Potential protective effects of the water-soluble Chinese propolis on experimental ulcerative colitis.

Zhou Hua, L I Hui, Wang Haihua
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Abstract

Objective: To investigate the outcome of Chinese water-soluble propolis (WSP) on the inflammatory response and oxidative stress (OS) of colonic mucosa in rats with ulcerative colitis.

Methods: Dextran sulfate sodium (DSS) was employed to establish the ucerative colitis (UC) rat model. Forty-eight male rats were arbitrarily separated into six groups, namely control, UC, low-dose water-soluble propolis (L-WSP), medium-dose water-soluble propolis (M-WSP), high-dose water-soluble propolis (H-WSP), and sulfasalazine (Sulfa). In this study, we adopted a method of pre-administration and reconstruction of the model that assessed the water-soluble propolis mediated protection against DSS-induced UC rats. Moreover, we examined the body weight (BW), disease activity index (DAI), bloody stool, colon length, and intestinal mucosal injury index of rats. In addition, using enzyme linked immunosorbent assays, we assessed indicators, such as, colonic myeloperoxidase (MPO), interleukin-6 (IL-6), interleukin-9 (IL-9), tumor necrosis factor-ɑ (TNF-ɑ), superoxide dismutase (SOD), malondialdehyde, and glutathione peroxidase (GSH-Px) levels.

Results: The pro-inflammatory cytokine expression, as well as OS, was increased in the model rats. However, upon WSP intervention, both pro-inflammatory cytokine levels and OS reduced dramatically, and the therapeutic effect was dose-dependent.

Conclusion: WSP downregulates OS by enhancing the function of endogenous antioxidant enzymes like SOD and GSH-Px, that inhibit neutrophil activity, as well as diminish pro-inflammatory cytokines like TNF-ɑ, IL-6, and IL-9, along with mechanisms that attenuate intestinal inflammation in UC rat model.

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水溶性蜂胶对实验性溃疡性结肠炎的潜在保护作用。
目的:观察水溶性蜂胶对溃疡性结肠炎大鼠结肠黏膜炎症反应和氧化应激的影响。方法:采用葡聚糖硫酸钠(DSS)建立大鼠溃疡性结肠炎(UC)模型。48只雄性大鼠随机分为6组,即对照组、UC组、低剂量水溶性蜂胶(L-WSP)组、中剂量水溶型蜂胶(M-WSP)、高剂量水溶式蜂胶(H-WSP)和柳氮磺吡啶(Sulfa)组。在本研究中,我们采用了一种预给药和重建模型的方法,评估了水溶性蜂胶介导的对DSS诱导的UC大鼠的保护作用。此外,我们还检测了大鼠的体重(BW)、疾病活动指数(DAI)、血便、结肠长度和肠粘膜损伤指数。此外,使用酶联免疫吸附测定法,我们评估了结肠髓过氧化物酶(MPO)、白细胞介素-6(IL-6)、白介素-9(IL-9)、肿瘤坏死因子-α(TNF-α)、超氧化物歧化酶(SOD)、丙二醛和谷胱甘肽过氧化物酶(GSH-Px)水平等指标。结果:模型大鼠的促炎细胞因子表达和OS均增加。然而,WSP干预后,促炎细胞因子水平和OS均显著降低,且治疗效果呈剂量依赖性。结论:WSP通过增强内源性抗氧化酶如SOD和GSH-Px的功能来下调OS,这些抗氧化酶抑制中性粒细胞活性,并减少促炎细胞素如TNF-、IL-6和IL-9,以及减轻UC大鼠模型中肠道炎症的机制。
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