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增强型局部麻醉药新沙甲毒素与布比卡因或肾上腺素联合应用:长效止痛阻滞剂的研发。

Potentiation of local anesthetic activity of neosaxitoxin with bupivacaine or epinephrine: development of a long-acting pain blocker.

机构信息

Membrane Biochemistry Laboratory, Programme of Physiology and Biophysics, ICBM, Faculty of Medicine, University of Chile, P.O. Box 70005, Santiago 7, Chile.

出版信息

Neurotox Res. 2009 Nov;16(4):408-15. doi: 10.1007/s12640-009-9092-3. Epub 2009 Jul 28.

Abstract

Local anesthetics effectively block and relieve pain, but with a relatively short duration of action, limiting its analgesic effectiveness. Therefore, a long-acting local anesthetic would improve the management of pain, but no such agent is yet available for clinical use. The aim of this study is to evaluate the potentiation of the anesthetic effect of neosaxitoxin, with bupivacaine or epinephrine in a randomized double-blind clinical trial. Ten healthy males were subcutaneously injected into the left and right forearms with a randomized pair of the following treatments: (i) bupivacaine (5 mg); (ii) neosaxitoxin (10 microg); (iii) neosaxitoxin (10 microg) plus bupivacaine (5 mg), and (iv) neosaxitoxin (10 microg) plus epinephrine (1:100.000), but all participant received all four formulations (in 2 ml; s.c.), with 1 month elapsing between the two round of experiments. A validated sensory and pain paradigm was used for evaluating the effect of the treatment 0-72 h after the injections, measuring sensory, pain, and mechanical touch perception threshold. The duration of the effect produced by combined treatments was longer than that by the single drugs. In conclusion, bupivacaine and epinephrine potentiate the local anesthetic effect of neosaxitoxin in humans when co-injected subcutaneously. The present results support the idea that neosaxitoxin is a new long-acting local pain blocker, with highly potential clinical use.

摘要

局部麻醉剂可有效阻断和缓解疼痛,但作用持续时间相对较短,限制了其镇痛效果。因此,长效局部麻醉剂将改善疼痛管理,但目前尚无此类药物可供临床使用。本研究旨在评估新沙海毒素与布比卡因或肾上腺素联合应用对麻醉效果的增强作用,采用随机双盲临床试验进行评估。10 名健康男性被随机分为两组,分别在左右前臂皮下注射以下治疗药物:(i)布比卡因(5mg);(ii)新沙海毒素(10μg);(iii)新沙海毒素(10μg)加布比卡因(5mg);(iv)新沙海毒素(10μg)加肾上腺素(1:100000),但所有参与者均接受了所有四种制剂(2ml;皮下注射),两次实验之间间隔 1 个月。采用已验证的感觉和疼痛范式评估注射后 0-72 小时的治疗效果,测量感觉、疼痛和机械触觉感知阈值。联合治疗的作用持续时间长于单一药物。总之,当皮下共注射时,布比卡因和肾上腺素增强了新沙海毒素在人体中的局部麻醉效果。本研究结果支持新沙海毒素是一种新型长效局部疼痛阻断剂,具有很高的临床应用潜力的观点。

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