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一项关于 5-羟色胺和去甲肾上腺素作为佐剂改善皮肤刺痛反应时,提高美西律皮肤镇痛作用的比较研究。在大鼠中。

A comparative study of serotonin and norepinephrine as adjuncts to improve cutaneous antinociception of mexiletine in response to skin pinpricks in rats.

机构信息

Department of Anesthesiology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.

出版信息

Int J Immunopathol Pharmacol. 2021 Jan-Dec;35:20587384211016129. doi: 10.1177/20587384211016129.

Abstract

As adrenaline, serotonin and norepinephrine are two other vasoconstrictors and both of which have been proved to increase the quality and duration of local anesthetics when added as adjuvants. However, the difference in the improvement of the nociception of local anesthetics between the two adjuvants remains unclear. The purpose of this study was to assess the cutaneous nociception of mexiletine by coadministration with serotonin and norepinephrine. Subcutaneous injection of drugs or combinations includes mexiletine 0.6, 1.8, 6.0 μmol, serotonin 1.6500 μmol, noradrenaline 0.8895 nmol, saline, mexiletine 1.8 and 6.0 μmol, respectively combined with serotonin 0.4125, 0.8250, 1.6500 μmol and noradrenaline 0.0356, 0.1779, 0.8895 nmol, with each injection dose of 0.6 ml. The nociception of mexiletine alone and mexiletine coadministered with serotonin and norepinephrine was assessed after subcutaneous injection. Subcutaneous injections of mexiletine elicited dose-related cutaneous antinociception ( < 0.05, 0.01, or 0.001). Compared with mexiletine (1.8 μmol), adding norepinephrine (except for lowest dose) and serotonin to mexiletine (1.8 μmol) solutions for skin nociceptive block potentiated and prolonged the action ( < 0.01 or 0.001). Mexiletine (6.0 μmol) combined with norepinephrine and serotonin extended the duration of cutaneous antinociception when compared with mexiletine (6.0 μmol) alone ( < 0.05, 0.01, or 0.001). Both serotonin and norepinephrine improve the sensory block and enhances the nociceptive block duration of mexiletine, and serotonin is superior to that of norepinephrine.

摘要

作为肾上腺素、血清素和去甲肾上腺素的另外两种血管收缩剂,当作为佐剂添加时,它们都已被证明可以提高局部麻醉剂的质量和持续时间。然而,这两种佐剂在改善局部麻醉剂的痛觉方面的差异仍不清楚。本研究旨在评估佐剂给予血清素和去甲肾上腺素后,对美西律的皮肤痛觉的影响。皮下注射药物或组合包括美西律 0.6、1.8、6.0 μmol、血清素 1.6500 μmol、去甲肾上腺素 0.8895 nmol、生理盐水、美西律 1.8 和 6.0 μmol 分别与血清素 0.4125、0.8250、1.6500 μmol 和去甲肾上腺素 0.0356、0.1779、0.8895 nmol 联合,每次注射剂量为 0.6ml。单独皮下注射美西律和同时皮下注射美西律和血清素与去甲肾上腺素后,评估美西律的痛觉。皮下注射美西律可引起剂量相关的皮肤镇痛作用( <0.05、0.01 或 0.001)。与美西律(1.8 μmol)相比,将去甲肾上腺素(除最低剂量外)和血清素加入美西律(1.8 μmol)溶液中,可增强和延长皮肤痛觉阻断作用( <0.01 或 0.001)。与单独使用美西律(6.0 μmol)相比,美西律(6.0 μmol)与去甲肾上腺素和血清素联合使用可延长皮肤镇痛持续时间( <0.05、0.01 或 0.001)。血清素和去甲肾上腺素均可改善美西律的感觉阻滞作用,并延长其痛觉阻滞时间,且血清素优于去甲肾上腺素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1fe/8132083/c5b0410b0ad3/10.1177_20587384211016129-fig1.jpg

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