Department of Pharmacology, College of Pharmacy, Jouf University, Sakaka, Al Jouf Province, Saudi Arabia; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University Putra Malaysia, Serdang, 43400, Selangor Darul Ehsan, Malaysia; Department of Pharmacology, Anwarul Uloom College of Pharmacy Affiliated to Jawaharlal Nehru Technological University, Hyderabad, Telangana State, India.
Department of Pharmacology, Anwarul Uloom College of Pharmacy Affiliated to Jawaharlal Nehru Technological University, Hyderabad, Telangana State, India; Department of Pharmacology, College of Pharmacy, Taibah University, Al-Madinah Al-Munawwarah, 30001, Saudi Arabia.
Food Chem Toxicol. 2018 May;115:523-531. doi: 10.1016/j.fct.2018.03.021. Epub 2018 Mar 17.
In view of the report on anti-nociceptive activity of Leathery Murdah, Terminalia coriacea {Roxb.} Wight & Arn. (Combretaceae) leaves, the present study was conducted to isolate the active constituents and identify the underlying mechanisms. The methanolic extract of T. coriacea leaves (TCLME) at doses 125, 250 and 500 mg/kg orally, was subjected to various in-vivo assays in acetic acid induced writhing and formalin induced paw-licking tests with aspirin (100 mg/kg) and morphine (5 mg/kg) as reference drugs. Three flavonoids, rutin, robinin and gossypetin 3-glucuronide 8-glucoside were isolated and characterized from TCLME for the first time. The extract showed significant (p < 0.001) dose-dependent anti-nociceptive activity in glutamate induced paw licking in mice. The involvement of opioid pathway was confirmed as naloxone (5 mg/kg, i.p) treatment blocked the analgesic activity of the test extract. Similarly, glibenclamide (an ATP - sensitive potassium channel inhibitor) at dose of 10 mg/kg, i.p increased writhing in acetic acid model. It reversed the inhibitory effects of TCLME when administered in combination. Treatment of TCLME alone and in combination with l-arginine (100 mg/kg, i.p) significantly (p < 0.001) reduced writhing while pre-treatment with l-NAME (20 mg/kg, i.p) further enhanced the analgesic action of TCLME indicating involvement of nitric oxide pathway.
鉴于关于 Leathery Murdah(Terminalia coriacea {Roxb.} Wight & Arn.,使君子科)叶的抗伤害作用的报告,本研究旨在分离活性成分并确定潜在机制。以阿司匹林(100mg/kg)和吗啡(5mg/kg)为参比药物,用浓度为 125、250 和 500mg/kg 的 Terminalia coriacea 叶甲醇提取物(TCLME)进行体内试验,在醋酸诱导的扭体和福尔马林诱导的舔足试验中进行各种体内试验。首次从 TCLME 中分离并鉴定出三种类黄酮,芦丁、罗宾素和棉子糖 3-葡萄糖醛酸 8-葡萄糖苷。提取物在谷氨酸诱导的小鼠舔足试验中表现出显著的(p<0.001)剂量依赖性镇痛活性。阿片途径的参与得到了证实,纳洛酮(5mg/kg,ip)治疗阻断了测试提取物的镇痛活性。同样,给予 10mg/kg,ip 的格列本脲(一种 ATP 敏感性钾通道抑制剂)在醋酸诱导的扭体模型中增加扭体。当与 TCLME 联合给药时,它逆转了 TCLME 的抑制作用。TCLME 单独和与 l-精氨酸(100mg/kg,ip)联合治疗可显著(p<0.001)减少扭体,而 l-NAME(20mg/kg,ip)预处理进一步增强了 TCLME 的镇痛作用,表明一氧化氮途径的参与。