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Pharmacological assessments of nitric oxide synthase isoforms and downstream diversity of NO signaling in the maintenance of thermal and mechanical hypersensitivity after peripheral nerve injury in mice.小鼠外周神经损伤后热和机械超敏反应维持过程中一氧化氮合酶亚型的药理学评估及NO信号的下游多样性
Neuropharmacology. 2009 Mar;56(3):702-8. doi: 10.1016/j.neuropharm.2008.12.003. Epub 2008 Dec 16.
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Pathological and protective roles of glia in chronic pain.神经胶质细胞在慢性疼痛中的病理及保护作用
Nat Rev Neurosci. 2009 Jan;10(1):23-36. doi: 10.1038/nrn2533.
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A prolonged nitric oxide-dependent, opioid-mediated antinociceptive effect of hyperbaric oxygen in mice.高压氧对小鼠产生的一种依赖一氧化氮、由阿片类介导的持久抗伤害感受作用。
J Pain. 2009 Feb;10(2):167-72. doi: 10.1016/j.jpain.2008.08.003. Epub 2008 Oct 31.
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Spinal nerve ligation reduces nitric oxide synthase activity and expression: effect of resveratrol.
Pharmacol Biochem Behav. 2008 Oct;90(4):742-7. doi: 10.1016/j.pbb.2008.05.024.
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Transient early expression of TNF-alpha in sciatic nerve and dorsal root ganglia in a mouse model of painful peripheral neuropathy.在疼痛性周围神经病变小鼠模型中,肿瘤坏死因子-α在坐骨神经和背根神经节中的短暂早期表达。
Neurosci Lett. 2008 May 9;436(2):210-3. doi: 10.1016/j.neulet.2008.03.023. Epub 2008 Mar 14.
6
Hyperbaric oxygen treatment is comparable to acetylsalicylic acid treatment in an animal model of arthritis.在关节炎动物模型中,高压氧治疗与乙酰水杨酸治疗效果相当。
J Pain. 2007 Dec;8(12):924-30. doi: 10.1016/j.jpain.2007.06.005. Epub 2007 Aug 9.
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Hyperbaric oxygen treatment decreases inflammation and mechanical hypersensitivity in an animal model of inflammatory pain.高压氧治疗可减轻炎性疼痛动物模型中的炎症和机械性超敏反应。
Brain Res. 2006 Jul 7;1098(1):126-8. doi: 10.1016/j.brainres.2006.04.088. Epub 2006 Jun 5.
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Hyperbaric oxygen therapy in chronic pain management.
Curr Pain Headache Rep. 2006 Apr;10(2):95-100. doi: 10.1007/s11916-006-0019-x.
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Immune and inflammatory mechanisms in neuropathic pain.神经病理性疼痛中的免疫和炎症机制。
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Mechanisms of hyperbaric oxygen and neuroprotection in stroke.高压氧与中风神经保护的机制
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高压氧对神经病理性疼痛大鼠模型疼痛相关行为和一氧化氮合酶的影响。

Effects of hyperbaric oxygen on pain-related behaviors and nitric oxide synthase in a rat model of neuropathic pain.

机构信息

Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang, China.

出版信息

Pain Res Manag. 2013 May-Jun;18(3):137-41. doi: 10.1155/2013/147043.

DOI:10.1155/2013/147043
PMID:23748254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3673931/
Abstract

BACKGROUND

Neuropathic pain is complex, and a satisfactory therapeutic method of treatment has yet to be developed; therefore, finding a new and effective therapeutic method is an important issue in the field of neuropathic pain.

OBJECTIVE

To determine the effects of hyperbaric oxygen (HBO) on pain-related behaviours and nitric oxide synthase (NOS) expression in a rat model of neuropathic pain.

METHODS

Forty male Sprague Dawley rats were randomly divided into five groups (eight rats per group) including control, sham operation, sciatic nerve with chronic constriction injury (CCI), HBO pretreatment (pre-HBO) and HBO post-treatment (post-HBO) groups. Pain-related behaviours and NOS expression in the spinal cord were compared among the five groups.

RESULTS

Compared with the CCI group, the mechanical withdrawal threshold was significantly increased and thermal withdrawal latency was significantly extended in the pre-HBO and post-HBO groups (all P<0.05). After CCI, expression of spinal neuronal NOS and inducible NOS were increased. Expression of spinal neuronal NOS and inducible NOS were significantly decreased in the pre-HBO and post-HBO groups compared with the CCI group (all P<0.05). Spinal eNOS expression changed very little.

DISCUSSION

HBO has been used as an effective and noninvasive method for the treatment of spinal cord injuries and high-altitude sickness, and in immunosuppression and stem-cell research; however, it has yet to be applied to the treatment of neuropathic pain. The present study indicated that HBO effectively increased mechanical withdrawal threshold and thermal withdrawal latency, demonstrating that HBO has therapeutic effects on neuropathic pain.

CONCLUSION

HBO inhibits pain in rats with CCI through the regulation of spinal NOS expression.

摘要

背景

神经病理性疼痛较为复杂,目前尚未开发出满意的治疗方法,因此寻找新的有效治疗方法是神经病理性疼痛领域的重要课题。

目的

观察高压氧(HBO)对神经病理性疼痛大鼠疼痛相关行为学及一氧化氮合酶(NOS)表达的影响。

方法

40 只雄性 SD 大鼠随机分为对照组、假手术组、坐骨神经慢性缩窄性损伤(CCI)组、HBO 预处理组(pre-HBO 组)和 HBO 后处理组(post-HBO 组),每组 8 只。比较五组大鼠的疼痛相关行为学及脊髓 NOS 表达。

结果

与 CCI 组比较,pre-HBO 组和 post-HBO 组大鼠机械缩足阈值升高,热缩足潜伏期延长(均 P<0.05)。CCI 后,大鼠脊髓神经元型 NOS 和诱导型 NOS 表达均升高,pre-HBO 组和 post-HBO 组大鼠脊髓神经元型 NOS 和诱导型 NOS 表达均低于 CCI 组(均 P<0.05),脊髓内皮型 NOS 表达变化不大。

讨论

HBO 已应用于脊髓损伤和高原病、免疫抑制及干细胞研究等的治疗,尚未应用于神经病理性疼痛的治疗。本研究发现 HBO 可有效提高机械缩足阈值和热缩足潜伏期,提示 HBO 对神经病理性疼痛具有治疗作用。

结论

HBO 通过调节脊髓 NOS 表达抑制 CCI 大鼠疼痛。