Two flavonoids, baicalein and naringin, are effective as anti-inflammatory and anti-oxidant agents in a rat model of polymicrobial sepsis.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Pinar Bayram, Selina Aksak Karamese, Bengul Ozdemir, Cagatay Salum, Huseyin Serkan Erol, Murat Karamese
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引用次数: 2

Abstract

Introduction: In this study, our aim was to investigate the possible protective and therapeutic effects of these two flavonoids, baicalein, and naringin, in 50 and 100 mg/kg doses applied both before and after cecal ligation and puncture (CLP) procedures in a polymicrobial sepsis rat model, and evaluate the possible contribution of oxidative and inflammatory markers by immunological, biochemical, molecular, and histopathological methods.

Methods: Sixty-six Wistar albino rats were divided into 11 groups. The pro-inflammatory (TNF-alpha, IL-1-beta, and IL-6) and anti-inflammatory (TGF-beta and IL-10) cytokine levels were measured by ELISA technique. CD3, CD68, and nuclear factor kappa B positivity rates were detected by immunohistochemical methods. Oxidative stress parameters (MDA, SOD, and GSH) were measured by tissue biochemistry.

Results: Sepsis caused a significant increase in all pro-inflammatory cytokine levels and MDA activity. Also, it led to an increase in the positivities of CD3, CD68, and NF-κB markers. However, especially pre-CLP doses of baicalein and naringin inhibited the inflammation process by suppressing pro-inflammatory and increasing anti-inflammatory cytokine levels, as well as regulating the oxidative stress process by normalizing the oxidant/anti-oxidant enzyme levels.

Conclusion: Both pre- and post-application of baicalein and naringin are quite effective to prevent sepsis-caused cellular processes. This protective and therapeutic effects by baicalein and naringin in animals with sepsis seems to be originated from the high antioxidant capacity and inhibition of pro-inflammatory cytokine production. Thus, those natural agents may prove to be valuable protective agent against septic shock.

黄芩苷和柚皮苷两种黄酮类化合物在多菌败血症大鼠模型中具有抗炎和抗氧化作用。
引言:在本研究中,我们的目的是研究这两种黄酮类化合物,黄芩苷和柚皮苷,对50和100 在多微生物败血症大鼠模型中,在盲肠结扎和穿刺(CLP)程序前后应用mg/kg剂量,并通过免疫学、生物化学、分子和组织病理学方法评估氧化和炎症标志物的可能贡献。方法:将66只Wistar白化大鼠分为11组。通过ELISA技术测量促炎(TNF-α、IL-1-β和IL-6)和抗炎(TGF-β和IL-10)细胞因子水平。免疫组织化学方法检测CD3、CD68和核因子κB的阳性率。通过组织生物化学测定氧化应激参数(MDA、SOD和GSH)。结果:脓毒症导致所有促炎细胞因子水平和MDA活性显著升高。此外,它还导致CD3、CD68和NF-κB标记物的阳性率增加。然而,特别是CLP前剂量的黄芩苷和柚皮苷通过抑制促炎和增加抗炎细胞因子水平来抑制炎症过程,以及通过使氧化/抗氧化酶水平正常化来调节氧化应激过程。结论:黄芩苷和柚皮苷应用前后均能有效预防败血症引起的细胞过程。黄芩苷和柚皮苷对败血症动物的这种保护和治疗作用似乎源于其高抗氧化能力和抑制促炎细胞因子的产生。因此,这些天然制剂可能被证明是对抗感染性休克的有价值的保护剂。
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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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