PMID- 28721088 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 1178-7090 (Print) IS - 1178-7090 (Electronic) IS - 1178-7090 (Linking) VI - 10 DP - 2017 TI - Forced exercise attenuates neuropathic pain in chronic constriction injury of male rat: an investigation of oxidative stress and inflammation. PG - 1457-1466 LID - 10.2147/JPR.S135081 [doi] AB - BACKGROUND AND OBJECTIVE: Initial peripheral/central nerve injuries, such as chronic constriction injury (CCI)/spinal cord injury, are often compounded by secondary mechanisms, including inflammation and oxidative stress, which may lead to chronic neuropathic pain characterized by hyperalgesia or allodynia. On the other hand, exercise as a behavioral and non-pharmacological treatment has been shown to alleviate chronic neuropathic pain. Therefore, this study was conducted to examine whether or not exercise reduces neuropathic pain through modifying oxidative stress and inflammation in chronic constriction injury of the sciatic nerve. MATERIALS AND METHODS: Wistar male rats weighing 200+/-20 g were randomly divided into five groups (normal, sham, CCI, pre-CCI exercise, and post-CCI exercise group). Sciatic nerve of anesthetized rats was loosely ligated to induce CCI, and they were then housed in separate cages. The rats ran on treadmill at a moderate speed for 3 weeks. Mechanical allodynia and thermal hyperalgesia were determined using von Frey filament and plantar test, respectively. Tumor necrosis factor-alpha (TNF-alpha) assayed in the cerebrospinal fluid, malondialdehyde, and total antioxidant capacity were measured in the serum using Western blot test, thiobarbituric acid, and ferric reducing ability of plasma (FRAP), respectively. RESULTS: The mechanical allodynia (P=0.024) and thermal hyperalgesia (P=0.002) in the CCI group were higher than those in the sham group. Exercise after CCI reduced (P=0.004) mechanical allodynia and thermal hyperalgesia (P=0.025) compared with the CCI group. Moreover, the level of FRAP in the CCI group was (P=0.001) lower than that in the sham group, and post-CCI exercise reversed FRAP amount toward the control level (P=0.019). The amount of malondialdehyde did not differ between groups. Level of TNF-alpha increased in the CCI group (P=0.0002) compared with sham group and post-CCI exercise could reverse it toward the level of control (P=0.005). CONCLUSION: Post CCI-exercise but not pre CCI-exercise reduces CCI-induced neuropathic pain. One of the possible involved mechanisms is increasing the total antioxidant capacity and reducing the amount of TNF-alpha. FAU - Safakhah, Hossein Ali AU - Safakhah HA AD - Department of Physiology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. AD - Research Center of Physiology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. FAU - Moradi Kor, Nasroallah AU - Moradi Kor N AD - Research Center of Physiology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. AD - Student Research Committee, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. FAU - Bazargani, Atiyeh AU - Bazargani A AD - Student Research Committee, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. FAU - Bandegi, Ahmad Reza AU - Bandegi AR AD - Department of Biochemistry, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. FAU - Gholami Pourbadie, Hamid AU - Gholami Pourbadie H AD - Department of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran. FAU - Khoshkholgh-Sima, Baharak AU - Khoshkholgh-Sima B AD - Department of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran. FAU - Ghanbari, Ali AU - Ghanbari A AD - Research Center of Physiology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran. LA - eng PT - Journal Article DEP - 20170623 PL - New Zealand TA - J Pain Res JT - Journal of pain research JID - 101540514 PMC - PMC5499951 OTO - NOTNLM OT - CCI OT - TNF-alpha OT - neuropathic pain OT - oxidative stress OT - treadmill exercise COIS- Disclosure The authors report no conflicts of interest in this work. EDAT- 2017/07/20 06:00 MHDA- 2017/07/20 06:01 PMCR- 2017/06/23 CRDT- 2017/07/20 06:00 PHST- 2017/07/20 06:00 [entrez] PHST- 2017/07/20 06:00 [pubmed] PHST- 2017/07/20 06:01 [medline] PHST- 2017/06/23 00:00 [pmc-release] AID - jpr-10-1457 [pii] AID - 10.2147/JPR.S135081 [doi] PST - epublish SO - J Pain Res. 2017 Jun 23;10:1457-1466. doi: 10.2147/JPR.S135081. eCollection 2017.