Oxidative profile, inflammatory responses and δ-aminolevulinate dehydratase enzyme activity in influenza B virus infection.

IF 2.7 4区 医学 Q3 IMMUNOLOGY
Jovana Simonetti Bulegon, Andressa de Azambuja Pias Weber, Manoela Dias de Souza, Fernanda Tibolla Viero, Micheli Mainardi Pillat, Thissiane de Lima Gonçalves
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引用次数: 0

Abstract

The aim of the current study was to determine the activity of the delta-aminolevulinate dehydratase (δ-ALA-D) enzyme, oxidative stress biomarkers and the expression of cytokines in those infected with influenza B virus (IBV). To evaluate the activity of the δ-ALA-D enzyme, lipid peroxidation was estimated as levels of thiobarbituric acid reactive substances, protein and non-protein thiol groups, ferric-reducing antioxidant power (FRAP), vitamin C concentration and cytokine levels in IBV-infected individuals (n  = 50) and a control group (n = 30). δ-ALA-D activity was significantly lower in IBV-infected individuals compared with controls, as well as levels of thiols, vitamin C and FRAP. Lipid peroxidation and cytokine levels of IL-6, IL-10, IL-17A and IFN-y were statistically higher in the IBV group. In conclusion, we found evidence of the generation of oxidants, the depletion of the antioxidant system, decrease in the activity of the δ-ALA-D enzyme and an increase in the synthesis of cytokines, thus contributing to a better understanding of oxidative and inflammatory pathways during IBV infection.

乙型流感病毒感染的氧化特性、炎症反应和δ-氨基乙酰丙酸脱水酶活性。
背景:测定乙型流感病毒(IBV)感染者δ-氨基乙酰丙酸脱水酶(δ-ALA-D)的活性、氧化应激生物标志物和细胞因子的表达,IBV感染个体的铁还原抗氧化能力(FRAP)、维生素C浓度(VIT C)和细胞因子水平(n = 50)和对照组(n=30)。结果:IBV感染者的δ-ALA-D活性以及硫醇、维生素C和FRAP水平均显著低于对照组。IBV组的脂质过氧化和细胞因子水平IL-6、IL-10、IL-17A和IFN-y在统计学上更高。结论:我们发现了氧化剂的产生、抗氧化系统的耗竭、δ-ALA-D酶活性的降低和细胞因子合成的增加,从而有助于更好地了解IBV感染期间的氧化和炎症途径。
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来源期刊
Pathogens and disease
Pathogens and disease IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
7.40
自引率
3.00%
发文量
44
期刊介绍: Pathogens and Disease publishes outstanding primary research on hypothesis- and discovery-driven studies on pathogens, host-pathogen interactions, host response to infection and their molecular and cellular correlates. It covers all pathogens – eukaryotes, prokaryotes, and viruses – and includes zoonotic pathogens and experimental translational applications.
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