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叶绿醇在体内和体外模型中的抗伤害感受及抗氧化活性

Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models.

作者信息

Santos Camila Carolina de Menezes Patrício, Salvadori Mirian Stiebbe, Mota Vanine Gomes, Costa Luciana Muratori, de Almeida Antonia Amanda Cardoso, de Oliveira Guilherme Antônio Lopes, Costa Jéssica Pereira, de Sousa Damião Pergentino, de Freitas Rivelilson Mendes, de Almeida Reinaldo Nóbrega

机构信息

Unity Academy of Hearth, Federal University of Campina Grande (UFCG), 58109-900 Cuité, PB, Brazil.

Health Sciences Center, Federal University of Paraíba (UFPB), 58051-900 João Pessoa, PB, Brazil.

出版信息

Neurosci J. 2013;2013:949452. doi: 10.1155/2013/949452. Epub 2013 Jun 11.

Abstract

The objective of the present study was to evaluate the antinociceptive effects of phytol using chemical and thermal models of nociception in mice and to assess its antioxidant effects in vitro. Phytol was administered intraperitoneally (i.p.) to mice at doses of 25, 50, 100, and 200 mg/kg. In the acetic acid-induced writhing test, phytol significantly reduced the number of contortions compared to the control group (P < 0.001). In the formalin test, phytol reduced significantly the amount of time spent in paw licking in both phases (the neurogenic and inflammatory phases), this effect being more pronounced in the second phase (P < 0.001). Phytol also provoked a significant increase in latency in the hot plate test. These antinociceptive effects did not impaire the motor performance, as shown in the rotarod test. Phytol demonstrated a strong antioxidant effect in vitro in its capacity to remove hydroxyl radicals and nitric oxide as well as to prevent the formation of thiobarbituric acid reactive substances (TBARS). Taken as a whole, these results show the pronounced antinociceptive effects of phytol in the nociception models used, both through its central and peripheral actions, but also its antioxidant properties demonstrated in the in vitro methods used.

摘要

本研究的目的是利用小鼠伤害感受的化学和热模型评估叶绿醇的抗伤害感受作用,并在体外评估其抗氧化作用。将叶绿醇以25、50、100和200mg/kg的剂量腹腔注射给小鼠。在醋酸诱导的扭体试验中,与对照组相比,叶绿醇显著减少了扭体次数(P<0.001)。在福尔马林试验中,叶绿醇在两个阶段(神经源性和炎症性阶段)均显著减少了舔足时间,在第二阶段这种作用更为明显(P<0.001)。叶绿醇在热板试验中还显著延长了潜伏期。如在转棒试验中所示,这些抗伤害感受作用并未损害运动性能。叶绿醇在体外表现出强大的抗氧化作用,能够清除羟自由基和一氧化氮,并防止硫代巴比妥酸反应性物质(TBARS)的形成。总体而言,这些结果表明,叶绿醇在所使用的伤害感受模型中具有显著的抗伤害感受作用,这是通过其中枢和外周作用实现的,同时也在体外方法中表现出抗氧化特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f46a/4437258/34f33510601e/NEUROSCIENCE2013-949452.001.jpg

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