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Effects of Glutathione on Mechanical Allodynia and Central Sensitization in Chronic Postischemic Pain Rats.

1. Introduction

Complex regional pain syndrome type I (CRPS I) is a devastating condition that usually affects a limb and is not accompanied by a clinically verifiable nerve injury [1]. CRPS I commonly develops following sprains, arthroscopic surgery, overly tight casting, and edematous soft tissue injuries. Many different mechanisms of action for the development of CRPS I have been suggested. These include an inflammatory process, centrally mediated sympathetic stimulation, central sensitization of pain, an autoimmune process, neurogenic inflammation, and ischemia-reperfusion injury [2].

The chronic postischemia pain (CPIP) is an animal model that mimics the symptoms of CRPS I [3]. In this model, a hind paw ischemia-reperfusion (IR) injury produces persistent mechanical and cold allodynia, edema, and microvascular dysfunction in rat hind paw without evidence of accompanying nerve damage. IR injury occurs when the blood supply returns to a tissue following a period of insufficient blood flow. Prolonged ischemia results in the accumulation of nitric oxide (NO) and hypoxanthine in the affected tissue [4]. The reintroduction of molecular O2 to ischemic tissue upon reperfusion results in the production of superoxide ([O.sup.-.sub.2]) and xanthine through the action of xanthine oxygenase [5]. The reaction of NO with [O.sup.-.sub.2] results in the production of peroxynitrite ([ONOO.sup.-]) [6]. [ONOO.sup.-] is a strong oxidant that exerts its toxic effects through lipid peroxidation, mitochondrial damage, protein nitration and oxidation, depletion of glutathione (GSH) reserve, and DNA damage [7]. The formation of [ONOO.sup.-] in the ischemic tissue leads to vascular dysfunction and tissue damage [8]. [ONOO.sup.-] is also known to be involved in such physiological processes as inflammation, nerve injury, opioid induced hyperalgesia, and IR injury [9, 10]. In CPIP rats, [ONOO.sup.-] is involved in development of allodynia and N-methyl-D-aspartate (NMDA) receptor mediated central sensitization [11].

GSH is the most abundant antioxidant in the cell. Ischemia-reperfusion injury depletes GSH in the tissue and supplementation with GSH has been found to reduce associated tissue damage [12, 13]. GSH has also been found to reduce [ONOO.sup.-] associated injury [14]. However, no previous studies have evaluated the effect of GSH on the development of mechanical allodynia following IR injury. We hypothesized that the protective effect of GSH on [ONOO.sup.-] associated injury could attenuate the development of mechanical allodynia and central sensitization in CPIP rats that mimics the symptoms of human CRPS I. Therefore, we conducted this study to investigate the protective effect of GSH in CPIP rats via changes in withdrawal threshold following mechanical stimulation of a hind limb and in the spinal activation of the N-methyl-D-aspartate (NMDA) receptor subunit GluN1 (pGluN1).

2. Materials and Methods

2.1. Animals. Forty-five male Sprague-Dawley rats (320-340 g) were used in this study (Koatech, Gyeonggi-do, Korea). All rats were housed at the animal care facility under specific pathogen-free conditions. They were allowed free access to food and water and were exposed to a light-and-dark cycle of 12 hours each. Care was provided according to National Institutes of Health guidelines on laboratory animal welfare. The rats acclimated to their cages for 7 days prior to the start of the experiment.

2.2. Experimental Protocol. The Institutional Animal Care and Use Committee at Kyungpook National University approved the experimental protocol. A total of 45 male rats were evenly distributed between five groups, with nine rats per group: (1) sham group, (2) CPIP group, (3) CPIP + GSH 100 mg/kg group, (4) CPIP + GSH 200 mg/kg group, and (5) CPIP + GSH 500 mg/kg group. The rats in sham group underwent a sham procedure, while the rats in the other groups underwent the CPIP procedure. Rats in the sham group and the CPIP group received intraperitoneal injections of 1 cc of normal saline 30 minutes prior to reperfusion. Rats in the CPIP + GSH 100 mg/kg group, CPIP + GSH 200 mg/kg group, and CPIP + GSH 500 mg/kg group received intraperitoneal injections of the designated dose of GSH mixed with 1 cc of normal saline 30 minutes prior to reperfusion (Figure 1).

2.3. Hind Paw Ischemia and Reperfusion. The CPIP procedure was performed as described by Coderre et al. [3]. Anesthesia was induced in all rats with an intraperitoneal injection of 50 mg/kg of sodium phenobarbital. Anesthesia was maintained with an infusion of sodium phenobarbital at 20 mg/kg/hr. Once anesthetized, a Nitrile 70 Durometer O-Ring (O-Rings West, Seattle, WA) with a 5.5 mm internal diameter was placed around the left hind limb just proximal to the medial malleolus of each rat in the CPIP groups. Three hours after placement of the O-Ring, it was removed and reperfusion was allowed to occur. An O-Ring was placed identically on the rats in the sham group, but the device was cut so that it surrounded the ankle loosely and did not occlude blood flow to the paw. All rats recovered fully within 30 minutes of O-Ring removal (Figure 2).

2.4. Hind Paw Mechanical Allodynia. To allow acclimation to the environment, the rats were placed individually in a testing cage (23 x 16 x 24 [cm.sup.3]) with a mesh metal floor for 1 hour daily beginning 2 days before the start of the experiment. Thirty minutes before the experiment began the rats were again allowed to acclimate. The ipsilateral hind limb was then evaluated for mechanical allodynia. The mechanical threshold for allodynia was assessed by measuring the 50% withdrawal response to von Frey filaments (Stoelting, Wood Dale, IL, USA) using a modification of the up/down method [15]. Von Frey filaments were applied to the center of the plantar surface of the hind paw for 10 seconds or less if the rat responded to the stimulus by withdrawing, flicking, stamping, or licking its paw. The experiment was started with a filament producing a force of 2g and was continued in either ascending (after a negative response) or descending (after a positive response) order. The minimum stimulus intensity utilized was 0.25 g and the maximum was 15 g. A 50% response threshold (g) was calculated from the response pattern and the force produced by the final filament. Both hind limbs were tested. A baseline recording of the withdrawal threshold was obtained 1 hour before infliction of the IR injury. On the first, third, and seventh days after CPIP injury, we evaluated the withdrawal threshold to determine the effects of GSH. All testing was performed by a researcher blinded to the treatments.

2.5. Western Blot Analysis. Three days after the procedure, three rats were randomly selected from each group. All rats were fully anesthetized and then rapidly sacrificed. The L4-5 spinal cord segment was harvested from each rat and then divided into a left and right side. The spinal cord sections were placed immediately in liquid nitrogen. The left side of the spinal cord sample was homogenized in 100 [micro]l of lysis buffer (20 mM Tris-HCl pH 8.0,150 mM NaCl, 1 mM EDTA, 2 mM [Na.sub.3]V[O.sub.4], 0.5 mM DTT, 10% glycerol, and 1% Nonidet P-40) plus a protease inhibitor cocktail tablet (Roche Diagnostics, Mannheim, Germany). The lysates were centrifuged at 13,000 xg for 25 min at 4[degrees]C. The supernatants were collected and the proteins were quantified using the Bradford method (Protein Assay Kit I, Bio-Rad, Hercules, Ca, USA). Protein samples (40 [micro]g) were dissolved in a buffer solution (0.1 M Tris-HCl, 10%glycerol, 2%SDS, and 0.1% bromophenol blue). The protein samples were heated at 100[degrees]C for 5 minutes and then loaded into 10% SDS-polyacrylamide gels. After separation by SDS-polyacrylamide gel electrophoresis, the proteins were transferred to a nitrocellulose membrane and blocked with Tris-buffered saline (50 mM Tris-HCl pH 7.4 and 10 mM NaCl) in 3% skim milk at room temperature for 1 hour. The blots were incubated with anti-phospho-NR1 antibody (1: 500, Ser897, ABN99, Millipore, Billerica, MA, USA) and anti [beta]-actin antibody (1: 5000, [beta]-actin, sc-47778, Santa Cruz Biotechnology, Dallas, TX, USA) at 4[degrees]C overnight. The blots were washed with washing buffer (50 mM Tris pH 7.4 and 10 mM NaCl) and then incubated with antimouse horseradish peroxidase conjugated secondary antibodies (1: 2000, anti-mouse IgG-HRP, 7076S, Cell Signaling Technology, Danvers, MA, USA) for 1 hour at 21[degrees] C. The blots were developed with an enhanced chemiluminescence kit (Amersham Pharmacia Biotech, Amersham, UK). [beta]-Actin was used as an internal control. The densities of the protein blots were quantified using Image J 1.50i software (National Institutes of Health, Bethesda, MD, USA).

2.6. Statistical Analyses. The measured data are presented as the mean [+ or -] standard error of the mean (SEM) and were analyzed using the statistical program SPSS statistics for Windows, version 21.0 (SPSS, IBM Corp., Armonk, NY, USA.). Analysis of change over time for multiple groups was performed using a two-way ANOVA with one repeated measure (time) followed by the Tukey test. Differences in values between multiple groups were tested using the one-way ANOVA (when comparing more than two groups) followed by the Tukey test. Change over time in a single group was tested using the one-way repeated measures ANOVA. P < 0.05 indicated statistical significance.

3. Results

3.1. Hind Paw Mechanical Allodynia. The withdrawal thresholds for both hind paws at baseline did not differ between the groups. There were no significant changes in the withdrawal thresholds of the ipsilateral and contralateral hind paws in the sham group during the entire study period. GSH treatment 30 minutes before reperfusion was associated with a significant increase in the withdrawal thresholds of both hind paws following reperfusion. The withdrawal thresholds of both hind paws in the CPIP and CPIP + GSH in the dose of 100 mg/kg, 200 mg/kg, and GSH 500 mg/kg groups on the first, third, and seventh days following reperfusion were significantly reduced as compared to the sham group at these same time points (P < 0.05). The CPIP + GSH 500 mg/kg group showed a significant increase in the withdrawal threshold as compared to the CPIP + GSH 100 mg/kg group (P < 0.05) in both hind paws at first, third, and seventh days after reperfusion (Figure 3).

3.2. Measurement of pNR1 in the Spinal Cord. The relative densities of pGluN1 in the CPIP and CPIP + GSH 100 mg/kg groups were significantly higher than that in the sham group. The relative densities of pGluN1 in the CPIP + GSH 200 mg/kg and CPIP + GSH 500 mg/kg groups were significantly lower than that in the CPIP group. The relative density of pGluN1 in the CPIP + GSH 500 mg/kg group was significantly lower than that in the CPIP + GSH 100 mg/kg group (Figure 4).

4. Discussion

Our study has showed that the treatment with GSH prior to reperfusion attenuated mechanical allodynia and suppressed spinal phosphorylation of GluN1 in CPIP rats dose-dependently. These findings suggest that the development of allodynia in the CPIP rats results from central sensitization secondary to GluN1 phosphorylation, and treatment with GSH suppressed sensitization in a dose-dependent manner.

The proposed pathogenesis of CRPS I is microvascular injury that results from a persistent deep tissue ischemia and subsequent inflammatory reaction after reperfusion [16]. Microvascular injury in the affected limb activates peripheral nociceptors and initiates and maintains NMDA mediated central sensitization [17]. The CPIP model involves complete occlusion of blood flow to the hind paw and results in prolonged reactive hyperemia and edema following reperfusion. The rats in this model develop cold allodynia, mechanical hyperalgesia, and vascular abnormalities without evidence of nerve injury, which is similar to the findings in CRPS I patients [18]. Prolonged ischemia in CPIP rats results in the accumulation of oxidases. Accumulated xanthine oxidase is responsible for the overproduction of superoxide during reperfusion. Activation of nitric oxide synthase during ischemia results in the production of nitric oxide (NO) from vascular endothelium and neutrophils [19]. Superoxide is rapidly removed by superoxide dismutase (SOD), and NO diffuses rapidly into red blood cells [6]. The proximity of NO and superoxide in the vascular space may promote the generation of [ONOO.sup.-] during early reperfusion [20].

[ONOO.sup.-] is an extremely short-lived cytotoxic oxidant. It has a half-life of 1.9 seconds at pH 7.4, which is even shorter in vivo [21]. In spite of its short half-life, [ONOO.sup.-] is able to diffuse through several cells and induce lipid peroxidation and DNA and protein damage [22]. [ONOO.sup.-] damages capillary endothelial cells and arterial smooth muscle cells following IR injury. Injured endothelial cells swell and occlude the capillary lumen. Capillary occlusion and reperfusion of the tissue produce IR injury [23]. Endothelial cell dysfunction decreases NO production and results in arterial vasospasm [18, 24]. Microvascular dysfunction following IR injury results in ischemia of the paw muscle, and allodynia has been correlated with muscle ischemia in CPIP rats [25]. [ONOO.sup.-] reportedly contributes to the development of chronic pain, and peripheral administration of [ONOO.sup.-] has been shown to induce inflammatory hyperalgesia [9]. Peripheral nerve injury results in the production of [ONOO.sup.-], and scavenging of [ONOO.sup.-] has been shown to alleviate hyperalgesia and nerve degeneration [10]. Pretreatment of CPIP rats with an [ONOO.sup.-] decomposition catalyst has been shown to decrease allodynia and prevent central sensitization by attenuating NMDA receptor activation [11].

GSH is an intracellular tripeptide thiol. It is a major water-soluble antioxidant and plays a central role in the modulation of nitric oxide [9, 26]. GSH converts [ONOO.sup.-] to less harmful by-products such as S-nitrosoglutathione [27]. In the presence of [ONOO.sup.-], GSH (1) relaxes vessel walls, (2) stimulates the activity of guanylate cyclase in endothelial cells, (3) attenuates [ONOO.sup.-] induced hemolysis, and (4) inhibits platelet aggregation [14]. These actions by GSH may reduce endothelial cell damage and improve microcirculation. Exogenously administered GSH is reported to increase intracellular GSH levels, and infusion of GSH has been shown to decrease pain and improve microcirculation in patients with peripheral artery disease [28]. In our study, GSH injection 30 minutes prior to reperfusion resulted in an increase in the withdrawal threshold and suppression of pGluN1 expression in a dose-dependent manner. These results suggest that GSH decreased pain and central sensitization after IR injury by decreasing [ONOO.sup.-] induced toxicity in CPIP rats.

In this study, we did not evaluate the dose-dependent effect of GSH on muscle ischemia and microvascular injury. However, IR injury is known to reduce the concentration of GSH in skeletal muscle [29], and the extent of hind paw muscle ischemia following CPIP injury is correlated with the development of mechanical allodynia [25]. In this study, supplementation with GSH prior to reperfusion suppressed the development of allodynia. This result suggests that GSH might attenuate pain by reducing microvascular damage after IR injury.

In conclusion, the results of the present study indicate that administration of GSH prior to reperfusion alleviates mechanical allodynia and spinal phosphorylation of GluN1 in CPIP rats. Our findings suggest that GSH counteracted microvascular dysfunction following IR injury. Further studies are needed to gain significant translatability by evaluating the antinociceptive potential of GSH analogs in ongoing clinical trials in the CPIP rats and CRPS I patients.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors' Contributions

Jinseok Yeo participated in the conception and design of the study and wrote and critically revised the manuscript. Hoon Jung performed animal experiment and sample collection. Hyerim Lee critically revised the manuscript and performed statistical analysis.


This work was supported by a Biomedical Research Institute grant, Kyungpook National University Hospital (2014).


[1] M. Stanton-Hicks, W. Janig, S. Hassenbusch, J. D. Haddox, R. Boas, and P. Wilson, "Reflex sympathetic dystrophy: changing concepts and taxonomy," PAIN, vol. 63, no. 1, pp. 127-133, 1995.

[2] A. Goebel, "Complex regional pain syndrome in adults," Rheumatology, vol. 50, no. 10, Article ID ker202, pp. 1739-1750, 2011.

[3] T. J. Coderre, D. N. Xanthos, L. Francis, and G. J. Bennett, "Chronic post-ischemia pain (CPIP): a novel animal model of complex regional pain syndrome-Type I (CRPS-I; reflex sympathetic dystrophy) produced by prolonged hindpaw ischemia and reperfusion in the rat," PAIN, vol. 112, no. 1-2, pp. 94-105, 2004.

[4] A. Khanna, P. A. Cowled, and R. A. Fitridge, "Nitric oxide and skeletal muscle reperfusion injury: Current controversies (research review)," Journal of Surgical Research, vol. 128, no. 1, pp. 98-107, 2005.

[5] J. M. McCord, "Oxygen-derived free radicals in postischemic tissue injury," The New England Journal of Medicine, vol. 312, no. 3, pp. 159-163, 1985.

[6] P. Pacher, J. S. Beckman, and L. Liaudet, "Nitric oxide and peroxynitrite in health and disease," Physiological Reviews, vol. 87, no. 1, pp. 315-424, 2007.

[7] C. Szabo, "Multiple pathways of peroxynitrite cytotoxicity," Toxicology Letters, vol. 140-141, pp. 105-112, 2003.

[8] R. S. Ronson, M. Nakamura, and J. Vinten-Johansen, "The cardiovascular effects and implications of peroxynitrite," Cardiovascular Research, vol. 44, no. 1, pp. 47-59, 1999.

[9] M. M. Ndengele, S. Cuzzocrea, E. Esposito et al., "Cyclooxygenases 1 and 2 contribute to peroxynitrite-mediated inflammatory pain hypersensitivity," The FASEB Journal, vol. 22, no. 9, pp. 3154-3164, 2008.

[10] T. Liu, K. R. Knight, and D. J. Tracey, "Hyperalgesia due to nerve injury-role of peroxynitrite," Neuroscience, vol. 97, no. 1, pp. 125-131, 2000.

[11] K.-H. Kwak, H. Jung, J. M. Park et al., "A peroxynitrite decomposition catalyst prevents mechanical allodynia and NMDA receptor activation in the hind-paw ischemia reperfusion injury rats," Experimental and Therapeutic Medicine, vol. 7, no. 2, pp. 508-512, 2014.

[12] P.-Y. Cheung, W. Wang, and R. Schulz, "Glutathione protects against myocardial ischemia-reperfusion injury by detoxifying peroxynitrite," Journal of Molecular and Cellular Cardiology, vol. 32, no. 9, pp. 1669-1678, 2000.

[13] F. Xue, G. Wang, Z. Pang, C. Liu, and T. Liang, "Protective effect of glutathione against liver warm ischemia-reperfusion injury in rats is associated with regulation of P-selectin and neutrophil infiltration," Anatomical Record, vol. 291, no. 8, pp. 1016-1022, 2008.

[14] M. Nakamura, V H. Thourani, R. S. Ronson et al., "Glutathione reverses endothelial damage from peroxynitrite, the byproduct of nitric oxide degradation, in crystalloid cardioplegia," Circulation, vol. 102, 3, no. 19, pp. 332-338, 2000.

[15] S. R. Chaplan, F. W. Bach, J. W. Pogrel, J. M. Chung, and T. L. Yaksh, "Quantitative assessment of tactile allodynia in the rat paw," Journal of Neuroscience Methods, vol. 53, no. 1, pp. 55-63, 1994.

[16] T. J. Coderre and G. J. Bennett, "A hypothesis for the cause of complex regional pain syndrome-type I (reflex sympathetic dystrophy): Pain due to deep-tissue microvascular pathology," Pain Medicine, vol. 11, no. 8, pp. 1224-1238, 2010.

[17] C. J. Woolf and S. W. N. Thompson, "The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation; implications for the treatment of post-injury pain hypersensitivity states," PAIN, vol. 44, no. 3, pp. 293-299, 1991.

[18] D. N. Xanthos, G. J. Bennett, and T. J. Coderre, "Norepinephrine-induced nociception and vasoconstrictor hypersensitivity in rats with chronic post-ischemia pain," PAIN, vol. 137, no. 3, pp. 640-651, 2008.

[19] M. C. Carreras, G. A. Pargament, S. D. Catz, J. J. Poderoso, and A. Boveris, "Kinetics of nitric oxide and hydrogen peroxide production and formation of peroxynitrite during the respiratory burst of human neutrophils," FEBS Letters, vol. 341, no. 1, pp. 65-68, 1994.

[20] W. Yasmin, K. D. Strynadka, and R. Schulz, "Generation of peroxynitrite contributes to ischemia-reperfusion injury in isolated rat hearts," Cardiovascular Research, vol. 33, no. 2, pp. 422-432, 1997.

[21] W. H. Koppenol, J. J. Moreno, W. A. Pryor, H. Ischiropoulos, and J. S. Beckman, "Peroxynitrite, a cloaked oxidant formed by nitric oxide and superoxide," Chemical Research in Toxicology, vol. 5, no. 6, pp. 834-842, 1992.

[22] C. Szabo and V L. Dawson, "Role of poly(ADP-ribose) synthetase in inflammation and ischaemia- reperfusion," Trends in Pharmacological Sciences, vol. 19, no. 7, pp. 287-298, 1998.

[23] M. D. Menger, "Capillary dysfunction in striated muscle ischemia/reperfusion: On the mechanisms of capillary "no-reflow"," Shock, vol. 8, no. 1, pp. 2-7, 1997

[24] W.-Z. Wang, G. Anderson, J. T. Fleming et al., "Lack of nitric oxide contributes to vasospasm during ischemia/reperfusion injury," Plastic and Reconstructive Surgery, vol. 99, no. 4, pp. 1099-1108, 1997.

[25] A. Laferriere, M. Millecamps, D. N. Xanthos et al., "Cutaneous tactile allodynia associated with microvascular dysfunction in muscle," Molecular Pain, vol. 4, article no. 49, 2008.

[26] D. Ghigo, P Alessio, A. Foco et al., "Nitric oxide synthesis is impaired in glutathione-depleted human umbilical vein endothelial cells," American Journal of Physiology--Cell Physiology, vol. 265, no. 3, pp. C728-C732, 1993.

[27] B. Mayer, A. Schrammel, P Klatt, D. Koesling, and K. Schmidt, "Peroxynitrite-induced accumulation of cyclic GMP in endothelial cells and stimulation of purified soluble guanylyl cyclase: dependence on glutathione and possible role of S-nitrosation," The Journal of Biological Chemistry, vol. 270, no. 29, pp. 17355-17360, 1995.

[28] E. Arosio, S. De Marchi, M. Zannoni, M. Prior, and A. Lechi, "Effect of glutathione infusion on leg arterial circulation, cutaneous microcirculation, and pain-free walking distance in patients with peripheral obstructive arterial disease: a randomized, double-blind, placebo-controlled trial," Mayo Clinic Proceedings, vol. 77, no. 8, pp. 754-759, 2002.

[29] J. T. Prem, M. Eppinger, G. Lemmon, S. Miller, D. Nolan, and J. Peoples, "The role of glutamine in skeletal muscle ischemia/reperfusion injury in the rat hind limb model," The American Journal of Surgery, vol. 178, no. 2, pp. 147-150, 1999.

Jinseok Yeo, Hoon Jung, and Hyerim Lee

Department of Anesthesiology and Pain Medicine, Chilgok Hospital, School of Medicine,

Kyungpook National University, Daegu, Republic of Korea

Correspondence should be addressed to Jinseok Yeo;

Received 28 June 2017; Revised 8 September 2017; Accepted 18 September 2017; Published 25 October 2017

Academic Editor: Fletcher A. White

Caption: FIGURE 1: Flow of the study. CPIP: chronic postischemia pain, GSH: glutathione, IP: intraperitoneal injection, and POD: postoperative day.

Caption: FIGURE 2: Photographs of the left hind paw in chronic postischemic pain rats. (a) Normal hind paw. (b) Hind paw during ischemic event: a tight-fitting O-Ring has been placed just proximal to the ankle joint; the paw shows cyanosis. (c) Hind paw 10 minutes after reperfusion: the paw shows swelling and hyperemia. (d) Hind paw 3 days after reperfusion: swelling and hyperemia are decreased; the paw appears dry and shiny.

Caption: FIGURE 3: Withdrawal threshold in CPIP and sham rats. Rats in the sham and CPIP groups received saline. Rats in the CPIP + GSH100, CPIP + GSH 200, and CPIP + GSH 500 groups received GSH 100 mg/kg, 200 mg/kg, and 500 mg/kg, respectively. CPIP: chronic postischemia pain; GSH: glutathione. *P < 0.05, repeated measurements ANOVA followed by the Tukey test compared to the sham group. [dagger] P < 0.05, repeated measurement ANOVA followed by the Tukey test compared to the CPIP group. [double dagger] P < 0.05, repeated measurement ANOVA followed by the Tukey test compared to the CPIP + GSH 100 group.

Caption: FIGURE 4: Changes in the relative density of pGluNl protein in the ipsilateral (left) spinal cord segment (L4-5). Expression of pGluN1 was measured by western blot on post-op day 3. Three rats were randomly selected from each group and sacrificed. Data are expressed as mean [+ or -] standard error of the mean. * indicates values significantly different from the sham group. [dagger] indicates values significantly different from the CPIP group. [double dagger] indicates values significantly different from the CPIP + GSH 100 group. P < 0.05 was considered statistically significant. CPIP: chronic postischemic pain, GSH: glutathione, and pGluN1: phosphorylated N-methyl-D-aspartate receptor subunit 1.
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Title Annotation:Research Article
Author:Yeo, Jinseok; Jung, Hoon; Lee, Hyerim
Publication:Pain Research and Management
Article Type:Report
Date:Jan 1, 2017
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