptin is a potent stimulator of GnRH neuron activity and release (15–17). Kisspeptin neurons of the arcuate nucleus are a strong candidate for a neuronal input that may mediate both of these processes, as they express estrogen receptor α (18), and contact GnRH neuron terminals in median eminence as well as other kisspeptin neurons (19). Arcuate kisspeptin neurons are often called kisspeptin, neurokinin B, and dynorphin (KNDy) neurons because in addition to kisspeptin, they coexpress two peptides that alter reproductive neuroendocrine function: neurokinin B (NKB; or Tac2) and dynorphin (20–26). KNDy neurons express NKB receptor type 1 and NKB receptor type 3 (NK3R) and the dynorphin receptor κ-opioid receptor (KOR), but not kisspeptin receptor 1 (kissR1), whereas GnRH neurons express kissR1, and NK3R (27–30). Consistent with this receptor expression, kisspeptin does not alter arcuate nucleus MUA but increases GnRH neuron activity, as well as GnRH and LH release, suggesting its role may be limited to output to GnRH neurons (8, 15, 31). In contrast, agonists of both NK3R and KOR alter arcuate MUA (31).

These observations have led to a model for the generation of GnRH pulses by KNDy neurons (22, 25, 32, 33). In this model, KNDy neurons are activated by NKB action on NK3R, resulting in kisspeptin output to GnRH neurons to initiate GnRH release. This is followed by subsequent release of dynorphin from KNDy neurons, which acts on KOR expressed by those cells and terminates their activity and release of kisspeptin, thus ceasing the signal for GnRH neuron activation. Elements of this model have been tested in brain slices from mice, demonstrating activating effects of NK3R agonists, inhibition by dynorphin, and modulation of these effects by sex steroids (30, 34–36). Optogenetic stimulation of KNDy neurons was recently shown to depolarize/increase firing in other KNDy neurons (37).These studies have provided important information about the short-term response of KNDy neurons to their peptides and other secretory products; however, studies of the long-term firing pattern and steroid modulation of KNDy neuron activity patterns are lacking. In the present report, we used targeted extracellular recordings of green fluorescent protein (GFP)–identified KNDy neurons to begin to fill this gap.

Materials and Methods

All reagents were purchased from Sigma-Aldrich (St. Louis, MO) unless noted.

Animals

Kiss1-hrGFP transgenic mice (generous gift of Dr. Carol Elias) and Tac2-enhanced GFP transgenic mice [015495-UCD/STOCK Tg (Tac2-EGFP)381Gsat] obtained from the Mouse Mutant Regional Resource Center (www.mmrrc.org/) were propagated in our colony. GFP expression within the arcuate nucleus in both of these models is confined to KNDy neurons (30, 38). Mice were maintained under a 14-hour light, 10-hour dark photoperiod with 2916 chow (Envigo, Madison, WI) and water available ad libitum. Male mice (70-100 days old) were either left intact or castrated under isoflurane anesthesia with local bupivacaine as an analgesic. Some mice received Silastic (Dow Corning, Midland, MI) implants containing estradiol (0.625 µg) or dihydrotestosterone (DHT; 400 µg × 2) in the scapular region at the time of castration (39). Studies were conducted 5 to 10 days postsurgery; no differences were noted with time after steroid manipulation. DHT implants produce an androgen milieu capable of restoring seminal vesicle mass in castrate mice to that of intact males (39). Estradiol in the circulation 5 to 10 days after implantation provides effective negative feedback but is not able to induce an LH surge (40). The Institutional Animal Care and Use Committee at the University of Michigan approved all procedures.

Brain slice preparation

All solutions were bubbled with 95% O₂/5% CO₂ throughout the experiments and for at least 30 minutes before exposure to tissue. Brain slices (400 µm) were prepared through the hypothalamus as previously described (41). The brain was rapidly removed and placed in ice-cold sucrose saline solution containing (in mM): 250 sucrose, 3.5 KCl, 26 NaHCO₃, 10 D-glucose, 1.25 Na₂HPO₄, 1.2 MgSO₄, and 3.8 MgCl₂. Coronal slices were cut with a Leica VT1200S (Leica Biosystems, Buffalo Grove, IL). Slices were incubated for 30 minutes at room temperature (approximately 21°C to 23°C) in 50% sucrose saline and 50% artificial cerebrospinal fluid (ACSF) containing (in mM) 135 NaCl, 3.5 KCl, 26 NaHCO₃, 10 d-glucose, 1.25 Na₂HPO₄, 1.2 MgSO₄, and 2.5 CaCl₂ (pH 7.4). After this time, the slices were transferred to 100% ACSF at room temperature for 0.5 to 4.5 hours before recording.

Electrophysiological recordings

Targeted single-unit extracellular recordings were used. This configuration has minimal impact on the cell’s intrinsic properties (42, 43). Recording pipettes (2 to 4 MΩ) were pulled from borosilicate glass (Schott no. 8250; World Precision Instruments, Sarasota, FL) with a Sutter P-97 puller (Sutter Instrument, Novato, CA). Pipettes were filled with HEPES-buffered solution containing (in mM) 150 NaCl, 10 HEPES, 10 D-glucose, 2.5 CaCl₂, 1.3 MgCl₂, and 3.5 KCl, and low-resistance (21 ± 6.4 MΩ) seals were formed between the pipette and neuron. Recordings were made in a voltage clamp with a 0-mV pipette holding potential and signals filtered at 10 kHz using an EPC8 or one channel of an EPC10 dual patch-clamp amplifier using PatchMaster software (HEKA Elektronic, Lambrecht, Germany).

Experimental design

Slices were transferred to a recording chamber with constant perfusion of carboxygenated ACSF at 29°C to 32°C at a rate of approximately 3 mL/min. Slices were allowed to equilibrate in the chamber for 5 to 10 minutes before initiating the recording. After a 5-minute recording stabilization period, spontaneous neuronal activity was recorded from a GFP-positive cell within the arcuate nucleus. Recordings lasted from 1 to 5 hours. In some cells, a loss of recording stability was observed after 3.5 hours; analysis was thus terminated at this point for all cells, when all recordings were still of high quality. At the end of each experiment, inactive cells were treated with high-potassium ACSF (20 mM K⁺), 4-aminopyridine (5 mM), or senktide (300 to 500 nM; Phoenix Pharmaceuticals, Burlingame, CA). Cells that exhibited action currents in response were verified to be alive and recordable, and all data were used. For cells not responding to K⁺, 4-aminopyridine or senktide, data analysis was truncated at the last observed action current. No more than two cells from the same animal were included, and at least six animals were studied per group.

To compare firing patterns in different steroid milieu, four groups were studied: intact (n = 12 cells), castrated (n = 9), castrated + estradiol (n = 9), and castrated + DHT (n = 7). To test the hypothesis that NK3R activation is required for KNDy neuron activity patterns, recordings of cells from castrated mice were made with the NK3R antagonist SB222200 (10 µM; Tocris/Bio-techne, Minneapolis, MN) in the ACSF (n = 8). To test the hypothesis that activation of KOR reduces activity of KNDy neurons, recordings of cells from intact mice were made with the KOR antagonist NorBNI (10 µM; Tocris/Bio-techne) in the ACSF (intact + NorBNI; n = 7). All ACSF solutions were replaced every hour to minimize changes in osmolarity and provide fresh drug; changes in firing pattern were not associated with solution exchange.

Data analysis

The extracellular approach records action currents, which are the currents underlying action potentials. Their frequency thus reflect action potential firing rate. Action currents (events) were identified using custom software written in IgorPro (WaveMetrics, Inc., Lake Oswego, OR). To analyze the long-term pattern of the firing activity, we updated the code for Cluster8 [generously provided by Dr. Michael Johnson, University of Virginia (44)] to run in IgorPro; peak detection was verified to be the same as the native version when the same parameters were used. Error was estimated from the local standard deviation. For this analysis, firing rate was binned at 2-minute intervals and cluster sizes of 2 for peak and 2 for nadir and a T-score increase greater or equal to 2. Varying the binning interval (1 to 2.5 minutes) and the cluster sizes (1 to 3 points) yielded similar results that revealed the same statistical differences among groups. A minimum peak size of 4% of the maximal amplitude reached by the cell (or 4 events for cells with a peak under 100 events/2 min) was defined to avoid the detection of nonsubstantial elevations of firing rate as peaks. Detected peaks separated by nadirs of only 1 point (2 minutes) were manually concatenated.

In addition to the long-term pattern activity, the short-term pattern of action potentials can affect neurosecretion (45, 46). Action potential grouping [referred to here as “bursts,” for convenience, although the frequency of spikes within a burst is noticeably lower than that in other neurons (47)] was detected as previously reported (48) using software that systematically adjusted the maximum time between events (burst window) for inclusion in a burst from 0.01 to 5 seconds in 10-ms intervals. A burst window of 230 ms was chosen for comparison among groups because it is the burst window in which the maximum number of bursts was detected.

Data are reported as mean ± standard error of the mean (SEM); n indicates number of cells. Statistical analysis was performed using Prism (GraphPad, La Jolla, CA). Data were tested for normal distribution using Shapiro-Wilk normality test. Comparisons among groups were made using tests appropriate for data distribution, and number of groups are detailed in the results. Mean, median, 25th percentile, 75th percentile, and interquartile range for all data are reported in Table 1. Significance was set at P < 0.05.

Results

Spontaneous firing activity of KNDy neurons is episodic and regulated by steroid milieu

Short-term firing frequency of KNDy neurons is influenced by in vivo steroid treatment in male mice (30). Here we studied the long-term spontaneous firing pattern of KNDy neurons from intact and castrated adult male mice, as well as castrated mice supplemented with estradiol or DHT, an androgen that cannot be converted into estradiol by aromatase (49). Figure 1A–1D show representative extracellular recording traces of KNDy neurons from each group during a nadir and a peak in firing activity, as well as firing rate of that cell plotted over time. KNDy neurons from all groups exhibited a succession of peaks and nadirs in action current frequency, but the patterns were strikingly different among groups. Specifically, peaks in firing rate were more frequent in cells from castrated mice (2.5 ± 0.3 peaks/h, n = 9) than in intact mice (1 ± 0.2 peaks/h, n = 12, P < 0.05, Kruskal-Wallis/Dunn test; Fig. 1F). Duration of nadirs was also reduced in cells from castrated compared with intact mice (P < 0.05, Kruskal-Wallis/Dunn test; Fig. 1G). Both peak frequency and nadir duration were restored to levels observed in gonadal intact mice by either estradiol (n = 9) or DHT (n = 7) (Fig. 1C–1G; all P > 0.1 vs intact mice, Kruskal-Wallis/Dunn test). Mean firing rate was not different among cells from intact, castrated, and castrated + DHT groups but was reduced in castrated + estradiol mice (P < 0.05, Kruskal-Wallis/Dunn test; Fig. 1E), suggesting the negative feedback effects of estradiol may be stronger than those of DHT. Together these observations suggest both androgens and estrogens affect the long-term firing pattern of KNDy neurons.

Burst firing activity is steroid dependent in KNDy neurons

Although the long-term firing pattern is important to understand for a system that is episodically active with the period of LH release, the short-term patterns of neuronal activity with spikes occurring in rapid succession (bursts) are also likely to be associated with neurotransmitter and neuromodulator release (47, 50). The maximum time between two spikes to be considered part of the same burst varies with neuron type and has not been defined for KNDy neurons. We examined the short-term pattern of firing using burst windows ranging from 0.01 to 5 seconds at 10-ms intervals. This analysis revealed a peak in the number of bursts detectable when spikes were separated by ≤ 230 ms.

Burst characteristics were analyzed and compared between groups using this definition; neurons that did not fire bursts were excluded from this analysis (two cells from intact, two cells from castrated, three cells from castrated + estradiol, and one cell from castrated + DHT group). KNDy neurons from castrated males (n = 7) had a higher burst frequency than intact males (n = 10, P < 0.05, Kruskal-Wallis/Dunn test; Fig. 2B). Burst frequency was restored to that of cells from intact mice by either estradiol or DHT. In parallel, interevent interval, which is inversely correlated to burst frequency, was reduced in cells from castrated compared with intact mice (P < 0.05, Kruskal-Wallis/Dunn test; Fig. 2C). This was restored to intact levels by DHT. In cells from estradiol-treated mice, interevent interval appeared to be increased relative to that in cells from intact mice, but the P value is just over that accepted for significance (n = 6, P = 0.054, Kruskal-Wallis/Dunn test; Fig. 2C). The mean burst duration was increased in cells from castrated compared with intact males [P < 0.05, one-way analysis of variance (ANOVA)/Fisher least significant difference (LSD); Fig. 2D] and was rescued by either estradiol or DHT. The number of spikes per burst was not different among groups (Fig. 2E). Finally, the intraburst interval was not different among cells from intact, castrated, and castrated + DHT but was reduced in castrated + estradiol group (P < 0.05, Kruskal-Wallis/Dunn test; Fig. 2F). The observation that burst duration is increased in the castrate group with no significant change in spikes per burst or intraburst interval is likely attributed to changes in the latter two parameters that do not reach the level traditionally accepted as significant combining to generate a significant increase in burst duration. Together these data indicate that spikes are organized in bursts in KNDy neurons from male mice, that several burst parameters are regulated by gonadal status, and that estrogens and androgens may differentially regulate some of these parameters.

The NK3R, but not the KOR, signaling affects episodic activity of KNDy neurons

Activation of NK3R increases, whereas activation of KOR decreases, the short-term firing rate of KNDy neurons (34). These effects depend on gonadal status in male mice (35). To test the hypotheses that endogenous NKB and dynorphin regulate the episodic activity of KNDy neurons, we used pharmacology to prevent these receptors from being activated by endogenous ligand released in the slice. We first did a pilot study to determine a dose of the NK3R antagonist SB222200 that could effectively block response to the NK3R agonist senktide. Addition of 10 µM SB222200 to ACSF effectively blocked the increase in KNDy neuron firing rate in response to 100 nM senktide (control, n = 3; SB222200, n = 5; P < 0.01, two-way repeated-measures ANOVA/Sidak’s test; Fig. 3A). The KOR antagonist NorBNI was used at 10 µM, a dose previously shown to effectively block response to dynorphin (30).

To test if blocking NK3R would reduce firing, we tested SB222200 effects on KNDy neurons from castrated mice because they have the highest activity. To test if blocking KOR would increase firing, we tested NorBNI effects on KNDy neurons from intact mice, which have relatively low activity. Data from both of these trials were compared with the intact and castrated data displayed in Figs. 1 and 2 as controls. Bath application of SB222200 restored peak frequency and nadir duration of cells from castrated mice to intact levels (n = 8, castrated + SB222200, P < 0.05, Kruskal-Wallis/Dunn test; Fig. 3C and 3D). Similarly, burst frequency, interevent interval, and burst duration were restored to intact levels by the SB222200 (n = 5, castrated + SB222200 cells exhibiting bursts; burst frequency and interevent interval, P > 0.5, Kruskal-Wallis/Dunn; burst duration, P > 0.2, both vs intact one-way ANOVA/Fisher LSD; Fig. 3E–3G). Spikes per burst and intraburst interval did not differ among groups (Fig. 3H and 3I). In contrast, and consistent with previous observations (30), NorBNI had no effect on either long- or short-term firing properties of cells from intact mice (intact + NorBNI, n = 7; peaks/h, P > 0.9; mean firing rate, P = 0.0804; nadir duration, P > 0.9 vs intact controls, Kruskal-Wallis/Dunn test; Fig. 3B–3F). These observations suggest activation of NK3R, but not KOR, may affect the long-term episodic and short-term activity of KNDy neurons.

Discussion

Arcuate kisspeptin neurons are an important candidate for both steroid feedback signaling to and coordination of GnRH neuron activity. In this context, a better understanding of KNDy neuron activity and its modulation by gonadal steroids is essential. Here we investigated the spontaneous long-term activity of KNDy neurons in acutely prepared brain slices from male mice in different steroid feedback conditions. KNDy neurons exhibit a long-term pattern of episodic activity, characterized by a succession of increases (peaks) and decreases (nadirs) in firing activity over time. Further, gonadal steroids in vivo and blocking NK3R in vitro modulated both the frequency of peaks in the long-term firing pattern and the short-term burst firing characteristics.

This is the first description, to our knowledge, of spontaneous succession of periods of low and high activity in KNDy neurons. These long-term shifts in firing over time may explain the variability in firing rate that has been reported in short-duration recordings of KNDy neurons from males and females (30, 35, 51, 52). That is, with a short-duration recording (5 to 15 minutes), one is more likely to capture solely a peak or a nadir depending on what phase of its activity rhythm a cell is in at the time the recording is performed. Long-term changes observed in individual KNDy neurons encompass the range of different short-term firing patterns described for these cells, such as “silent,” “irregular,” or “burst firing” (51), with transitory phases of acceleration and deceleration of the firing rate. Of interest, short-term KNDy neuron activity is also sensitive to both estradiol and DHT (35). In long-term recordings, the mean firing rate was not a parameter that discriminated effectively among groups, perhaps attributable to the higher variability observed in the castrated group, in which cells released from negative feedback may have a greater range of possible firing activity. The lack of a difference in mean firing rate is not surprising, as averaging firing rate over hours will obscure the details of peaks and nadirs.

In contrast to the effect of blocking NK3R on peak frequency, blocking KOR had no effect. This is consistent with a previous study that showed no effect of KOR antagonist on short-term activity of KNDy neurons (30). This difference may be explained by the observation that fewer KNDy neurons express KOR than NK3R (36). The effects of blocking neuropeptide receptors on firing pattern are of interest, but we urge some caution in interpretation of these data. In addition to immediate effects on activity, dynorphin and NKB could act through signaling pathways that ultimately regulate gene expression. Even with long-term recordings, it may not be possible to capture changes subsequent to blocking these processes if they have a long half-life. For these studies, we chose to compare cells with drug present for the entire recording to control cells, rather than examine a more acute drug treatment part way through a recording, for two reasons. First, this increased the observation time during treatment. Second, although individual KNDy neurons clearly show long-term changes in firing rate, the interval between peaks in firing rate within a cell is variable. This is in contrast to relative stability over several hours of GnRH and LH pulses and multiunit activity associated with LH release in vivo (5–7). One possibility is that the irregularity of peaks in the current study is an artifact of removal of important control elements in a brain slice vs the whole animal. Another possibility is that pulse generation arises as a network property in which the individual KNDy neurons contribute to a steady episodic pattern but may not themselves be active during each episodic event. Of interest in this regard, a similar irregularity in peaks of firing was observed in immortalized GnRH neurons (GT1 cells) cultured on multiunit electrode arrays. The ability to observe multiple cells simultaneously with that method revealed that when activity of individual cells was added together, peaks became much more regular (53). Continued development of methods such as calcium imaging that permit coincident measures from multiple KNDy neurons will help resolve this question.

Interestingly, a similar pattern of peaks and nadirs in firing rate was observed in long-term extracellular recordings of GnRH neurons from male mice (39). The steroid modulation, however, appears to be different between these cell types. Specifically, in GnRH neurons, the number of peaks/h in castrated males is restored to normal levels by estradiol but not DHT (39), whereas both androgens and estrogens were effective in KNDy neurons. In GnRH neurons from females, estradiol negative feedback likewise reduces the frequency of peaks in firing rate (54, 55) and estradiol in combination with DHT results in activation, rather than inhibition, of GnRH neurons (39). If these cell types work together as part of a steroid-sensitive, pulse-generating network, these observations suggest a principal role for estradiol in inhibition of KNDy and GnRH peak frequency and a possible role for androgens in activating parallel pathways that may send signals to the GnRH neuron that can “override” androgen inhibition of KNDy neurons (Fig. 4). In this regard, castration in males increases γ-aminobutyric acid transmission to GnRH neurons (56), which provides an excitatory input via the γ-aminobutyric acid receptor subtype A (57, 58). KNDy neurons are primarily glutamatergic, thus the γ-aminobutyric acid afferents are likely from different cells (38).

Despite the apparent different steroid sensitivities, the similarities in long-term firing pattern are consistent with the postulate that KNDy neurons are a source of GnRH neuron pulse generation. A likely mediator is kisspeptin, which is a strong activator of GnRH neurons via activation of kissR1. In addition to kisspeptin, activation of NK3R can also induce the release of GnRH neurons in the median eminence of male mice (59). Dynorphin is unlikely to act directly on GnRH neuron activity as KOR expression has not been detected (60, 61). The main projections from KNDy neurons to GnRH neurons are detected at the level of the terminals of these cells, in the median eminence (19). KNDy neurons also project to anteroventral periventricular (AVPV) kisspeptin neurons (19), and to other KNDy neurons on both sides of the brain. A recent study showed that optogenetic activation of KNDy neurons in one hemisphere increases KNDy neuron firing in the other (37). The postulate of KNDy neurons generating a rhythm for GnRH release does not exclude the existence of intrinsic activity of GnRH neurons, which exhibit episodic activity when fast synaptic transmission is blocked in female mice (55) and GnRH release in the absence of kisspeptin in males and females (17). The response of GnRH neurons to exogenous kisspeptin increases over the prepubertal period as organized LH pulses become detectable (62). Together these observations raise the possibility of a pulse generation signal from KNDy neurons, imposing organization and steroid responsiveness to endogenous activity of GnRH neurons.

In addition to the long-term pattern of firing activity that may be associated with the LH pulse pattern, the short-term pattern action potential grouping (bursts) is classically linked to, and perhaps required for, the release of neuropeptides such as kisspeptin (63–65). We iteratively examined how spontaneous spikes in KNDy neurons are grouped; this analysis revealed a peak in the number of bursts at a maximum intraburst interval of 230 ms. This is similar to the interval identified in current-clamp recordings of GnRH neurons when a definition of continuous depolarization from the peak of the afterhyperpolarization to the next action potential threshold was used [210 ms (66)] and to studies of GnRH neurons using the same analysis on extracellular recordings (320 ms; Phumsatitpong and Moenter, unpublished observations). The firing rate during bursts in both KNDy and GnRH neurons is lower than that in cortical and thalamic neurons and may thus be considered “nonclassical” bursts (47). Of interest, firing rates during bursts in AVPV kisspeptin neurons are also relatively low (50).

Several burst parameters were regulated by gonadal status in KNDy neurons, demonstrating a different organization of action potentials between intact and castrated mice. Burst firing is linked to neuropeptide release; thus the same number of spikes organized in bursts could trigger more neuropeptide release in castrated mice. Although a number of studies have investigated membrane properties of arcuate kisspeptin neurons (34, 67–71), relatively few have examined directly the influence of sex steroids. In females, optogenetic stimulation of firing in these cells induces a slow depolarization, the magnitude of which is enhanced in low steroid conditions (37). In males, membrane properties of KNDy neurons appeared to be regulated by gonadal status (68). This study concludes that KNDy neurons are intrinsically less excitable in the absence of steroid feedback, which is in contrast with the present findings. It is possible that the whole-cell configuration used in the previous work resulted in dialysis of factors important for mediating steroid feedback effects on neuronal activity. KNDy neurons express hyperpolarization-activated cyclic nucleotide-gated channels and the low-threshold voltage-gated calcium channel Cav.3, which often underlie burst firing (64, 69). The former is regulated by steroid feedback in AVPV kisspeptin neurons (72) but has not yet been studied in KNDy neurons. The present results indicate that KNDy neurons generate “nonclassical bursts” that are regulated by gonadal status and may contribute to steroid-dependent activity and release from these cells.

Castration augmented both the long-term and the burst-firing patterns of KNDy neurons, with both patterns restored toward intact values by either estradiol or DHT. DHT acts via androgen receptor, as it cannot be converted into estradiol by aromatase (49), and thus permits segregation of steroid action via androgen receptor or estrogen receptor, both of which are expressed by KNDy neurons (73). These data support and extend previous short-term recording studies in which estradiol and DHT restore initial firing rate and quiescence in castrated mice (35) and are consistent with studies showing both androgens and estrogens inhibit arcuate kisspeptin messenger RNA expression in mice (18, 73), suggesting steroid negative feedback acts via multiple pathways.

The present observations add to the growing body of evidence that arcuate kisspeptin neurons are likely important for both pattern generation and steroid sensitivity of GnRH pulse generation. The mechanisms underlying a “KNDy pulse generator” remain to be determined and are likely critical to the central control of reproduction.

Abbreviations:

 
• ACSF

  artificial cerebrospinal fluid

 
• ANOVA

  analysis of variance

 
• AVPV

  anteroventral periventricular

 
• DHT

  dihydrotestosterone

 
• GFP

  green fluorescent protein

 
• kissR1

  kisspeptin receptor 1

 
• KNDy

  kisspeptin, neurokinin B, and dynorphin

 
• KOR

  κ-opioid receptor

 
• LH

  luteinizing hormone

 
• LSD

  least significant difference

 
• MUA

  multiunit electrical activity

 
• NK3R

  neurokinin type 3 receptor

 
• NKB

  neurokinin B

 
• SEM

  standard error of the mean.

Acknowledgments

We thank Elizabeth Wagenmaker and Laura Burger for expert technical assistance and Jacob DeFazio and Jonathon Penix for recoding Cluster and software interface development, respectively.

Financial Support: This work was supported by the National Institutes of Health/Eunice Kennedy Shriver National Institute of Child Health and Human Development Grant R01 HD34860 (to S.M.M.) and a Lalor Foundation Postdoctoral Fellowships (to M.R.M. and C.V.).

Current Affiliation: M. R. Moya’s current affiliation is Núcleo de Ciencias Biológicas, Facultad de Ciencias Universidad Mayor, Santiago 8550745, Chile.

Disclosure Summary: The authors have nothing to disclose.

References