Krishnakumar Neenthamadathil Mohandas, Manikantan Kuttapetty, Suja Somasekharan Nair Rajam, Latha Panickamparambil Gopalakrishnan, Ceasar Stanislaus Antony
Department of Biosciences, Rajagiri College of Social Sciences (Autonomous), Kalamassery, Kochi, Kerala 683104, India.
Division of Ethnomedicine and Ethnopharmacology, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Palode, Thiruvananthapuram, Kerala 695562, India.
Toxicol Res (Camb). 2022 Sep 8;11(5):841-851. doi: 10.1093/toxres/tfac063. eCollection 2022 Oct.
L. is a woody climber or liana distributed in south East Asia. It is a traditional medicinal plant with excellent curative effects against diarrhea, dysentery, and other stomach disorders. The present study was aimed to assess the effect of active fraction (MUAF) on various inflammatory mediators using lipopolysaccharide (LPS) induced model in Wistar rats. The effect of MUAF on secretion of TNF-α, IL-1β, and IL-6 were evaluated in LPS-induced experimental animals. The expression of α, and genes were also evaluated. The gas chromatography-mass spectrometry (GC-MS) analysis of the active fraction was carried out to identify the active compounds present in MUAF. The results of oral acute toxicity suggested the non-toxic nature of MUAF. GC-MS analysis of the MUAF leaves revealed the presence of 8 compounds. The study demonstrated that the proinflammatory cytokines such as TNF-α, IL-1β, and IL-6 were significantly inhibited by MUAF in a dose-dependent manner. Moreover, MUAF down-regulated the expression of α, and genes. Our research findings suggest that the presence of anti-inflammatory compounds in MUAF can effectively inhibit LPS-induced proinflammatory cytokines TNF-α, IL-β, and IL-6 . It also suppressed the over expression of α, , , , and possibly via downregulating activation.
L.是一种分布于东南亚的木质攀缘植物或藤本植物。它是一种传统药用植物,对腹泻、痢疾和其他胃部疾病具有出色的治疗效果。本研究旨在使用脂多糖(LPS)诱导的Wistar大鼠模型评估活性成分(MUAF)对各种炎症介质的影响。在LPS诱导的实验动物中评估了MUAF对肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)分泌的影响。还评估了α和相关基因的表达。对活性成分进行气相色谱-质谱(GC-MS)分析以鉴定MUAF中存在的活性化合物。口服急性毒性结果表明MUAF无毒。MUAF叶片的GC-MS分析显示存在8种化合物。研究表明,MUAF以剂量依赖性方式显著抑制TNF-α、IL-1β和IL-6等促炎细胞因子。此外,MUAF下调了α和相关基因的表达。我们的研究结果表明,MUAF中抗炎化合物的存在可有效抑制LPS诱导的促炎细胞因子TNF-α、IL-β和IL-6。它还可能通过下调相关激活来抑制α、、、和的过度表达。