Glucocorticoid regulation of ATP release from spinal astrocytes underlies diurnal exacerbation of neuropathic mechanical allodynia

Koyanagi, Satoru; Kusunose, Naoki; Taniguchi, Marie; Akamine, Takahiro; Kanado, Yuki; Ozono, Yui; Masuda, Takahiro; Kohro, Yuta; Matsunaga, Naoya; Tsuda, Makoto; Salter, Michael W.; Inoue, Kazuhide; Ohdo, Shigehiro

doi:10.1038/ncomms13102

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Published: 14 October 2016

Glucocorticoid regulation of ATP release from spinal astrocytes underlies diurnal exacerbation of neuropathic mechanical allodynia

Satoru Koyanagi^1,2^na1,
Naoki Kusunose¹^na1^nAff9,
Marie Taniguchi¹,
Takahiro Akamine¹,
Yuki Kanado¹,
Yui Ozono³,
Takahiro Masuda⁴,
Yuta Kohro⁴,
Naoya Matsunaga^1,2,
Makoto Tsuda⁴,
Michael W. Salter ORCID: orcid.org/0000-0001-6897-6585^5,6,7,
Kazuhide Inoue³ &
…
Shigehiro Ohdo¹

Nature Communications volume 7, Article number: 13102 (2016) Cite this article

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Abstract

Diurnal variations in pain hypersensitivity are common in chronic pain disorders, but the underlying mechanisms are enigmatic. Here, we report that mechanical pain hypersensitivity in sciatic nerve-injured mice shows pronounced diurnal alterations, which critically depend on diurnal variations in glucocorticoids from the adrenal glands. Diurnal enhancement of pain hypersensitivity is mediated by glucocorticoid-induced enhancement of the extracellular release of ATP in the spinal cord, which stimulates purinergic receptors on microglia in the dorsal horn. We identify serum- and glucocorticoid-inducible kinase-1 (SGK-1) as the key molecule responsible for the glucocorticoid-enhanced release of ATP from astrocytes. SGK-1 protein levels in spinal astrocytes are increased in response to glucocorticoid stimuli and enhanced ATP release by opening the pannexin-1 hemichannels. Our findings reveal an unappreciated circadian machinery affecting pain hypersensitivity caused by peripheral nerve injury, thus opening up novel approaches to the management of chronic pain.

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Introduction

A variety of pathological conditions exhibit profound day–night changes in the symptom intensity with a large portion exacerbating and occurrence of grave events. Diurnal alterations in pain hypersensitivity have been confirmed in patients with cancer^1,2, rheumatoid arthritis³, diabetic neuropathy⁴, fibromyalgia⁵ and multiple sclerosis⁶; however, the underlying mechanism remains unknown.

Pain hypersensitivity is often caused by peripheral nerve injury, which is associated with the hyperexcitability of neurons in the dorsal horn of the spinal cord^7,8,9. Extracellular ATP in the spinal cord has been implicated in the development and maintenance of pain hypersensitivity after nerve injury^{10,11,12,13,14}. This pain hypersensitivity is even evoked by a simple touch, pressure from clothing or gentle massage, which is also known as ‘mechanical allodynia’^15,16.

In mammals, diurnal rhythms in physiological functions are governed by an internal self-sustained molecular oscillator referred to as the circadian clock^16,17. The circadian clock system in mammals is composed of a master pacemaker, which is located in the suprachiasmatic nuclei (SCN) of the anterior hypothalamus, and subsidiary oscillators in other brain regions, as well as many peripheral tissues^18,19. The times of the day-dependent changes in the secretion of glucocorticoids from the adrenal glands are controlled by the SCN²⁰, which, in turn, synchronizes subsidiary oscillators to coordinate various biological processes, thereby generating daily rhythms in physiology and behaviour^21,22.

Since the glucocorticoid receptor (GCR) is expressed in most cell types, including spinal neurons, microglia and astrocytes^23,24,25, we investigated whether the diurnal secretion of adrenal glucocorticoids affects the threshold of mechanical allodynia in peripheral nerve-injured mice. Temporal elevations in glucocorticoid levels enhance the extracellular release of ATP in the spinal cord, which stimulates purinergic receptors on microglia in the dorsal horn. The stimuli of purinergic receptors decrease the threshold of mechanical allodynia. Serum- and glucocorticoid-inducible kinase-1 (SGK-1) mediates the glucocorticoid-enhanced release of ATP from astrocytes by opening the pannexin-1 hemichannels. Therefore, our findings reveal an underlying mechanism of diurnal exacerbation of neuropathic mechanical allodynia and also provide novel approaches to the management of chronic pain.

Results

Glucocorticoids govern diurnal exacerbation of mechanical allodynia

To determine the pathological relevance of the diurnal secretion of adrenal glucocorticoids in neuropathic hypersensitivity, we investigated the influence of adrenalectomy on the threshold of mechanical allodynia in nerve-injured mice. To achieve this, we prepared adrenalectomized (ADX) and sham-operated (sham) male ICR mice (Fig. 1). To induce neuropathic pain hypersensitivity, ADX mice underwent partial sciatic nerve ligation (PSL) in the right hindlimb. PSL is a well-established nerve injury model which produces pain hypersensitivity lasting >3 weeks²⁶. All animals were maintained on a 12-h light–dark cycle (ZT, zeitgeber time; ZT0, lights on; ZT12, lights off). Plasma CORT (corticosterone) concentrations in animals that had not been subjected to nerve injury—naive mice—showed significant diurnal oscillations (F_5,30=13.128, P<0.001; Fig. 1a, upper panel). The CORT levels increased from the late light phase to the early dark phase. A significant diurnal oscillation in plasma CORT levels was also observed in male sham+PSL mice on day 7 after nerve injury (F_5,30=6.592, P<0.001; Fig. 1b, upper panel). No significant differences were observed in the rhythmicity of plasma CORT levels between sham+PSL and naive male mice.

**Figure 1: Glucocorticoids regulate the diurnal oscillations in the threshold of mechanical allodynia in PSL mice.**

We found that the withdrawal threshold of the ipsilateral hindpaw, but not that of the contralateral hindpaw, of male sham+PSL mice exhibited a significant diurnal oscillation (F_5,30=5.482, P=0.011; Fig. 1b, lower panel). By contrast, no diurnal variation was noted in the paw withdrawal threshold in male naive mice (Fig. 1a, lower panel). The lowest level of paw withdrawal, that is, maximum pain hypersensitivity, in male sham+PSL mice occurred from the late light phase to the early dark phase (Fig. 1b, lower panel). The trough level of paw withdrawal corresponded to the peak in plasma CORT levels in male sham+PSL mice. This inverse relationship was observed between the threshold of mechanical allodynia and plasma CORT levels, for the entire 3-week observation period after PSL (Fig. 1e).

In contrast to naive and sham+PSL mice, there was no diurnal oscillation in plasma CORT levels male ADX+PSL mice (F_5,24=1.271, P=0.309; Fig. 1c, upper panel); CORT levels remained low throughout the day. Furthermore, the withdrawal threshold of the ipsilateral hindpaw in male ADX+PSL mice did not decrease even after nerve injury (F_5,24=1.131, P=0.371; Fig. 1c, lower panel), which was similar to the paw withdrawal threshold in the contralateral side. Although we continued to assess the paw withdrawal threshold of male ADX+PSL mice for 3 weeks after nerve injury, no decreases in the pain threshold were observed during the duration of the experimental period (Fig. 1f).

To determine whether pain hypersensitivity could be reproduced in male ADX+PSL mice, we administered CORT (500 μg kg⁻¹ h⁻¹, s.c.) to animals starting 3 days after PSL. We found that the withdrawal threshold of the ipsilateral paw decreased to a level that was not different from the minimum level in sham+PSL mice (Fig. 1d). By contrast, the administration of CORT had no effect on the withdrawal threshold in the contralateral paw. In these experiments, CORT was administered continuously and neither plasma CORT levels nor the withdrawal threshold of the ipsilateral hindpaw in CORT-administered male ADX+PSL mice showed a significant diurnal oscillation (F_5,24=1.073, P=0.408 for CORT levels, F_5,24=0.591, P=0.707 for pain threshold; Fig. 1d). We also detected significant diurnal variations in the threshold of pain hypersensitivity of female sham+PSL mice (Supplementary Fig. 1). Consistent with males, diurnal variations in pain intensity was dampened by adrenalectomy. Therefore, the decrease observed in the threshold of pain hypersensitivity in PSL mice and the diurnal variations in the hypersensitivity appeared to be dependent on diurnal oscillations in glucocorticoid levels.

Since purinergic receptors on microglia in the spinal cord are responsible for the induction of pain hypersensitivity evoked by a peripheral nerve injury^12,13, the stimulation of spinal microglia by ATP is required for the development and maintenance of neuropathic pain hypersensitivity. Although an increase in the number of Iba1-positive cells, a marker of microglia, was observed in the ipsilateral side of the spinal cord in male sham+PSL mice (F_7,32=6.550, P<0.001; Fig. 2a), no significant time-dependent changes were noted in the number of Iba1-positive cells. We also detected elevations in the mRNA levels of interferon regulatory factor 8 (Irf8; F_7,36=13.307, P<0.001; Fig. 2c), P2ry6 (F_7,36=7.586, P<0.001; Fig. 2f) and P2ry12 (F_7,36=9.544, P<0.001; Fig. 2g). We found no change in the mRNA levels for GCR encoded by Nr3c1 gene (F_7,36=0.347, P=0.926; Fig. 2b), P2rx4 (F_7,36=1.325, P=0.267; Fig. 2d) or P2rx7 (F_7,36=0.809, P=0.586; Fig. 2e) in the ipsilateral side of the spinal cord in male sham+PSL mice; moreover, their mRNA levels did not show significant time-dependent variations. A significant time-dependent variation in CORT levels was also detected in the spinal cord of male sham+PSL mice (Supplementary Fig. 2; Supplementary Method). Time-dependent increases and decreases in CORT levels in the spinal cord were similar to those observed in plasma. Although the time-dependent variations in CORT levels in the spinal cord was dampened in male ADX+PSL mice (Supplementary Fig. 2), adrenalectomy had a negligible effect on the PSL-induced increase in the number of Iba1-positive cells, as well as the expression of neuropathic pain-related genes in the ipsilateral side of the spinal cord. We also found an increase in the mRNA levels for Irf8, P2ry6 and P2ry12 in the inpsilateral spinal cord of female sham+PSL mice, and the PSL-induced molecular alterations were not modified by adrenalectomy (Supplementary Fig. 3). These results indicate that temporal elevations in glucocorticoid levels cause the diurnal oscillations in the threshold of pain hypersensitivity without affecting morphological or molecular alterations in spinal microglia.

**Figure 2: Morphological and molecular alterations in the spinal cords of PSL mice.**

Glucocorticoids enhance ATP release from the spinal cord

Extracellular ATP in the spinal cord has been implicated in the development and maintenance of pain hypersensitivity after nerve injury^10,11,12,13. Therefore, we also investigated whether temporary changes in glucocorticoid levels affected extracellular ATP release in the spinal cord of PSL mice. We prepared contralateral and ipsilateral spinal slices from L4-L5 lumbar segments of sham+PSL and ADX+PSL male mice at six different time points. The amount of ATP in the perfusate of the slices after incubation for 20 min was measured as an increase in ATP release. The increased amount of ATP was normalized to protein contents of the slices. The release of ATP from spinal slices prepared from male sham+PSL mice exhibited a significant diurnal oscillation with a peak from the late light phase to the early dark phase (F_5,30=2.552, P=0.035 for the ipsilateral side; F_5,30=2.049, P=0.048 for the contralateral side; Fig. 3a, left panel). Similar time-dependent variations were also detected in ATP concentrations in the cerebrospinal fluid (CSF) of sham+PSL mice (P<0.05; Supplementary Fig. 4a; Supplementary Method). This may have been due to diurnal variations in the release of ATP from cells in the spinal cord. The rhythmic pattern of spinal ATP release in male sham+PSL mice resembled the overall oscillation in plasma and spinal CORT levels (Fig. 1b upper panel and Supplementary Fig. 2). In contrast, the oscillation in ATP release from spinal slices of male ADX+PSL mice was severely dampened (Fig. 3a, right panel); the release of ATP from both the ipsilateral and contralateral sides remained low throughout the day (F_5,28=1.158, P=0.369 for the ipsilateral side; F_5,28=0.492, P=0.779 for the contralateral side). Time-dependent variations in ATP concentrations in the CSF were also diminished in female ADX+PSL mice (Supplementary Fig. 4b). Since the single subcutaneous administration of CORT (30 mg kg⁻¹) to male ADX+PSL mice significantly enhanced ATP release from the ipsilateral and contralateral spinal slices (F_3,16=3.755, P=0.042 for the ipsilateral side, F_3,16=4.933, P=0.018 for the contralateral side; Fig. 3b), diurnal changes in glucocorticoid levels appear to govern the time-dependent oscillations in extracellular ATP release in the spinal cord.

**Figure 3: Glucocorticoids decrease the threshold of mechanical allodynia in PSL mice via P2Y₁₂ receptor in the ipsilateral spinal cord.**

The administration of CORT to male ADX+PSL mice significantly enhanced ATP release from both the ipsilateral and contralateral sides of the spinal cord. However, the withdrawal threshold of the ipsilateral hindpaw only decreased significantly after the administration of CORT (F_6,35=2.356, P=0.042 for the ipsilateral side; F_6,35=1.075, P=0.396 for the contralateral side; Fig. 3c). Due to the ability of glucocorticoids to enhance ATP release as well as produce mechanical allodynia in ADX+PSL mice, we also examined whether ATP was involved in the glucocorticoid-induced decrease in the threshold of pain hypersensitivity. The single intrathecal injection of ATP (30 nmol per mouse) to male ADX+PSL mice transiently, but significantly decreased the withdrawal threshold of the ipsilateral hindpaw (F_6,49=3.964, P=0.002; Fig. 3d); however, ATP-induced decreases in the withdrawal threshold were not detected in the contralateral hindpaw (F_6,49=0.518, P=0.792). Taken together, these results indicate the possibility that glucocorticoids decrease the threshold of mechanical allodynia in PSL mice by enhancing the extracellular release of ATP in the spinal cord.

To explore this possibility, we investigated whether CORT-evoked mechanical allodynia in ADX+PSL mice was attenuated by antagonists of purinergic receptors. In this experiment, all antagonists were intrathecally injected into ADX+PSL mice at 1 h before the administration of CORT (30 mg kg⁻¹, s.c.). The withdrawal threshold of ispilateral hindpaw of male ADX+PSL mice after the CORT treatment was significantly decreased (F_23,90=1.012, P=0.046; Fig. 3e), which was consistent with the results described above. The CORT-induced decrease in the pain threshold of the ipsilateral hindpaw in male ADX+PSL mice was prevented by pretreatment with the P2Y₁₂ receptor antagonists, AR-C69931 (ref. 13) or AZD6140 (ref. 27) (P<0.05, respectively). On the other hand, neither 2′,3′-O-(2,4,6-trinitrophenyl) adenosine 5-triphosphate (TNP-ATP) (ref. 12), an antagonist of P2X1–4 receptors, nor MRS2578 (ref. 28), an antagonist of P2Y₆ receptor, suppressed CORT-evoked mechanical allodynia in male ADX+PSL mice (Fig. 3f). The single intrathecal injection of AR-C69931 or AZD6140 also prevented PSL-induced decreases in the withdrawal threshold of ipsilateral hindpaw of male mice (F_14,75=1.965, P=0.033; Fig. 3g). We also found that the P2Y₁₂ receptor antagonists, AR-C69931, alleviated CORT- or PSL-induced mechanical allodynia in female mice (Supplementary Fig. 5). Since, the mRNA levels of P2ry12 were significantly elevated in the ipsilateral spinal cord of both male and female ADX+PSL mice (Fig. 2g), P2Y12 receptors appeared to be involved in the glucocorticoid-induced decrease in the threshold of mechanical allodynia in ADX+PSL mice.

Glucocorticoids induce exacerbation of mechanical allodynia via SGK-1

Glucocorticoids modulate the physiology of the cell by activating or repressing the expression of its target genes²⁹. Therefore, we hypothesized that glucocorticoids caused diurnal oscillations in spinal ATP release by inducing specific genes. To screen for glucocorticoid-regulated genes whose expression in the spinal cord exhibited diurnal oscillations, we performed oligonucleotide microarray analyses using RNA isolated from the spinal cords of male sham+PSL or ADX+PSL mice at ZT10 and ZT22, times at which plasma glucocorticoid levels in sham+PSL mice peaked and declined, respectively (Fig. 1b). Three criteria were applied to select diurnal cycle-dependent glucocorticoid-regulated genes in the spinal cord. (1) Sham+PSL at ZT10>Sham+PSL at ZT22; (2) ADX+PSL at ZT10≒ADX+PSL at ZT22; and (3) Sham+PSL>ADX+PSL. From this analysis, we identified 25 genes as candidates for diurnal time-dependent glucocorticoid-regulated genes expressed in the spinal cord (Table 1). The glucocorticoid-regulated gene Sgk-1 was included as a diurnal time-dependent spinal gene. Since typical glucocorticoid response elements are located in the upstream promoter region of both mouse and human Sgk-1 genes, we focused on this gene to examine whether SGK-1 was involved in the glucocorticoid-regulated diurnal release of ATP in the spinal cord as well as time-dependent oscillations in the threshold of mechanical allodynia in PSL mice.

Table 1 Candidates for glucocorticoid-regulated genes in spinal cords of mice.

Full size table

The expression of Sgk-1 mRNA and its protein exhibited a significant diurnal oscillations in both the ipsilateral (F_5,24=33.233, P<0.001 for mRNA; F_5,24=4.808, P=0.006 for protein) and contralateral (F_5,24=14.996, P<0.001 for mRNA; F_5,24=4.591, P=0.007 for protein) sides of the spinal cord of male sham+PSL mice (Fig. 4a). However, oscillations were not detected in the ipsilateral (P=0.995 for mRNA, P=0.979 for protein) side of male ADX+PSL mice (Fig. 4b). Disruption of diurnal variation in Sgk-1 mRNA levels was also detected in female ADX+PSL mice (Supplementary Fig. 6). The results of the chromatin immunoprecipitation analysis indicated that diurnal oscillations in the spinal expression of Sgk-1 were associated with enhanced binding of the GCR to the promoter region of the gene (Fig. 4c). The induction of the spinal expression of Sgk-1 and enhancements in GCR binding to the promoter region were also detected when male ADX+PSL mice were subcutaneously administered with 30 mg kg⁻¹ CORT (Supplementary Fig. 7). The single intrathecal injection of the SGK-1 inhibitor GSK650394 (0.5 nmol per mouse) to male sham+PSL mice increased the threshold of mechanical allodynia (F_9,40=8.876, P<0.001; Fig. 4d), and this was accompanied by the suppression of extracellular ATP release in the spinal cord (F_3,16=12.454, P<0.001). Furthermore, the intrathecal injection of GSK650394 (0.5 nmol per mouse) to male ADX+PSL mice prevented the CORT-induced decrease in the threshold of mechanical allodynia (F_23,96=3.599, P<0.001), as well as spinal ATP release (F_7,36=5.735, P<0.001; Fig. 4e). Similar inhibitory effects of GSK650394 on CORT- or PSL-induced mechanical allodynia were also observed in female mice (Supplementary Fig. 5). These results suggest that the glucocorticoid-induced exacerbation of neuropathic pain hypersensitivity depends on SGK-1.

**Figure 4: SGK-1 mediates the glucocorticoid-regulated diurnal oscillations in the threshold of mechanical allodynia in PSL mice.**

SGK-1 mediates the glucocorticoid-enhanced ATP release from astrocytes

In an attempt to identify the types of cells expressing SGK-1, we performed double immunofluorescence labelling for SGK-1 and cell type-specific markers: for neurons, neuronal nuclei (NeuN); for microglia, CD11b; and for astrocytes, glial fibrillary acidic protein (GFAP). In the dorsal horn of the spinal cord in male sham+PSL mice, cells showing SGK-1 immunofluorescence were not double-labelled for NeuN or CD11b (Fig. 5a). Instead, most SGK-1-positive cells were double-labelled with GFAP, and their number in the dorsal horn was significantly higher at ZT10 than at ZT22 (51.78±6.11% for ZT10; 20.42±4.22% for ZT22; n=5, mean±s.e.m.; t₈=4.031, P=0.004, unpaired t-test, two-sided). Consistent with previous observation¹⁴, the immunoreactivity of GFAP were significantly increased in the ipsilateral spinal cord of male sham+PSL mice, whereas the number of GFAP-positive cells were similar between the two time points (Supplementary Fig. 8). Therefore, SGK-1 in the spinal cord of PSL mice appears to be mainly expressed in astrocytes and exhibits diurnal variation. The treatment of primary cultures of astrocytes with 100 ng ml⁻¹ CORT significantly induced the expression of Sgk-1 mRNA (F_11,48=25.461, P<0.001; Fig. 5b), and this was suppressed by a concomitant treatment with the GCR antagonist RU486 (F_2,12=55.500, P<0.001; Fig. 5c). The treatment with CORT for 4 h also enhanced ATP release from astrocytes (F_5,24=6.175, P=0.017; Fig. 5d). The enhancing effects of CORT appeared to be mediated by SGK-1, because the treatment of cells with GSK650394 resulted in the suppression of the CORT-induced release of ATP (P<0.01). The ability of SGK-1 to enhance ATP release from astrocytes was further confirmed by the transfection of cells with Sgk-1-expressing vectors (Fig. 5e). The amount of ATP released from Sgk-1-expressing vector-transfected cells was approximately five-fold higher than that from empty (pcDNA3.1) vector-transfected cells (F_2,12=13.508, P=0.002). The enhancing effect of SGK-1 was also prevented in cells treated with GSK650394 (P<0.05).

**Figure 5: The expression of SGK-1 enhances ATP release from astrocytes.**

SGK-1 enhances ATP release from astrocytes via pannexin-1

Several possible pathways have been suggested for ATP release in astrocytes^30,31. To identify which pathway is involved in the SGK-1-induced enhancement in ATP release, we tested the sensitivity of CORT-treated astrocytes to inhibitors on the proteins contributing to possible ATP-releasing pathways. As demonstrated above (Fig. 5d), a significant increase in ATP release from astrocytes was detected when cells were treated with 100 ng ml⁻¹ CORT for 4 h (P<0.05, F_9,45=3.094, P=0.005; ANOVA with Tukey–Kramer’s PHT; Fig. 5f). We then investigated the effects of different inhibitors by adding them to media at concentrations that were previously reported to be effective. The CORT-induced enhancement in astrocytic ATP release was unaffected by the treatments with 10 μM verapamil (P=0.999) or 1 mM probenecid (P=0.998), which are known to inhibit the transporting activity of p-glycoprotein³² and multidrug resistance protein 1 (ref. 33), respectively. Similarly, the treatment of cells with 200 μM glibenclamide, an inhibitor of the cystic fibrosis transmembrane conductance regulator anion channel³⁴, also failed to prevent the CORT-induced enhancement in ATP release (P=0.999). An inhibitor of the P2X₇ receptor (ref. 35), brilliant blue G (1 μM), did not have a significant effect on the release of ATP (P=0.778). Max-ion channels are shown to be responsible for the hypotonicity-induced ATP release from mouse astrocytes³⁶. However, the treatment of cells with 50 μM GdCl₃, an inhibitor of max-ion channels, did not suppress the CORT-induced enhancement in ATP release (P=0.989). Although no significant effects were observed when cells were treated with 2 mM 1-octanol (P=0.971), an inhibitor of connexins³⁷ or 100 μM carbenoxolone (P=0.786), an inhibitor of both connexins and pannexins³⁸, the selective pannexin-1 inhibitor, ¹⁰Panx-1 (100 μM) (ref. 39), significantly inhibited CORT-enhanced astrocytic ATP release (P<0.05). Since ¹⁰Panx-1 also inhibited the enhancement effects of SGK-1 on the astrocytic ATP release (Supplementary Fig. 9a; Supplementary Method), we further investigated the ability of this channel to mediate ATP release in response to glucocorticoids.

The treatment of primary cultured astrocytes with 100 ng ml⁻¹ CORT for 4 h did not change the protein levels of pannexin-1 (Fig. 6a) despite enhancing ATP release (t₈=3.087, P=0.021; unpaired t-test, two-sided). On the other hand, the downregulation of this hemichannel by siRNA (Fig. 6b) significantly attenuated the CORT-induced enhancement in ATP release from astrocytes (F_3,16=19.130, P<0.001; Fig. 6c). The transfection of primary cultured astrocytes with Sgk-1-expressing vectors had a negligible effect on the protein levels of pannexin-1 (Supplementary Fig. 9b). Therefore, we considered that CORT-induced SGK-1 to enhance the release of ATP from astrocytes by opening of pannexin-1 hemichannels.

**Figure 6: Induction of SGK-1 by glucocorticoid enhances ATP release from astrocytes via pannexin-1 hemichannels.**

The opening of pannexin-1 is gated by cellular signals such as membrane depolarization and intracellular calcium⁴⁰. Since SGK-1 has the ability to increase the activity of Orai1 (ref. 41), the pore-forming unit of store-operated calcium entry, we investigated whether the inhibition of Orai1-mediated intracellular calcium entry also suppressed the CORT-enhanced release of ATP from astrocytes. The results of a Fluo-8 fluorescence analysis revealed that the treatment of astrocytes with 100 ng ml⁻¹ CORT-enhanced store-operated calcium entry (Fig. 6d), and the enhancing effects of CORT were suppressed by treating of cells with 10 μM Cpd5J-4, an inhibitor on Orai1 (ref. 42). This Orai1 inhibitor also prevented the release of ATP from CORT-treated cells (F_3,16=19.323, P<0.001; Fig. 6e). Cpd5J-4 exerted similar inhibitory effects on intracellular calcium entry and ATP release were also observed in SGK-1 overexpressing astrocytes (Supplementary Fig. 10; Supplementary Method). These results suggest that glucocorticoid-induced SGK-1 enhances ATP release from astrocytes through pannexin-1 hemichannels gated by store-operated calcium entry.

Discussion

Although the extracellular ATP release in the spinal cord is considered to activate the microglia and produce neuropathic pain behaviour⁹, the results of the present study suggest that the glucocorticoid-induced release of ATP from spinal astrocytes is involved in the diurnal decrease in the threshold of mechanical allodynia in PSL mice. Astrocytes play an active role in cell-to-cell signalling in the central nervous system through their release of gliotransmitters, which form neuron–glia and glia–glia networks^31,43. Astrocytes have been shown to release ATP in response to mechanical stress, osmotic swelling, the deprivation of extracellular calcium, and stimulations with noradrenaline, nitrogen monoxide and uridine triphosphate³¹. In addition to these endogenous compounds, we found that glucocorticoids enhanced astrocytic ATP release by inducing the expression of SGK-1. A previous study reported that SGK-1 was expressed in both neurons and astrocytes⁴⁴. The L5 spinal nerve ligation (SNL) of male Sprague–Dawley rats is known to induce the phosphorylation of SGK-1 in the ipsilateral dorsal horn without changing its total protein level⁴⁵. Although there is no direct evidence for SGK-1 expression in neural cells in the spinal cord, phosphorylated SGK-1 has been suggested to be associated with mechanical allodynia in SNL rats through the activation of glutamatergic N-methyl-D-aspartate receptors⁴⁵. In the present study, we used a PSL model in mice, because they exhibited diurnal oscillations in the threshold of mechanical allodynia⁴⁶. The results of immunofluorescence analysis indicated that SGK-1 in the spinal cord of PSL mice was expressed in astrocytes rather than in neurons. Glucocorticoids have been shown to induce the expression of SGK-1 more selectively in astrocytes than in neurons⁴⁴. We detected coincident immunoreactivity for SGK-1 and GFAP in the spinal cord of sham+PSL mice around the peak time of diurnal glucocorticoid secretion. These results indicate that the diurnal expression of SGK-1 in the spinal cord is attributable to its temporal accumulation in astrocytes.

The times of the day-dependent changes in the adrenal secretion of glucocorticoids are controlled by the master circadian clock, which is located in the SCN of the hypothalamus, and, in turn, coordinates various biological processes in peripheral tissues in a diurnal cycle-dependent manner^19,20,21. The most parsimonious explanation for our results is that temporal elevations in glucocorticoid levels induce the expression of SGK-1 in spinal astrocytes, thereby enhancing extracellular ATP release through pannexin-1 hemichannels (Fig. 6f). The glucocorticoid-controlled diurnal release of ATP was detected in both contralateral and ipsilateral spinal cords of sham+PSL mice, whereas the number of microglia and expression of the P2ry12 gene increased only in the ipsilateral side. Consequently, the glucocorticoid-enhanced release of ATP from astrocytes may stimulate P2Y12 receptors on microglia in the ipsilateral spinal cord, which then evoke mechanical allodynia in the nerve-injured hindpaw during a certain time of day.

SGK-1 is a member of the AGC kinase family and participates in the regulation of cell physiology through the phosphorylation of its target proteins⁴⁷. Since elevations in the abundance of the SGK-1 protein in cultured astrocytes had negligible effects on the membrane expression of pannexin-1, this kinase appears to enhance extracellular ATP release through the opening of pannexin-1 hemichannels. The opening of pannexin-1 is known to be gated by various cellular signals⁴⁰. As described above, SGK-1 has the ability to increase the activity of Orai1 (ref. 41). In fact, an inhibitor of Orai1 significantly suppressed the SGK-1-enhanced release of ATP from astrocytes, and this inhibitor also prevented the store-operated calcium entry. Therefore, we suggest that astrocytic ATP release by this mechanism may be responsible for the glucocorticoid-induced decrease in the threshold of mechanical allodynia in PSL mice.

The involvement of GCR in the development of mechanical allodynia has been demonstrated in rats following chronic constriction nerve injury⁴⁸. The development of pain hypersensitivity in chronic constriction nerve injury rats has been implicated in the increase in the spinal expression of GCR, which is induced by interleukin-6 and protein kinase C. We also detected significant elevations in GCR mRNA levels in the ipsilateral spinal cord of male PSL model rats (Supplementary Fig. 11; Supplementary Method); however, an increase in GCR mRNA levels was not observed in the spinal cords of PSL mice (Fig. 2b). It is therefore possible that differences among animal species is reflected in the distinct expression patterns of GCR in the spinal cords of nerve-injured rats and mice. This may also be applicable to the absence of significant alterations in the spinal expression of the P2X4 receptor in PSL mice, because we observed elevations in the mRNA levels of both P2rx4 and P2ry12 in the ipsilateral spinal cord in male PSL rats (Supplementary Fig. 11). Consistent with previous findings in rats following SNL^12,13, the development of pain hypersensitivity in PSL rats also appears to be associated with the activation of P2X₄ and P2Y₁₂ receptors in the spinal cord. Alternatively, we detected elevations in P2rx4 mRNA levels in the ipsilateral spinal cord of C57BL mice following L4 spinal nerve transection (Supplementary Fig. 12; Supplementary Method). The transection of spinal nerves also tended to increase P2rx4 mRNA expression in the ipsilateral spinal cord of ICR mice. In addition to the animal species and strain, the spinal expression of the P2X₄ receptor may also be dependent on the nerve injury procedures.

A recent study has demonstrated that microglial involvement in mechanical allodynia is dependent on sex⁴⁹. Nerve-injured female mice achieve similar levels of pain hypersensitivity as those in males, but this may be caused by proalgesic mediators released from T cells⁴⁹. We also found that diurnal variation in the threshold of pain hypersensitivity of female sham+PSL mice was dependent on diurnal oscillation in glucocorticoid levels (Supplementary Fig. 1). Glucocorticoids also play a key role in conveying circadian signals from the SCN to the immune system⁵⁰. Diurnal variations in plasma glucocorticoid levels show a negative correlation with 24-h changes in blood lymphocyte counts⁵¹. Elevations of glucocorticoid levels decrease the number of lymphocytes in the blood by enhancing the migration of these cells to tissues⁵². Time-dependent elevations in plasma CORT levels may also enhance the infiltration of immune cells into the inflammatory sites during a certain time of day, which causes diurnal variations in pain hypersensitivity in nerve-injured female mice. In addition to this possible mechanism, ATP release in the spinal cord appears to be partially involved in the mechanism underlying PSL-induced mechanical allodynia in female mice. As observed in males, female sham+PSL mice also exhibited diurnal variations in ATP concentrations in the CSF, accompanied by elevations in P2ry12 mRNA levels in the ipsilateral spinal cord (Supplementary Fig. 3 and Fig. 4). Although the anti-allodynic effects were less as compared with those observed in males, the P2Y12 receptor antagonist AR-C69931 or SGK-1 inhibitor GSK650394 alleviated CORT- and PSL-induced mechanical allodynia in female mice (Supplementary Fig. 5). Taken together, glucocorticoids may also govern diurnal variations in pain hypersensitivity in female PSL mice by controlling extracellular ATP release in the spinal cord and activation of the P2Y₁₂ receptor.

In clinical situation, high doses of synthetic glucocorticoids are used in the management of neuropathic pain⁵³. Synthetic glucocorticoids are considered to reduce the symptoms of neuropathic pain through their anti-inflammatory and immunosuppressive actions. On the other hand, the role of endogenous glucocorticoids in nerve injury-induced pain hypersensitivity had been enigmatic. Under certain conditions, physiological levels of endogenous glucocorticoids have enhancing effects on the immune system⁵⁴, while similar levels of glucocorticoids suppress autoimmune and inflammatory reactions under other conditions. These differential effects of glucocorticoids on the immune system may be due to the differences in the duration of their exposure⁵⁵.

Diurnal rhythms in pain hypersensitivity have been demonstrated clinically^1,2,3,4,5,6. However, the temporal pattern of the exacerbation of pain is distinct in a manner that is dependent on the cause of the pain. For example, cancer-associated pain is exacerbated around the morning¹ or during the daytime², but the intensity of spontaneous pain in patients with diabetic neuropathy or post-herpetic neuralgia has been reported to decrease during the night⁴. Although the rhythmic phase of adrenal glucocorticoid secretion is controlled by the circadian clock machinery, the secretion pattern is sometimes modulated under pathological conditions^56,57. The understanding of such patterns is necessary for research on the mechanisms and triggers of chronic pain, and for appropriate patient care, including optimal timing of analgesic treatment. Our findings reveal an unappreciated circadian machinery affecting pain hypersensitivity caused by peripheral nerve injury, and also provide novel approaches to the management of chronic pain.

Methods

Animals and treatments

Male ICR mice (5–6 weeks old) were housed in groups (from 6 to 10 per cage for mice and from 3 to 4 per cage for rats) in a light-controlled room (lights on from ZT0 to ZT12) at 24±1 °C and humidity of 60±10% with food and water ad libitum. We prepared ADX mice under sodium pentobarbital (40 mg kg⁻¹, i.p.) and isoflurane anaesthesia. The adrenals were removed via a dorsal approach using an aseptic technique. ADX mice were given 0.9% NaCl to drink during the duration of the experiment. Sham adrenalectomy was performed using the same procedure to expose the adrenals without their removal. Mouse models of PSL were also prepared under anaesthesia. The right thigh was shaved and the sciatic nerve was exposed through an incision. Half of the nerve was tightly ligated with 8-0 silk thread and the wound was sutured (Ipsilateral side; right hindpaw). The sciatic nerve of the left hindpaw was also exposed by the same procedure; however, the wound was sutured without nerve ligation (Contralateral side; left hindpaw). ADX+PSL mice were anaesthetized and an osmotic pump (Model 2001, Alzet, Alza Corp., Palo Alto, CA) was implanted in the subcutaneous pocket over the back. These osmotic pumps were designed to deliver a flow rate of 1 μl h⁻¹ for 7 days and were filled with CORT dissolved in water and propylene glycol (1:1 volume) with 5% DMSO and 5% ethanol. AR-C69931 (AdooQ Bioscience, Irvine, CA), AZD6140 (Cayman Chemical, Ann Arbor, MI), and TNP-ATP (Sigma-Aldrich, St Louis, MO) were dissolved in phosphate-buffered saline (PBS) with 0.01% DMSO and 0.01% ethanol. A solution of MRS2578 (Sigma-Aldrich) was prepared by dissolving in 5% DMSO and 95% olive oil. Drugs were intrathecally injected using a 30-gauge needle. A volume of 10 μl drug solution was injected over 30 s. All experimental procedures were performed under the approval and guidelines of Kyushu University.

Measurement of plasma CORT levels

Blood samples were drawn by orbital sinus collection and plasma samples were obtained after centrifugation at 3,000 r.p.m. for 3 min. CORT concentrations were measured using a corticosterone enzyme immunoassay kit (Cayman Chemical) validated for mouse plasma samples according to the manufacturer’s protocol.

Assessment of mechanical allodynia

To assess mechanical allodynia, mice were placed individually in an opaque plastic cylinder, which was placed on a wire mesh and habituated for 0.5 h to allow acclimatization to the new environment. Calibrated von Frey filaments (0.02–2.0 g, North Coast Medical) were then applied to the plantar surfaces of the hindpaws of mice. The paw withdrawal threshold was evaluated using the up-down method^12,13. Observers were blinded to the drug treatment.

Quantitative RT-PCR analysis

To extract mRNA from the spinal cord of mice, contralateral and ipsilateral spinal slices from lumbar segments L4 to L5 were prepared. RNA was extracted using RNAiso reagent (Takara Bio Inc., Osaka, Japan). cDNA was synthesized using a ReverTra Ace qPCR RT Kit (Toyobo, Osaka, Japan) and amplified by PCR. A real-time PCR analysis was performed on diluted cDNA samples using the THUNDERBIRDTM SYBR qPCR Mix (Toyobo) with the 7500 Real-time PCR system (Applied Biosystems). Data were normalized using ‘18s’ and ‘β-actin’ mRNAs as a controls because spinal expression was constant throughout the day. Primer sequences were listed in Supplementary Table 1.

Western blotting

Nuclear and cytosolic fractions of the spinal cords of mice were prepared at six time points. Membrane and cytosolic fractions of cultured astrocytes were also prepared by the same procedure. A total of 20 μg protein lysates was then resolved by 10% SDS-PAGE, transferred to a PVDF membrane, and probed with rabbit monoclonal antibodies against SGK-1 (1:1,000; ab32374, Abcam, Cambridge, UK), GCR (1:1,000; sc1002, Santa Cruz Biotechnology, Santa Cruz, CA), Pannexin-1 (1:1,000; ab124131, Abcam), Actin (1:1,000; sc1616-HRP, Santa Cruz Biotechnology) or POL2 (1:1,000; sc900, Santa Cruz Biotechnology). The specificities of antibodies for their target proteins have been validated in previous studies^58,59,60. Specific antigen–antibody complexes were visualized using horseradish peroxidase-conjugated secondary antibodies and a chemiluminescence reagent (Nacalai Tesque, Kyoto, Japan).

Measurement of ATP

To determine ATP concentrations in CSF, mice were anaesthetized using isoflurane and oxygen. CSF was collected by direct cisterna-magna puncture and diluted with 10-fold volume of artificial CSF (ACSF). The diluted samples were used for the ATP assay. Samples contaminated with erythrocytes or visibly haemolysed were not used for ATP measurements. To measure extracellular ATP release in the spinal cord, contralateral and ipsilateral spinal slices (500-μm-thick) from lumbar segments L4 to L5 were prepared and incubated in 300 μl of oxygenized ACSF for 20 min. Before and after incubation, 10 μl of ACSF was collected for the ATP assay. The residual slices in ACSF were homogenized and protein concentrations were measured using Lowry’s method (DC protein assay; Bio-Rad). An increase in the amount of ATP released from the spinal slices was expressed as nmol mg⁻¹ protein. To determine the release of ATP from cultured astrocytes, cells were seeded on 24-well culture plate and then incubated until they were in a semi-confluent state. For assessment of ATP release, culture media were replaced with 500 μl of assay butter containing 125 mM NaCl, 4.8 mM KCl, 5.6 mM D-glucose, 1.2 mM CaCl₂, 1.2 mM KH₂PO₄, 1.2 mM MgSO₄ and 25 mM HEPES (pH 7.4), and cells were incubated for 30 min. The assay buffer was also collected for the ATP assay. ATP levels were mesured using a bioluminescent ATP assay kit (Promega, Madison, WI). The ectonucleotidase inhibitor 6-N,N-diethyl-β-γ-dibromomethylene-D-adenosine-5-triphosphate FPL 67156 (ARL 67156 trisodium salt, Sigma-Aldrich) was added to ACSF or the assay buffer (100 μM final concentration) throughout the experiment to decrease ATP hydrolysis.

Microarray analysis

Spinal slices (500-μm-thick) from lumber segments L4 to L5 were prepared from sham+PSL and ADX+PSL mice at ZT10 and ZT22. Total RNA (250 ng) was extracted from these slices using RNAiso (Takara Bio Inc.). The quality of the extracted RNA was analysed using an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA). cRNA was amplified and labelled using a low-input quick amp labelling kit. Labelled cRNA was hybridized to a 44K Agilent 60-mer oligomicroarray (Whole Mouse Genome Microarray kit version 2.0) according to the manufacturer’s instructions. All hybridized microarray slides were washed and scanned using an Agilent scanner. Relative hybridization intensities and background hybridization values were calculated using Agilent Feature Extraction software (version 9.5.1.1). Raw signal intensities and flags for each probe were calculated from hybridization intensities and spot information according to the procedures recommended by Agilent. The raw signal intensities of two samples were log2-transformed and normalized by a quantile algorithm in the ‘preprocessCore’ library package of the Bioconductor software. This produced a gene expression matrix consisting of 55,681 probe sets, and differentially expressed genes between samples were selected by calculating Z-scores and ratios (non-log-scaled fold change) as follows: for upregulated genes: a Z-score of 2.0 or more and a ratio of twofold or more; and for downregulated genes: a Z-score of -2.0 or less and a ratio of 0.5 or less.

Chromatin immunoprecipitation analysis

Cross-linked chromatin in the spinal cord was sonicated on ice, and nuclear fractions were obtained by centrifugation at 10 000g for 5 min. Supernatants were incubated with antibodies against GCR (1:500; sc1002, Santa Cruz Biotechnology) or rabbit IgG (1:500; sc66931, Santa Cruz Biotechnology). DNA was purified using a DNA purification kit (Promega) and amplified by PCR for the surrounding GRE in the 5′-flanking region of the Sgk-1 gene. The primer sequences for amplification of the surrounding GRE were as follows: 5′-CTCACGTGTTCTTGGCATGG-3′ and 5′-TGGCCAAAACTAAGCAAGGC-3′. The quantitative reliability of PCR was evaluated by a kinetic analysis of the amplified products to ensure that signals were only derived from the exponential phase of amplification. This analysis also proceeded in the absence of an antibody or in the presence of rabbit IgG as negative controls. Ethidium bromide staining did not detect any PCR products in these samples.

Immunofluorescent histochemical staining

Animals were anaesthetized and perfused transcardially with 4% paraformaldehyde in PBS, pH 7.4. The L4 spinal cord was removed and postfixed at 4 °C for 5 h. The postfixed spinal cord was transferred to 15% sucrose in PBS for 24 h and then 30% sucrose in PBS for 24 h. Floating transverse sections (30-μm-thick) were blocked in solution containing 10 % normal goat serum and 0.1% Triton X-100 for 2 h at 4 °C. The sections were then incubated for 48 h at 4 °C with primary antibodies against Iba1 (1:1,000; 019-19741, Wako Pure Chemicals), SGK-1 (1:1,000; ab32374, Abcam), NeuN (1:5,000, MAB377, Millipore Bioscience Research Reagents, Temecula, CA), CD11b (1:500; MCA711G, AbD Serotec, Oxford, UK) and GFAP (1:5,000; 13-0300, Invitrogen, Carlsbad, CA). The specificities of antibodies for their target proteins have been validated in previous studies^12,13,58. After washing, the sections were incubated with a fluorescent-conjugated secondary antibody (Alexa 488 or Alexa 546, 1:1,000; Jackson ImmunoResearch, Laboratories, West Grove, PA) at 4 °C for 2 h. The sections were mounted with Vectashield (Vector Laboratories, Burlingame, CA). Fluorescent images were obtained with confocal fluorescence microscopy. The numbers of Iba1-positive microglial cells and GFAP-positive astrocytic cells were quantified with the Image J cell counter analysis tool in defined area of interest on the spinal cord dorsal horn. The score was blinded to sampling times and animal treatments.

Preparation and treatment of primary cultures of astrocytes

A dissociated cell suspension was prepared from the cerebral cortex of neonatal mouse pups (2 days old). Cells were plated in tissue culture flasks at a concentration of 1 × 10⁵ cells per ml and incubated in DMEM supplemented with 10% fetal bovine serum (FBS) and antibiotics at 37 °C in a humidified 5% CO₂ atmosphere for 72 h, which allowed the cells sufficient time to adhere and begin multiplying. Medium was changed every 72 h during the growth of cells. After incubating the primary cultures for 7–9 days, medium was changed completely and culture flasks were shaken to remove oligodendrocytes from the cultures. Fresh medium was added to the shaken flasks and the shaking process was repeated at least four times. The purification of primary cultures of astrocytes was confirmed by immunohistochemistry for the expression of GFAP. Astrocytes were treated with CORT for 4-h in the presence or absence of each inhibitor. The Sgk-1-expressing astrocytes were prepared by transfecting with Flag-tagged Sgk-1-expressing vectors, which were kindly provided by Dr Ono (Kyushu University). Vectors were transfected into cells using a squarewave electroporater (Model CUY21, Nepa Gene, Chiba, Japan). Transfection efficacy was confirmed by immunofluorescent staining by using anti-Flag monoclonal antibodies (F1804, Sigma-Aldrich). Approximately 70% of GFAP-positive cells merged with Flag-tagged SGK-1. Astrocytes were also transfected with 150 pmol siRNA against pannexin-1 (sc61288, Santa Cruz Biotechnology) using Lipofectamine 2000 reagent (Invitrogen Life Technologies) and used for experiments 72 h after transfection. The downregulated efficacy of this siRNA was confirmed, as shown in Fig. 6b.

Calcium mobilization assay

Astrocytes (2 × 10⁴) were seeded on a 96-well plate. After 24 h, CORT was added to culture media at a final concentration of 100 ng ml⁻¹. Four hours after the treatment, cells were loaded with 4 μM Fluo-8 AM (Abcam) in 100 μl of Hank’s balanced salt solution containing 20 mM HEPES (pH 7.4) supplemented with 0.04% Pluronic F-127 and 1% FBS at 37 °C for 30 min, followed by a further incubation at room temperature for 30 min. Intracellular calcium mobilization was assessed by monitoring the fluorescence intensity (excitation at 490 nm and emission at 525 nm) using FlexStation 3 (Molecular Devices, Sunnyvale, CA, USA).

Statistical and data analyses

The values presented are expressed as the means±s.e.m. The significance of the 24-h variations in each parameter was tested by ANOVA. The statistical significance of differences among groups was analysed by ANOVA followed by Tukey–Kramer’s PHT. Equal variances were not formally tested. P<0.05 was considered significant. No statistical method was used to predetermine sample sizes; however, our sample sizes were similar to those reported in previous studies^13,36,46. Experiments were not randomized.

Data availability

All data supporting the results of the present study are included in the article, either in the main figures or the Supplementary Information Files. Microarray data were submitted to the Gene Expression Omnibus at the National Center for Biotechnology Information (accession # GSE65756).

Additional information

How to cite this article: Koyanagi, S. et al. Glucocorticoid regulation of ATP release from spinal astrocytes underlies diurnal exacerbation of neuropathic mechanical allodynia. Nat. Commun. 7, 13102 doi: 10.1038/ncomms13102 (2016).

References

Gagnon, B. et al. The impact of delirium on the circadian distribution of breakthrough analgesia in advanced cancer patients. J. Pain Symptom Manage. 22, 826–833 (2001).
Article CAS Google Scholar
Saini, A. et al. Circadian variation of breakthrough pain in cancer patients. Eur. J. Pain 17, 264–270 (2013).
Article CAS Google Scholar
Yazici, Y., Pincus, T., Kautiainen, H. & Sokka, T. Morning stiffness in patients with early rheumatoid arthritis is associated more strongly with functional disability than with joint swelling and erythrocyte sedimentation rate. J. Rheumatol. 31, 1723e6 (2004).
Google Scholar
Odrcich, M., Bailey, J. M., Cahill, C. M. & Gilron, I. Chronobiological characteristics of painful diabetic neuropathy and postherpetic neuralgia: diurnal pain variation and effects of analgesic therapy. Pain 120, 207–212 (2006).
Article Google Scholar
Bellamy, N., Sothern, R. B. & Campbell, J. Aspects of diurnal rhythmicity in pain, stiffness, and fatigue in patients with fibromyalgia. J. Rheumatol. 31, 379–389 (2004).
PubMed Google Scholar
Solaro, C., Uccelli, M. M., Guglieri, P., Uccelli, A. & Mancardi, G. L. Gabapentin is effective in treating nocturnal painful spasms in multiple sclerosis. Mult. Scler. 6, 192–193 (2000).
Article CAS Google Scholar
McMahon, S. B. & Malcangio, M. Current challenges in glia-pain biology. Neuron 64, 46–54 (2009).
Article CAS Google Scholar
Baron, R. Mechanisms of disease: neuropathic pain—a clinical perspective. Nat. Clin. Pract. Neurol. 2, 95–106 (2006).
Article Google Scholar
Tsuda, M., Inoue, K. & Salter, M. W. Neuropathic pain and spinal microglia: a big problem from molecules in “small” glia. Trends Neurosci. 28, 101–107 (2005).
Article CAS Google Scholar
Nakatsuka, T. & Gu, J. G. ATP P2X receptor-mediated enhancement of glutamate release and evoked EPSCs in dorsal horn neurons of the rat spinal cord. J. Neurosci. 21, 6522–6531 (2001).
Article CAS Google Scholar
Bardoni, R., Goldstein, P. A., Lee, C. J., Gu, J. G. & MacDermott, A. B. ATP P2X receptors mediate fast synaptic transmission in the dorsal horn of the rat spinal cord. J. Neurosci. 17, 5297–5304 (1997).
Article CAS Google Scholar
Tsuda, M. et al. P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury. Nature 424, 778–783 (2003).
Article ADS CAS Google Scholar
Tozaki-Saitoh, H. et al. P2Y12 receptors in spinal microglia are required for neuropathic pain after peripheral nerve injury. J. Neurosci. 28, 4949–4956 (2008).
Article CAS Google Scholar
Tsuda, M. et al. JAK-STAT3 pathway regulates spinal astrocyte proliferation and neuropathic pain maintenance in rats. Brain 134, 1127–1139 (2011).
Article Google Scholar
von Hehn, C. A., Baron, R. & Woolf, C. J. Deconstructing the neuropathic pain phenotype to reveal neural mechanisms. Neuron 73, 638–652 (2012).
Article CAS Google Scholar
Reppert, S. M. & Weaver, D. R. Coordination of circadian timing in mammals. Nature 418, 935–941 (2002).
Article ADS CAS Google Scholar
Wijnen, H. & Young, M. W. Interplay of circadian clocks and metabolic rhythms. Annu. Rev. Genet. 40, 409–448 (2006).
Article CAS Google Scholar
Hastings, M. H., Reddy, A. B. & Maywood, E. S. A clockwork web: circadian timing in brain and periphery, in health and disease. Nat. Rev. Neurosci. 4, 649–661 (2003).
Article CAS Google Scholar
Akhtar, R. A. et al. Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus. Curr. Biol. 12, 540–550 (2002).
Article CAS Google Scholar
Moore, R. Y. & Eichler, V. B. Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Res. 42, 201–206 (1972).
Article CAS Google Scholar
Meyer-Bernstein, E. L. et al. Effects of suprachiasmatic transplants on circadian rhythms of neuroendocrine function in golden hamsters. Endocrinology 140, 207–218 (1999).
Article CAS Google Scholar
Cuesta, M., Cermakian, N. & Boivin, D. B. Glucocorticoids entrain molecular clock components in human peripheral cells. FASEB J. 29, 1360–1370 (2015).
Article CAS Google Scholar
Yan, P. et al. Glucocorticoid receptor expression in the spinal cord after traumatic injury in adult rats. J. Neurosci. 19, 9355–9363 (1999).
Article CAS Google Scholar
Blanco, C. E., Peltz, A., Staley, R. & Kim, F. Effects of pharmacologic androgen treatment duration on glucocorticoid receptor alpha immunoreactivity of lumbosacral motor neurons in the male rat. Neuroscience 115, 941–949 (2002).
Article CAS Google Scholar
Tanaka, J. et al. Glucocorticoid- and mineralocorticoid receptors in microglial cells: the two receptors mediate differential effects of corticosteroids. Glia 20, 23–37 (1997).
Article CAS Google Scholar
Kim, K. J., Yoon, Y. W. & Chung, J. M. Comparison of three rodent neuropathic pain models. Exp. Brain Res. 113, 200–206 (1997).
Article CAS Google Scholar
van Giezen, J. J. & Humphries, R. G. Preclinical and clinical studies with selective reversible direct P2Y12 antagonists. Semin. Thromb. Hemost. 31, 195–204 (2005).
Article CAS Google Scholar
Barragán-Iglesias, P. et al. Role of spinal P2Y6 and P2Y11 receptors in neuropathic pain in rats: possible involvement of glial cells. Mol. Pain 10, 29 (2014).
Article Google Scholar
Schaaf, M. J. & Cidlowski, J. A. Molecular mechanisms of glucocorticoid action and resistance. J. Steroid Biochem. Mol. Biol. 83, 37–48 (2002).
Article CAS Google Scholar
Corriden, R. & Insel, P. A. Basal release of ATP: an autocrine-paracrine mechanism for cell regulation. Sci. Signal. 3, re1 (2010).
Article Google Scholar
Koizumi, S., Fujishita, K. & Inoue, K. Regulation of cell-to-cell communication mediated by astrocytic ATP in the CNS. Purinergic Signal. 1, 211–217 (2005).
Article CAS Google Scholar
Roman, R. M. et al. Evidence for multidrug resistance-1 P-glycoprotein-dependent regulation of cellular ATP permeability. J. Membr. Biol. 183, 165–173 (2001).
Article CAS Google Scholar
Ballerini, P. et al. Glial cells express multiple ATP binding cassette proteins which are involved in ATP release. NeuroReport 13, 1789–1792 (2002).
Article CAS Google Scholar
Sheppard, D. N. & Welsh, M. J. Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents. J. Gen. Physiol. 100, 573–591 (1992).
Article CAS Google Scholar
Suadicani, S. O., Brosnan, C. F. & Scemes, E. P2X7 receptors mediate ATP release and amplification of astrocytic intercellular Ca2+ signaling. J. Neurosci. 2, 1378–1385 (2006).
Article Google Scholar
Liu, H. T., Toychiev, A. H., Takahashi, N., Sabirov, R. Z. & Okada, Y. Maxi-anion channel as a candidate pathway for osmosensitive ATP release from mouse astrocytes in primary culture. Cell Res. 18, 558–565 (2008).
Article CAS Google Scholar
Ye, Z. C., Wyeth, M. S., Baltan-Tekkok, S. & Ransom, B. R. Functional hemichannels in astrocytes: a novel mechanism of glutamate release. J. Neurosci. 23, 3588–3596 (2003).
Article CAS Google Scholar
Bruzzone, R., Barbe, M. T., Jakob, N. J. & Monyer, H. Pharmacological properties of homomeric and heteromeric pannexin hemichannels expressed in Xenopus oocytes. J. Neurochem. 92, 1033–1043 (2005).
Article CAS Google Scholar
Woehrle, T. et al. Hypertonic stress regulates T cell function via pannexin-1 hemichannels and P2X receptors. J. Leukoc. Biol. 88, 1181–1189 (2010).
Article CAS Google Scholar
MacVicar, B. A. & Thompson, R. J. Non-junction functions of pannexin-1 channels. Trends Neurosci. 33, 93–102 (2010).
Article CAS Google Scholar
Eylenstein, A. et al. Stimulation of Ca²⁺-channel Orai1/STIM1 by serum- and glucocorticoid-inducible kinase 1 (SGK1). FASEB J. 25, 2012–2021 (2011).
Article CAS Google Scholar
Kim, K. D. et al. Calcium signaling via Orai1 is essential for induction of the nuclear orphan receptor pathway to drive Th17 differentiation. J. Immunol. 192, 110–122 (2014).
Article CAS Google Scholar
Fields, R. D. & Burnstock, G. Purinergic signalling in neuron-glia interactions. Nat. Rev. Neurosci. 7, 423–436 (2006).
Article CAS Google Scholar
Slezak, M. et al. Astrocytes are a neural target of morphine action via glucocorticoid receptor-dependent signaling. Glia 61, 623–635 (2013).
Article Google Scholar
Peng, H. Y., Chen, G. D., Lai, C. Y., Hsieh, M. C. & Lin, T. B. Spinal serum-inducible and glucocorticoid-inducible kinase 1 mediates neuropathic pain via kalirin and downstream PSD-95-dependent NR2B phosphorylation in rats. J. Neurosci. 33, 5227–5240 (2013).
Article CAS Google Scholar
Kusunose, N. et al. Molecular basis for the dosing time-dependency of anti-allodynic effects of gabapentin in a mouse model of neuropathic pain. Mol. Pain. 6, 83 (2010).
Article CAS Google Scholar
Frödin, M. et al. A phosphoserine/threonine-binding pocket in AGC kinases and PDK1 mediates activation by hydrophobic motif phosphorylation. EMBO J. 21, 5396–5407 (2002).
Article Google Scholar
Wang, S. et al. Expression of central glucocorticoid receptors after peripheral nerve injury contributes to neuropathic pain behaviors in rats. J. Neurosci. 24, 8595–8605 (2004).
Article CAS Google Scholar
Sorge, R. E. et al. Different immune cells mediate mechanical pain hypersensitivity in male and female mice. Nat. Neurosci. 18, 1081–1083 (2015).
Article CAS Google Scholar
Scheiermann, C., Kunisaki, Y. & Frenette, P. S. Circadian control of the immune system. Nat. Rev. Immunol. 13, 190–198 (2013).
Article CAS Google Scholar
Oishi, K. et al. Clock mutation affects circadian regulation of circulating blood cells. J. Circadian Rhythms 4, 13 (2006).
Article Google Scholar
Scheiermann, C. et al. Adrenergic nerves govern circadian leukocyte recruitment to tissues. Immunity 37, 290–301 (2012).
Article CAS Google Scholar
Rijsdijk, M., van Wijck, A. J., Kalkman, C. J. & Yaksh, T. L. The effects of glucocorticoids on neuropathic pain: a review with emphasis on intrathecal methylprednisolone acetate delivery. Anesth. Analg. 118, 1097–1112 (2014).
Article CAS Google Scholar
Dhabhar, F. S. & McEwen, B. S. Enhancing versus suppressive effects of stress hormones on skin immune function. Proc. Natl Acad. Sci. USA 96, 1059–1064 (1999).
Article ADS CAS Google Scholar
Dhabhar, F. S. Enhancing versus suppressive effects of stress on immune function: implications for immunoprotection and immunopathology. Neuroimmunomodulation 16, 300–317 (2009).
Article CAS Google Scholar
Touitou, Y., Bogdan, A., Lévi, F., Benavides, M. & Auzéby, A. Disruption of the circadian patterns of serum cortisol in breast and ovarian cancer patients: relationships with tumour marker antigens. Br. J. Cancer 74, 1248–1252 (1996).
Article CAS Google Scholar
Lederbogen, F. et al. Flattened circadian cortisol rhythm in type 2 diabetes. Exp. Clin. Endocrinol. Diabet. 19, 573–575 (2011).
Article Google Scholar
Ronchi, C. L. et al. Low SGK1 expression in human adrenocortical tumors is associated with ACTH-independent glucocorticoid secretion and poor prognosis. J. Clin. Endocrinol. Metab. 97, E2251–E2260 (2012).
Article CAS Google Scholar
Wiper-Bergeron, N., Wu, D., Pope, L., Schild-Poulter, C. & Haché, R. J. Stimulation of preadipocyte differentiation by steroid through targeting of an HDAC1 complex. EMBO J. 22, 2135–2145 (2003).
Article CAS Google Scholar
Mühlbauer, M., Chilton, P. M., Mitchell, T. C. & Jobin, C. Impaired Bcl3 up-regulation leads to enhanced lipopolysaccharide-induced interleukin (IL)-23P19 gene expression in IL-10(−/−) mice. J. Biol. Chem. 283, 14182–14189 (2008).
Article Google Scholar

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Acknowledgements

We thank Dr Yamashita for technical assistance with calcium imaging, and Mr. Tsurudome for their technical support in the preparation of animal models and gene analyses. We are also grateful for the technical support provided by the Research Support Center, Graduate School of Medical Sciences, Kyushu University. This work was supported by a Grant-in-Aid for Scientific Research B from the Japan for the Promotion of Science (15H04765 to S.K.), a Grant-in-Aid from the Mochida Memorial Foundation (to S.K.), and a Grant-in-Aid from Kyushu University Interdisciplinary Programs in Education and Projects in Research Development. This work was also supported in part by a Grant-in-Aid for Scientific Research A (16H02636 to S.O.) from the Japan for the Promotion of Science.

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Naoki Kusunose
Present address: Present address: Department of Ophthalmology, Faculty of Medicine, Oita University, 1-1 Idaigaoka Hasamamachi Yufu-shi, Oita 879-5593, Japan,
Satoru Koyanagi and Naoki Kusunose: These authors contributed equally to this work

Authors and Affiliations

Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan
Satoru Koyanagi, Naoki Kusunose, Marie Taniguchi, Takahiro Akamine, Yuki Kanado, Naoya Matsunaga & Shigehiro Ohdo
Department of Glocal Healthcare, Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan
Satoru Koyanagi & Naoya Matsunaga
Department of Molecular and System Pharmacology, Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan
Yui Ozono & Kazuhide Inoue
Department of Life Innovation, Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan
Takahiro Masuda, Yuta Kohro & Makoto Tsuda
Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, M5G 1X8, Ontario, Canada
Michael W. Salter
Department of Physiology, University of Toronto, Toronto, M5S 1A8, Ontario, Canada
Michael W. Salter
University of Toronto Centre for the Study of Pain, Toronto, M5T 1P8, Ontario, Canada
Michael W. Salter

Authors

Satoru Koyanagi
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Naoki Kusunose
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Marie Taniguchi
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Takahiro Akamine
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Yuki Kanado
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Yui Ozono
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Takahiro Masuda
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Yuta Kohro
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Naoya Matsunaga
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Makoto Tsuda
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Michael W. Salter
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Kazuhide Inoue
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Shigehiro Ohdo
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Contributions

S.K., N.K., M.T. and S.O. designed the research; S.K., N.K., M.T., T.A., Y.K., Y.O., T.M., Y.K. and M.T. acquired the data; N.M., M.T. and T.A. supplied the experimental materials; S.K., N.K., M.T., M.W.S., K.I. and S.O. drafted the manuscript.

Corresponding author

Correspondence to Shigehiro Ohdo.

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The authors declare no competing financial interests.

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Supplementary Figures 1-17, Supplementary Table 1, Supplementary Methods and Supplementary Reference. (PDF 2009 kb)

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Koyanagi, S., Kusunose, N., Taniguchi, M. et al. Glucocorticoid regulation of ATP release from spinal astrocytes underlies diurnal exacerbation of neuropathic mechanical allodynia. Nat Commun 7, 13102 (2016). https://doi.org/10.1038/ncomms13102

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Received: 15 December 2015
Accepted: 02 September 2016
Published: 14 October 2016
DOI: https://doi.org/10.1038/ncomms13102

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