基础研究

脉冲射频对坐骨神经慢性压迫大鼠降钙素基因相关肽表达的远期影响

  • 付淼 ,
  • 任浩 ,
  • 罗芳
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  • 1.北京大学肿瘤医院暨北京市肿瘤防治研究所,恶性肿瘤发病机制及转化研究教育部重点实验室麻醉科,北京市 100142;
    2.首都医科大学附属北京天坛医院麻醉科,北京市 100050
付淼(1988-),女,汉族,北京市人,医师,主要研究方向:疼痛治疗与麻醉。通讯作者:罗芳(1971-),女,四川人,主任医师、教授,主要研究方向:急慢性疼痛的治疗。

收稿日期: 2018-02-07

  修回日期: 2018-03-14

  网络出版日期: 2018-05-24

基金资助

北京市卫生系统高层次人才培养计划(学科骨干)项目(No. 2014-3-035)

Long-term Effect of Pulsed Radiofrequency on Expression of Calcitonin Gene-related Peptide in Chronic Constriction Injured Rats

  • FU Miao ,
  • REN Hao ,
  • LUO Fang
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  • 1. Department of Anesthesiology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China;
    2. Department of Anesthesiology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China;

Received date: 2018-02-07

  Revised date: 2018-03-14

  Online published: 2018-05-24

Supported by

Supported by Beijing Health System Excellent Professional Program (Core) (No. 2014-3-035)

摘要

目的 探讨脉冲射频对坐骨神经慢性压迫模型大鼠背根神经节中降钙素基因相关肽(CGRP)表达的长期影响。方法 Sprague-Dawley大鼠36只随机分为假手术组(n=12)、模型组(n=12)和治疗组(n=12)。模型组和治疗组结扎坐骨神经,治疗组予脉冲射频治疗坐骨神经结扎部位120 s。治疗前及治疗后7 d、14 d、21 d、28 d测量缩足反射阈值(HWT),治疗后28 d取大鼠右L4-6背根神经节,采用RT-qPCR和ELISA方法检测CGRP表达。结果 治疗后治疗组大鼠HWT逐渐升高,7 d起即高于模型组(P<0.05),21 d、28 d与假手术组无显著性差异(P>0.05)。治疗组CGRP转录及翻译水平均明显低于模型组(P<0.01)。结论 脉冲射频治疗可长时间缓解神经病理性疼痛,可能与下调背根神经节中CGRP表达有关。

本文引用格式

付淼 , 任浩 , 罗芳 . 脉冲射频对坐骨神经慢性压迫大鼠降钙素基因相关肽表达的远期影响[J]. 中国康复理论与实践, 2018 , 24(5) : 526 -529 . DOI: 10.3969/j.issn.1006-9771.2018.05.007

Abstract

Objective To investigate the long-term effect of pulsed radiofrequency on the expression of calcitonin gene-related peptide (CGRP) in dorsal root ganglion of rats with chronic constriction injury. Methods A total of 36 Sprague-Dawley rats were randomly divided into sham group (n=12), model group (n=12) and treatment group (n=12). The sciatic nerve was ligated in the model group and the treatment group, and the treatment group was treated with pulsed radiofrequency on the injured nerve for 120 seconds. Hindpaw withdrawl threshold (HWT) was measured before treatment, and seven days, 14 days, 21 days and 28 days after treatment. After HWT, the right L4-6 dorsal root ganglions were tested the CGRP expression using RT-qPCR and ELISA. Results HWT gradually increased in the treatment group after treatment, and was higher than that in the model group since seven days after treatment (P<0.05), similar to that of the sham group 21 days and 28 days after treatment (P>0.05). The transcription and translation levels of CGRP were both significantly lower in the treatment group than in the model group (P<0.01).Conclusion Pulsed radiofrequency might relieve the neuropathic pain through reducing CGRP expression in dorsal root ganglion in a long term.

参考文献

[1] Treede RD, Jensen TS, Campbell JN, et al.Neuropathic pain: redefinition and a grading system for clinical and research purposes[J]. Neurology, 2008, 70(18): 1630-1635.
[2] Sluijter ME. Pulsed radiofrequency [J]. Anesthesiology, 2005, 103(6): 1313; author reply 1313-1314.
[3] Abd-Elsayed A, Anis A, Kaye AD.Radio frequency ablation and pulsed radiofrequency for treating peripheral neuralgias[J]. Curr Pain Headache Rep, 2018, 22(1): 5.
[4] Kim K, Jo D, Kim E.Pulsed Radiofrequency to the dorsal root ganglion in acute herpes zoster and postherpetic neuralgia[J]. Pain Physician, 2017, 20(3): E411-E418.
[5] Albayrak I, Apiliogullari S, Dal CN, et al.Efficacy of pulsed radiofrequency therapy to dorsal root ganglion adding to TENS and exercise for persistent pain after total knee arthroplasty[J]. J Knee Surg, 2017, 30(2): 134-142.
[6] Schou WS, Ashina S, Amin FM, et al.Calcitonin gene-related peptide and pain: a systematic review[J]. J Headache Pain, 2017, 18(1): 34.
[7] Russell FA, King R, Smillie SJ, et al.Calcitonin gene-related peptide: physiology and pathophysiology[J]. Physiol Rev, 2014, 94(4): 1099-1142.
[8] Hamann W, Abou-Sherif S, Thompson S, et al.Pulsed radiofrequency applied to dorsal root ganglia causes a selective increase in ATF3 in small neurons[J]. Eur J Pain, 2006, 10(2): 171-176.
[9] Ren H, Jin H, Jia Z, et al.Pulsed radiofrequency applied to the sciatic nerve improves neuropathic pain by down-regulating the expression of calcitonin gene-related peptide in the dorsal root ganglion[J]. Int J Med Sci, 2018, 15(2): 153-160.
[10] Bennett GJ, Xie YK.A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man[J]. Pain, 1988, 33(1): 87-107.
[11] 孙臣琛,刘金锋. 背根神经节介入治疗带状疱疹后神经痛研究进展[J]. 中国疼痛医学杂志, 2017, 23(2): 130-134.
[12] 韩卫江,李霞,方梅,等. 半月神经节重复脉冲射频治疗三叉神经痛的临床观察[J]. 中国疼痛医学杂志, 2017, 23(5): 392-394.
[13] 贾怡童,罗芳. 脉冲射频技术用于神经病理性疼痛的治疗参数研究进展[J]. 中国疼痛医学杂志, 2017, 23(7): 481-486.
[14] Pope JE, Deer TR, Kramer J.A systematic review: current and future directions of dorsal root ganglion therapeutics to treat chronic pain[J]. Pain Med, 2013, 14(10): 1477-1496.
[15] 贾子普,任浩,李倩,等. 脉冲射频对慢性坐骨神经缩窄伤大鼠坐骨神经超微结构和胶质细胞源性神经营养因子表达的影响[J]. 中国康复理论与实践, 2016, 22(1): 53-57.
[16] Fang L, Ying S, Tao W, et al.3D CT-guided pulsed radiofrequency treatment for trigeminal neuralgia[J]. Pain Pract, 2014, 14(1): 16-21.
[17] Hirose K, Iwakura N, Orita S, et al.Evaluation of behavior and neuropeptide markers of pain in a simple, sciatic nerve-pinch pain model in rats[J]. Eur Spine J, 2010, 19(10): 1746-1752.
[18] Sugawara S, Okada S, Katagiri A, et al.Interaction between calcitonin gene-related peptide-immunoreactive neurons and satellite cells via P2Y12R in the trigeminal ganglion is involved in neuropathic tongue pain in rats[J]. Eur J Oral Sci, 2017, 125(6): 444-452.
[19] Ishikawa T, Miyagi M, Yamashita M, et al.In-vivo transfection of the proopiomelanocortin gene, precursor of endogenous endorphin, by use of radial shock waves alleviates neuropathic pain[J]. J Orthop Sci, 2013, 18(4): 636-645.
[20] La Rana G, Russo R, D'Agostino G, et al. AM404, an anandamide transport inhibitor, reduces plasma extravasation in a model of neuropathic pain in rat: role for cannabinoid receptors[J]. Neuropharmacology, 2008, 54(3): 521-529.
[21] Iyengar S, Ossipov MH, Johnson KW.The role of calcitonin gene-related peptide in peripheral and central pain mechanisms including migraine[J]. Pain, 2017, 158(4): 543-559.
[22] McMahon SB, Cafferty WB, Marchand F. Immune and glial cell factors as pain mediators and modulators[J]. Exp Neurol, 2005, 192(2): 444-462.
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