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不同电针方案对鼠骨肿瘤诱导痛觉过敏的影响:性别差异和炎症的作用。

Effects of different electroacupuncture scheduling regimens on murine bone tumor-induced hyperalgesia: sex differences and role of inflammation.

机构信息

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, MN 55108, USA.

出版信息

Evid Based Complement Alternat Med. 2012;2012:671386. doi: 10.1155/2012/671386. Epub 2012 Dec 20.

DOI:10.1155/2012/671386
PMID:23320035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3541553/
Abstract

Previous studies have shown that electroacupuncture (EA) is able to reduce hyperalgesia in rodent models of persistent pain, but very little is known about the analgesic effects and potential sex differences of different EA treatment regimens. In the present study, we examined the effects of five different EA treatments on tumor-induced hyperalgesia in male and female mice. EA applied to the ST-36 acupoint either twice weekly (EA-2X/3) beginning on postimplantation day (PID) 3 or prophylactically three times prior to implantation produced the most robust and longest lasting antinociceptive effects. EA treatment given once per week beginning at PID 7 only produced an antinociceptive effect in female animals. The analgesic effect of EA-2X/3 began earlier in males, but lasted longer in females indicating sex differences in EA. We further demonstrate that EA-2X/3 elicits a marked decrease in tumor-associated inflammation as evidenced by a significant reduction in tumor-associated neutrophils at PID 7. Moreover, EA-2X/3 produced a significant reduction in tumor-associated PGE(2) as measured in microperfusate samples. Collectively, these data provide evidence that EA-2X/3 treatment reduces tumor-induced hyperalgesia, which is associated with a decrease in tumor-associated inflammation and PGE(2) concentration at the tumor site suggesting possible mechanisms by which EA reduces tumor nociception.

摘要

先前的研究表明,电针(EA)能够减轻持续性疼痛的啮齿动物模型中的痛觉过敏,但对于不同的 EA 治疗方案的镇痛效果和潜在的性别差异知之甚少。在本研究中,我们检查了五种不同的 EA 治疗方法对雄性和雌性小鼠肿瘤诱导性痛觉过敏的影响。从植入后第 3 天(PID)3 开始,每周两次(EA-2X/3)应用于 ST-36 穴位,或在植入前预防性地进行三次,产生了最强烈和最持久的镇痛作用。从 PID 7 开始每周一次的 EA 治疗仅在雌性动物中产生镇痛作用。EA-2X/3 的镇痛作用在雄性中更早开始,但在雌性中持续时间更长,表明 EA 存在性别差异。我们进一步证明,EA-2X/3 引起肿瘤相关炎症的明显减少,这表现在 PID 7 时肿瘤相关中性粒细胞的显著减少。此外,EA-2X/3 还导致肿瘤相关 PGE(2)在微灌流样本中的显著减少。总的来说,这些数据提供了证据表明,EA-2X/3 治疗可减轻肿瘤诱导的痛觉过敏,这与肿瘤部位的肿瘤相关炎症和 PGE(2)浓度的降低有关,提示了 EA 减轻肿瘤伤害感受的可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/10f7f52853f9/ECAM2012-671386.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/481d7764a6c9/ECAM2012-671386.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/1fc0c389d9e4/ECAM2012-671386.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/277085bd7b54/ECAM2012-671386.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/2ba0c9b914c4/ECAM2012-671386.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/ee3f9cc73593/ECAM2012-671386.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/10f7f52853f9/ECAM2012-671386.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/481d7764a6c9/ECAM2012-671386.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/1fc0c389d9e4/ECAM2012-671386.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/277085bd7b54/ECAM2012-671386.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/2ba0c9b914c4/ECAM2012-671386.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/ee3f9cc73593/ECAM2012-671386.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b4/3541553/10f7f52853f9/ECAM2012-671386.006.jpg

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