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通过人中性粒细胞和无细胞体系中的化学发光抑制法测定百里酚的抗氧化潜力。

Antioxidant potential of thymol determined by chemiluminescence inhibition in human neutrophils and cell-free systems.

作者信息

Braga Pier Carlo, Dal Sasso Monica, Culici Maria, Galastri Laura, Marceca Maria Teresa, Guffanti Enrico Eugenio

机构信息

Center of Respiratory Pharmacology, Department of Pharmacology, School of Medicine, University of Milan, Via Vanvitelli 32, IT-20129 Milan, Italy.

出版信息

Pharmacology. 2006;76(2):61-8. doi: 10.1159/000089719. Epub 2005 Nov 11.

Abstract

Thyme essential oil and thymol have antimicrobial, antifungal and antioxidant activities. Their antioxidant activity has been studied almost exclusively by means of chemical testing in order to be able to use it for food preservation purposes. The aim of this luminol amplified chemiluminescence (LACL) study was to investigate whether thymol can interfere with the production of reactive oxygen species, nitric oxide and the nitric oxide-derived peroxynitrite released by human neutrophils after activation by fMLP and PMA with and without the addition of the L-arginine (L-Arg) nitric oxide donor to the medium. The lowest thymol concentration that was still active in reducing LACL was 2.73 microg/ml, and there was a progressive linear inhibition of LACL from this concentration to 21.87 microg/ml, the highest thymol concentration investigated. This was also observed in the case of both fMLP and PMA stimulation with or without L-Arg. In cell-free systems using H(2)O(2)/HOCl(-) and SIN-1 as radical producers, a significant scavenging activity of thymol was present already at 0.08 and 0.68 microg/ml respectively, and these are very low concentrations. These findings can be related to the phenolic structure of thymol, because phenolic compounds have redox properties and play an important role in adsorbing and neutralizing free radicals and peroxynitrite, and in decomposing peroxides. Our findings in human neutrophils are pharmacologically relevant as they imply that thymol is a potential antioxidant and anti-inflammatory agent in human cells.

摘要

百里香精油和百里香酚具有抗菌、抗真菌和抗氧化活性。为了将其用于食品保鲜目的,几乎完全通过化学测试研究了它们的抗氧化活性。本鲁米诺增强化学发光(LACL)研究的目的是调查百里香酚是否会干扰人中性粒细胞在fMLP和PMA激活后产生的活性氧、一氧化氮以及一氧化氮衍生的过氧亚硝酸盐的释放,实验中分别在培养基中添加和不添加L-精氨酸(L-Arg)一氧化氮供体。仍能有效降低LACL的最低百里香酚浓度为2.73微克/毫升,从该浓度到所研究的最高百里香酚浓度21.87微克/毫升,LACL呈现出逐渐的线性抑制。在有或没有L-Arg的fMLP和PMA刺激情况下均观察到这种现象。在使用H(2)O(2)/HOCl(-)和SIN-1作为自由基产生剂的无细胞系统中,百里香酚分别在0.08和0.68微克/毫升时就已具有显著的清除活性,而这些浓度非常低。这些发现可能与百里香酚的酚类结构有关,因为酚类化合物具有氧化还原特性,在吸附和中和自由基及过氧亚硝酸盐以及分解过氧化物方面发挥着重要作用。我们在人中性粒细胞中的发现具有药理学相关性,因为这表明百里香酚在人体细胞中是一种潜在的抗氧化剂和抗炎剂。

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