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The Anti-Inflammatory and Antioxidative Effects of Ningmitai Capsule in the Experimental Autoimmune Prostatitis Rat Model

机译:宁迈泰胶囊在实验性自身免疫前列腺炎大鼠模型中的抗炎和抗氧化作用

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Objective. Ningmitai (NMT) capsule has been widely prescribed for the treatment of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS), but the mechanism remains unclear. This study aims to evaluate the therapeutic effects of the NMT capsule in the experimental autoimmune prostatitis (EAP) rat models and explore its possible mechanisms. Methods. A total of fifty male Sprague Dawley rats were used in this study. Prostate extract was obtained for the induction of EAP rat models. The EAP rats were randomly divided into the model group, NMT low-dose group (0.45?g/kg/d), NMT medium-dose group (0.90?g/kg/d), and NMT high-dose group (1.80?g/kg/d), with six rats per group. Three NMT treatment groups were administered with the NMT capsule by gavage for 30?days. HE staining was used for histopathological analyses of prostate tissues. Western blotting was used to measure the expression of proinflammatory factors IL-1β and TNF-α. The MDA level was detected to reflect the level of oxidative stress. The bilateral dorsal root ganglia of T3/L1 to S4 were dissected to measure the substance P expression. Results. EAP rat models were successfully constructed, in which extensive infiltration of inflammatory cells was found. Treatment of NMT capsule for 30?days and the infiltration of inflammatory cells were significantly mitigated (P0.05), especially in the NMT medium-dose group and NMT high-dose group. Moreover, the expression of IL-1β and the level of MDA were significantly decreased (P0.05). In addition, NMT treatment could significantly alleviate substance P expression in dorsal root ganglia. Conclusion. Our findings demonstrate that the NMT capsule can alleviate inflammatory response and oxidative stress and reduce the production of substance P in EAP rats. This provides a theoretical basis for the clinical application of NMT capsule for CP/CPPS treatment.
机译:客观的。宁米特(NMT)胶囊已被广泛规定治疗慢性前列腺炎/慢性盆腔疼痛综合征(CP / CPP),但该机制仍不清楚。本研究旨在评估NMT胶囊在实验性自身免疫前列腺炎(EAP)大鼠模型中的治疗效果,并探索其可能的机制。方法。在这项研究中使用了总共​​五十只雄性Sprague Dawley大鼠。获得前列腺提取物用于EAP大鼠模型的诱导。将EAP大鼠随机分为模型组,NMT低剂量组(0.45〜G / kg / d),NMT中剂量组(0.90〜G / kg / d)和NMT高剂量组(1.80? g / kg / d),每组六只大鼠。通过Gavage将三个NMT处理基团与NMT胶囊施用30?天。他染色用于前列腺组织的组织病理学分析。用于测量促炎因子IL-1β和TNF-α的表达的蛋白质印迹。检测MDA水平以反映氧化胁迫水平。解剖T3 / L1至S4的双侧背根神经节以测量物质P表达。结果。成功构建了EAP大鼠模型,其中发现了炎症细胞的广泛浸润。将NMT胶囊的处理持续30?天,炎症细胞的渗透被显着减轻(P <0.05),特别是在NMT中剂型组和NMT高剂量组中。此外,IL-1β的表达和MDA的水平显着降低(P <0.05)。此外,NMT治疗可显着减轻背根神经节中的物质P表达。结论。我们的研究结果表明,NMT胶囊可以减轻炎症反应和氧化应激,并减少EAP大鼠物质的生产。这为NMT胶囊进行了临床应用,为CP / CPPS处理提供了理论依据。

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