Ullah Rahim, Badshah Waseem, Ali Gowhar, Ullah Aman, Khan Saleem Ullah, Ahmad Nisar, Shahid Muhammad, Naveed Muhammad, Ullah Sami, Bangash Sudhair Abbas, Althobaiti Yusuf S
Faculty of Life Science, Department of Pharmacy Sarhad University of Science and Information Technology, Peshawar, Khyber Pakhtunkhwa, Pakistan; Department of Pharmacy, University of Peshawar, Peshawar 25120, Khyber Pakhtunkhwa, Pakistan.
Department of Pharmacy, Abdul Wali Khan University, Mardan, Khyber Pakhtunkhwa, Pakistan.
Biomed Pharmacother. 2022 May;149:112834. doi: 10.1016/j.biopha.2022.112834. Epub 2022 Mar 23.
Cassia plants have a considerable position in conventional systems of medicine. The possible anti-nociceptive, anti-inflammatory, and anti-neuropathic properties of Cassia artemisiodes (CAD) extract were tested using the standard animal models. In this study, in vitro antioxidant, cyclooxygenase (COX-1 and 2), and 5-lipoxygenase (5-LOX) inhibitory assays were performed. The anti-inflammatory activity was evaluated using carrageenan, histamine, and serotonin-induced paw edema models. Antipyretic activity, thermally and chemically-induced nociception, and naloxone antagonistic activities were carried out. The CAD extract was tested for anti-neuropathic activity in the streptozotocin-induced diabetic neuropathy model. Suppressing the effect of CAD extract on the mRNA level of inducible nitric oxide synthase (iNOS), COX-2, and pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) was determined by performing RT-PCR. The CAD extract inhibited COX-2 and 5-LOX enzymes, paw inflammation, and reduced nociceptive behaviors. The mRNA gene expression of iNOS, COX-2, and inflammatory cytokines was reduced significantly with increased DPPH scavenging activity. The extract significantly reduced the diabetes-induced neuropathic pain. In a nutshell, these results recommended that the CAD extract has anti-nociceptive and anti-neuropathic activities due to inhibition of inflammatory and oxidative signaling.
决明属植物在传统医学体系中占有相当重要的地位。使用标准动物模型测试了青蒿决明(CAD)提取物可能具有的抗伤害感受、抗炎和抗神经病理性特性。在本研究中,进行了体外抗氧化、环氧化酶(COX-1和2)以及5-脂氧合酶(5-LOX)抑制试验。使用角叉菜胶、组胺和5-羟色胺诱导的爪肿胀模型评估抗炎活性。进行了解热活性、热和化学诱导的伤害感受以及纳洛酮拮抗活性试验。在链脲佐菌素诱导的糖尿病神经病变模型中测试了CAD提取物的抗神经病理性活性。通过进行逆转录-聚合酶链反应(RT-PCR)来确定CAD提取物对诱导型一氧化氮合酶(iNOS)、COX-2和促炎细胞因子(TNF-α、IL-1β、IL-6)mRNA水平的抑制作用。CAD提取物抑制了COX-2和5-LOX酶、爪部炎症,并减少了伤害感受行为。随着二苯基苦味酰基自由基(DPPH)清除活性的增加,iNOS、COX-2和炎性细胞因子的mRNA基因表达显著降低。该提取物显著减轻了糖尿病诱导的神经病理性疼痛。简而言之,这些结果表明,由于抑制了炎症和氧化信号传导,CAD提取物具有抗伤害感受和抗神经病理性活性。