Abstract
The control of the excitability in magnocellular neurosecretory cells (MNCs) of the supraoptic nucleus has been attributed mainly to synaptic inputs from circunventricular organs. However, nitric oxide (NO), a gaseous messenger produced in this nucleus during isotonic and short-term hypertonic conditions, is an example of a modulator that can act directly on MNCs to modulate their firing rate. NO inhibits the electrical excitability of MNCs, leading to a decrease in the release of vasopressin and oxytocin. Although the effects of NO on MNCs are well established, the mechanism by which this gas produces its effect is, so far, unknown. Because NO acts independently of synaptic inputs, we hypothesized that ion channels present in MNCs are the targets of NO. To investigate this hypothesis, we used the patch-clamp technique in vitro and in situ to measure currents carried by hyperpolarization-activated and nucleotide-gated cation (HCN) channels and establish their role in determining the electrical excitability of MNCs in rats. Our results show that blockade of HCN channels by ZD7288 decreases MNC firing rate with significant consequences on the release of OT and VP, measured by radioimmunoassay. NO induced a significant reduction in HCN currents by binding to cysteine residues and forming S-nitrosothiol complexes. These findings shed new light on the mechanisms that control the electrical excitability of MNCs via the nitrergic system and strengthen the importance of HCN channels in the control of hydroelectrolyte homeostasis.
SIGNIFICANCE STATEMENT Cells in our organism live in a liquid environment whose composition and osmolality are maintained within tight limits. Magnocellular neurons (MNCs) of the supra optic nucleus can sense osmolality and control the synthesis and secretion of vasopressin (VP) and oxytocin (OT) by the neurohypophysis. OT and VP act on the kidneys controlling the excretion of water and sodium to maintain homeostasis. Here we combined electrophysiology, molecular biology, and radioimmunoassay to show that the electrical activity of MNCs can be controlled by nitric oxide (NO), a gaseous messenger. NO reacts with cysteine residues (S-nitrosylation) on hyperpolarization-activated and nucleotide-gated cation channels decreasing the firing rate of MNCs and the consequent secretion of VP and OT.
- electrolyte homeostasis
- electrophysiology
- HCN channels
- magnocellular neurons
- nitric oxide
- S-nitrosylation
Introduction
Maintenance of hydroelectrolyte homeostasis requires complex interactions between peripheral and CNS circuits in several mammalian species. The central control of hydroelectrolyte balance involves highly organized hypothalamic structures that operate to maintain the extracellular fluid osmolality within tight limits. Among these structures, the hypothalamic supraoptic nucleus (SON), composed of magnocellular neurosecretory cells (MNCs), plays a critical role in the synthesis and secretion of vasopressin (VP) and oxytocin (OT). These neuropeptides are involved in several processes, including memory, vasoconstriction, reproduction, and prevention of osmotic stress via renal control of sodium and water reabsorption (Poulain et al., 1977; Antunes-Rodrigues et al., 2004). Their release is directly correlated with MNC firing rate.
Although the control of MNC electrical excitability can be influenced by synaptic inputs (Bourque, 2008), local modulators have been shown to directly interfere in the final responses of these cells (Ruginsk et al., 2015). Indeed, previous reports from our group (Ventura et al., 2008; da Silva et al., 2013) and others (Ventura et al., 2005; Coletti et al., 2015; Reis et al., 2015) indicate the participation of gaseous signaling molecules in the control of MNC excitability and neurohypophyseal secretion, both under physiological conditions and during short-term increases in plasma osmolality. One of these gaseous messengers is nitric oxide (NO). NO decreases MNC excitability and the release of neuropeptides (Ventura et al., 2005; Reis et al., 2010), although the corresponding underlying mechanism remains unknown.
Members of the cyclic nucleotide-gated family of ion channels, such as the hyperpolarization-activated and nucleotide-gated cation (HCN) channel, are strong candidates for controlling MNC excitability (Ghamari-Langroudi and Bourque, 2000). First described in the heart (DiFrancesco, 1993) and later in the CNS (Pape, 1996), HCN channels are involved in numerous intrinsic neuronal functions, such as regulation of resting membrane potential, spontaneous firing in pacemaker cells, synaptic transmission, and regulation of membrane resistance (Kase and Imoto, 2012). Four subtypes of HCN channels (HCN1-HCN4) are expressed in mammals with ∼60% molecular identity between them. Once open, these channels allow the flow of a cationic current, termed Ih, carried by both Na+ and K+ with permeability ratio = 0.2 to 0.4 (Pape, 1996). In addition to being voltage-dependent, HCN channels are also known to be controlled by cAMP and cGMP (Biel et al., 2009). The latter is also the major second messenger used by NO (Denninger and Marletta, 1999; Matulef and Zagotta, 2003; Zagotta et al., 2003). Based on this evidence, the present study aimed to analyze the mechanisms by which NO acts on HCN channels and influences the intrinsic activity of MNCs. We demonstrated that blockade of HCN channels results in important changes in MNC firing frequency, resting membrane potential, and peptides release into the circulation. Furthermore, NO modulates the intrinsic activity of these channels via a cGMP-independent mechanism involving post-translational modification of ion channel proteins by oxidation of cysteine residues, a mechanism known as S-nitrosylation.
Materials and Methods
Ethics.
We used male Wistar rats (80–100 g) to perform all experiments, which were approved by the Ethical Committee on Animal Experimentation of Ribeirão Preto Medical School, University of São Paulo (protocols 064/2010 and 023/2012).
Hypothalamic supraoptic brain slices.
Hypothalamic brain slices were obtained as previously described (da Silva et al., 2013). In short, Wistar rats (100–120 g) were killed by decapitation, and the brain was quickly removed from the skull and placed in an ice-cold (0°C) ACSF solution containing the following (in mm): 121 NaCl, 2.5 KCl, 25 glucose, 26 NaHCO3, 2 CaCl2, 1 MgCl2, saturated with carbogen (95% O2/5% CO2), with pH 7.35, osmolality 310 mosm/kg H2O.
A block of tissue containing the hypothalamus was placed on the platform of a Vibratome (VT 1200, Leica), and coronal slices (230-μm-thick) containing the SON were obtained. Slices were incubated for 60 min at 36°C in modified ACSF with the following composition (in mm): 121 NaCl, 4 KCl, 10 glucose, 26 NaHCO3, 2 CaCl2, 1 MgCl2, constantly gassed with carbogen, pH 7.35, osmolality 295 mosm/kg H2O. A single slice was transferred to the recording chamber placed on the stage of a microscope (Nikon, E-600FN), and neurons were identified using infrared differential contrast optics with images captured by a CCD digital camera (Sensicam qe, Cooke).
Isolation of magnocellular neurons.
MNCs were isolated from cylindrical punches made laterally to the optic chiasm in hypothalamic coronal slices (230-μm-thick), using a 16 gauge sharpened needle. The tissue fragments containing the SON were washed and incubated in Hanks solution (in mm) as follows: 121 NaCl, 4 KCl, 5 NaHCO3, 10 HEPES, 10 glucose (constantly gassed with 100% oxygen; pH 7.35, osmolality 295 mosm/kg H2O) and trypsin (7 mg/ml, Sigma Chemical) for 30 min at 37°C. Then, the tissue fragments were washed again with Hanks solution and incubated for 10 min with 0.05% trypsin inhibitor (Sigma Chemical). Subsequently, the solution was substituted with Neurobasal Medium supplemented with 2% B27 (Serum Free, Invitrogen), 0.5 mm glutamine, 1% penicillin and streptomycin, and the cells were gently dispersed by aspiration and flushing with fire-polished Pasteur pipettes with decreasing diameters. The cells were then plated on plastic dishes with glass bottoms, and electrophysiology was performed after 24 h. The OT and/or VP phenotype of the isolated neurons was recognized using single-cell qRT-PCR (for details, see below).
In situ brainstem-hypothalamus preparation.
In this set of experiments, we simultaneously measured electrophysiological parameters and hormone release using a precollicularly decerebrated preparation, as originally described by Antunes et al. (2006). Briefly, Wistar rats (100–120 g) were deeply anesthetized with halothane (Itapira), bisected below the fifth rib and decorticated. At this point, anesthesia was terminated. The preparation was transferred to a recording chamber, and a double-lumen catheter was placed into the aortic arch through the left ventricle, for hypothalamus perfusion with ACSF solution containing the following (in mm): 121 NaCl, 4 KCl, 10 glucose, 26 NaHCO3, 2 CaCl2,1 MgCl2 (pH 7.35, osmolality 295 mosm/kg H2O) saturated with 95% O2/5% CO2. Ficoll (molecular weight 20,000; 1.25%) was added as an oncotic agent and vecuronium bromide (4 μg/ml Cristália, Itapira) as a muscle relaxant. The superior vena cava was cannulated to collect samples from the hypophyseal circulation for measurement of peptide concentrations by radioimmunoassay (see below).
MNCs intrinsic electrical activity was measured with the blind patch-clamp technique in the whole-cell configuration (one neuron per preparation). Biocytin (0.2%, Invitrogen) was added to the patch pipette solution to label the recorded neurons by immunofluorescence (for details, see below). The micropipettes were mounted on a micromanipulator (MHW-3; Narishige) and positioned onto the dorsal surface of the hypothalamus under visual control by a binocular microscope (Seiler Precision Microscope, SSI-202/402).
Infusion of ZD7288 (30 μm) into the SON was made through the inner aperture (1 mm in diameter) of a perforated ring secured on the hypothalamus dorsal surface and placed directly above the SON neurons. This allowed a local bath-like application of drugs, which diffused to the SON neurons within 3–5 min. Infusion of isotonic ACSF was used as a control for ZD7288.
At the end of the experimental procedures, the preparations were perfused with 4% PFA and the brains were removed and postfixed in 4% PFA for 2–5 d. Transverse sections (40-μm-thick) were cut through the SON with a vibrating microtome (Leica), collected into a cryoprotectant solution, and stored at −20°C for further processing. The immunofluorescence was performed with free-floating sections. After three PBS (0.1 m PBS) washes, the sections were incubated with Alexa-488-conjugated streptavidin (1:1.000; Invitrogen) for 1 h at room temperature. Slices were washed three times in PBS and mounted with Fluoromount (Sigma-Aldrich) on glass slides. Images were collected on a Leica TCS SP5 confocal microscope equipped with 488 nm laser line and tunable emission wavelength detection. For each preparation, biocytin-positive neurons were identified and confocal z-stacks were sequentially collected.
Whole-cell recordings.
Whole-cell recordings of both in vitro and in situ preparation were done using borosilicate glass micropipettes with resistance ranging from 4 to 5 mΩ when filled with the following pipette solution (in mm): 140 potassium gluconate, 10 KCl, 0.3 CaCl2, 1.0 MgCl2, 10 HEPES, 1.0 EGTA, 2.0 Na-ATP, 0.25 Na-GTP, 0.2 mm cAMP, pH adjusted to 7.35 with KOH and osmolality ranging from 285 to 295 mosm/kg H2O. Milli Q water used to prepare pipette solution was treated overnight with diethylpyrocarbonate (Sigma-Aldrich) for subsequent single-cell qRT-PCR procedures. The junction potential between pipette and bath solution was calculated using Clampex (Molecular Devices), and the value (−15 mV) was subtracted from baseline during data analysis. Voltages or currents were measured at room temperature using an Axon 200B patch-clamp amplifier (Molecular Devices), filtered at 2 kHz, and digitized at 10 kHz with a Digidata 1440A (Molecular Devices) controlled by Clamplex (pClamp 10, Molecular Devices). Capacitance and access resistance (compensated by 40%–60% when necessary) were electronically measured using the amplifier settings. Ih currents were evoked by 3 s hyperpolarizing voltage pulses ranging from −50 to −120 mV (in −10 mV steps) every 8 s, as described previously (Ghamari-Langroudi and Bourque, 2000). To avoid synaptic effects on Ih currents and other conductances, all measurements reported in this paper were made in the presence of synaptic blockers (glutamate antagonists = 10 μm CNQX and 30 μm dl-AP5, GABA antagonist = 30 μm picrotoxin) and potassium channels blockers (1 mm tetraethylammonium chloride and 1 mm 4-aminopiridine).
For acute hypertonic stimulation, 35 mm mannitol was added to the isotonic ACSF recording solution to obtain 330 mosm/kg H2O as final osmolality. For hypotonic stimulation, 116 mm NaCl was used instead of 121 mm, and the final osmolality was 285 mosm/kg H2O.
Real time qRT-PCR.
Single-cell qRT-PCR was used for both characterizing HCN channel subtypes expressed in single MNCs and phenotyping the recorded cell. For this purpose, we followed the same procedures described previously (da Silva et al., 2015). In brief, after electrophysiological recordings, the cytoplasm of each neuron, diluted into the pipette solution, was collected for mRNA reverse transcription (High Capacity cDNA Reverse Transcription Kit, Invitrogen). mRNA reverse transcription was performed before a preamplification step, using the TaqMan PreAmp Master Mix Kit (Invitrogen) and the following hydrolysis probes: Rn00564446_g1 (vasopressin), Rn00566449_ml (oxytocin), Rn00670384_ml (HCN1), Rn01408572_mh (HCN2), Rn00586666_m1 (HCN3), and Rn00572232_ml (HCN4). β-Actin was used as an endogenous reference gene (NM_031144.2).
Finally, the reactions for the single-cell RT-PCR were performed in simplex and in triplicate (StepOne Plus System, Applied Biosystems) using the probes described before and a TaqMan Universal PCR Master Mix kit (Invitrogen) according to the manufacturer's recommendations.
Analysis of single-cell qRT-PCR phenotypes.
The relative quantification of HCN gene expression was done using the 2−ΔΔCT method (Livak and Schmittgen, 2001). However, MNC phenotypes (VP or OT or intermediate) were determined based on the ratio analysis described previously (da Silva et al., 2015) following the principles outlined by Heid et al. (1996). The equation below was used to analyze the results. Where is the ratio of the initial amount of vasopressin cDNA to the initial amount of oxytocin cDNA, Eot and Evp are the amplification efficiencies for each gene, and Cqot and Cqvp are the quantities of oxytocin and vasopressin cDNA in the quantification cycle, respectively.
According to the above protocol, neurons with a ratio >1 were considered vasopressinergic, whereas neurons with a ratio <1 were considered oxytocinergic. A ratio equal to 1 suggested expression of both peptides and the neuron was classified as intermediate.
Radioimmunoassay.
VP and OT were quantified in the effusate collected from the superior vena cava in heparinized tubes during isotonic condition and after hypertonic stimulation, preceded by either ACSF or ZD7288 local infusion. Remaining blood cells were separated from ACSF by centrifugation (20 min, 3000 rpm at 4°C) and samples were stored at −20°C until hormone extraction and radioimmunoassay procedures. The effusate was treated with acetone and petroleum ether and VP and OT were measured using specific antibodies, rabbit anti-VP-RAS 8103, 1:120,000, and rabbit anti-OT-HIC8152, 1:80,000 (Peninsula Laboratories). The assay sensitivity was 0.1 pg/ml for both hormones and interassay variability were 1.8% for OT and 1.4% for VP.
Drugs.
l-Arginine monohydrochloride, d-arginine monohydrochloride, N-nitro-l-arginine methyl ester hydrochloride (l-NAME), N-nitro-d-arginine methyl ester hydrochloride (d-NAME), dl-2-amino-5-phosphonovaleric acid (dl-AP5), and tetraethylammonium chloride (TEA), 4-aminopiridine (4-AP) were purchased from Sigma Chemical, and CNQX, picrotoxin, N-ethylmaleimide (NEM), and ZD7288 were purchased from Tocris Bioscience.
Analysis and statistics.
Ih currents were isolated by digital subtraction of traces recorded in the absence and presence of ZD7288, a HCN channel blocker, to eliminate other time- and voltage-dependent currents. All electrophysiological data were analyzed off-line using the Clampfit (Molecular Devices) and Origin 8 (Origin Laboratory) programs. Averaged data are expressed as mean ± SEM and compared using Student's paired or unpaired t test, and repeated-measures ANOVA followed by Bonferroni post hoc test using Prism 6 (GraphPad Software). Values of p ≤ 0.05 were considered statistically significant differences.
Results
HCN channels and the excitability of MNCs
Single-cell qRT-PCR experiments showed that VP- and OT-secreting cells express all types of HCN channel isoforms. Although HCN3 and HCN4 had higher levels of expression in all tested cells, they are not statistically different from each other (Fig. 1A). No differential expression was observed when comparing VP and OT neurons (Fig. 1B,C). The role played by HCN channels in determining the electrical activity of MNCs is shown in Figure 2. ZD7288 (30 μm), a known Ih current blocker (Harris and Constanti, 1995), induced a decrease in MNC intrinsic firing frequency (control = 4.3 ± 0.5 Hz; ZD7288 = 2.7 ± 0.4 Hz, n = 12, p < 0.05). Furthermore, 9 of 12 recorded neurons showed a significant hyperpolarization in the resting membrane potential when treated with ZD7288 in comparison with control cells (Fig. 2B,B1; control = −56.5 ± 1.1 mV vs ZD7288= −60.6 ± 1.8 mV, n = 9, p < 0.05). These results indicate that HCN channels determine MNC electrical activity.
Nitrergic modulation of HCN channels
Because HCN channels seem to be involved in MNC excitability, we performed experiments to analyze whether the nitrergic modulation occurred through a direct action on Ih currents. Results shown in Figure 3A, B demonstrate that 500 μm l-arginine, an NO substrate, significantly decreased instantaneous Ih currents (−20.4 ± 1 pA vs −13.7 ± 1 pA; at −135 mV), as well as steady-state current amplitude (−37.1 ± 7.9 pA vs −16.9 ± 4.2 pA; measured at −135 mV, n = 9; p < 0.05). In contrast, 100 μm l-NAME (NO synthase inhibitor) significantly increased instantaneous Ih (−17.7 ± 1 pA vs −37.5 ± 2 pA, measured at −135 mV) and steady-state Ih current (from −26.5 ± 9 pA in control to −71.7 ± 14 pA; measured at −135 mV, n = 6; p < 0.05) pointing to an endogenous action of NO on HCN channels. The specificity of NO effects was tested using both inactive isomers and remaining current analysis (Fig. 4).
Nitrergic modulation of HCN channels in isolated neurons
Experiments in this section were devised to test the hypothesis that NO acts directly on MNCs. As shown in Figure 5A, B, l-arginine induced the same type of effect observed on slices, decreasing Ih current amplitude (control = −19.9 ± 5.9 pA/pF; l-arginine = −6.8 ± 1.9 pA/pF, n = 8; p < 0.05 at −135 mV) and also increased the time constant of activation of the current (Fig. 5C) (τ = 109 ± 6.2 ms in the control and τ = 167.8 ± 32.2 ms with l-arginine, at −135 mV, n = 8, p < 0.05). These results clearly show that synaptic connections are not a prerequisite for NO effect on MNCs.
Nitrergic signaling pathway
Because cGMP is reported to be implicated in the effects of NO (Arnold et al., 1977; Denninger and Marletta, 1999) and HCN channels have a cytoplasmatic binding site for cGMP, we investigated whether the nitrergic modulation of Ih currents could involve cGMP synthesis. To this end, a selective inhibitorqj of soluble guanylate cyclase (sGC), H-(1,2,4) oxadiazole [4,3-a] quinoxalin-1-one (ODQ), was used in different concentrations (3, 30, and 100 μm). Inhibition of sGC did not change the steady-state value of Ih currents in concentrations up to 100 μm (3 μm = −33.3 ± 7 pA vs −33 ± 6 pA, n = 8, p > 0.05; 30 μm = −30.6 ± 4 pA vs −37.2 ± 5 pA, n = 8, p > 0.05; 100 μm = −48.7 ± 8 pA vs −45.3 ± 13.3 pA n = 8 p > 0.05; values measured at −135 mV). Furthermore, when l-arginine was added to the bath solution, a significant decrease in Ih currents was still observed, even in the presence of ODQ 30 μm (−47.6 ± 14 pA vs −24.7 ± 10 pA, n = 5, p < 0.05, at −135 mV), suggesting a cGMP-independent effect (Fig. 6).
In view of the results shown above, we asked whether NO could interact with cysteine residues in HCN channels to form S-nitrosothiol complexes. For this purpose, we used NEM to specifically oxidize cysteine residues and avoid S-nitrosylation (Paulech et al., 2013). As shown in Figure 7A, 300 μm NEM blocked the effects of l-arginine on instantaneous (Iinst) and steady state (Iss) currents (Iinst = −32.2 ± 5 pA vs −38.8 ± 7 pA, Iss = control = −33 ± 10 pA, NEM = −59.2 ± 15 pA, l-Arg = −59 ± 11 pA, values measured at −135 mV; n = 10, p > 0.05).
Although NEM is a specific cysteine oxidant, it does not remove the NO already linked to cysteine residues. Therefore, ascorbate, a reducing agent, was used to release endogenous NO eventually linked to HCN channels (Stamler and Toone, 2002). As shown in Figure 7B, B1, ascorbate induced a significant increase in the magnitude of both Ih current components (Iinst = −21.7 ± 4 pA vs −41.9 ± 5 pA, at −135 mV; Iss= −16.8 ± 8.5 pA vs −69.8 ± 14 pA, at −135 mV; n = 6, p < 0.05). This set of results strongly supports the hypothesis that NO modulates HCN channels via an S-nitrosylation-dependent mechanism.
HCN channels are modulated by NO upon osmotic stimulation
Small changes in plasma osmolality are known to affect vasopressin and oxytocin production and release and also to increase NO synthesis by the MNCs (da Silva et al., 2013). Therefore, we analyzed whether acute hypertonic or hypotonic challenges can change Ih currents and whether these responses can be modulated by NO. As shown in Figure 8, hypertonicity increased instantaneous and steady-state Ih currents in relation to the isotonic situation (Iinst = −10 ± 1 pA vs −29 ± 3 pA; Iss = −20.1 ± 7 pA vs −50.3 ± 9 pA; n = 8; p < 0.05; values measured at −135 mV). Furthermore, an additional increase in Ih currents was observed during hypertonicity when NO synthesis was blocked by l-NAME (Iinst = −29 ± 3 pA vs −48.3 ± 3 pA; Iss= −50.3 ± 9 pA to −91.7 ± 14 pA; at −135 mV; n = 8, p < 0.05). On the other hand, Figure 8C shows that short-term hypotonic challenge did not change Ih currents (Iinst = −18.5 ± 1 pA vs −19 ± 1 pA; Iss = −40.5 ± 8 pA vs −36 ± 6 pA, at −135 mV, n = 7; p > 0.05). These data indicate that hypertonicity, but not hypotonicity, acts via NO to modulate HCN channels.
Physiological implications of HCN channels function in MNCs
Because MNC firing frequency is affected by osmotic challenges and determines release of peptides by the neurohypophysis, we used the in situ brainstem-hypothalamus preparation of rats to analyze the physiological role played by HCN channels during acute hypertonic stimulation. For this purpose, the MNC membrane potential was recorded during basal condition, after local infusion of ZD7288 or isotonic ACSF into the SON, followed by perfusion of the preparation with hypertonic ACSF. At the same time, the effusate from the vena cava was collected for radioimmunoassay of VP and OT (for details, see Materials and Methods). As shown in Figure 9, MNC firing rate increased during acute hypertonic perfusion as expected (3.9 ± 0.3 Hz vs 6.3 ± 0.2 Hz, n = 5, p < 0.001). In addition, the concentration of VP and OT increased in the effusate (VP = 1 ± 0.1 pg/ml vs 3.2 ± 0.1 pg/ml; OT = 3.59 ± 0.6 pg/ml vs 5.3 ± 0.2 pg/ml, n = 5, p < 0.005 and p < 0.05 for VP and OT, respectively). On the other side, blockade of HCN channels with ZD7288 decreased MNC firing rate (control = 4 ± 0.2 Hz, ZD7288 = 2.4 ± 0.1 Hz, Hyper + ZD = 2.2 ± 0.1 Hz; n = 5 rats, p < 0.05) and prevented VP and OT release induced by the hypertonic stimulation (VP = 1 ± 1.1 pg/ml vs 1.1 ± 0.2 pg/ml, OT = 3.8 ± 0.3 vs 3.7 ± 0.5 pg/ml; n = 5 rats, p > 0.05). These results suggest that HCN channels are critical in determining MNC electrical activity, even in situations where homeostasis is disturbed.
Discussion
MNCs exposed to long term or acute hypertonicity have their electrical excitability readily modulated by NO (Ventura et al., 2008; da Silva et al., 2013). However, the molecular mechanisms involved in this response were, so far, unknown. Here HCN channels were identified as important players in determining MNC electrical excitability and as targets of nitrergic modulation via a nonconventional signaling pathway, the S-nitrosylation.
Role of Ih currents in the control of MNC excitability and NO effects
Unlike the vast majority, HCN channels are hyperpolarization-activated (Wahl-Schott and Biel, 2009) and responsible for carrying an ionic current termed Ih. Our results, using single-cell qRT-PCR, show that the four isoforms of HCN are expressed in the SON, with HCN-3 and HCN-4 mRNAs showing the highest expression levels (Fig. 1). Our data are in accordance with in situ hybridization studies of Monteggia et al. (2000) and of immunohistochemical labeling performed by Notomi and Shigemoto (2004). HCN channels are involved in several basic electrophysiological processes, such as resting membrane potential control, dendritic integration, synaptic transmission, and neuronal electrical oscillations (Maccaferri and McBain, 1996; Gasparini and DiFrancesco, 1997; Beaumont et al., 2002; Fan et al., 2005; Rodrigues and Oertel, 2006). HCN tonic activation places the resting membrane potential at a somewhat depolarized level, whereas their inactivation leads to hyperpolarization (Robinson and Siegelbaum, 2003). Our results, both in slices and in the in situ brainstem-hypothalamus preparation (Figs. 2, 9), show that blockade of HCN channels decreases MNCs spontaneous firing rate and hyperpolarizes the resting membrane potential, in agreement with Ghamari-Langroudi et al. (2000). Similar results are also reported for other excitable cell types (Maccaferri and McBain, 1996; Rodrigues and Oertel, 2006; Deng et al., 2015). In addition, the role played by HCN channels in MNCs seems critical in situations where the hydroelectrolyte homeostasis is disrupted (Fig. 8).
Previous results from our laboratory have shown that NO can modulate MNC resting membrane potential (Ventura et al., 2008; da Silva et al., 2013). Although NO can quickly diffuse from its site of production and interfere presynaptically with GABA release (Stern and Ludwig, 2001), its hyperpolarizing effects are present, even when synaptic transmission is blocked (Ventura et al., 2008; da Silva et al., 2013). Those results point to a direct effect of NO on the MNCs. Indeed, as shown in Figure 3, NO reduces Ih current amplitudes by negatively modulating HCN channels. The same result was observed in isolated cells (Fig. 5), strengthening the idea that NO acts on MNCs independently of synaptic transmission.
Ih currents are clearly involved in the after-hyperpolarizing potential (HAP) of MNCs and other cell types (Armstrong et al., 1994; Greffrath et al., 1998; Roper et al., 2003; da Silva et al., 2013). HAP sets the firing frequency of neurons by keeping the membrane potential at the appropriate value in relation to threshold for a certain time. Although MNCs Ih currents are of relatively small magnitude (∼30–50 pA) they can significantly change the MNCs membrane potential due to the large input resistance observed in these cells (1.1 ± 0.5 GΩ; n = 12, data not shown). Therefore, in the absence of this small current, HAP amplitude increases, hyperpolarizing the membrane potential and taking more time to reach threshold and trigger a new action potential. Reinforcing this hypothesis, ZD7288 changed MNCs firing pattern (Figs. 2, 9) similarly to what has been shown by Oswald et al. (2009).
It is also interesting to note that hypertonicity per se was able to increase Ih (Fig. 8) and to reduce the peak of the HAP (da Silva et al., 2013), both effects leading to increases in the firing rate of neurons. l-NAME enhanced the effect of hypertonicity, indicating that the nitrergic system is actively participating in the control of MNC excitability during osmotic challenges. However, no changes were observed with the hypotonic challenge because there is no NO production above the basal level as shown by da Silva et al. (2013). Therefore, the inhibitory effects of NO on HCN channels and on the MNC excitability, during hypertonic stimulation, reinforce the hypothesis that NO is part of a negative feedback mechanism preventing MNC hyperactivity (Liu et al., 1997; da Silva et al., 2013).
NO signaling pathway in the modulation of HCN channels
NO effects in a number of cell types are mostly due to activation of GC, increasing the synthesis of cGMP and modulation of HCN channels (Bredt and Snyder, 1989; Archer et al., 1994; Zha et al., 2008).
Although MNCs from the SON express both α1 and β1 subunits of GC (Furuyama et al., 1993; Koesling et al., 2000; Ding et al., 2004), Southam et al. (1993) demonstrated that cGMP expression in animals perfused with sodium nitroprusside was not detected in MNCs but found in populations of smaller cells and fibers. These results were later confirmed by Vacher et al. (2003). cGMP was found only in GABA, tyrosine hydroxylase, glutamate-positive fibers, as well as in GFAP-stained cells, and was abolished by incubation of the brain slices with l-NAME. Based on these facts, it is reasonable to suggest that NO signaling may involve other pathways, such as the covalent binding of NO to thiol side chains (Qin et al., 2013). NO binds directly to cysteine residues forming nitrosothiol adducts, increasing its availability and modifying the activity of proteins (Mannick et al., 1997; Lang et al., 2000; Ahern et al., 2002). This mechanism was first described for NMDA receptors where cysteine 399 of NR2A subunit can be nitrosylated (Choi et al., 2000). Because there is no specific blocker of S-nitrosylation, here we used NEM to oxidize MNCs cysteine residues, and evaluated whether nitrergic modulation could be explained through this signaling pathway. NEM blocked the effects of l-arginine (Fig. 7), consistent with results in hypoglossal motoneurons (Wenker et al., 2012) showing that NO modulates HCN channels via S-nitrosylation.
Given the diversity and ubiquity of proteins whose function can be regulated by S-nitrosylation (Lander et al., 1997; Lang et al., 2000), its physiological importance cannot be ignored. The advantage of this mechanism can be related to the stability conferred to the NO molecule, which could be stored and transported to long distances in its nitrosylated form. Although binding of NO to cysteine occurs in a covalent way, denitrosylation by S-glutathione, tyrosine nitration, and ascorbate can reverse this interaction (Derakhshan et al., 2007; Benhar et al., 2009). Our results show that ascorbate significantly increased Ih current amplitudes, implying that HCN channels are endogenously S-nitrosylated (Fig. 7).
Physiological implications
Physiological responses to changes in the extracellular osmolality must operate synergistically to control salt and water reabsorption by the kidneys. Much evidence indicates that SON is a central player in these responses due to its ability to sense changes in the extracellular osmolality (Oliet and Bourque, 1992) and to integrate input signals related to the maintenance of hydroelectrolyte balance. Accordingly, during imbalances in osmolality, MNC electrical activity determines the rate of VP and OT release to the circulation (Brimble and Dyball, 1977; Wakerley et al., 1978; Bourque et al., 1994). Here we show that blockade of HCN channels prevented the increase in the release of peptides, even during an acute hypertonic challenge (Fig. 9). Therefore, we can infer that HCN channels, together with other ion channels (Bourque et al., 2002; Zaelzer et al., 2015), are crucial in determining the MNC electrical activity, and that its blockade alters the osmoregulatory mechanisms responsible for the correction of short-term increases in plasma osmolality.
In conclusion, our results show that NO controls MNC electrical excitability by acting on HCN channels. Furthermore, our results also reinforce the idea that cGMP is not the exclusive mediator of nitrergic modulation: S-nitrosylation is also an important mechanism to control ion channel activity.
Footnotes
M.P.d.S. was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior fellowship. The laboratory of W.A.V. was supported by Fundacao de Amparo a Pesquisa do Estado de Sao Paulo Grant 2012/19750-7. D.J.d.A.M. was supported by Fundacao de Amparo a Pesquisa do Estado de Sao Paulo Grant 2013/10484-5.
The authors declare no competing financial interests.
- Correspondence should be addressed to Dr. Melina Pires da Silva, Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, 14049-900, Ribeirão Preto, São Paulo, Brazil. melina{at}rfi.fmrp.usp.br