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Preclinical evidence for quercetin against inflammatory bowel disease: a meta-analysis and systematic review

机译:槲皮素抗炎症性肠病的临床前证据:荟萃分析和系统评价

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Background Inflammatory bowel disease (IBD) is a chronic, potentially cancerous disease with limited treatment options. Quercetin may be a novel treatment for IBD. However, its efficacy and safety are unknown. Our goal was to conduct a systematic evaluation to summarize the preclinical effects of quercetin, which may help guide future studies. Methods The literature was drawn from three English databases (PubMed, Embase, and Web of Science), and the quality of the included literature was assessed using the SYRCLE list (10 items). The meta-analysis was performed using STATA 15.1 software. Results A total of 11 animal studies with 199 animals were involved. The current meta-analysis showed that quercetin could reduce histological score (HS), Disease Activity Index (DAI), interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha (TNF-alpha), nitric oxide(NO), malondialdehyde (MDA), myeloperoxidase (MPO) activity and increase colon length (CL), weight change degree (WCD), interleukin-10 (IL-10), glutathione (GSH), superoxide dismutase (SOD) activity and catalase (CAT) activity, which may involve anti-inflammatory, anti-oxidative stress, cytoprotective, barrier protection, flora regulation. Conclusions In conclusion, preclinical evidence suggests that quercetin is an ideal agent for IBD treatment. However, the validity of the findings may be compromised by the low methodological quality and the small number of studies included. There may be some discrepancies between the results of the current analysis and the real situation. More rigorous experimental designs and more comprehensive studies are needed to test the protection of quercetin against IBD.
机译:背景 炎症性肠病 (IBD) 是一种慢性、潜在的癌性疾病,治疗选择有限。槲皮素可能是治疗IBD的一种新方法。然而,其疗效和安全性尚不清楚。我们的目标是进行系统评估,总结槲皮素的临床前效果,这可能有助于指导未来的研究。方法 从3个英文数据库(PubMed、Embase和Web of Science)中抽取文献,采用SYRCLE列表(10项)对纳入文献的质量进行评价。使用STATA 15.1软件进行meta分析。结果 共纳入动物研究11项,共199只动物。目前的荟萃分析表明,槲皮素可降低组织学评分(HS)、疾病活动指数(DAI)、白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、一氧化氮(NO)、丙二醛(MDA)、髓过氧化物酶(MPO)活性,增加结肠长度(CL)、体重变化度(WCD)、白细胞介素-10(IL-10)、谷胱甘肽(GSH)、超氧化物歧化酶(SOD)活性和过氧化氢酶(CAT)活性,这可能涉及抗炎、 抗氧化应激,细胞保护,屏障保护,菌群调节。结论 临床前证据表明,槲皮素是治疗IBD的理想药物。然而,研究结果的有效性可能会因方法学质量低和纳入的研究数量少而受到影响。当前分析的结果与实际情况之间可能存在一些差异。需要更严格的实验设计和更全面的研究来测试槲皮素对IBD的保护作用。

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