Thermally active TRPV1 tonically drives central spontaneous glutamate release

Abstract

Central synapses spontaneously release neurotransmitter at low rates. In brainstem, cranial visceral afferent terminals in caudal solitary tract nucleus (NTS) display pronounced activity-dependent asynchronous release of glutamate and this extra release depends on TRPV1 receptors (TRPV1+). Asynchronous release is absent for afferents lacking TRPV1 (TRPV1-) and resting EPSC frequency was greater in TRPV1+. Here, we studied this basal activity difference by assessing thermal sensitivity of spontaneous and miniature synaptic events in TRPV1+ and TRPV1- second order NTS neurons. The spontaneous EPSC rate decreased when temperature was decreased, increased steeply between 30 and 42°C only in TRPV1+ neurons and was calcium-dependent. TRPV1-specific antagonist SB366791, but not TTX, strongly attenuated thermal responses. Temperature changes failed to alter EPSC frequency in TRPV1- neurons. EPSC amplitudes and decay kinetics changed little with temperature. IPSCs in these second order NTS neurons were unaltered by temperature. Such results suggest that activated presynaptic TRPV1+ receptors trigger continuous, resting release of glutamate vesicles at physiological temperatures only in capsaicin-responsive terminals. In mechanically isolated individual neurons harvested from medial NTS, increases in temperature increased the rate of glutamate release only in TRPV1+ neurons whereas IPSC rates were unaffected. Cadmium failed to block thermal increases in glutamate release suggesting that calcium entry through TRPV1 channels may trigger glutamate release independent of voltage activated calcium channels. Together our findings indicate a new form of afferent signaling in which TRPV1 channels within central terminals of peripheral afferents tonically generate glutamate release in NTS at 37°C in the absence of afferent action potentials.

INTRODUCTION

Quiescent central synaptic terminals often spontaneously release neurotransmitter at low rates and these events are thought to reflect the stochastic release of primed, docked synaptic vesicles. Rates of spontaneous release at rest are generally a thousand fold lower than quantal release rates evoked by depolarization and it remains uncertain whether these two types of release are derived from a common or separate pool of vesicles (Wasser & Kavalali, 2009). TRPV1 is an ion channel activated in somatosensory primary afferent neurons during noxious heat and peripheral tissue damage (Lumpkin & Caterina, 2007). TRPV1 is also expressed at most presynaptic primary afferent terminals within the brainstem at the solitary tract nucleus (NTS) (Patterson et al., 2003; Sun et al., 2009) – a location unlikely to meet harsh TRPV1 gating requirements including thermal thresholds of ~43°C (Julius & Basbaum, 2001). Recently, we found that TRPV1 regulates activity-dependent asynchronous release from a distinct pool of solitary tract (ST) afferent glutamate vesicles and the basal, pre-stimulation release rates from TRPV1+ was greater (Peters et al., 2010). This TRPV1 sensitive asynchronous pool of vesicles could be specifically isolated pharmacologically or by decreasing temperature and was independent of the synchronous glutamate release responsible for ST-evoked EPSCs. The presence of a unique pool of TRPV1-dependent glutamate vesicles raises fundamental questions about the nature of the coupling between TRPV1, glutamate release and presynaptic activity.

To investigate this unique vesicle population, we studied the mechanisms governing the unsynchronized or “autonomous” release of glutamate in second order NTS neurons in relation to TRPV1 expression and temperature. We assessed the roles of action potentials, local circuits and calcium entry in the genesis of unsynchronized synaptic activity. Cooling and TRPV1 antagonism suppressed spontaneous EPSCs suggesting that TRPV1 actively accelerates tonic release of glutamate from TPRV1+ afferent terminals. Glutamate release onto TRPV1- neurons or GABAergic transmission was thermally insensitive. Block of afferent terminal depolarization with TTX or voltage-activated calcium entry with cadmium did not prevent thermally evoked, calcium-dependent release of glutamate so that the calcium entry for vesicle fusion and release likely occurred through TRPV1 channels. Thus, since the majority of cranial visceral afferents are unmyelinated (Andresen et al., 2004), the presence of active TRPV1 in most cranial afferent terminals provides a new form of phenotype-specific control over synaptic signaling that generates a tonic stream of glutamate release even in the absence of peripheral afferent activation.

MATERIALS AND METHODS

Brainstem slices

Horizontal brain stem slices (250 μm) were prepared from adult male Sprague Dawley rats (>160 g) under isoflurane anesthesia as previously described using cooled artificial cerebrospinal fluid (aCSF) containing (mM): 125 NaCl, 3 KCl, 1.2 KH₂PO₄, 1.2 MgSO₄, 25 NaHCO₃, 10 dextrose, and 2 CaCl₂, bubbled with 95% O₂–5% CO₂. at 300 mOsm (Doyle & Andresen, 2001; Peters et al., 2008). All animal procedures were approved by the Institutional Animal Care and Use Committee and conform to the guidelines of the National Institutes of Health publication “Guide for the Care and Use of Laboratory Animals”.

Slice recordings

NTS slices were perfused with aCSF 34–35°C with temperature controlled using an in-line system (TC2BIP with HPRE2, Cell MicroControls, Norfolk, VA). Bath temperature was continuously measured immediately downstream to the slice. Details for visualized recordings were as previously (Peters et al., 2010). Recording electrodes (2.1–3.2MΩ) were filled generally with a low Cl⁻ (10mM, E_Cl = −69 mV), intracellular solution which contained (mM): 6 NaCl, 4 NaOH, 130 K-gluconate, 11 EGTA, 1 CaCl₂, 1 MgCl₂, 10 HEPES, 2 Na₂ATP, and 0.2 Na₂GTP. The intracellular solution was pH 7.3 and 296 mOsm. Neurons were voltage clamped at V_H = −60 mV with a MultiClamp 700B amplifier (Axon Instruments, Foster City, CA) in open, whole cell configuration. Liquid junction potentials were not corrected. Signals were filtered at 10 kHz and sampled at 30 kHz using p-Clamp (version 9.4, Axon Instruments). In experiments targeting GABA-mediated IPSCs, glutamate receptor antagonists, NBQX (20 μM, 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline-2,3-dione) and AP-5 (50 μM, D-2-amino-5-phosphonopentanoate) were added and pipette Cl- content of the intracellular solution was adjusted to 54 mM and IPSCs were inward (E_Cl = −22 mV). Distal ST shocks (200 μm concentric electrode, Frederick Haer Co., Bowdoinham, ME) identified second order neurons by analysis of latency SD (jitter) of <200 μsec (Doyle & Andresen, 2001) with ST shocks delivered every 6 sec (duration 100 μsec, Master-8, AMPI, Jerusalem, Israel). At the end of each recording, capsaicin (100 nM) determined vanilloid sensitivity - TRPV1+ or TRPV1-.

Isolated neurons

Neurons were mechanically dissociated from horizontal slices (Jin et al., 2009). Standard external solution contained (in mM): 150 NaCl, 5 KCl, 1 MgCl₂, 2 CaCl₂, 10 HEPES, and 10 glucose (pH was adjusted to 7.4 with Tris-OH). A fine vibrated pipette dispersed neurons from the same region as recorded in slices (Jin et al., 2004). All experiments began at room temperature (~22–23°C). Neurons were continuously superfused with a Y-tube system with complete exchanges within 20 msec (Murase et al., 1989). The in-line heating element controlled bath temperature which was detected at the cell’s location with a miniature temperature probe (TH-10Kmp, Cell MicroControls). Testing suggested that this probe likely underestimated temperature shifts experienced by cells. The probe sensing dimensions (0.45 × 2 mm) were much larger than neurons and temperature dropped steeply lateral to the flow center. Recordings utilized MultiClamp 700B, pClamp and electrodes filled with (in mM): 70 CsMeSO₄ 70 CsCl, 5 TEA-Cl, 10 EGTA, 2 NaATP, 0.3 NaGTP; and pH adjusted to 7.2 with Tris-OH. Neurons were voltage clamped to −60 mV and currents sampled at 20 kHz.

Data analysis

pClamp 9 and Mini Analysis (Synaptosoft, Decatur, GA) analyzed data off-line. Synaptic waveform values (decay-time constant and amplitude) and baseline values across each group were compared statistically using a minimum of one min. at each condition using the Friedman repeated measures ANOVA on ranks (frequency, decay time constant and amplitude) or repeated measures ANOVA (baseline, amplitude and latency) with post hoc pairwise multiple comparisons (Holm-Sidak method, SigmaStat, San Jose, CA). All data are represented as mean ± SEM and p<0.05 was considered significant.

Drugs

Capsaicin, NBQX, AP-5, tetrodotoxin (1 μM TTX) and SB366791 were obtained from Tocris (Ellisville, Missouri) and gabazine (SR-95531, GABA_A antagonist) from Sigma-RBI (Natick, MA). Except where specifically noted otherwise, all recordings were made in 10 μM gabazine to isolate glutamatergic EPSCs.

RESULTS

Glutamate vesicles released from ST afferent terminals produce a background of spontaneous EPSC (sEPSC) activity that was higher in certain second order NTS neurons under equivalent conditions (33°C, Figure 1A). Neurons contacted by ST afferents that were activated by 100 nM capsaicin (TRPV1+) had higher rates of sEPSCs than TRPV1- neurons (Peters et al., 2010). Compared to controls at 33°C, sEPSC activity decreased in TRPV1+ neurons when bath temperature was decreased and increased when temperature was raised. Thus, the rate of spontaneous EPSCs closely followed changes in bath temperature only in TRPV1+ NTS neurons (Figure 1B) with the greatest changes nearest a physiological 37°C. In contrast in TRPV1- NTS neurons, the sEPSC rate was typically low at 33–34°C and changed little with temperature changes. Temperature induced changes in frequency were rapid, showed no signs of diminishing over time and were fully reversible. Event amplitudes and decay time constants – postsynaptic measures –changed similarly with weak associations with TRPV1 subtype suggesting that presynaptic properties of TRPV1+ terminals were the most temperature sensitive (Figure 1C). Consistent with this idea, the TRPV1-selective antagonist SB366791 attenuated temperature-induced increases in sEPSC rate in TRPV1+ neurons (n=5, p<0.001, 2-way RM-ANOVA, Figure 1D).

Figure 1.

Temperature strongly augmented spontaneous glutamate release in TRPV1+ compared to TRPV1- second order NTS neurons. A. Original traces of sEPSCs from representative neurons (TRPV1+, left; TRPV1- right) show that TRPV1+ neurons typically had higher spontaneous EPSC rates than TRPV1- neurons at each temperature. B. Temperature (upper trace) rapidly and reversibly changed spontaneous EPSC rates in a TRPV1+ (filled circles) but not in a TPRV1- neuron (unfilled circles). Frequency points are counts over 10 sec bins expressed as average frequency. Note that A and B are from same neurons. C. Aggregate summary for temperature responses of seven TRPV1+ (filled circles) and six TRPV1- neurons (unfilled circles) displayed as means±SEM. On average (2-way, RM-ANOVA), temperature increased frequency in TRPV1+ (p<0.001) but not in TRPV1- (p>0.2). sEPSC amplitudes increased slightly in TRPV1+ (p<0.001). Decay time constants of sEPSCs (single exponentials, not shown) declined similarly (p=0.15) in both TRPV1+/− decreasing from 3.12 to 1.78±0.09 ms from 25 to 38°C. D. In the absence of action potentials (1 μM TTX), mEPSC frequency increased with temperature. The TRPV1-selective antagonist SB366791 (10 μM, left, unfilled squares, n=5) significantly decreased mEPSC activity at temperatures >33°C (p<0.001, 2-way RM-ANOVA). In separate TRPV1+ neurons (right, n=7,) temperature sensitivity of mEPSC frequency was reduced (p<0.001, 2-way RM-ANOVA) by reducing bath Ca⁺⁺ (right) from control of 2 mM (filled circles) to 1 mM (unfilled squares) Average values within neurons were binned in 3°C intervals and represented by their midrange. Asterisks mark significant differences. E. In a representative current clamp example of five TRPV1+ neurons, synaptic potential rates increased substantially with temperature (expanded plots in ovals, right) and action potentials increased accordingly. Two of five neurons inactivated at the highest temperatures.

The inward flux of cations through open TRPV1 channels should promote glutamate release by depolarizing ST synaptic terminals triggering voltage-activated processes and/or calcium permeation via TRPV1. To test whether voltage-activated Na⁺ channels contributed to basal release, we applied 1 μM TTX and measured spontaneously occurring miniature EPSCs (mEPSCs, Figure 1D). Similar to sEPSCs, changes in temperature produced new steady levels of mEPSC activity that persisted at each temperature in TRPV1+ neurons. Although the mean sEPSC and mEPSC results are based on separate studies of two different groups of TRPV1+ neurons, the mEPSC average temperature relationship was quantitatively similar to that for sEPSCs. Like the sEPSCs, mEPSC amplitudes increased only slightly and decay time constants decreased with temperature (p<0.001, not shown). Reduction of external calcium from 2 mM to 1 mM decreased the mEPSC rate and the response to temperature (Figure 1D). Under current clamp, synaptic potential activity increased steeply with temperature in all cells and increased action potential activity in most (3 of 5 neurons, Figure 1E). Together our results suggest that temperature acts on TRPV1 at ST afferents to promote vesicular glutamate release independent of action potential activity.

Second order NTS neurons generally receive both excitatory and inhibitory synaptic contacts. To test whether IPSCs were temperature sensitive, we recorded miniature synaptic events in TRPV1+ neurons (Figure 2A). Counts of total synaptic activity – mEPSCs and mIPSCs – increased in direct proportional to temperature (Figure 2B, right). However, blockade of glutamate receptors with NBQX and AP5 reduced synaptic activity to a low level of remaining IPSCs that were insensitive to temperature changes (Figure 2A, B). On average (n=4), mIPSC frequency, amplitudes and kinetics were minimally altered within the range of 25°C to 38°C (Figure 2C). Together these results in slices indicate that substantial temperature sensitivity in NTS required TRPV1– a factor only expressed presynaptically within one type of ST afferent terminal but not present postsynaptically or in presynaptic GABAergic terminals.

Figure 2.

Temperature did not alter GABA release at second order NTS neurons. A. Application of NBQX and AP-5 at 25°C greatly reduced total spontaneous synaptic activity (sEPSCs + sIPSCs, upper trace) and increases in temperature failed to substantially alter the remaining sIPSCs (lower three traces). B. Counts of spontaneous IPSCs (triangles) changed little with temperature. At right, temperature-evoked increases in total synaptic events (mEPSCs+mIPSCs, circles) were prevented by glutamate antagonists indicating that in this neuron, sIPSCs were temperature insensitive (triangles). Note that gabazine eliminated the remaining events (not shown) and these IPSCs were inward in our conditions. C. On average across TRPV1+ second order neurons (n=4), temperature produced no significant changes in mIPSC (triangles) frequency (p=0.18) or amplitude (p=0.27) and small decreases in time constant (tau, p=0.01). Asterisks mark significant differences.

To better understand the mechanisms of action of TRPV1 and reduce the possibility of interactions with adjacent neurons, we mechanically isolated medial NTS neurons using a microharvesting approach that retained functioning synaptic terminals (Jin et al., 2010). All neurons displayed glutamatergic and GABAergic events. Raising temperature of the perfusion solution increased mEPSC activity substantially in many isolated neurons (Figure 3A, B). The timing of temperature changes was estimated using a probe placed close to the recorded neuron. The frequency of mEPSC activity closely followed changes in temperature (Figure 3B, C). The values for temperature registered at the cell location were consistently lower by ~5°C in single cell experiments than in slices and we likely underestimate actual temperatures at the cells. Outflow temperatures of 35°C reached 29–30°C near the cell location but moving the probe closer to the outlet did not reduce the difference and we conclude that most likely the probe is too large to accurately register the temperature. Note that all neurons with highly temperature dependent mEPSCs also responded to capsaicin with increases in mEPSC frequency (Figure 3B, lower right). Temperature-insensitive neurons were capsaicin insensitive (results not shown). On average across neurons (Figure 3D), temperature selectively increased mEPSC frequency of TRPV1+ neurons (n=10) but not in TRPV1- neurons (n=5). The mIPSC frequency was not changed by temperature whether recorded in TRPV1+ or TRPV1-neurons (Figure 3D). The amplitudes of mEPSCs or mIPSCs in isolated neurons were insensitive to temperature (Figure 3D). TRPV1 channels are more permeable to Ca⁺² than to Na⁺ (Caterina et al., 1997; Chung et al., 2008). Capsaicin activation of TRPV1 triggered glutamate release onto NTS neurons independent of voltage-activated Ca⁺² channels (VACC) (Jin et al., 2004). To test whether VACC contributed to temperature-activated glutamate release, we measured mEPSC increases to temperature step increases in isolated NTS neurons and added Cd²⁺ (100 μM) to block all VACCs non-selectively. Raising temperature evoked rapid increases in mEPSCs frequency (Figure 4) even in the presence of Cd²⁺. Temperature-evoked increases in mEPSC rates on average (Figure 4B, n=7) more than doubled (p<0.02) and these increases were similar with and without Cd²⁺ present (p=0.80). Amplitudes of mEPSCs were unaltered by temperature or Cd²⁺ (p>0.1). Together, our results suggest that temperature activates TRPV1 channels which allow calcium entry into the terminals to increase the rate of glutamate release and this process does not require VACCs.

Figure 3.

Temperature-sensitive TRPV1+ synaptic responses were preserved in isolated NTS neurons. A. Rates of mEPSC activity (1 μM TTX) in mechanically dispersed NTS neurons at room temperature (23°C) increased substantially with temperature. A probe placed close to the position of the isolated cell registered a rise and then fall in temperature that evoked an increase and decrease of mEPSC rate in this representative TRPV1+ neuron. B. Temperature increases reversibly increased mEPSCs (columns) and as did capsaicin (100 nM, CAP, far right, broken axis). C. The average mEPSC rate (20 s bin) increased linearly with temperature in this range for this neuron. Gabazine (10 μM) was present throughout. A, B, and C taken from same neuron. Note that the large probe likely underestimated actual temperature at neuron. D. In aggregate average, only mEPSC frequency for TRPV1+ (filled circles, n=10 neurons) was steeply temperature-sensitive while TRPV1- mEPSCs (unfilled circles, n=5 neurons) and mIPSCs (triangles, n=8 neurons) from both TRPV1+/− types were insensitive. Amplitudes were uniformly unaltered. Group data are means±SEM. * is p<0.02. EPSCs isolated using gabazine (10 μM) and IPSCs isolated in NBQX and AP-5.

Figure 4.

Temperature-activated TRPV1 release of glutamate is calcium dependent. Raising temperature substantially increased mEPSC frequency in this representative isolated TRPV1+ neuron (p<0.01) even in the presence of the nonselective calcium channel antagonist Cd²⁺ (100 μM, broken box). On average (n=7 neurons), Cd²⁺ did not change the evoked increase in mEPSC rate to raising temperature from 23 to 30°C (p>0.7). Amplitudes were unaltered by Cd²⁺ (p>0.2). Gabazine (10 μM) present throughout. CAP response not shown. * is p<0.02 from control.

DISCUSSION

The present results revealed profound differences in the regulation of autonomous release of glutamate vesicles between two classes of afferent terminals at second order NTS neurons. Our new findings include: 1. physiological temperatures (~36–38°C) drive high rates of spontaneous glutamate release only from TRPV1+ afferent terminals. 2. TRPV1- and GABAergic terminals were nearly temperature insensitive. 3. Temperature responses involved calcium dependent, tonic glutamate release without a requirement for voltage-gated Na⁺ or Ca²⁺ channel activity. 4. TRPV1-specific antagonism attenuated thermally evoked glutamate release suggesting that TRPV1 controls this pool of vesicles.

Thermally driven TRPV1 glutamate release

TRPV1 receptors on presynaptic ST terminals confer prominent temperature sensitivity to spontaneous glutamate release. The steep sensitivity of sEPSC and mEPSC regulation between 30 and 40°C only in TRPV1+ terminals contrasts with similar evoked synchronous release at these same ST terminals (Peters et al., 2010). In fact, regulation of the synchronous vesicle pool is indistinguishable in most respects between TRPV1+ and TRPV1- ST terminals (Andresen & Peters, 2008; Peters et al., 2010). The temperature sensitivity of mEPSC rates from TRPV1+ terminals on NTS neurons greatly exceeds that of AMPA-mediated EPSCs in other central neurons (Hestrin et al., 1990) and the peripheral discharge from cranial afferents including baroreceptors is much less temperature sensitive (McQueen & Eyzaguirre, 1974). At physiological temperatures, the absolute sEPSC rate at TRPV1+ ST neurons averaged about 25 mEPSCs per sec – a rate 20–30 fold greater than TRPV1- neurons whose rates were typical of most central synapses (Wasser & Kavalali, 2009). This high rate of release was diagnostic of TRPV1+ terminals in NTS. Single ST afferent axons contribute ~20 somatodendritic synaptic contacts whether from TRPV1+ or TRPV1-afferents (Andresen & Peters, 2008). The attenuation of autonomous release to low levels during cooling and TRPV1 block suggests that most sEPSCs arise from ST afferents. Likely other glutamate terminals including from NTS interneurons contributed to our total activities but evidence suggests that their numbers are relatively low compared to ST contacts (McDougall et al., 2009). FM1-43 tracking of multiple individual terminals on NTS neurons shows that capsaicin and potassium depolarization activated the same terminals (Jin et al., 2010), a finding consistent with co-localization of the TRPV1-dependent pool with the depolarization-evoked vesicle pool.

TRPV1 contains a non-selective cation pore that is gated by heat (typically >40°C), protons (pH=~5) and/or vanilloid chemicals to transduce potentially harmful conditions (Lumpkin & Caterina, 2007) – conditions unlikely to exist within the normal CNS. Interestingly, TRPV1 blockers are multi-modal with different potencies for thermal vs. vanilloid gating (Garami et al., 2010) and this may explain why there is only partial block of release by SB-366791 (Peters et al., 2010). TRPV1 thermosensitivity likely arises from a unique portion of the pore that functions independently of the capsaicin binding/gating motif (Yang et al., 2010). We found previously that low temperature was always more effective than pharmacological blockade (Peters et al., 2010). This is consistent with a relative resistance of TRPV1 thermal responses to many high affinity vanilloid blockers (Garami et al., 2010) and the more complete block at low temperatures suggests that most glutamate terminals are likely afferent in origin. Our results suggest important distinctions among evoked, asynchronous and spontaneous vesicle release but with certain common elements in their control. All glutamate release modes show similar dependence on external Ca²⁺ entry (Peters et al., 2010). However, VACCs similarly contribute to synchronous and asynchronous release but are not required for spontaneous release. Spontaneous synaptic events are considered to be random vesicle fusions that closely correlate with evoked events (Hestrin, 1992). Our present results show that activity-independent release from ST terminals is actively controlled by TRPV1. Spontaneous synaptic signals influence dendritic protein synthesis patterns and postsynaptic receptivity to subsequent evoked events (Sutton et al., 2004). The much higher rates of TRPV1+ sEPSCs and their regulation by peptides (Peters et al., 2008; Appleyard et al., 2005) may represent a robust ST afferent signal that helps to phenotypically differentiate NTS neurons (Bailey et al., 2002).

The physiological consequences of spontaneous glutamate signaling in NTS are not clear, but contrasts between A- and C-fiber afferents are apparent. First, this tonic glutamate signal arises from C-type afferents that are often physiologically silent under normal circumstances. Second, unmyelinated cranial visceral afferents represent up to 90% of all afferents arising from different organs (Jammes et al., 1982; Kubin & Davies, 1995; Andresen et al., 1978). From one typical visceral afferent source common to medial NTS, 75% of aortic baroreceptors were unmyelinated and inactive at normal blood pressures (Andresen & Kunze, 1994). Thus C-fiber baroreceptors represent physiologically silent afferents (Jones & Thoren, 1977); a finding similar for other organs (Coleridge & Coleridge, 1984). Since activity-dependent processes importantly shape and maintain patent synaptic connections (Sutton et al., 2004; McKinney et al., 1999; Poo, 2001), TRPV1-dependent, activity-independent generation of glutamate transmission may maintain the afferent signaling from C-type axons.