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来自巴西藤黄的氧化还原活性双黄酮作为中性粒细胞氧化爆发和人红细胞膜损伤的抑制剂。

Redox-active biflavonoids from Garcinia brasiliensis as inhibitors of neutrophil oxidative burst and human erythrocyte membrane damage.

作者信息

Saroni Arwa Phanuel, Zeraik Maria Luiza, Ximenes Valdecir Farias, da Fonseca Luiz Marcos, Bolzani Vanderlan da Silva, Siqueira Silva Dulce Helena

机构信息

Department of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P.O. Box 355, 14800-900 Araraquara, São Paulo, Brazil.

Department of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P.O. Box 355, 14800-900 Araraquara, São Paulo, Brazil.

出版信息

J Ethnopharmacol. 2015 Nov 4;174:410-8. doi: 10.1016/j.jep.2015.08.041. Epub 2015 Aug 29.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Garcinia brasiliensis, a plant native to the Brazilian Amazon Rainforest, is used in traditional medicine to treat inflammation of the urinary tract, peptic ulcers, arthritis and other conditions.

AIM OF THE STUDY

The purposes of this study were to analyze the chemical constituents of G. brasiliensis branches and leaves and to evaluate the potential of isolated compounds to act as inhibitors of both the oxidative burst of stimulated neutrophils and oxidative damage in human erythrocyte membranes to verify the antioxidant and anti-inflammatory effects of this plant.

MATERIALS AND METHODS

Neutrophils were isolated from the blood of healthy donors by Ficoll-Paque density gradient centrifugation. Superoxide anion and total reactive oxygen species (ROS) produced by stimulated neutrophils were measured by WST-1 reduction and luminol-enhanced chemiluminescence assays, respectively. Radical-induced lipoperoxidation and hemolysis were performed using erythrocytes from the blood of healthy donors. Compounds were isolated from G. brasiliensis branches and leaves by HPLC microfractionation, and structure elucidation of the isolated compounds was performed based on NMR and HR-MS analyses.

RESULTS

The biflavonoids procyanidin, fukugetin, amentoflavone and podocarpusflavone isolated from G. brasiliensis showed potent inhibitory effects on the oxidative burst of human neutrophils, inhibiting ROS production by 50% at 1 μmol L(-1). These biflavonoids also proved to be potent inhibitors of hemolysis (with 88 ± 7% inhibition at 50 µmol L(-1) for procyanidin) and lipid peroxidation in human erythrocytes, with a malondialdehyde level (a biomarker of oxidative stress) of 8.5 ± 0.3 nmol/mg Hb at 50 µmol L(-1) for procyanidin.

CONCLUSIONS

These findings indicate that the biflavonoids extracted from G. brasiliensis branches and leaves modulate oxidative stress via inhibition of NADPH oxidase and ROS production by stimulated human neutrophils. Furthermore, the biflavonoids exhibited potent inhibition of oxidant hemolysis and lipid peroxidation induced by AAPH in human erythrocytes. Therefore, these studies suggest the use of G. brasiliensis extract as an antioxidant and anti-inflammatory agent.

摘要

民族药理学相关性

巴西藤黄是一种原产于巴西亚马逊雨林的植物,在传统医学中用于治疗尿路感染、消化性溃疡、关节炎和其他病症。

研究目的

本研究的目的是分析巴西藤黄枝叶的化学成分,并评估分离出的化合物作为刺激的中性粒细胞氧化爆发抑制剂和人红细胞膜氧化损伤抑制剂的潜力,以验证该植物的抗氧化和抗炎作用。

材料与方法

通过Ficoll-Paque密度梯度离心从健康供体的血液中分离中性粒细胞。分别采用WST-1还原法和鲁米诺增强化学发光法测定刺激的中性粒细胞产生的超氧阴离子和总活性氧(ROS)。使用健康供体血液中的红细胞进行自由基诱导的脂质过氧化和溶血实验。通过HPLC微分离从巴西藤黄枝叶中分离化合物,并基于NMR和HR-MS分析对分离出的化合物进行结构解析。

结果

从巴西藤黄中分离出的双黄酮原花青素、福木苷、穗花杉双黄酮和罗汉松黄酮对人中性粒细胞的氧化爆发具有显著抑制作用,在1 μmol L(-1)时可抑制ROS产生50%。这些双黄酮还被证明是有效的溶血抑制剂(原花青素在50 µmol L(-1)时抑制率为88 ± 7%)和人红细胞脂质过氧化抑制剂,原花青素在50 µmol L(-1)时丙二醛水平(氧化应激生物标志物)为8.5 ± 0.3 nmol/mg Hb。

结论

这些发现表明,从巴西藤黄枝叶中提取的双黄酮通过抑制NADPH氧化酶和刺激的人中性粒细胞产生ROS来调节氧化应激。此外,双黄酮对AAPH诱导的人红细胞氧化溶血和脂质过氧化具有显著抑制作用。因此,这些研究表明巴西藤黄提取物可作为抗氧化剂和抗炎剂使用。

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