Department of Orthopaedic Surgery, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
The Division of Pulmonary and Critical Care Medicine, Guangzhou Institute of Respiratory Health, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, National Center for Respiratory Medicine, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Bioengineered. 2021 Dec;12(1):6240-6250. doi: 10.1080/21655979.2021.1969194.
Although the mechanism of osteoarthritis (OA) has been widely studied and the use of quercetin for OA therapy is well documented, the relevant characteristics of the microbiome and metabolism remain unclear. This study reports changes in the gut microbiota and metabolism during quercetin therapy for OA in a rat model and provides an integrative analysis of the biomechanism. In this study, the rats were categorized into 3 different groups: the OA model, quercetin treatment, and control groups. The OA rats was conducted using a monoiodoacetate (MIA) injection protocol. The rats in the quercetin group received daily intragastric administration of quercetin from day 1 to day 28. Stool samples were collected, and DNA was extracted. We used an integrated approach that combined the sequencing of whole 16S rRNA, short-chain fatty acid (SCFA) measurements and metabolomics analysis by mass spectrometry (MS) to characterize the functional impact of quercetin on the gut microbiota and metabolism in a rat model of OA. The use of quercetin partially abrogated intestinal flora disorder and reversed fecal metabolite abnormalities. Compared with the control rats, the OA rats showed differences at both the class level (, and ) and the genus level ( and ). Acetic acid, propionic acid and 24 metabolites were significantly altered among the three groups. However, the changes were significantly abrogated in quercetin-treated OA rats. Consequently, this study provided important evidence regarding perturbations of the gut microbiome and the function of these changes in a potential new mechanism of quercetin treatment.
虽然骨关节炎 (OA) 的发病机制已得到广泛研究,并且已有大量文献报道槲皮素可用于 OA 治疗,但微生物组和代谢相关的特征仍不清楚。本研究报告了在 OA 大鼠模型中,槲皮素治疗 OA 期间肠道微生物组和代谢的变化,并对其生物力学机制进行了综合分析。在这项研究中,将大鼠分为 3 个不同组:OA 模型组、槲皮素治疗组和对照组。OA 大鼠采用单碘乙酸 (MIA) 注射方案。槲皮素组大鼠从第 1 天到第 28 天每天接受胃内给予槲皮素。收集粪便样本并提取 DNA。我们采用了一种综合方法,将 16S rRNA 全长测序、短链脂肪酸 (SCFA) 测量和通过质谱 (MS) 进行代谢组学分析相结合,以表征槲皮素对 OA 大鼠模型肠道微生物组和代谢的功能影响。槲皮素的使用部分减轻了肠道菌群失调,并逆转了粪便代谢物异常。与对照组大鼠相比,OA 大鼠在纲水平(,和)和属水平(和)上均表现出差异。乙酸、丙酸和 24 种代谢物在三组间有显著差异。然而,在槲皮素治疗的 OA 大鼠中,这些变化显著减轻。因此,本研究为槲皮素治疗的潜在新机制中肠道微生物组的变化及其功能的改变提供了重要证据。