Abstract
Mesocorticolimbic dopaminergic (DA) neurons have been implicated in regulating nociception in chronic pain, yet the mechanisms are barely understood. Here, we found that chronic constructive injury (CCI) in mice increased the firing activity and decreased the KCNQ channel-mediated M-currents in ventral tegmental area (VTA) DA neurons projecting to the nucleus accumbens (NAc). Chemogenetic inhibition of the VTA-to-NAc DA neurons alleviated CCI-induced thermal nociception. Opposite changes in the firing activity and M-currents were recorded in VTA DA neurons projecting to the medial prefrontal cortex (mPFC) but did not affect nociception. In addition, intra-VTA injection of retigabine, a KCNQ opener, while reversing the changes of the VTA-to-NAc DA neurons, alleviated CCI-induced nociception, and this was abolished by injecting exogenous BDNF into the NAc. Taken together, these findings highlight a vital role of KCNQ channel-mediated modulation of mesolimbic DA activity in regulating thermal nociception in the chronic pain state.
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Introduction
Chronic pain has become an enormous health care issue, affecting >15% of the world population [1, 2]. The literature suggests that the mesolimbic reward system plays a critical role in regulating chronic pain [3,4,5,6]. The ventral tegmental area (VTA), a core part of the mesolimbic reward system, contains predominantly dopaminergic (DA) neurons [7]. The VTA sends DA projections to both limbic and cortical areas and forms two important circuits: the mesolimbic circuit (VTA to the nucleus accumbens, VTA-to-NAc) and the mesocortical circuit (VTA to the medial prefrontal cortex, VTA-to-mPFC) [8, 9].
Both increases and decreases in the firing activity of VTA DA neurons have been reported in chronic pain states [10,11,12]. Theses discrepancies may be explained by the intricate heterogeneity of the different DA projection neurons. There is evidence that the firing activity of VTA DA neurons modulates the functional output of the reward system through its downstream targets [13, 14]. As such, the VTA-to-NAc and VTA-to-mPFC DA neurons may undergo differential adaptations in chronic pain states. Furthermore, the NAc and the mPFC, at the single-brain-region level, have been studied extensively for their roles in the processing of nociception under physiological and pathological pain conditions [11, 15,16,17,18]. Therefore, we speculated that the mesolimbic and mesocortical circuits play different roles in regulating nociceptive responses in chronic pain states.
The roles of the mesolimbic DA neurons in regulating nociception are strongly associated with their neuronal activity [19]. We previously reported that the increased firing activity of the VTA-to-NAc DA neurons mediates the thermal hyperalgesia induced by chronic constriction injury (CCI) of the sciatic nerve by releasing brain-derived neurotrophic factor (BDNF) into the NAc [19]. However, the mechanisms underlying the changes of DA neuronal activity remain largely unknown.
K+ voltage-gated channel subfamily Q (KCNQ) channels are widely expressed in neurons and have been implicated in pain [20,21,22,23,24]. Several studies have shown that KCNQ channels are involved in the modulation of hyperalgesia by regulating neuronal activity in peripheral nerve [20, 21]. A recent report demonstrated that overexpression of KCNQ channels normalizes the hyperactivity of VTA DA neurons [25]. These findings led us to hypothesize that that KCNQ channels of the VTA DA neurons might be involved in the regulation of nociception in chronic pain states.
Using electrophysiological, chemogenetics, and pharmacological approaches, we explored the roles of the VTA-to-NAc and VTA-to-mPFC DA neurons in an animal model of CCI-induced neuropathic pain and further investigated the underlying cellular mechanism.
Materials and Methods
Animals
Male C57BL/6J mice aged 7–8 weeks were provided by the Experimental Animal Center of Xuzhou Medical University and were acclimated to the housing facility for 1 week prior to experiments. These mice were group-housed (5 per cage) and maintained on a 12-h light/dark cycle with controlled humidity and temperature, and ad libitum access to food and water. All experiments were performed during the light cycle and all the behavioral tests were conducted by double-blind randomization in a silent room. All procedures followed the recommendations of the National Institutes of Health Guide for Care and Use of Laboratory Animals as well as the Committee for Research and Ethical Issues of the International Association for the Study of Pain.
CCI Surgery
CCI surgery was performed following a method described previously [26]. Briefly, mice were anesthetized with 1% pentobarbital sodium (40 mg/kg, i.p.) and the skin on the lateral surface of the left thigh was incised. The left sciatic nerve was exposed at mid-thigh level and a unilateral constriction injury just proximal to the trifurcation was performed with three loose ligatures using 4–0 silk (spaced at 1-mm intervals). In sham-operated animals, the nerve was exposed but not ligated. The incision was closed in layers, and the wound was treated with topical penicillin.
Stereotaxic Injections
Mice were anesthetized with 1% pentobarbital sodium (40 mg/kg, i.p.) and then placed in a stereotaxic apparatus (RWD, China). The cranium was exposed with the periosteum removed by 3% hydrogen peroxide. To label the projection-specific VTA DA neurons, lumafluor (0.5 μL, Lumafluor Inc., Durham, NC) was injected either into the NAc (in mm): anterior/posterior (AP), +1.40; medial/lateral (ML), +0.60; dorsal/ventral (DV), −4.70 or into the mPFC (in mm): AP, +1.95; ML, +0.27; DV, −2.00. Retigabine (20 µmol/L, MB1200, Melone Pharmaceutical Co., Ltd., China) was injected into the VTA (in mm): AP, −3.30; ML, +1.05; DV, −4.60; 7º, in a volume of 0.3 μL to investigate the effect of retigabine on behavior associated with neuropathic pain. The viruses were from BrainVTA (Wuhan, China). To evaluate the expression of KCNQ2 and KCNQ3 in VTA-to-NAc and VTA-to-mPFC DA neurons, rAAV-TH-NLS-Cre-WPRE-pA (0.2 μL, 2/R, 5.65 × 1012 genomic copies per mL) and rAAV-Eflα-DIO-EGFP-WPRE-pA (0.2 μL, 2/9, 6.86 × 1012 genomic copies per mL) were respectively injected into the NAc or mPFC and the VTA. To modulate projection-specific VTA DA neurons by chemogenetics, rAAV-TH-NLS-Cre-WPRE-pA (0.2 μL, 2/R, 5.65 × 1012 genomic copies per mL) was injected into the NAc or mPFC, while rAAV-Eflα-DIO-hM4D(Gi)-mCherry-WPRE-pA (0.2 μL, 2/9, 5.67 × 1012 genomic copies per mL) or rAAV-Eflα-DIO-hM3D(Gq)-mCherry-WPRE-pA (0.2 μL, 2/9, 5.65 × 1012 genomic copies per mL) was injected into the VTA contralateral to the CCI surgery. To overexpress KCNQ2 in projection-specific DA neurons, rAAV-TH-NLS-Cre-WPRE-pA (0.2 μL, 2/R, 5.65 × 1012 genomic copies per mL) was injected into the NAc or mPFC, and rAAV-CMV-DIO-KCNQ2-EGFP (0.2 μL, 2/R, 5.65 × 1012 genomic copies per mL) into the VTA. To elucidate the role of BDNF signaling in retigabine-induced behavioral outcomes in the mesocorticolimbic system, 0.2 μL BDNF (10 ng, B3795; Sigma-Aldrich) was injected into the NAc or mPFC. All the reagents were microinjected using a Hamilton syringe needle (33-gauge) at 0.1 µL/min with a pump (Harvard Apparatus).
Measurement of Thermal Nociception
The Hargreaves test [27] was performed to evaluate the thermal nociceptive response by using an IITC plantar analgesia meter (IITC Life Science, Inc.). In brief, mice were placed in plastic cages on a glass platform and allowed to acclimatize for 30 min before testing. A radiant heat source was positioned directly beneath the glass and focused on the plantar surface of the left hind paw. The nociceptive endpoint in the radiant heat test was the lifting or licking of the hind paw. The time from onset of the radiant heat to the reaction was considered as the paw withdrawal latency (PWL). The radiant heat intensity was adjusted at the beginning of the experiment to obtain a basal PWL of 12–15 s and the cutoff time for exposure was set at 25 s to prevent tissue damage. The measurements were repeated five times at 5-min intervals and the average of the five measurements was calculated. For the chemogenetic-mediated behavioral test, the animals were injected intraperitoneally with clozapine-N-oxide (CNO; 1 mg/kg, dissolved in saline; HY-17366, MCE) 30 min prior to the test.
Ex-vivo Electrophysiological Recordings
All recordings were carried out blind to the experimental conditions of behavioral, drug, and viral treatments. Mice were anesthetized with isofluorane and perfused immediately with ice-cold aCSF (artificial cerebrospinal fluid) for 40–60 s, which contained (in mmol/L): 128 NaCl, 3 KCl, 1.25 NaH2PO4, 10 D-glucose, 24 NaHCO3, 2 CaCl2, and 2 MgCl2 (oxygenated with 95% O2 and 5% CO2, pH 7.4, 295–305 mOsm). Acute brain slices containing VTA DA neurons were cut on a microslicer (DTK-1000, Ted Pella) in ice-cold sucrose aCSF, in which the NaCl was fully replaced with 254 mmol/L sucrose and saturated by 95% O2 and 5% CO2. Slices were maintained in holding chambers with aCSF for 1 h recovery at 37°C. For experiments, slices were transferred to the recording chamber and perfused (2–2.5 mL/min) with oxygenated aCSF at 35°C.
Patch pipettes (3–5 MΩ) for whole-cell current-clamp, voltage-clamp, and cell-attached recordings were filled with internal solution containing the following (in mmol/L): 115 potassium gluconate, 20 KCl, 1.5 MgCl2, 10 phosphocreatine, 10 HEPES, 2 magnesium ATP, and 0.5 GTP (pH 7.2, 285 mOsm). VTA DA neurons were identified by their location and infrared differential interference contrast microscopy and recordings were made from lumafluor-positive neurons for projection-specific recordings.
Cell-attached recordings were used for measurements of the spontaneous activity of VTA DA neurons. Signals were band-pass filtered at 300 Hz–1 kHz to identify DA neurons and were then Bessel filtered at 10 kHz (gain 50) using a Multiclamp 700B amplifier (Molecular Devices). For chemogenetics validations, the spontaneous activity of VTA DA neurons was recorded continuously before, during, and after CNO perfusion (5 mmol/L).
To measure M-current, whole-cell recordings were carried out in voltage-clamp mode. The neurons were recorded in the presence of 1 μmol/L tetrodotoxin (TTX; Alomone Labs), at a holding potential of −20 mV, and 1-s repolarizing steps were then applied to −40 mV. To measure the intrinsic membrane properties of VTA DA neurons, whole-cell recordings were carried out in current-clamp mode and spikes were induced by 100-pA current injection.
Retigabine (10 µmol/L, MB1200, Melone Pharmaceutical Co., Ltd., China) was used to investigate the role of KCNQ channels in regulating the activity of VTA DA neurons. Series resistance was monitored during all recordings. Data were acquired and analyzed using a Digidata 1440 A digitizer and pClamp 10.2 (Molecular Devices).
Immunohistochemistry
Under general anesthesia with 1% pentobarbital sodium (40 mg/Kg, i.p.), the mice were intracardially perfused with 30 mL cold PBS (pH 7.4) and 30 mL 4% paraformaldehyde. The brains were removed and post-fixed at 4°C overnight, then kept in 30% sucrose for 2 days. Coronal sections (30 µm) were cut on a freezing microtome (VT1000S, Leica Microsystems). VTA sections were directly imaged for lumafluor, EGFP, and mCherry expression on a laser scanning confocal microscope (FluoView FV1000; Olympus).
For immunofluorescence staining, the sections were blocked for 1 h with 3% donkey serum and 0.25% Triton X-100 in PBS at room temperature. Then they were incubated with the primary antibodies rabbit anti-Kv7.2 (KCNQ2, 1:100; APC-050, Alomone Labs), rabbit anti-Kv7.3 (KCNQ3, 1:100; APC-051, Alomone Labs), and mouse anti-tyrosine hydroxylase (1:600, 318; Millipore), at 4°C overnight. The sections were then incubated for 2 h at room temperature with the secondary antibodies Alexa Fluor 488 anti-rabbit (A-11034), AlexaFluor 594 anti-mouse (A-11032), and AlexaFluor 488 anti-mouse (A-32723) (1:200, Molecular Probes), and rinsed three times with PBS before mounting. Afterwards, the sections were visualized under an Olympus confocal microscope.
Western Blot
NAc and mPFC tissue blocks were harvested with 12-gauge punches and then sonicated in 30 μL homogenization buffer containing 320 mmol/L sucrose, 5 nmol/L HEPES, 1% sodium dodecyl sulfate (v/v), phosphatase inhibitor cocktails I and II (Sigma-Aldrich), and protease inhibitors (Roche Diagnostics). Protein concentrations were determined with a DC protein assay (Bio-Rad). Proteins (20–40 μg protein per lane) were electrophoresed in 10% SDS-PAGE gel and transferred onto PVDF membranes. The membranes were incubated at 4°C overnight with the primary rabbit anti-BDNF (1:1000, sc-546, Santa Cruz) and mouse anti-GAPDH (1:1000, E021010, Earthox) antibodies. The membranes were rinsed and then incubated for 2 h at room temperature with the secondary antibodies conjugated to alkaline phosphatase (1:500; Santa Cruz). The immune complexes were detected with a BCIP/NBT kit (Beyotime). Blots were analyzed with Photoshop software (Adobe Systems, Inc.), and the gray-scale values of protein bands were normalized to those of GAPDH.
Statistical Analysis
Data are presented as mean ± SEM. Statistical analyses were performed with GraphPad Prism 6.0 software (Graph Pad Software, Inc.). Differences among three or more groups were compared with one-way ANOVA followed by Tukey’s post hoc test. The unpaired t test was used if only two groups were compared. The significance of any difference in thermal PWLs in the behavioral tests was assessed with a two-way ANOVA with repeated measures and Bonferroni’s post hoc test. All P values given are based on two-tailed tests. For all analyses, P <0.05 was considered to be statistically significant.
Results
Changes of Firing Rates in Mesocorticolimbic DA Neurons Under Chronic Pain
PWLs were used to assess nociceptive responses [27]. CCI mice exhibited a significant decrease in the PWLs of the affected hind paws, which lasted for at least 14 days (Fig. 1A, B). To investigate the firing activity of the VTA-to-NAc and VTA-to-mPFC DA neurons in a state of CCI-induced chronic neuropathic pain, we injected the retrograde tracer lumafluor into the NAc or mPFC 7 days before CCI surgery to label projection-specific VTA neurons. Cell-attached electrophysiological recordings were performed in these labeled neurons, and the DA neurons were identified by their waveforms under signal-filtered condition (see Methods) (Fig. 1C). The ex-vivo recordings showed that CCI induced a significant increase in the firing activity in the contralateral, but not the ipsilateral, VTA-to-NAc DA neurons (Fig. 1D). In contrast, the firing activity of contralateral VTA-to-mPFC DA neurons was dramatically decreased (Fig. 1E). These data indicate that the VTA-to-NAc and VTA-to-mPFC DA neurons respond differentially to CCI-induced neuropathic pain.
Roles of the Mesocorticolimbic Circuits in Regulation of CCI-Induced Thermal Nociception
To answer the question whether these activity changes of the mesocorticolimbic DA neurons are implicated in regulation of thermal nociception in CCI-induced neuropathic pain, we first chemogenetically decreased the activity of VTA-to-NAc DA neurons by injection of a retrograde AAV, rAAV-TH-NLS-Cre-WAPE-pA, into the NAc, and a cre-dependent AAV, rAAV-Eflα-DIO-hM4D(Gi)-mCherry-WPRE-pA, into the VTA (Fig. 2A, B). The expression of hM4Di in VTA DA neurons was confirmed by co-localization of TH and mCherry (Fig. 2B) and its function was validated as a decreased firing rate of mCherry-labeled VTA DA neurons in acute slices induced by CNO perfusion (5 mmol/L) (Fig. 2C). CCI surgery was conducted 2 weeks following the microinjections, and 7 days after that, PWLs were measured. CCI mice with CNO injection (1 mg/kg, i.p.) showed increased PWLs (Fig. 2D), suggesting that the chemogenetic inhibition of VTA-to-NAc DA neurons reversed CCI-induced thermal hyperalgesia.
Next, we tested whether the decreased firing activity of the VTA-to-mPFC DA neurons contributed to the thermal nociception in CCI mice. To upregulate the firing activity in these neurons, we injected rAAV-TH-NLS-Cre-WAPE-pA into the mPFC, and rAAV-Eflα-DIO-hM3D(Gq)-mCherry-WPRE-pA into the VTA (Fig. 2A, E). The viral expression and its function were confirmed by immunofluorescence staining and cell-attached recordings (Fig. 2E, F). Unlike inhibition of the VTA-to-NAc DA neurons, this chemogenetic activation by CNO injection did not change the PWLs in CCI mice (Fig. 2G). These results suggest an involvement of the VTA-to-NAc, but not the VTA-to-mPFC DA neurons, in regulating thermal nociception under a state of chronic neuropathic pain.
Changes of M-current (I M) in Mesocorticolimbic DA Neurons Under Chronic Pain
IM, a voltage-gated K+ current, is involved in the physiological and pathological modulation of neuronal activity [28,29,30]. It is mediated by KCNQ-type K+ channels [28, 31] and thus measurement of IM reflects the function of KCNQ channels. We used the retrograde tracer lumafluor to label VTA-to-NAc and VTA-to-mPFC neurons and performed ex-vivo whole-cell recordings to measure IM in these labeled cells from CCI mice. The results showed that CCI mice exhibited decreased M-current density in the contralateral VTA-to-NAc DA neurons (Fig. 3A) and increased density the contralateral VTA-to-mPFC DA neurons (Fig. 3B), suggesting that CCI differentially modulates the KCNQ channels of mesocorticolimbic DA neurons, and thus may lead to the opposite changes of firing activity in the VTA-to-NAc and VTA-to-mPFC DA neurons.
Location of KCNQ2/3 Channels in Mesocorticolimbic DA Neurons
Immunohistochemical studies have shown that KCNQ2 and KCNQ3 channels are present in VTA neurons [30, 32,33,34]. Thus, we investigated the location of KCNQ2/3 channels in mesocorticolimbic DA neurons. To do this, we labeled the two DA populations by microinjection of a retrograde AAV, rAAV-TH-NLS-Cre-WAPE-pA, into the NAc or mPFC, and a cre-dependent AAV, rAAV-Eflα-DIO-EGFP-WPRE-pA, into the VTA. The EGFP- and TH-positive cells were concerned as the putative circuit-specific DA populations. KCNQ2-labeled cells constituted 91.69% of VTA-to-NAc DA neurons (Fig. 4A, C), and 96.23% of VTA-to-mPFC neurons (Fig. 4B, D). Meanwhile, 81.65% of the VTA-to-NAc DA neurons (Fig. 4E, G) and 82.66% of the VTA-to-mPFC population (Fig. 4F, H) were KCNQ3-positive.
We further analyzed the proportions of KCNQ2- or KCNQ3-positive cells in VTA-to-NAc or VTA-to-mPFC DA neurons. No significant differences were seen between the CCI mice and the sham counterparts (Fig. 4A–H). These data suggest no quantitative changes of the DA neurons that contain KCNQ2/KCNQ3 channels in CCI-induced chronic pain. It is worth noting that this result does not deny differential expression of KCNQ2/KCNQ3 channels in the two VTA DA projections in chronic neuropathic pain.
Roles of Circuit-Specific KCNQ2 Overexpression in Regulating Thermal Nociception
Changes in both KCNQ expression and channel status may contribute to IM alterations. To explore the roles of KCNQ channels in regulating thermal nociception in a chronic pain state, we overexpressed KCNQ2 in each of the two specific DA populations by injecting rAAV-TH-cre into the NAc or mPFC, and rAAV-CMV-DIO-KCNQ2-EGFP into the VTA (Fig. 5A, B, F). After validation of viral expression (Fig. 5B, F), whole-cell recordings confirmed that this projection-selective overexpression of KCNQ2 increased the M-current density (Fig. 5C) and decreased the firing activity (Fig. 5D). Behavioral results showed that KCNQ2 overexpression in the VTA-to-NAc DA neurons reversed the established thermal hyperalgesia in CCI mice as evidenced by the increased PWLs (Fig. 5E). This reversal was not seen in the mice with KCNQ2 overexpression in the VTA-to-mPFC DA neurons (Fig. 5G), These results indicate that functional modulation of KCNQ2 channels in the VTA-to-NAc, rather than the VTA-to-mPFC circuit contributes to regulating thermal nociception in chronic neuropathic pain.
Relief of CCI-Induced Thermal Nociception by Retigabine
Given that the functional status of KCNQ channels may also affect IM, we further investigated their effects on thermal nociception by activating KCNQ channels. The KCNQ opener retigabine, an FDA-approved agent for anticonvulsant therapy [35,36,37], was used here. The results from ex-vivo whole-cell recordings in VTA slices showed that perfusion of retigabine significantly increased the M-current density and membrane potential (Fig. 6A–F), and decreased the firing rate (Fig. 6G, H) in both VTA-to-NAc and VTA-to-mPFC DA neurons as compared with the vehicle controls, suggesting its non-selective effects on the mesocorticolimbic circuits. Furthermore, intra-VTA injection of retigabine (10 μmol/L, 0.15 μL) produced a clear anti-nociceptive response as evidenced by the increased PWLs (Fig. 6I). Combined with our previous finding, we suggest that retigabine exerts its anti-nociceptive effects by decreasing the activity of the VTA-to-NAc DA neurons by activating KCNQ channels.
Mesocorticolimbic BDNF Signaling in the Anti-nociceptive Effect of Retigabine
BDNF plays important roles in regulating synaptic plasticity and neuronal survival [38, 39]. Previous studies have suggested that VTA DA neurons release BDNF into the targeted areas in an activity-dependent manner [38, 40]. Our recent work showed that BDNF in the VTA-to-NAc circuit is increased, thus mediating thermal nociception in mice with CCI-induced neuropathic pain [19]. Therefore, we asked whether BDNF signaling in the VTA-NAc circuit is involved in the anti-nociceptive effect of retigabine. Western blot assays showed that the BDNF protein levels in the NAc were drastically increased in CCI mice and this increase was reversed by intra-VTA injection of retigabine (Fig. 7A), suggesting that intra-VTA injection of retigabine decreased BDNF levels in the NAc under chronic pain. Furthermore, exogenous administration of BDNF into the NAc abolished the anti-nociceptive effect of intra-VTA retigabine injection in CCI mice (Fig. 7C). Unlike that in the NAc, CCI induced a significant decrease of BDNF protein levels in the mPFC (Fig. 7B). Intra-VTA injection of retigabine further lowered the BDNF levels in the mPFC in CCI mice (Fig. 7B). Exogenous BDNF injected into the mPFC did not alter the anti-nociceptive effect induced by intra-VTA retigabine injection (Fig. 7D). These data imply a potential role of BDNF signaling in the VTA-to-NAc DA circuit in the anti-nociceptive effect of retigabine on chronic neuropathic pain.
Discussion
Our current results demonstrate that: (1) CCI differentially modulated the firing activity of the VTA-to-NAc and VTA-to-mPFC DA circuits, and of the two, the former is involved in thermal nociception regulation; (2) both KCNQ2 overexpression in the VTA-to-NAc DA neurons and intra-VTA injection of the KCNQ opener retigabine corrected mesolimbic KCNQ channel-mediated M-currents and DA neuronal activity, and relieved CCI-induced thermal nociception; and (3) BDNF signaling in the VTA-to-NAc DA circuit may be involved in the anti-nociceptive effect of retigabine. These findings reveal a novel KCNQ channel-based ionic and circuit mechanism for the regulatory roles of mesocorticolimbic circuits in chronic neuropathic pain-induced thermal nociception.
VTA DA neurons are a heterogeneous population divided into several subgroups in terms of their targets [13, 41]. Among them, the VTA-to-NAc and the VTA-to-mPFC DA neurons have been shown to have distinct properties: for example, these subpopulations have different firing properties [42, 43]. Specifically, the VTA-to-mPFC DA neurons discharge faster than the VTA-to-NAc DA neurons [42, 43], as confirmed by our current results (Fig. 1C–E).
Pain is a stressor, causing multiple adaptive changes in the brain [44, 45]. A growing body of literature suggests that the mesocorticolimbic DA circuits are implicated in chronic pain [3, 6, 19, 25, 46]. Similar stress can induce different firing alterations in these projection-specific VTA DA neurons [47]. For instance, recent studies have shown that the VTA-to-NAc and VTA-to-mPFC DA neurons exhibit distinct properties and actions in regulating stress-related depression [48,49,50,51]. Likewise, our current study reports such heterogeneity in CCI-induced chronic neuropathic pain. In line with our previous study [19], the current results suggest that the mesolimbic DA circuit is required for the regulation of thermal nociception in a state of chronic pain (Fig. 1, 2). Although the firing activity of VTA-to-mPFC DA neurons was decreased by CCI (Fig. 1E), activation of these neurons did not change the thermal nociceptive threshold (Fig. 2E–G). This result does not support an involvement of VTA-to-mPFC DA neurons in regulating the thermal nociception underlying chronic pain. It should be noted that the function of the decreased activity in the mesocortical DA neurons remains unknown. Based on recent studies [50, 52], we speculate that this adaptive change may be involved in regulating chronic pain-related negative emotions and cognitive impairments.
It has been shown that KCNQ channels serve as a brake to suppress abnormal ectopic discharges of neurons and control neuronal hyperexcitability [25, 28, 33]. These channels and related M-currents set the resting membrane potential [53], and exert an inhibitory effect on neuronal discharges in brain slice, spinal cord, and dorsal root ganglion neurons [20, 25, 54]. Structurally, KCNQ channels consist of five subunits as homo- or hetero-tetramers [28, 31, 33]. Among them, KCNQ2/3 channels are well recognized to form the molecular basis for M-currents [31], and have been found to affect DA neuronal activity within the VTA [32, 55]. It is known that the KCNQ2/3 heteromers exhibit an 11-fold larger current than the KCNQ2 or KCNQ3 homomers [56]. Based on their abundant distribution (Fig. 4), we speculate that the majority of KCNQ2 and KCNQ3 channels form heteromers in the VTA. Furthermore, both KCNQ2 overexpression and microinjection of the KCNQ opener retigabine corrected the CCI-induced changes of M-currents and firing activity in the VTA-to-NAc DA neurons and reversed thermal hyperalgesia. These data support the hypothesis that chronic neuropathic pain may heterogeneously modulate the expression and/or functional status of KCNQ channels in mesocorticolimbic DA circuits, resulting in the distinct firing properties. Although KCNQ4 and KCNQ5 may contribute to M-currents likewise, we did not test their roles due to their locations [57, 58].
The functional heterogeneity of the mesocorticolimbic DA circuits is largely dependent on changes of the firing activity in the VTA DA subpopulations [50, 51], and yet various ion channels expressed within these neurons play an important role as intrinsic factors in regulating firing activity [59]. Studies have shown that hyperpolarization-activated cation channel-mediated currents (Ih) provide an excitatory driving force [60,61,62] and K+ channel-mediated currents provide an inhibitory driving force in VTA DA neurons [30, 63], and the balance between them is essential for normal function of the mesocorticolimbic DA circuits [55, 63, 64]. External stimuli may shift this balance towards an excitatory or inhibitory state in different projecting circuits [55], and then result in heterogeneous functional phenotypes. The ion channel-related heterogeneous alterations in mesocorticolimbic DA circuits have been well studied in the social defeat stress-induced depression model [25, 55]. We report similar ion channel-mediated functional heterogeneity of the mesocorticolimbic DA circuits in chronic pain processing. In detail, KCNQ channel-mediated M-type K+ currents, as an inhibitory driving force [30, 63], display heterogeneous alterations in the mesocorticolimbic DA circuits in mice with CCI-induced neuropathic pain (Fig. 3), which may result in changes of the firing activity of DA neurons.
Our previous study has shown that the VTA-to-NAc DA neurons exhibit an increase of the excitatory driving force Ih current in CCI mice and pharmacologically inhibiting VTA DA neuron firing with Ih blockers reverses CCI-induced NAc neuronal activation and thermal hyperalgesia in CCI mice [19]. Thus, we speculate that long-lasting nociceptive inputs with chronic pain shift the balance towards an excitatory state in the VTA-to-NAc DA circuit via modulating Ih and M-type K+ currents and therefore increase the firing activity of these neurons. These studies strongly support the conclusion that the intrinsic firing activity of VTA DA neurons serves as an important mechanism underlying the adaptations involved in chronic pain, and may provide valuable therapeutic targets for chronic pain.
Retigabine is an FDA-approved anticonvulsant drug for partial epilepsies. It reduces neuronal excitability in animals and humans by enhancing IM via the activation of KCNQ channels [35]. Recent studies have also implicated this drug in treating lateral sclerosis [65], alcohol addiction [66], chronic pain [20,21,22], and depression [25]. Administration of retigabine has been reported to reverse mechanical and thermal hypersensitivity in inflammatory, neuropathic, and cancer pain and chemotherapy-induced peripheral neuropathy models [20,21,22, 24]. Retigabine exerts an analgesic effect through peripheral mechanisms including inhibiting the excitability of nociceptive neurons and C-type nerve fibers [20, 24]. Studies have also reported that intra-thalamic or intra-cerebral ventricular injection of retigabine produce an analgesic effect [67, 68], suggesting that a supraspinal mechanism may be involved in the anti-nociceptive effect of retigabine. In the present study, intra-VTA injection of retigabine alleviated CCI-induced thermal nociception, in parallel with increased M-currents and decreased firing activity in VTA DA neurons (Fig. 6). Combined with the finding that the adaptive changes in the VTA-to-NAc DA neurons contribute to CCI-induced thermal nociception, we speculate that correction of the KCNQ-mediated firing activity in VTA-to-NAc DA neurons may underlie the anti-nociceptive effect of retigabine.
Previous studies have demonstrated that BDNF is a critical nociceptive modulator in the mesolimbic reward circuit [19, 51]. There is a strong association between VTA DA neuronal firing rates and BDNF levels in the target regions [19, 38, 40]. We provide evidence that intra-VTA injection of retigabine corrected BDNF protein levels in the NAc in CCI mice (Fig. 7A, B). As BDNF levels in the NAc may reflect the VTA DA neuronal activity, this change in BDNF levels is in line with the finding that retigabine decreased the firing activity of the VTA DA neurons in CCI mice (Fig. 6G, H). In addition, exogenous BDNF in the NAc abolished the effect of retigabine on thermal nociception in CCI mice (Fig. 7C). These results reflect a possible role of BDNF signaling of the VTA-to-NAc DA circuit in the anti-nociceptive effect of retigabine. It is worth noting that retigabine similarly changed the BDNF levels in the mPFC, whereas exogenous BDNF delivered to the mPFC had no effect on thermal nociception (Fig. 7B, D). This point needs future investigations on the part played by the retigabine-induced decrease in BDNF levels in the mPFC.
Since pain is a distressing experience with emotional and cognitive components, a limitation of this study is that we only focused on thermal pain sensation. Whether and how this system is involved in processing pain-related negative emotions and cognition impairments remain to be explored. Limitations in viral expression may also occur due to nonspecific expression and the influence of injection sites.
In summary, our study reveals the functional heterogeneity of the mesocorticolimbic DA circuits in regulating thermal nociception in the chronic pain state, and unmasks a novel mechanism by which mesolimbic KCNQ channels regulate thermal nociception by modulating the VTA-to-NAc DA neuronal firing activity.
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Acknowledgements
This work was supported by grants from the National Natural Science Foundation of China (31771161, 81720108013, 81230025, 81200859 and 81801096), Key Project of Nature Science Foundation of Jiangsu Education Department (17KJA320005), Natural Science Foundation of Jiangsu Province (BK20171159), the Qing-Lan Project of Jiangsu, the Six Talent Summit Project of Jiangsu, the 333 High-level Personnel Training Project of Jiangsu, the Priority Academic Program Development of Jiangsu Higher Education Institutions, the Jiangsu Provincial Special Program of Medical Science (BL2014029), and the Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX19–2241 and KYCX20_2449), China.
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Wang, HR., Hu, SW., Zhang, S. et al. KCNQ Channels in the Mesolimbic Reward Circuit Regulate Nociception in Chronic Pain in Mice. Neurosci. Bull. 37, 597–610 (2021). https://doi.org/10.1007/s12264-021-00668-x
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DOI: https://doi.org/10.1007/s12264-021-00668-x