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提取物对炎性疼痛的疗效:小鼠体内研究

Efficacy of Extract against Inflammatory Pain: In Vivo Studies in Mice.

作者信息

Micheli Laura, Vasarri Marzia, Barletta Emanuela, Lucarini Elena, Ghelardini Carla, Degl'Innocenti Donatella, Di Cesare Mannelli Lorenzo

机构信息

Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA)-Pharmacology and Toxicology Section, University of Florence, Viale Gaetano Pieraccini, 6, 50139 Florence, Italy.

Department of Experimental and Clinical Biomedical Sciences, University of Florence, Viale Morgagni 50, 50134 Florence, Italy.

出版信息

Mar Drugs. 2021 Jan 21;19(2):48. doi: 10.3390/md19020048.

DOI:10.3390/md19020048
PMID:33494253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7909763/
Abstract

(L.) Delile is traditionally used for its beneficial properties. Recently, promising antioxidant and anti-inflammatory biological properties emerged through studying the in vitro activity of the ethanolic leaves extract (POE). The present study aims to investigate the anti-inflammatory and analgesic role of POE in mice. Inflammatory pain was modeled in CD-1 mice by the intraplantar injection of carrageenan, interleukin IL-1β and formalin. Pain threshold was measured by von Frey and paw pressure tests. Nociceptive pain was studied by the hot-plate test. POE (10-100 mg kg) was administered per os. The paw soft tissue of carrageenan-treated animals was analyzed to measure anti-inflammatory and antioxidant effects. POE exerted a dose-dependent, acute anti-inflammatory effect able to counteract carrageenan-induced pain and paw oedema. Similar anti-hyperalgesic and anti-allodynic results were obtained when inflammation was induced by IL-1β. In the formalin test, the pre-treatment with POE significantly reduced the nocifensive behavior. Moreover, POE was able to evoke an analgesic effect in naïve animals. Ex vivo, POE reduced the myeloperoxidase activity as well as TNF-α and IL-1β levels; further antioxidant properties were highlighted as a reduction in NO concentration. POE is the candidate for a new valid strategy against inflammation and pain.

摘要

传统上,德利莱(L. Delile)因其有益特性而被使用。最近,通过研究乙醇叶提取物(POE)的体外活性,发现了其有前景的抗氧化和抗炎生物学特性。本研究旨在探讨POE在小鼠中的抗炎和镇痛作用。通过在CD-1小鼠足底注射角叉菜胶、白细胞介素IL-1β和福尔马林来模拟炎症性疼痛。通过von Frey和爪压力测试测量疼痛阈值。通过热板试验研究伤害性疼痛。POE(10 - 100毫克/千克)经口给药。分析角叉菜胶处理动物的爪软组织,以测量抗炎和抗氧化作用。POE发挥了剂量依赖性的急性抗炎作用,能够抵消角叉菜胶诱导的疼痛和爪水肿。当由IL-1β诱导炎症时,获得了类似的抗痛觉过敏和抗异常性疼痛的结果。在福尔马林试验中,POE预处理显著降低了伤害性防御行为。此外,POE能够在未处理的动物中诱发镇痛作用。在体外,POE降低了髓过氧化物酶活性以及TNF-α和IL-1β水平;进一步的抗氧化特性表现为NO浓度的降低。POE是对抗炎症和疼痛的新有效策略的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/f97bc69a6a3a/marinedrugs-19-00048-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/8e246ad8407b/marinedrugs-19-00048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/9f9dd763441a/marinedrugs-19-00048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/a5883968422e/marinedrugs-19-00048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/3ffe37742510/marinedrugs-19-00048-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/004bc1b5432f/marinedrugs-19-00048-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/25666b9f82e6/marinedrugs-19-00048-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/f97bc69a6a3a/marinedrugs-19-00048-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/8e246ad8407b/marinedrugs-19-00048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/9f9dd763441a/marinedrugs-19-00048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/a5883968422e/marinedrugs-19-00048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/3ffe37742510/marinedrugs-19-00048-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/004bc1b5432f/marinedrugs-19-00048-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/25666b9f82e6/marinedrugs-19-00048-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb6b/7909763/f97bc69a6a3a/marinedrugs-19-00048-g007.jpg

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