SUR1,newly expressed in astrocytes,mediates neuropathic pain in a mouse model of peripheral nerve injury

Ethics statement

The article was written in accordance with ARRIVE guidelines. ³⁹ We certify that all applicable institutional and governmental regulations concerning the ethical use of animals were followed during the course of this research. Animal experiments were performed under a protocol approved by the Institutional Animal Care and Use Committee of the University of Maryland, Baltimore, and in accordance with the relevant guidelines and regulations as stipulated in the National Research Council Publication, “Guide for the Care and Use of Laboratory Animals”, NIH Publication 86–23. All efforts were made to minimize the number of animals used and their suffering.

Subjects

Adult male C57BL/6 mice, 22–25 gm, were obtained from Envigo (Indianapolis, IN). Global Abcc8 knock-out (a.k.a., Abcc8–/–) mice and Abcc8-floxed mice were generated, validated and gifted by Dr. Joseph Bryan and colleagues.^40,41 Global Trpm4 knock-out (a.k.a., Trpm4–/–) mice were generated, validated and gifted by Prof. Dr. Marc Freichel and Prof. Dr. Veit Flockerzi. ⁴² Gfap-cre mice (B6.Cg-Tg(Gfap-cre)73.12Mvs/J; stock #012886) and GFAP-cre/ERT2 mice (B6.Cg-Tg(GFAP-cre/ERT2)505Fmv/J; stock #012849), in which Cre recombinase is under the control of the murine Gfap or human GFAP promoter, either constitutive or conditional, were obtained from The Jackson Laboratory (Bar Harbor, ME). Mice with constitutive deletion of Abcc8 driven by the Gfap promoter, i.e., Abcc8^fl/fl;+Gfap-cre (henceforth, pGfap-cre-driven Abcc8 deletion) and littermate controls (Abcc8^fl/fl;–Gfap-cre) were obtained by crossing homozygous Abcc8-floxed mice with transgenic Gfap-cre mice. Mice with conditional deletion of Abcc8 driven by the GFAP promoter, i.e., Abcc8^fl/fl;+GFAP-cre/ERT2 (henceforth, pGFAP-cre/ERT2-driven Abcc8 deletion) and littermate controls (Abcc8^fl/fl;–GFAP-cre/ERT2) were obtained by crossing homozygous Abcc8-floxed mice with transgenic GFAP-cre/ERT2 mice.

Genotyping of mice used for breeding and experiments was performed by Transnetyx (Cordova, TN). Mice were given free access to food and water, except during neurofunctional testing. They were housed in plastic cages in specially constructed rooms with controlled humidity, exchange of air and controlled lighting (12/12 hour light/dark cycle). Male mice were used for all experiments.

Surgery

Mice were anesthetized (100 mg/kg ketamine plus 10 mg/kg xylazine, intraperitoneal [IP]) and breathed room air spontaneously. Core temperature was maintained at 37 °C using a heating pad (Deltaphase® Isothermal Pad, Braintree Scientific, Braintree, MA, USA). Hair was clipped from the right proximal lateral thigh, and the surgical site was prepared using iodine and alcohol. A sterile environment was maintained throughout the procedure. Lidocaine solution (2%) was injected subcutaneously prior to making an incision.

The procedure for sciatic n. cuffing was as previously described,^37,38 with only minor modification, as we described. ⁴³ In this model, mechanical allodynia is sustained unabated for at least 9 weeks. ⁴³ Using a surgical microscope, the common branch of the right sciatic n. was exposed by separating the muscles and the nerve by blunt dissection. After isolation, the nerve was gently stretched for 15 minutes by placing a 5-mm diameter plastic rod beneath it, which caused the nerve to blanch. A 2-mm long section of PE-20 tubing, pre-split and sterilized, was placed around the nerve. Animals in the sham group received surgery identical to that described but without nerve manipulation or cuffing. After the surgical procedure, mice were nursed on a heating pad to maintain body temperature ∼37°C until they emerged from anesthesia. The day of surgery is called post-op day 0 (pod-0).

No mice became infected, required early euthanasia or died. No mice in the control groups failed to develop stable mechanical allodynia. There were no exclusions.

Glibenclamide treatment

A stock solution of glibenclamide (#G2539; meets USP testing; Sigma-Aldrich) of 2.5 mg/mL in dimethyl sulfoxide was prepared. We diluted 40 μL of the stock solution into 960 µL phosphate buffered saline (PBS); mice received 100 μL of the final solution (10 µg glibenclamide) or an equal volume of vehicle IP daily until the end of the experiment. IP injections were performed using a 27-gauge needle with the depth of the injection limited to 3 mm by a sleeve of PE20 tubing placed over the shaft of the needle.

Sample size calculation

For mechanical allodynia, we based our sample size calculation on a previous study that used the same model of neuropathic pain but tested a different drug. Values derived from Figure 2 of Yalcin et al. 38 suggested an effect size (Cohen’s d) of ≈2, where d = (M₁–M₂)/SD_pooled, M₁ and M₂ are the means, and SD_pooled = [(SD₁ + SD₂)/2]^½. Using the following assumptions: two-tailed hypothesis, α, 0.05; desired power, 80%; d, 2.1, sample size calculation indicated a minimum sample size of 5 mice per group. This group size is similar to other reports using this model.^37,43

Experimental series

In series 1, 8 WT mice underwent sciatic n. cuffing and, on pod-3, pod-7 and pod-14, 2–3 mice per time point were euthanized to examine SUR1 expression in the spinal cord; 3 uninjured sham mice were used as controls. In series 2, 5 mice with global deletion of Abcc8 and 5 WT littermate controls underwent sciatic n. cuffing and were assessed for pain behaviors until pod-14. In series 3, 10 mice with pGfap-cre-driven Abcc8 deletion and 10 littermate controls underwent sciatic n. cuffing and were assessed for pain behaviors until pod-14; tissues from these mice were used for immunohistochemistry and PLA for SUR1-TRPM4. In series 4, 5 mice with pGFAP-cre/ERT2-driven Abcc8 deletion and 5 littermate controls underwent sciatic n. cuffing, were assessed for pain behaviors until pod-35, and on pod-14–18, were administered tamoxifen in corn oil (75 mg/kg; 100 µL IP). In series 5, 7 mice with global deletion of Trpm4 and 7 WT littermate controls underwent sciatic n. cuffing and were assessed for pain behaviors until pod-14. In series 6 (prophylactic treatment), 20 WT mice underwent sciatic n. cuffing and were randomly divided into two groups, one receiving vehicle, the other, glibenclamide. Treatments were administered daily, beginning on pod-0, and pain behaviors were assessed up to pod-14. Tissues from these mice were used for immunohistochemical assessment of neuroinflammation in the affected dorsal horn. In series 7 (therapeutic treatment), 10 WT mice underwent sciatic n. cuffing and were randomly divided into two groups, one receiving vehicle, the other, glibenclamide. Treatments were administered daily, beginning on pod-21, after pain behaviors had been stably established. Pain behaviors were assessed up to pod-45.

In all cases, mice were handled 2–3× weekly for acclimatization to handlers, and the non-injured contralateral hind paw served as the control.^44,45 In series 3–7, outcomes were assessed by investigators blinded to treatment group; in series 2, blinding was not possible because Abcc8–/– mice are white and littermate WT controls are black.

Mechanical sensitivity

Mechanical sensitivity was assessed using von Frey filaments.^44,45 Mice were placed in elevated Perspex cages with a wire mesh floor (15 × 10 × 10 cm) (ITCC Life Science, Woodland Hill, CA, USA) and were acclimatized for 30 minutes prior to testing. The paw withdrawal threshold to mechanical stimulation of both the ipsilateral and contralateral hind paws was measured using a series of von Frey filaments that exerted forces ranging from 0.16–4 g (North Coast Medical, San Jose, CA, USA). The von Frey filaments were pressed perpendicularly onto the plantar surface of the hind paw for 2 seconds (five times for each filament), and a positive response was noted if there was a sharp flinching or licking of the hind paw. To determine the withdrawal threshold, we used the “ascending” method, to preclude potential aversive behavior associated with the “up-down” method. ⁴⁵ The Kolmogorov-Smirnow test for normality showed that, at the P = 0.05 level, the data on mechanical sensitivity were drawn from a normally distributed population.

Thermal sensitivity

Thermal sensitivity was assessed using the Hargreaves method^44,45 and a Hargreaves-type apparatus (Ugo Basile Thermal Plantar Test Instrument, Stoelting Co., Wood Dale, IL) that uses a fiber optic sensor to record time latency automatically. Unrestrained mice were placed in a Perspex enclosure atop of a glass pane and were acclimatized for 30 minutes prior to testing. An infrared generator placed below the glass pane was aimed at the plantar surface of the hind paw and the time to withdrawal was recorded automatically by the fiber optic sensor. Paw-withdrawal latency was calculated as the mean of 3–5 different measurements for each of three trials taken at 15-minute intervals.

Antibody validation

The custom anti-SUR1 and anti-TRPM4 antibodies used for immunolabeling were validated previously using lysates from appropriate SUR1 and TRPM4 expression systems, tissues from wild-type, Abcc8–/– and Trpm4–/– mice, and using mass spectrometry of immunoisolated proteins, ²⁹ in accordance with recommendations for antibody validation by Uhlen et al. ⁴⁶ In a previous publication, we further validated the specificity of the custom anti-SUR1 antibody for immunohistochemistry by comparing immunolabeling of adjacent sections using our custom polyclonal antibody, a monoclonal antibody (S289-16; Novus Biologicals, Littleton, CO) and a commercial polyclonal antibody (sc-5789; Santa Cruz Biotechnology, Dallas, TX). ⁴⁷

Immunohistochemistry, quantification of specific labeling

Under deep anesthesia, mice were euthanized, underwent trans-cardiac perfusion with normal saline (NS) (15 mL) followed by 10% neutral buffered formalin (15 mL). Spinal cord tissues at spinal segments L1–L5 were harvested and post-fixed. Tissues were cryoprotected with 30% sucrose, frozen in OCT and cryosectioned (10 µm).

Immunohistochemistry was performed as described in a non-blinded manner.^35,36 For SUR1 and TRPM4, sections were first processed for antigen retrieval in Epitope Retrieval Solution (cat# IW-1100; IHCWORLD, Woodstock, MD) using an Epitope Retrieval Steamer (cat# IW-1102; IHCWORLD) for 10–15 min, followed by cooling for 30 min, then washing in distilled H₂O. For all immunolabelings, sections were incubated at 4 °C overnight with primary antibodies, including: goat anti-SUR1 (1:600; custom); chicken anti-TRPM4 (1:600; custom); goat anti-TRPM4 (1:200; G-20, cat# 27540; Santa Cruz Biotechnology, Santa Cruz, CA); mouse anti-GFAP (1:300; conjugated Alexa Fluor 488, cat#53–9892-82; Invitrogen, Carlsbad, CA); rabbit anti-Iba1 (1:200; cat#019–19741; Wako, Osaka, Japan); rabbit anti-MBP (1:500; Ab40390; Abcam, Cambridge, UK); goat anti-IL-6 (1:100; cat# SC7920[H-183]; Santa Cruz Biotechnology); rabbit anti-CCL2 (1:200; cat# ab9669; Abcam); rabbit anti-CXCL1 (1:100; cat# PA1760; Boster, Pleasanton, CA). After several rinses in PBS, sections were incubated with species-appropriate fluorescent secondary antibodies (Alexa Fluor 488 and 555, Molecular Probes, Invitrogen) for 1 hour at room temperature. Controls for immunohistochemistry included the omission of primary antibodies.

Unbiased measurements of specific labeling within regions of interest (ROI) were obtained using NIS-Elements AR software (Nikon Instruments, Melville, NY) from sections (one section per mouse) immunolabeled as a single batch. All images for a given signal were captured using uniform parameters of magnification, area, exposure and gain. Segmentation analysis was performed by computing a histogram of pixel intensity for a particular ROI, and pixels were classified as having specific labeling based on signal intensity greater than 2× that of background. ROIs in coronal sections of the dorsal horn were defined by pixels with specific labeling for GFAP or Iba1 or MBP. Cell specific expression of the protein of interest within these ROIs was then determined as the fraction of pixels with specific labeling for the protein of interest (% ROI).

Proximity ligation assay (PLA) was used to detect SUR1-TRPM4 heteromers. Following antigen retrieval, as above, PLA was performed according to the manufacturer’s protocol using the Duolink (Sigma Aldrich) assay, including in situ PLA probe anti-goat plus (DUO92003), in situ PLA probe anti-rabbit minus (DUO92005), in situ wash buffer, fluorescent (DUO82049) and fluorescent detection reagent (orange) (DUO92007). Controls for PLA included the omission of primary antibodies.

Quantitative polymerase chain reaction

Tissues from the ipsilateral and contralateral dorsal quadrant of the spinal cord at L3–4 were processed using methods and primers as we described previously. ³²

Statistics

Nominal data are presented as mean ± SE. Nominal data were analyzed using a t-test, ANOVA or repeated measures ANOVA, as appropriate, with post-hoc Fisher correction. The Kolmogorov-Smirnow test was used to assess normality of the data on mechanical sensitivity. Statistical tests were performed using Origin Pro (V8; OriginLab, North Hampton, MA). Significance was assumed if P < 0.05.

PNI upregulates SUR1-TRPM4 in dorsal horn astrocytes of the spinal cord

WT mice underwent unilateral sciatic n. cuffing, a highly reproducible model of neuropathic pain.^37,38 On pod-3–14 after sciatic n. cuffing, spinal cord tissues from the dorsal horns at L3-4, which innervate the plantar surface of the hindpaw, ⁴⁸ were harvested to assess the expression of SUR1 and TRPM4 in various cell types.

SUR1 was minimal in the dorsal horns of normal WT controls and in the contralateral dorsal horns of mice with sciatic n. cuffing but was prominent in the dorsal horn ipsilateral to the PNI (Figure 1(a) and (b)), consistent with a prior report. ⁴⁹ Quantitative analysis of SUR1 immunopositivity confirmed a progressive increase in the ipsilateral dorsal horn over the course of 14 days (Figure 1(c)). Quantitative polymerase chain reaction (qPCR) confirmed upregulation of Abcc8 mRNA in ipsilateral dorsal horn tissues (Figure 1(d)).

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Figure 1.

De novo upregulation of SUR1-TRPM4 in dorsal horn astrocytes at spinal segment L3-4 after PNI. (a) and (b) Double immunolabeling for GFAP (red) and SUR1 (green) at low (a) and high (b) magnification, ipsilateral (Ipsi) and contralateral (Contra) to sciatic n. cuffing; superimposed images in (a), right and (b), right. (c) Quantification of SUR1 in the ipsilateral GFAP-positive region of interest in control (CTR) and on pod-1–14 after sciatic n. cuffing; data from 4 CTR mice and 11 with PNI, 2–3 mice/time point; **, P < 0.01. (d) Abcc8 mRNA upregulation relative to S18 shown by qPCR of ipsilateral dorsal horn (PNI) vs. sham; 3 mice/group; *, P < 0.05. (e) Double immunolabeling for SUR1 and Iba1 shows minimal overlap. (f) Analysis of SUR1 co-localization with GFAP, Iba1 and MBP after PNI using Pearson’s correlation coefficient, demonstrating a predominant astrocytic localization; 3 mice/group. (g) Double immunolabeling for SUR1 and TRPM4, ipsilateral to PNI; superimposed images are shown (right). (h) Quantification of TRPM4 in the ipsilateral GFAP-positive region of interest in control (CTR) and on pod-14 after sciatic n. cuffing; data from 4 CTR mice and 5 mice with PNI; **, P < 0.01. I,J: Proximity ligation assay (PLA) for SUR1 and TRPM4 (red) and GFAP immunolabeling (green), at low (i) and high (j) magnification, ipsilateral to sciatic n. cuffing in sham CTR, after PNI in WT mice, and after PNI in mice with pGfap-cre-driven Abcc8 deletion. (k) Quantification of SUR1-TRPM4 PLA in the ipsilateral dorsal horn on pod-14 after sciatic n. cuffing in sham CTR, after PNI in WT mice, and after PNI in mice with pGfap-cre-driven Abcc8 deletion; data from 4, 5 and 5 mice, respectively; **, P < 0.01 with respect to CTR; ##, P < 0.01 with respect to PNI in WT.

SUR1 expression was localized predominantly to cells with a stellate morphology that co-labeled for glial fibrillary acidic protein (GFAP), consistent with astrocytes (Figure 1(a) and (b)). Minimal SUR1 was observed in microglia/macrophages that co-labeled for ionized calcium binding adaptor molecule 1 (Iba1) (Figure 1(e)). Quantitative analysis of double immunolabeled sections revealed a high degree of co-localization of SUR1 with GFAP (Pearson’s correlation coefficient [PCC], 0.80), minimal co-localization of SUR1 with Iba1 (PCC, 0.12) and minimal co-localization of SUR1 with oligodendrocyte myelin basic protein (MBP) (PCC, 0.03) (Figure 1(f)), consistent with most of the newly upregulated SUR1 being localized to astrocytes.

SUR1 can assemble with TRPM4 to form SUR1-TRPM4 channels. ²⁹ As with SUR1, TRPM4 was minimal in the dorsal horns of normal WT controls and in the contralateral dorsal horns of mice with sciatic n. cuffing but was prominent in the dorsal horn ipsilateral to the PNI (Figure 1(g)). Quantitative analysis of SUR1 immunopositivity confirmed a significant increase in the ipsilateral dorsal horn at 14 days (Figure 1(h)). Double immunolabeling for SUR1 and TRPM4 showed prominent co-localization of the two channel subunits in cells with a stellate morphology, consistent with astrocytes (Figure 1(g)). ²⁹ Proximity ligation assay confirmed co-assembly of SUR1-TRPM4 heteromers in the ipsilateral dorsal horn (Figure 1(i) to (k)).

Deletion of Abcc8/SUR1

Uninjured mice with global deletion of Abcc8/SUR1 were previously reported to have a modest reduction (∼25%) in the withdrawal threshold to mechanical, but not thermal, stimulation. ¹⁷ However, this genotype has not been studied after PNI. Here, mice with global deletion of Abcc8/SUR1 and littermate WT controls underwent sciatic n. cuffing, which induces pain behaviors including mechanical allodynia and thermal hyperalgesia.^37,38 Von Frey filaments were used to assess ipsilateral and contralateral hindpaw withdrawal thresholds during the two weeks after PNI. In controls, sciatic n. cuffing gave rise to mechanical allodynia involving the ipsilateral hindpaw that developed over the course of 7 days and persisted on testing at pod-14 (Figure 2(a)). In mice with global deletion of Abcc8/SUR1, allodynia of the ipsilateral hindpaw to mechanical stimuli failed to develop, and withdrawal thresholds were not different from those of the contralateral uninjured hindpaw (Figure 2(a)).

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Figure 2.

Both global and pGfap-cre-driven Abcc8 deletion impedes the development of pain behaviors after PNI. A,B: Mice with global Abcc8 deletion and WT littermate controls (WT) underwent sciatic n. cuffing on pod-0 and were tested for mechanical sensitivity using von Frey filaments (a) and for thermal sensitivity using the automated Hargreaves test (b) on the days denoted on the abscissas; ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws were tested in both WT controls (squares) and with gene deletion (triangles); 5 mice/group; **, P < 0.01 by repeated measures ANOVA for ipsilateral hindpaws of WT vs. gene deletion. (c) Immunolabeling for SUR1 in the dorsal horn at spinal segment L3-4 from an uninjured mouse (naïve) and, following sciatic n. cuffing (PNI), in a littermate control mouse (CTR) and a mouse with pGfap-cre-driven Abcc8 deletion; a black signal denotes positive immunolabeling for SUR1; bar graph: quantification of SUR1 in ipsilateral and contralateral dorsal horns from the 3 experimental conditions: naïve (bar at left), PNI in CTR (middle bars), and PNI with pGfap-cre-driven Abcc8 deletion (bars at right); 5 mice/group; **, P < 0.01. (d)–(f) High magnification views of spinal cord sections immunolabeled for SUR1 ((d)–(f)) and double labeled for GFAP showing astrocyte expression of SUR in dorsal horn astrocytes from a control mouse (d), but not from a mouse with pGfap-cre-driven Abcc8 deletion (e); the ventral horns (VH) and DRG of the same mice show SUR1 expression in neurons of both genotypes (f). (g) and (h) Mice with pGfap-cre-driven Abcc8 deletion and littermate controls (CTR) underwent sciatic n. cuffing on pod-0 and were tested for mechanical sensitivity using von Frey filaments (g) and for thermal sensitivity using the automated Hargreaves test (h) on the days denoted on the abscissas; ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws were tested in both controls (squares) and with gene deletion (triangles); 10 and 5 mice/group in (g) and (h), respectively; **, P < 0.01 by repeated measures ANOVA for ipsilateral hindpaws of control vs. gene deletion.

The same mice were tested for thermal sensitivity using an automated Hargreaves apparatus. Compared to the contralateral hindpaw, the ipsilateral hindpaw of littermate controls exhibited significant thermal hyperalgesia (Figure 2(b)). By contrast, mice with global deletion of Abcc8/SUR1 exhibited ipsilateral thermal sensitivity that was not different from the contralateral uninjured hindpaw (Figure 2(b)).

We further explored the role of Abcc8/SUR1 specifically in astrocytes, since SUR1 is expressed not only in activated astrocytes, as shown above (Figure 1), but in other cell types within the CNS, including DRG^15,16 and other neurons, ⁵⁰ Schwann cells ¹⁶ and activated microglia.^32,51 Mice with pGfap-cre-driven Abcc8 deletion and littermate controls underwent sciatic n. cuffing. Compared to uninjured mice, littermate controls with sciatic n. cuffing showed prominent upregulation of SUR1 in ipsilateral dorsal horn that co-localized with the astrocyte marker, GFAP (Figure 2(c) and (d)). By contrast, in mice with pGfap-cre-driven Abcc8 deletion, sciatic n. cuffing resulted in minimal SUR1 upregulation (Figure 2(c) and (e)) and minimal PLA signal for SUR1-TRPM4 (Figure 1(k)) in the dorsal horn, whereas SUR1 expression in ventral horn neurons and DRG neurons was unaffected (Figure 2(f)).

In littermate controls, sciatic n. cuffing gave rise to mechanical allodynia involving the ipsilateral hindpaw that developed over the course of 7 days and persisted on testing at pod-14 (Figure 2(g)). In mice with pGfap-cre-driven Abcc8 deletion, allodynia of the ipsilateral hindpaw to mechanical stimuli failed to develop, and withdrawal thresholds were not different from those of the contralateral uninjured hindpaw (Figure 2(g)). On testing for thermal sensitivity, the ipsilateral hindpaw of controls exhibited significant thermal hyperalgesia (Figure 2(h)), whereas mice with pGfap-cre-driven Abcc8 deletion exhibited ipsilateral thermal sensitivity that was not different from the contralateral uninjured hindpaw (Figure 2(h)).

We also examined whether delayed silencing of Abcc8 in astrocytes could ameliorate pain behaviors after those behaviors had been established. Mice with Abcc8 deletion regulated by pGFAP-cre/ERT2 and littermate controls underwent sciatic n. cuffing and were tested for mechanical sensitivity. In all mice, mechanical allodynia developed in the ipsilateral hindpaw over the first 7 days and persisted through to pod-14 (Figure 3(a)). All mice were administered tamoxifen once daily on pod-14–18. Littermate controls continued to exhibit ipsilateral mechanical allodynia unabated until pod-35. By contrast, the ipsilateral hindpaw of mice with pGFAP-cre/ERT2-driven Abcc8 deletion slowly regained a significantly more normal mechanical sensitivity, although ipsilateral sensitivity did not reach that in the contralateral hindpaw (Figure 3(a)). On testing for thermal sensitivity, all mice demonstrated marked hyperalgesia through to pod-14 (Figure 3(b)). Subsequently, littermate controls showed partial loss of thermal hyperalgesia, as may occur over time with nerve constriction in mice ⁵² or which may have been due to tamoxifen. ⁵³ By contrast, mice with pGFAP-cre/ERT2-driven Abcc8 deletion showed complete reversion to the normal thermal sensitivity exhibited by the contralateral hindpaw (Figure 3(b)).

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Figure 3.

Delayed silencing of Abcc8 in astrocytes or constitutive global silencing of Trpm4 reduces pain behaviors after PNI. (a) and (b) Mice with pGFAP-cre/ERT2-driven Abcc8 deletion and littermate controls underwent sciatic n. cuffing on pod-0 and were tested for mechanical sensitivity using von Frey filaments (a) and for thermal sensitivity using the automated Hargreaves test (b) on the days denoted on the abscissas; all mice were administered tamoxifen once daily on pod-14–18; ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws were tested in both controls (squares) and with gene deletion (triangles); 5 mice/group; **, P < 0.01 by repeated measures ANOVA for ipsilateral hindpaws of control vs. gene deletion. (c) and (d) Mice with global Trpm4 deletion and WT littermate controls (WT) underwent sciatic n. cuffing on pod-0 and were tested for mechanical sensitivity using von Frey filaments (c) and for thermal sensitivity using the automated Hargreaves test (d) on the days denoted on the abscissas; ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws were tested in both WT controls (squares) and with gene deletion (triangles); 7 mice/group; **, P < 0.01 by repeated measures ANOVA for ipsilateral vs. contralateral hindpaws of WT.

Deletion of Tprm4/TRPM4

As shown above, sciatic n. cuffing was associated with upregulation of SUR1-TRPM4 in ipsilateral dorsal horn astrocytes. To assess the possible involvement of TRPM4 in neuropathic pain, mice with global deletion of Trpm4/TRPM4 and littermate WT controls underwent sciatic n. cuffing. In littermate controls, sciatic n. cuffing gave rise to mechanical allodynia involving the ipsilateral hindpaw that developed over the course of 7 days and persisted on testing at pod-14 (Figure 3(c)). In mice with global deletion of Trpm4/TRPM4, allodynia of the ipsilateral hindpaw to mechanical stimuli failed to develop, and withdrawal thresholds were not different from those of the contralateral uninjured hindpaw (Figure 3(c)). On testing for thermal sensitivity, the ipsilateral hindpaw of controls exhibited significant thermal hyperalgesia (Figure 3(d)), whereas mice with global deletion of Trpm4/TRPM4 exhibited ipsilateral thermal sensitivity that was not different from the contralateral uninjured hindpaw (Figure 3(d)).

Glibenclamide—Prophylactic treatment

The salutary effects of genetic deletion of Abcc8 suggested that pharmacological inhibition of SUR1 by glibenclamide might be beneficial. Moreover, glibenclamide is a potent blocker of SUR1-TRPM4 channls. ²⁹ Normally the blood-brain/blood-spinal barrier (BSB) is not permeable to glibenclamide. ⁵⁴ However, PNI leads to neuroinflammation in the dorsal horn^12,13 that is characterized by a BSB that is leaky, which allows the extravasation of serum proteins that persists for 4–8 weeks^6,7 and may facilitate the targeted entry of therapeutic drugs. Here, we confirmed that sciatic n. cuffing leads to BSB opening in the dorsal horn 2 weeks post-PNI, as shown by leakage of circulating IgG, and that the entry of glibenclamide into the involved tissues was facilitated (Figure 4(a) to (c)).

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Figure 4.

Single-dose glibenclamide enters the dorsal horn after PNI, but does not affect pain behaviors. (a) After sciatic n. cuffing, BSB leakage is shown by IgG extravasation in the ipsilateral dorsal horn (red). (b) Fluorescent bodipy-glibenclamide enters the ipsilateral (PNI) but not contralateral (Contra) dorsal horn at the level indicated by line in (a). (c) Quantification for extravasated IgG and bodipy-glibenclamide in the dorsal horn; 3 mice/group; **, P < 0.01. (d) Mechanical sensitivity tested using von Frey filaments in normal uninjured WT mice before and after administering vehicle (black filled square) or single-dose glibenclamide (green empty circles), and in the ipsilateral hindpaw of mice with established mechanical allodynia due to sciatic n. cuffing after administering single-dose glibenclamide (green filled circle); 3 mice/group, uninjured; 5 mice/group, mechanical allodynia.

Glibenclamide, when tested as a single-dose injection in the acute setting, has been used in neuropathic pain models with nerve injury to explore involvement of K_ATP channels in the mechanism of action of analgesics.^18–28 In these studies, single-dose glibenclamide had no effect on pain thresholds in the absence of analgesic, a finding that we confirmed here. Uninjured WT mice and WT mice with mechanical allodynia due to sciatic n. cuffing were administered a single dose of glibenclamide and were tested acutely using von Frey filaments. No effect of glibenclamide was detected following single-dose drug injection (Figure 4(d)).

In contrast to single-dose administration, a regimen of repeated daily dosing of glibenclamide over the course of many days is required to reduce neuroinflammation linked to astrocyte upregulation of SUR1 in the spinal cord.^35,36 Here, we assessed the effect of glibenclamide on neuropathic pain behaviors when drug was administered prophylactically, beginning on the day of PNI and repeated daily until the end of the experiment.

WT mice underwent sciatic n. cuffing and were randomly assigned to receive either vehicle or glibenclamide (10 µg IP) daily. In controls, sciatic n. cuffing gave rise to mechanical allodynia involving the ipsilateral hindpaw that developed during the first 7 days and persisted on testing at pod-14 (Figure 5(a)). In mice treated daily with glibenclamide, allodynia of the ipsilateral hindpaw to mechanical stimuli failed to develop, and withdrawal thresholds were not different from those of the contralateral uninjured hindpaw (Figure 5(a)).

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Figure 5.

Repeated-dose glibenclamide, administered either prophylactically or therapeutically, impedes or reverses the development of pain behaviors after PNI. (a) and (b) WT mice underwent sciatic n. cuffing on pod-0 and were tested for mechanical sensitivity using von Frey filaments (a) and for thermal sensitivity using the automated Hargreaves test (b) on the days denoted on the abscissas; the mice received daily administration of vehicle (red squares) or glibenclamide (green triangles); ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws were tested in both vehicle- (squares) and glibenclamide- (triangles) treated animals; 5 mice/group; **, P < 0.01 by repeated measures ANOVA for ipsilateral hindpaws of vehicle vs. glibenclamide. (c) and (e) Double immunolabeling for GFAP (red) plus IL-6 (c), CCL2 (d) or CXCL1 (e), ipsilateral (PNI) and contralateral (CTR) to PNI, in untreated WT mice. (f) Quantification in the GFAP-positive region of interest for IL-6, CCL2 and CXCL1 in untreated WT (PNI) mice and mice treated daily with glibenclamide (GLIB) ipsilateral to PNI; tissues were from the experiment in Panels A,B; 5 mice/group; **, P < 0.01. (g) WT mice underwent sciatic n. cuffing on pod-0 and on pod-21 began daily administration of vehicle (red squares) or glibenclamide (green triangles); mechanical sensitivity of ipsilateral (filled symbols) and contralateral (empty symbols) hindpaws was tested using von Frey filaments on the days denoted on the abscissa; 5 mice/group; **, P < 0.01 by repeated measures ANOVA for ipsilateral hindpaws of vehicle vs. glibenclamide.

The same mice were tested for thermal sensitivity. Compared to the contralateral hindpaw, the ipsilateral hindpaw of both vehicle controls and glibenclamide-treated animals exhibited significant thermal hyperalgesia on pod-7 (Figure 5(b)). However, by pod-14 glibenclamide-treated mice showed normal thermal sensitivity that was not different from the contralateral uninjured hindpaw, whereas vehicle-treated mice continued to show ipsilateral thermal hyperalgesia (Figure 5(b)).

Glibenclamide and neuroinflammation

After PNI, dorsal horn astrocytes exhibit a chronic activation state characterized by secretion of numerous pro-inflammatory cytokines, chemokines and other factors, including IL-6,^55–57 CCL2^58–60 and CXCL1.^61–64 Blockade of each of these individually results in significant attenuation of pain behaviors.

We studied tissues from mice from the foregoing experiment administered daily glibenclamide vs. vehicle. The involved spinal cord segment was immunolabeled for GFAP and co-labeled for either IL-6, CCL2 or CXCL1. After sciatic n. cuffing, ipsilateral but not contralateral dorsal horn astrocytes, identified by GFAP immunolabeling, showed prominent upregulation of IL-6, CCL2 and CXCL1 (Figure 5(c) to (e)), as reported.^{55,56,60–62,64} Co-labeling with Iba1 showed that cytokine and chemokine expression was absent in microglia/macrophages (not shown). The dorsal horns of mice administered glibenclamide showed less prominent immunolabeling for IL-6, CCL2 and CXCL1. Quantification of IL-6, CCL2 and CXCL1 immunoreactivity showed significant increases in vehicle-treated mice with sciatic n. cuffing compared to uninjured controls, and significantly smaller increases in mice with sciatic n. cuffing treated daily with glibenclamide (Figure 5(f)).

Glibenclamide—Therapeutic treatment

To examine a clinically relevant scenario, we studied the effect of glibenclamide when administered beginning after mechanical allodynia was established. WT mice underwent sciatic n. cuffing, following which mechanical allodynia involving the ipsilateral hindpaw developed over the course of 7 days and persisted unabated through to pod-21 (Figure 5(g)). Mice then were assigned randomly to receive either vehicle or glibenclamide (10 µg IP), beginning on pod-21 and repeated daily until the end of the experiment on pod-45. Vehicle-treated mice showed no extinction, continuing to exhibit mechanical allodynia for the full 45 days of the experiment. However, over the course of the next 14 days, mice receiving glibenclamide daily gradually reverted to mechanical sensitivity similar to the contralateral hindpaw (Figure 5(g)).

Glibenclamide vs. KATP in pain models

The effects of glibenclamide on sensory thresholds and pain are complex and context dependent. A considerable body of work has implicated the L-arginine/nitric oxide/cyclic GMP/K_ATP channel pathway in the mechanism of action of numerous analgesics, with glibenclamide and other SUR agonists and antagonists being used to implicate K_ATP channels. In models with neuropathic pain induced by chronic sciatic n. constriction or L5-L6 spinal n. ligation, single-dose administration of glibenclamide invariably blunted the anti-allodynic effects of numerous analgesics, including: gabapentin, ¹⁸ R-PIA, ¹⁹ mangiferin, ²⁰ Angeli’s salt, ²¹ nefopam ²² diosmin, ²³ zerumbone, ²⁴ [6]-gingerol, ²⁵ curcumin, ²⁶ JM-20 ²⁷ and astragaloside IV. ²⁸ However, in nearly all of these studies, when controls were performed without analgesic, it was found that pain thresholds were not affected by single-dose glibenclamide administered either intraperitoneally or intrathecally. Similarly, in a study not involving analgesics, whereas intraplantar or intrathecal injection of SUR1-subtype K_ATP channel agonists (diazoxide and NN414) reduced mechanical sensitivity after PNI, glibenclamide, as well as other K_ATP antagonists (tolbutamide, gliclazide) had no significant effect on mechanical or thermal thresholds. ¹⁷ In accordance with the foregoing, here we showed that a single dose of glibenclamide (10 µg IP; ∼0.3 mg/kg) had no effect on acute pain behaviors in either uninjured mice or mice with allodynia. Together, these findings indicate that, while K_ATP channels are important for the analgesic effect of many compounds, and may contribute to mechanical sensory thresholds, K_ATP channels may not be dominant under basal conditions of neuropathic pain.

Chronically activated, pro-inflammatory secretory phenotype

Neuroinflammation linked to glial cell activation is increasingly recognized to play a prominent role in the initiation and maintenance of pain hypersensitivity.^9–13 Microglia, astrocytes, and oligodendrocytes modulate CNS inflammation triggered by PNI. ⁶⁵ After PNI, dorsal horn astrocytes exhibit a chronically activated, pro-inflammatory secretory (CAPS) phenotype that is induced by activated microglia and damaged neurons. ⁹ The astrocytic CAPS phenotype is characterized by chronic activation and secretion of pro-inflammatory cytokines (TNF, IL-1β, IL-6), chemokines (CCL2, CCL7, CXCL1) and other factors.^66,67 Among the many factors secreted by astrocytes, several stand out including IL-6,^55–57 CCL2^58–60 and CXCL1.^61–64 In neuropathic pain models, blockade or gene deletion of each of these individually results in significant attenuation of pain behaviors. A major consequence of the astrocytic CAPS phenotype is neuroinflammation and neuronal hyperactivation. Chemokines such as CCL2 and CXCL1 are best known for recruiting leukocytes, but they also act on their cognate receptors, CCR2 and CXCR2, expressed on dorsal horn neurons (astrocyte-to-neuron signaling), resulting in synaptic hyperexcitability in the dorsal horn that leads to hypersensitivity following PNI.^9,68

Repeated dosing with glibenclamide

In different mouse models with neuroinflammation involving spinal cord astrocytes, neuroinflammation and its associated neurofunctional phenotype may be gradually extinguished by repeated daily dosing with glibenclamide. In a murine model of multiple sclerosis (MS) – experimental allergic encephalomyelitis (EAE) induced by myelin oligodendrocyte glycoprotein (MOG)_35–55 – repeated daily administration of glibenclamide beginning 24 days after MOG_35–55 immunization, well after clinical symptoms had plateaued, improved clinical motor function and reduced the expression of the proinflammatory factors TNF, BAFF, CCL2 and NOS2 in GFAP-positive astrocytes in the spinal cord.^35,36 Here we show that, in the sciatic n. cuff model of neuropathic pain, repeated daily administration of glibenclamide beginning 21 days after PNI, well after mechanical allodynia had developed, improved pain behaviors and, when used prophylactically, reduced the expression of the proinflammatory factors IL-6, CCL2 and CXCL1 in GFAP-positive astrocytes in the spinal cord. In both the EAE and PNI models, the effects of repeated prophylactic dosing with glibenclamide on GFAP-linked neuroinflammation and the associated neurofunctional phenotype were replicated by global deletion of Abcc8 and, as shown here, by pGfap-cre-driven Abcc8 deletion. These observations underscore the important pathological consequences of astrocytes that exhibit the CAPS phenotype, and the importance of SUR1 in sustaining this pathological astrocytic phenotype.

We did not examine the effect of sex in our experiments. Notably, sex differences in K_ATP subunit expression and sex-specific responses to K_ATP agonists have been reported in the trigeminal ganglion. ⁶⁹ However, previous work indicates that spinal microglia, not spinal astrocytes, are the dominant cell type in sex-dependent glial signaling in pathological pain, with treatments that target astrocytes showing similar efficacy in both sexes. ⁷⁰ The present work on neuroinflammation linked to spinal cord astrocytes in PNI, all carried out in males, and the previous work on neuroinflammation linked to spinal cord astrocytes in EAE, all carried out in females,^35,36 show that Abcc8/SUR1 is a druggable target in chronically activated astrocytes of both sexes.

The mechanism by which repeated dosing of glibenclamide and Abcc8 suppression reduce the expression of pro-inflammatory cytokines/chemokines by astrocytes in vivo remains to be elucidated, but may involve transcription that is regulated by intracellular calcium, such as nuclear factor of activated T-cells. ³² A transcriptional mechanism was previously implicated for glibenclamide inhibition of cytokine/chemokine expression by reactive astrocytes in vitro. ³⁶