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薰衣草精油的化学多样性与镇痛活性

Chemodiversity and Antinociceptive Activity of L. Essential Oil.

作者信息

Đorđević Zlatković Miljana R, Stojanović Nikola M, Zlatković Dragan B, Randjelović Pavle J, Radulović Niko S

机构信息

Department of Chemistry, Faculty of Sciences and Mathematics, University of Niš, 18000 Niš, Serbia.

Department of Physiology, Faculty of Medicine, University of Niš, 18000 Niš, Serbia.

出版信息

Plants (Basel). 2024 Oct 30;13(21):3045. doi: 10.3390/plants13213045.

Abstract

An essential oil dominated by germacrene D (19.3% by GC) was isolated from the fresh fruit of L. (Fabaceae). Agglomerative clustering and -means clustering were employed to compare the composition of the oil with the existing literature data, suggesting that the used in this study represents a new chemotype. The essential oil was evaluated for its antinociceptive activity using the acetic acid-induced writhing test in rats at doses of 400, 200, and 100 mg/kg. All tested doses reduced the number of writhes induced by the intraperitoneal injection of acetic acid. The 400 mg/kg dose of the oil demonstrated a 54.4% inhibition, which was statistically different from the positive control, aspirin, which showed 90.2% inhibition at a dose of 200 mg/kg. Since the injection of acetic acid produces the release of prostaglandins, such as PGE2α and PGF2α, as well as sympathetic nervous system mediators in peritoneal fluids, the results suggest that the inhibition of prostaglandin release might represent one of the possible mechanisms of action exerted by the oil.

摘要

从豆科植物L.的新鲜果实中分离出一种以杜松烯D为主(气相色谱法测定含量为19.3%)的精油。采用凝聚聚类法和K均值聚类法将该精油的成分与现有文献数据进行比较,表明本研究中使用的该植物代表一种新的化学型。采用乙酸诱导大鼠扭体试验,以400、200和100mg/kg的剂量对该精油的抗伤害感受活性进行评估。所有测试剂量均减少了腹腔注射乙酸诱导的扭体次数。该精油400mg/kg剂量组显示出54.4%的抑制率,这与阳性对照阿司匹林在统计学上存在差异,阿司匹林在200mg/kg剂量时显示出90.2%的抑制率。由于注射乙酸会导致前列腺素如PGE2α和PGF2α以及腹膜液中交感神经系统介质的释放,结果表明抑制前列腺素释放可能是该精油发挥作用的一种可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006d/11548152/06c1be3c4ad9/plants-13-03045-g001.jpg

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