Liu Lingling, Abouelfetouh Mahmoud M, Ding Yi, Qianghui Lei, Sun Rui, Salah Eman, Nan Sha, Ding Mingxing, Song Yuzhen
Henan University of Animal Husbandry and Economy, Zhengzhou, Henan Province, China.
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei Province, China.
Pain Rep. 2025 Sep 3;10(5):e1296. doi: 10.1097/PR9.0000000000001296. eCollection 2025 Oct.
Neuropathic pain severely affects patients' quality of life. Limited treatments offer relief but often involve long-term use and side effects.
This study aimed to explore the electroacupuncture (EA) and subanesthetic alfaxalone (ALF) combination as a novel therapeutic substitute for the treatment of neuropathic pain in a spared nerve injury (SNI) mouse model.
Sixty healthy C57BL/6 male mice were randomized into 5 equal-sized groups: sham (n = 12) group, spared nerve injury (SNI; n = 12) group, SNI-ALF (n = 12), SNI-EA (n = 12), and SNI-EA-ALF (n = 12). The SNI mice received the treatment regimens at 8 days postoperatively once every 2 days for 7 treatments in total. The mechanical and thermal pain thresholds were tested after each treatment. Spinal cord samples were collected after the fourth and seventh treatments for detection of diazepam-binding inhibitor (DBI) and γ-aminobutyrate A1 isoform receptor (GABAA1).
Mice in the SNI-EA-ALF group showed a significant increase in mechanical and thermal pain thresholds as compared to those in the SNI-ALF and SNI-EA groups during the treatment period ( < 0.05). A significant increase in GABAA1 expression was observed after the fourth and seventh treatments in the SNI-EA-ALF group compared to the SNI-ALF and SNI-EA groups ( < 0.05). In addition, the DBI expression level was significantly lower in the SNI-ALF-EA group than the SNI, SNI-ALF, and SNI-EA groups ( < 0.05).
Our results support the use of EA, combined with ALF, to synergistically relieve pain in preclinical models of NP.
神经性疼痛严重影响患者的生活质量。可用的治疗方法有限,虽能缓解疼痛,但往往需要长期使用且伴有副作用。
本研究旨在探索电针(EA)与亚麻醉剂量的阿法沙龙(ALF)联合使用,作为一种新型治疗替代方法,用于在 spared nerve injury(SNI)小鼠模型中治疗神经性疼痛。
将60只健康的C57BL/6雄性小鼠随机分为5组,每组大小相等:假手术组(n = 12)、 spared nerve injury组(SNI;n = 12)、SNI-ALF组(n = 12)、SNI-EA组(n = 12)和SNI-EA-ALF组(n = 12)。SNI小鼠在术后第8天开始接受治疗方案,每2天一次,共进行7次治疗。每次治疗后测试机械性和热痛阈值。在第4次和第7次治疗后收集脊髓样本,用于检测地西泮结合抑制剂(DBI)和γ-氨基丁酸A1亚型受体(GABAA1)。
与SNI-ALF组和SNI-EA组相比,SNI-EA-ALF组小鼠在治疗期间的机械性和热痛阈值显著升高(<0.05)。与SNI-ALF组和SNI-EA组相比,SNI-EA-ALF组在第4次和第7次治疗后观察到GABAA1表达显著增加(<0.05)。此外,SNI-ALF-EA组的DBI表达水平显著低于SNI组、SNI-ALF组和SNI-EA组(<0.05)。
我们的结果支持在神经性疼痛的临床前模型中使用EA联合ALF协同缓解疼痛。