Department of Histology and Embryology, Kafkas University, Kars, Turkey.
Department of Physiology, Kastamonu University, Kastamonu, Turkey.
Immunopharmacol Immunotoxicol. 2023 Oct;45(5):597-606. doi: 10.1080/08923973.2023.2197143. Epub 2023 Apr 11.
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.
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.
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.
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.
在这项研究中,我们的目的是研究两种黄酮类化合物,白杨素和柚皮苷,在 50 和 100mg/kg 剂量下,在盲肠结扎和穿刺(CLP)程序前后应用于多微生物脓毒症大鼠模型中的可能的保护和治疗作用,并通过免疫、生化、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。
将 66 只 Wistar 白化大鼠分为 11 组。通过酶联免疫吸附试验(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。通过免疫组织化学方法检测 CD3、CD68 和核因子 kappa B 的阳性率。通过组织生物化学方法测量氧化应激参数(MDA、SOD 和 GSH)。
脓毒症导致所有促炎细胞因子水平和 MDA 活性的显著增加。此外,它导致 CD3、CD68 和 NF-κB 标志物的阳性率增加。然而,特别是在 CLP 前给予白杨素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,以及通过使氧化酶/抗氧化酶水平正常化来调节氧化应激过程。
在脓毒症动物中,白杨素和柚皮苷的预应用和后应用都非常有效,可以预防脓毒症引起的细胞过程。白杨素和柚皮苷在脓毒症动物中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产生。因此,这些天然药物可能被证明是对抗感染性休克的有价值的保护剂。