首页> 外文期刊>Frontiers in Pharmacology >Anti-nociceptive Activity of Ethnomedicinally Important Analgesic Plant Isodon rugosus Wall. ex Benth: Mechanistic Study and Identifications of Bioactive Compounds
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Anti-nociceptive Activity of Ethnomedicinally Important Analgesic Plant Isodon rugosus Wall. ex Benth: Mechanistic Study and Identifications of Bioactive Compounds

机译:种族学上重要的止痛药植物 Isodon rugosus Wall的抗伤害感受活性。前Benth:生物活性化合物的机理研究和鉴定

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Isodon rugosus Wall. ex Benth. is extensively used as traditional medicine for the management of various types of pain including tooth ache, gastric pain, abdominal pain, ear ache, and generalized body pain. The current study is designed to scientifically verify the purported uses of I. rugosus as analgesic agent and to figure out its possible mechanism of action. Bioactive compounds responsible for analgesic activity were identified using GC and GC-MS analysis. Analgesic potentials were evaluated using acetic acid induced writhing, hot plate test, and formalin induced paw licking test. In acetic acid induced writhing chloroform fraction (Ir.Chf) exhibited 53% analgesia while formalin test displayed 61% inhibition at phase-I and 45% at phase-II respectively at a dose of 100 mg/kg. Similarly, in hot plate test Ir.Chf displayed average reaction time of 7 min at 15, 30, 45, and 60 min intervals. The possible mechanism of action was found to be the central pathway via opioidergic receptors as the mice showed morphine like analgesic activity at pre-administration of naloxone (opioid antagonist) in hot plate and formalin tests. In GC-MS analysis, 83 compounds were identified among which eight compounds including benzyl alcohol, sebacic acid, myristic acid, phytol, sugiol, Tocopherol, α-Amyrin, and stigmasterol were sorted out as previously reported analgesic compounds. Current study revealed that analgesic potential of I. rugosus can attributed to the presence of analgesic compounds. It may also be concluded that opioids receptors are involved in the analgesic mechanism of I. rugosus due to effective antagonism of nalaxone.
机译:Isodon rugosus墙。前Benth。被广泛用作管理各种疼痛的传统药物,包括牙痛,胃痛,腹痛,耳痛和全身性疼痛。当前的研究目的是科学地证实皱纹伊豆作为止痛剂的用途,并弄清其可能的作用机理。使用GC和GC-MS分析鉴定了负责镇痛活性的生物活性化合物。使用乙酸诱导的扭体法,热板试验和福尔马林诱导的爪舔试验评估镇痛潜力。在乙酸中,以100 mg / kg的剂量引起的扭曲的氯仿馏分(Ir.Chf)表现出53%的镇痛作用,而福尔马林试验分别在I期抑制61%,II期抑制45%。同样,在热板测试中,Ir.Chf以15、30、45和60分钟的间隔显示7分钟的平均反应时间。由于在热板法和福尔马林试验中,纳洛酮(阿片类拮抗剂)的预给药小鼠表现出吗啡样镇痛活性,因此发现其可能的作用机制是通过阿霉素受体的中枢途径。在GC-MS分析中,鉴定出83种化合物,其中包括八种化合物,包括苄醇,癸二酸,肉豆蔻酸,植醇,sugiol,生育酚,α-Amyrin和豆固醇。目前的研究表明,皱纹伊豆的止痛潜力可归因于止痛化合物的存在。还可以得出结论,由于纳拉酮的有效拮抗作用,阿片类药物受体参与了皱I的镇痛作用。

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