Kamau James Kimani, Ngugi Mathew Piero, Ngeranwa Joseph N
Department of Biochemistry and Biotechnology, School of Pure and Applied Sciences, Kenyatta University, P.O. Box 43844-00100, Nairobi, Kenya.
Inflammopharmacology. 2025 May 5. doi: 10.1007/s10787-025-01770-6.
This study determined the phytochemical profile and in vivo anti-arthritic potential and mechanistic effects of MeOH extract of Rhamnus prinoides. The liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS) were used in the phytochemical analysis of the extract. In the anti-arthritic assay, the rats were assigned into arthritic control, non-arthritic control, methotrexate control, and three extract-treated [100, 200, and 300 mg/kg body weight (bw)] groups. Complete Freund's adjuvant was used to induce polyarthritis. The treatments were orally administered from day 8 post-induction of polyarthritis. The experimental animals were euthanized and blood was drawn for hematological parameter analysis on day 29. The ankle joint tissue and liver were detached and utilized in gene expression using RT-qPCR and standard antioxidant assays, respectively. One-factorial ANOVA and Tukey's multiple comparisons were used to compute for statistical differences of the raw data. The LC-MS analysis identified phytochemicals of flavonoids, anthraquinones, lignans, and coumarins classes. Fatty acid methyl ester, benzofuran, and terpene were also detected using GC-MS. The extract significantly reduced ankle joint edema, reduced body weight loss and arthritis scores, improved elevated spleen and thymus indices, attenuated aberrant hematological parameters, lowered malonaldehyde levels, and enhanced enzymatic antioxidant activities in rats induced with polyarthritis (p < 0.05). The extract also significantly upregulated expression of I-κBα, IL-4, and IL-10 genes, as well as downregulated expression of STAT-3, NF-κB, RANKL, COX-2, TNF-α, and IL-6 genes in rats induced with polyarthritis (p < 0.05). The extract possesses phytochemicals with anti-arthritic potential and can be used as a potential lead in developing novel anti-arthritic agents.
本研究确定了鼠李的甲醇提取物的植物化学特征、体内抗关节炎潜力及其作用机制。采用液相色谱 - 质谱联用(LC - MS)和气相色谱 - 质谱联用(GC - MS)对提取物进行植物化学分析。在抗关节炎试验中,将大鼠分为关节炎对照组、非关节炎对照组、甲氨蝶呤对照组和三个提取物处理组[100、200和300毫克/千克体重(bw)]。使用完全弗氏佐剂诱导多关节炎。从多关节炎诱导后第8天开始口服给药。在第29天对实验动物实施安乐死并采血进行血液学参数分析。分离踝关节组织和肝脏,分别用于通过逆转录定量聚合酶链反应(RT - qPCR)进行基因表达分析和标准抗氧化测定。采用单因素方差分析和Tukey多重比较来计算原始数据的统计学差异。LC - MS分析鉴定出了黄酮类、蒽醌类、木脂素类和香豆素类植物化学物质。使用GC - MS还检测到了脂肪酸甲酯、苯并呋喃和萜类化合物。该提取物显著减轻了踝关节水肿,减少了体重减轻和关节炎评分,改善了升高的脾脏和胸腺指数,减轻了异常的血液学参数,降低了丙二醛水平,并增强了多关节炎诱导大鼠的酶促抗氧化活性(p < 0.05)。该提取物还显著上调了多关节炎诱导大鼠中I - κBα、IL - 4和IL - 10基因的表达,并下调了STAT - 3、NF - κB、RANKL、COX - 2、TNF - α和IL - 6基因的表达(p < 0.05)。该提取物含有具有抗关节炎潜力的植物化学物质,可作为开发新型抗关节炎药物的潜在先导物。