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基于使用健康个体外周血单个核细胞的酶促氧化应激基因表达,对古洛糖醛酸(G2013)的抗衰老作用进行体外评估。

An in vitro evaluation of anti-aging effect of guluronic acid (G2013) based on enzymatic oxidative stress gene expression using healthy individuals PBMCs.

作者信息

Taeb Mahsa, Mortazavi-Jahromi Seyed Shahabeddin, Jafarzadeh Abdollah, Mirzaei Mohammad Reza, Mirshafiey Abbas

机构信息

Department of Immunology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

Department of Cellular and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran.

出版信息

Biomed Pharmacother. 2017 Jun;90:262-267. doi: 10.1016/j.biopha.2017.03.066. Epub 2017 Mar 30.

DOI:10.1016/j.biopha.2017.03.066
PMID:28364598
Abstract

BACKGROUND

Aging is usually associated with increased levels of oxidants, and may result in damages caused by oxidative stress. There is a direct relationship between aging and increased incidence of inflammatory diseases. The present research intended to study the anti-aging and anti-inflammatory effects of the drug G2013 (guluronic acid) at low and high doses on the genes expression of a number of enzymes involved in oxidative stress (including SOD2, GPX1, CAT, GST, iNOS, and MPO) in peripheral blood mononuclear cells (PBMCs) of healthy individuals under in vitro conditions.

METHODS

Venous blood samples were taken from 20 healthy individuals, the PBMCs were isolated and their RNAs extracted and their cDNAs were synthesized, and the genes expression levels were measured using the qRT-PCR technique.

RESULTS

Our results indicated that this drug could, at both low and high doses, significantly reduce the expression of the genes for SOD2, GPX1, CAT, and GST compared to the LPS group (p<0.0001). Moreover, it was noticed that the drug is able to significantly reduce gene expression levels at the high dose and at both doses (low and high), for iNOS and MPO compared to the LPS group (p<0.0001), respectively.

CONCLUSIONS

The present research showed that G2013, as a novel NSAID drug with immunomodulatory properties, could modulate the expression levels of the genes for SOD2, GPX1, CAT, GST, iNOS, and MPO, to the level of healthy gene expression, and possibly it might reduce the pathological process of aging and age-related inflammatory diseases.

摘要

背景

衰老通常与氧化剂水平升高相关,并可能导致氧化应激引起的损伤。衰老与炎症性疾病发病率增加之间存在直接关系。本研究旨在体外条件下,研究低剂量和高剂量药物G2013(古洛糖醛酸)对健康个体外周血单个核细胞(PBMCs)中一些参与氧化应激的酶(包括SOD2、GPX1、CAT、GST、iNOS和MPO)基因表达的抗衰老和抗炎作用。

方法

采集20名健康个体的静脉血样本,分离PBMCs,提取RNA并合成cDNA,使用qRT-PCR技术测量基因表达水平。

结果

我们的结果表明,与LPS组相比,该药物的低剂量和高剂量均可显著降低SOD2、GPX1、CAT和GST基因的表达(p<0.0001)。此外,还发现与LPS组相比,该药物在高剂量以及低剂量和高剂量时,均可分别显著降低iNOS和MPO的基因表达水平(p<0.0001)。

结论

本研究表明,G2013作为一种具有免疫调节特性的新型非甾体抗炎药,可将SOD2、GPX1、CAT、GST、iNOS和MPO基因的表达水平调节至健康基因表达水平,并可能减轻衰老及与年龄相关的炎症性疾病的病理过程。

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