Welcome to visit Acta Anatomica Sinica! Today is
Chinese






P2X3 mRNA expression in L4-6 dorsal root ganglion at different times after the spared nerve injury
DU Jun-ying FANG Jun-fan FANG Jian-qiao* LE Xiao-qin XIAO Ting PAN Ning-fang YU Jie
Acta Anatomica Sinica ›› 2016 ›› Issue (3) : 297-302.
P2X3 mRNA expression in L4-6 dorsal root ganglion at different times after the spared nerve injury
Objective To observe the mRNA expression of P2X3 in L4-6 dorsal root ganglion (DRG) at different times after spared nerve injury (SNI), and to discuss the effect of periphery P2X3 in neuropathic pain. Methods Fifty-four healthy male SD rats were randomly divided into control group, sham surgery group, and surgery group. The spared nerve injury model was established by ligating the common peroneal and the tibial nerves and then cutting off the nerves but keeping the sural nerve intact. Bilateral paw withdrawal thresholds were dynamic observed before injury (base), at day 1, 3, 7 and day 14 after injury. P2X3 mRNA expression in L4-6 DRG at day 3, 7, and day 14 after injury was measured by fluorescence quantitative PCR method. Results Compared with control group, ispilateral paw withdrawal thresholds of surgery group were significantly decreased at day 1, 3, 7, and day 14 after injury (P<0.05), while that of sham surgery had no statistical significance (P>0.05). There was no difference of contralateral pain threshold among control group, surgery group, and sham surgery group (P>0.05). P2X3 mRNA expressions of L4, L5, and L6 DRG of surgery group were remarkable increased at day 3, 7 after injury (P<0.05), while that of L5, L6 DRG were decreased at 14d after injury (P<0.05), and that of L4 DRG were more than that of sham surgery at day 14 after injury (P<0.05). In addition, there was no difference of P2X3 mRNA expression in L4, L5, and L6 DRG at every time after injury between sham surgery group and surgery group. Conclusion Periphery P2X3 mRNA expression is involved in the initiation and maintenance of pain induced by SNI, which may play a different effect at different phases.
[1]Chen XM, Xu J, Song JG, et al. Electroacupuncture inhibits excessive interferon-gamma evoked up-regulation of P2X4 receptor in spinal microglia in a CCI rat model for neuropathic pain[J]. Br J Anaesth, 2015, 114(1): 150-157.
[2]Decosterd I, Woolf CJ. Spared nerve injury: an animal model of persistent peripheral neuropathic pain[J]. Pain, 2000, 87(2): 149-158.
[3]Guo J, Fu X, Cui X, et al. Contributions of purinergic P2X3 receptors within the midbrain periaqueductal gray to diabetes-induced neuropathic pain[J]. J Physiol Sci, 2015, 65(1): 99-104.
[4]Xiong W, Qiu SY, Xu LY, et al. Effects of intermedin on dorsal root ganglia in the transmission of neuropathic pain in chronic constriction injury rats[J]. Clin Exp Pharmacol Physiol, 2015, 42(7): 780-787.
[5]Wang WSh, Tu WZh, Xi HY, et al. The effect of electroacupuncture on the expression of P2X3 receptor in dorsal root ganglion and spinal cord in rats with neuropathic pain[J]. Chinese Journal of Pain Medicine, 2015, 21(2): 97-101. (in Chinese)
王万胜, 屠文展, 奚海艳, 等. 电针对神经病理性疼痛大鼠背根神经节及脊髓P2X3受体的影响[J]. 中国疼痛医学杂志, 2015, 21(2): 97-101.
[6]North RA. P2X3 receptors and peripheral pain mechanisms[J]. J Physiol, 2004, 554(Pt 2): 301-308.
[7]Du JY, Fang JF, Chen YT, et al. Parametric optimization of electroacupuncture against bone-cancer pain in rats and its intervention on mRNA expression of opioid receptor and precursor[J]. Chinese Acupuncture & Moxibustion, 2015, 35(2): 161-168. (in Chinese)
杜俊英, 房军帆, 陈宜恬, 等. 电针抗大鼠骨癌痛的参数优选及其对阿片受体和前体mRNA表达的干预[J]. 中国针灸, 2015, 35(2): 161-168.
[8]Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2-Delta Delta C(T) method [J]. Methods, 2001, 25(4): 402-408.
[9]Lin L, Tao GC, Yi B. Difference of the characteristics of pain proceeding and the level of oxidative stress between the three neuropathic pain models[J]. Chongqing Medicine, 2011, 40(1): 3-6. (in Chinese)
林露, 陶国才, 易斌. 3种神经病理性疼痛大鼠模型的评价[J]. 重庆医学, 2011, 40(1): 3-6.
[10]Ye JY, Yan SS, Jiang JL, 等. Difference of the characteristics of pain proceeding and the level of oxidative stress between the four neuropathic pain models[J]. Journal of Yunnan University of Traditional Chinese Medicine, 2015, 38(4): 92-95. (in Chinese)
叶佳瑜, 颜思思, 蒋永亮, 等. 4种常用神经病理痛动物模型的评价[J]. 云南中医学院学报, 2015, 38(4): 92-95.
[11]Hirai T, Enomoto M, Kaburagi H, et al. Intrathecal AAV serotype 9-mediated delivery of shRNA against TRPV1 attenuates thermal hyperalgesia in a mouse model of peripheral nerve injury[J]. Mol Ther, 2014, 22(2): 409-419.
[12]Ballini E, Virginio C, Medhurst SJ, et al. Characterization of three diaminopyrimidines as potent and selective antagonists of P2X3 and P2X2/3 receptors with in vivo efficacy in a pain model[J]. Br J Pharmacol, 2011, 163(6): 1315-1325.
[13]Burnstock G. Purinergic mechanisms and pain—an update[J]. Eur J Pharmacol, 2013, 716(13): 24-240.
[14]Pankratov Y, Lalo U, Krishtal O, et al. P2X receptormediated excitatory synaptic currents in somatosensory cortex[J]. Mol Cell Neurosci, 2003, 24(3): 842-849.
[15]Xiang Z, Xiong Y, Yan N, et al. Functional up-regulation of P2X 3 receptors in the chronically compressed dorsal root ganglion[J]. Pain, 2008, 140(1): 23-34.
[16]Ford AP. In pursuit of P2X3 antagonists: novel therapeutics for chronic pain and afferent sensitization[J]. Purinergic Signal, 2012, 8(Suppl 1): 3-26.
[17]Jarvis MF, Burgard EC, McGaraughty S, et al. A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat[J]. Proc Natl Acad Sci U S A, 2002, 99(26): 17179-17184.
[18]Jacobson KA, Costanzi S, Joshi BV, et al. Agonists and antagonists for P2 receptors[J]. Novartis Found Symp, 2006, 276:58-68.
[19]Honore P, Kage K, Mikusa J, et al. Analgesic profile of intrathecal P2X(3) antisense oligonucleotide treatment in chronic inflammatory and neuropathic pain states in rats[J]. Pain, 2002, 99(1-2): 11-19.
[20]Cui YY, Wu HH, Wang L, et al. Spatio-temporal expression of P2X3 receptor in rats with diabetic mechanical allodynia[J]. Acta Anatomica Sinica, 2014, 45(4): 540-544. (in Chinese)
崔媛媛, 吴黄辉, 王兰, 等. 糖尿病机械性痛模型大鼠P2X3 受体的时空表达[J]. 解剖学报, 2014, 45(4): 540-544.
[21]Ou S, Zhao YD, Xiao Z, et al. Effect of lappaconitine on neuropathic pain mediated by P2X3 receptor in rat dorsal root ganglion[J]. Neurochem Int, 2011, 58(5): 564-573.
[22]Gao Y, Xu C, Liang S, et al. Effect of tetramethylpyrazine on primary afferent transmission mediated by P2X3 receptor in neuropathic pain states[J]. Brain Res Bull, 2008, 77(1): 27-32.
[23]Meisner JG, Reid AR, Sawynok J. Adrenergic regulation of P2X3 and TRPV1 receptors: differential effects of spared nerve injury[J]. Neurosci Lett, 2008, 444(2): 172-175.
/
〈 |
|
〉 |