Nazir Muhammad Muzammil, Farzeen Iqra, Fasial Shahla, Ashraf Asma
Department of Zoology, Government College University, Faisalabad, 38000, Pakistan.
Department of Statistics, Government College University, Faisalabad, 38000, Pakistan.
Inflammopharmacology. 2025 Jan;33(1):215-229. doi: 10.1007/s10787-024-01612-x. Epub 2024 Dec 23.
Berberine (BBR), an alkaloid derivative mostly found in Oregon grapes and barberry shoots, has several medical properties, including anti-microbial, anti-tumorigenic, and anti-inflammatory properties. As such, it is a superior alternative to presently recommended medications. From previous researches, which showed that BBR has anti-arthritic qualities by blocking a number of inflammatory signalling pathways. Furthermore, it has been demonstrated that BBR attenuates Beclin-1, which reduces autophagy-mediated survival of mature adipocytes. BBR has also been identified as an AhR inducer and a promoter of Treg differentiation. Berberine has been shown in earlier studies to be useful in treating rheumatoid arthritis (RA) in animal models. The pharmacological effects and possible action pathway of Berberine were evaluated in this study. We looked through three databases-PubMed, Web of Science, and Google Scholar-for pertinent research published from the time the databases were created and August 2024. This risk-of-bias measure was used to evaluate the methodological quality. Utilising RevMan 5.4, the statistical analysis was conducted. There were 12 studies in this research with 175 animals. The findings showed that Berberine lowers the levels of IL-1β, IL-17, IL-6, IL-10, and TNF-α), paw swelling, and histopathological scores. These connected to the anti-inflammatory, anti-oxidative stress, and osteoprotective qualities of berberine. Nonetheless, further superior animal research is required to evaluate berberine impact on rheumatoid arthritis (RA). Additionally, more research is needed to validate berberine safety. Considering the significance of the active component, further research is needed to determine the best dose and increase berberine bioavailability.
黄连素(BBR)是一种主要存在于俄勒冈葡萄和小檗嫩枝中的生物碱衍生物,具有多种医学特性,包括抗菌、抗肿瘤和抗炎特性。因此,它是目前推荐药物的优质替代品。以往的研究表明,BBR通过阻断多种炎症信号通路具有抗关节炎的特性。此外,已经证明BBR可使Beclin-1衰减,从而降低自噬介导的成熟脂肪细胞的存活率。BBR还被确定为芳烃受体(AhR)诱导剂和调节性T细胞(Treg)分化的促进剂。早期研究表明黄连素可用于治疗动物模型中的类风湿性关节炎(RA)。本研究评估了黄连素的药理作用和可能的作用途径。我们在三个数据库——PubMed、科学网和谷歌学术搜索中,查找了从数据库创建之时到2024年8月发表的相关研究。采用这种偏倚风险评估方法来评价方法学质量。使用RevMan 5.4进行统计分析。本研究中有12项研究,涉及175只动物。结果表明,黄连素可降低白细胞介素-1β(IL-1β)、白细胞介素-17(IL-17)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)和肿瘤坏死因子-α(TNF-α)的水平、爪肿胀和组织病理学评分。这些与黄连素的抗炎、抗氧化应激和骨保护特性有关。尽管如此,仍需要进一步高质量的动物研究来评估黄连素对类风湿性关节炎(RA)的影响。此外,还需要更多研究来验证黄连素的安全性。考虑到该活性成分的重要性,需要进一步研究以确定最佳剂量并提高黄连素的生物利用度。