Relationship between G9a and Slack in spinal cord dorsal horn during remifentanil-induced hyperalgesia in a rat model of incisional pain

Q4 Medicine
Yi-ze Li, M. Han, Lin-lin Zhang, Lin Su, Xin Wang, K. Xie, Yonghao Yu, Guolin Wang
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Abstract

Objective To evaluate the relationship between euchromatic histone-lysine N-methyltransferase (G9a) and sodium-dependent activation of potassium channel (Slack) in the spinal cord dorsal horn during remifentanil-induced hyperalgesia in a rat model of incisional pain. Methods Clean-grade healthy male Sprague-Dawley rats, aged 1 month, weighing 100-120 g, were divided into 4 groups (n=6 each) by a random number table method: normal saline group (S group), vector group (V group), vector plus remifentanil plus incisional pain group (VRI group), and G9a-siRNA plus remifentanil plus incisional pain group (DRI group). In VRI group and DRI group, vector 1 μl was injected into the L4-5 spinal dorsal horn, 3 days later remifentanil 1 μg·kg-1·min-1 was intravenously infused via the tail vein for 60 min, and the model of incisional pain was established simultaneously.The equal volume of normal saline was given instead in S and V groups.The mechanical paw withdrawal threshold (MWT) and thermal paw withdrawal latency (TWL) were measured at 24 h before remifentanil infusion (T0) and 2, 6, 24 and 48 h after infusion (T1-4). Rats were sacrificed after behavioral tests, and the L4, 5 segments of spinal dorsal horns were taken for determination of the expression of G9a, H3K9me2 and Slack by Western blot. Results Compared with S group, TWL was significantly shortened, and MWT was decreased at T1-4, the expression of G9a and H3K9me2 was up-regulated, and the expression of Slack was down-regulated in VRI group (P<0.05). Compared with VRI group, the TWL was significantly prolonged and MWT was increased at T1-4, the expression of G9a and H3K9me2 was down-regulated, and Slack expression was up-regulated in DRI group (P<0.05). Conclusion The mechanism by which remifentanil induces hyperalgesia is related to up-regulating G9a and H3K9me2 expression and down-regulating Slack expression in the spinal dorsal horn of rats with incisional pain. Key words: Piperidines; Hyperalgesia; Spinal cord; Histone-lysine N-methyltransferase; Potassium channels
瑞芬太尼致痛觉过敏大鼠切口痛模型中脊髓背角G9a与松弛的关系
目的探讨瑞芬太尼致痛觉过敏大鼠脊髓背角钠依赖性钾通道激活与常染色组蛋白-赖氨酸n -甲基转移酶(G9a)的关系。方法1月龄、体重100 ~ 120 g的清洁级健康雄性sd - dawley大鼠,采用随机数字表法分为生理盐水组(S组)、载体组(V组)、载体加瑞芬太尼加切口疼痛组(VRI组)、G9a-siRNA加瑞芬太尼加切口疼痛组(DRI组),每组n=6。VRI组和DRI组大鼠腰4 ~ 5脊背角注射载体1 μl, 3 d后经尾静脉滴注瑞芬太尼1 μg·kg-1·min-1,持续60 min,同时建立切口疼痛模型。S组和V组改为等量生理盐水。在瑞芬太尼输注前24 h (T0)和输注后2、6、24、48 h (T1-4)测量机械足戒断阈值(MWT)和热足戒断潜伏期(TWL)。行为学实验后处死大鼠,取脊髓背角L4、5节段,Western blot法检测G9a、H3K9me2、Slack的表达。结果与S组比较,VRI组在T1-4时TWL显著缩短,MWT降低,G9a、H3K9me2表达上调,Slack表达下调(P<0.05)。与VRI组相比,DRI组在T1-4时TWL显著延长,MWT升高,G9a、H3K9me2表达下调,Slack表达上调(P<0.05)。结论瑞芬太尼诱导痛觉过敏的机制与上调切口痛大鼠脊髓背角G9a和H3K9me2表达,下调Slack表达有关。关键词:哌啶类;痛觉过敏;脊髓的;Histone-lysine N-methyltransferase;钾离子通道
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来源期刊
中华麻醉学杂志
中华麻醉学杂志 Medicine-Anesthesiology and Pain Medicine
CiteScore
0.10
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0.00%
发文量
11211
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