Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Department of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad, Azad Kashmir, Pakistan.
Inflammopharmacology. 2018 Aug;26(4):1037-1049. doi: 10.1007/s10787-018-0446-4. Epub 2018 Feb 22.
Chronic inflammation is pathologically associated with various clinical conditions such as rheumatoid arthritis. Several anti-inflammatory and analgesic drugs currently available in market presents a wide range of problems. Therefore, the current study was aimed to evaluate anti-inflammatory and analgesic activities of newly synthesized compound 2-(5-mercapto-1,3,4-oxadiazol-2-yl)-N-propylbenzenesulphonamide (MOPBS). Carrageenan and CFA-induced models were developed for evaluation of anti-inflammatory and analgesic activity. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of inflammatory mediators. Pain behaviours were evaluated by performing Von Frey, Randall Selitto, cold acetone and hot plate test respectively. X-ray imaging and haematoxylin and eosin (H&E) staining were performed for examination of soft tissues of treated mice paw. Additionally, Kodzeila's screen test and weight test were performed for determination of any side effects on motor function and muscle strength. Acute pretreatment of animals with MOPBS (1, 10, 50 and 100 mg/kg, i.p.) produced a significant reduction of paw oedema against carrageenan-induced acute inflammation as well as notable inhibition of mechanical hyperalgesia, allodynia and thermal hyperalgesia. Similarly, in chronic inflammation model, administration of MOPBS (50 mg/kg, i.p.) produced a remarkable reduction of paw oedema. Additionally, MOPBS pretreatment showed a significant inhibition of thermal hyperalgesia, mechanical allodynia, and mechanical hyperalgesia in chronic arthritis model. Several pro-inflammatory mediators such as nitric oxide (NO), vascular endothelial growth factor (VEGF), interleukins (IL-1β, IL-6) and tumor necrosis factor-α (TNF-α) were inhibited by MOPBS treatment in blood plasma and paw tissues, respectively. MOPBS also enhanced the mRNA expression levels of nuclear factor (erythroid-derived 2)-like 2 (Nrf2), superoxide dismutase (SOD2) and heme oxygenase (HO-1) and in turn reduced arthritis severity and inflammation. Furthermore, anti-inflammatory data were confirmed by X-rays and histological analysis. MOPBS pretreatment did not produce any apparent toxic effect on gastric, kidney and liver function and on muscle strength and motor function. Hence, the present data suggest that MOPBS might be a candidate for several chronic inflammatory diseases such RA and other auto-immune diseases.
慢性炎症与类风湿关节炎等多种临床病症在病理学上有关联。目前市场上有许多抗炎和镇痛药物,但存在各种问题。因此,本研究旨在评估新合成的化合物 2-(5-巯基-1,3,4-恶二唑-2-基)-N-丙基苯磺酰胺(MOPBS)的抗炎和镇痛活性。采用角叉菜胶和 CFA 诱导模型来评估抗炎和镇痛活性。通过定量实时 PCR(qRT-PCR)测定炎症介质的 mRNA 表达水平。通过进行 Von Frey、Randall Selitto、冷丙酮和热板试验分别评估疼痛行为。进行 X 射线成像和苏木精和伊红(H&E)染色以检查治疗后小鼠爪子的软组织。此外,进行 Kodzeila 筛选试验和体重试验以确定对运动功能和肌肉力量的任何副作用。动物急性预处理 MOPBS(1、10、50 和 100mg/kg,ip)可显著减轻角叉菜胶诱导的急性炎症引起的足肿胀,并显著抑制机械性痛觉过敏、痛觉过敏和热痛觉过敏。同样,在慢性炎症模型中,MOPBS(50mg/kg,ip)给药可显著减轻足肿胀。此外,MOPBS 预处理可显著抑制慢性关节炎模型中的热痛觉过敏、机械性痛觉过敏和机械性痛觉过敏。MOPBS 处理分别在血浆和爪子组织中抑制几种促炎介质,如一氧化氮(NO)、血管内皮生长因子(VEGF)、白细胞介素(IL-1β、IL-6)和肿瘤坏死因子-α(TNF-α)。MOPBS 还增强了核因子(红系衍生 2)样 2(Nrf2)、超氧化物歧化酶(SOD2)和血红素加氧酶(HO-1)的 mRNA 表达水平,从而减轻关节炎严重程度和炎症。此外,抗炎数据通过 X 射线和组织学分析得到证实。MOPBS 预处理对胃、肾和肝功能以及肌肉力量和运动功能没有产生任何明显的毒性作用。因此,本研究数据表明,MOPBS 可能是类风湿关节炎和其他自身免疫性疾病等几种慢性炎症性疾病的候选药物。