首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Anti-nociceptive effect of total alkaloids isolated from the seeds of Areca catechu L (Arecaceae) in mice
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Anti-nociceptive effect of total alkaloids isolated from the seeds of Areca catechu L (Arecaceae) in mice

机译:从儿茶槟榔种子中提取的总生物碱对小鼠的镇痛作用

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Purpose: To investigate the antinociceptive effect of the total alkaloids (TA) isolated from the seeds of Areca catechu L. (SAC) and to elucidate the probable mechanism of action. Methods: TA extraction conditions including concentration of ethanol, extraction temperature, liquid–solid ratio and designed pH were optimized by an orthogonal experiment {L 9 (3) 4 } test. The anti-nociceptive effect of the extract in mice was evaluated by acetic acid writhing reflex test, hot plate test, capsaicin-induced nociception test, tail-flick test and formalin-induced pain test in mice. Furthermore, pretreatment of the animals with naloxone (2 mg/kg) was performed to investigate whether the anti-nociceptive effect involved the opioid route or not. The locomotor activity of TA in mice were also assessed. Results: The optimum extraction conditions of TA were as follows: solid-liquid ratio of 1: 15 (w/v), ethanol concentration of 80 %, pH of 9.0 and extraction temperature of 70 °C. Oral administration of TA produced a marked anti-nociceptive activity in mice, and pretreatment with naloxone did not reverse the anti-nociceptive activity of TA in mice. Also, the locomotor activity of mice was not affected by TA. In addition, TA significantly down-regulated the ex pression levels of COX-2 in the dorsal root of mice spinal cord at 100, 200 and 400 mg/kg doses. Conclusion: The results demonstrate that TA possesses significant anti-nociceptive effects, and the mechanisms are closely related to suppression of COX-2 ex pression. Overall, the results provided scientific support for the use of TA in treatment of pain.
机译:目的:研究从槟榔(SAC)种子中分离的总生物碱(TA)的抗伤害作用,并阐明其可能的作用机理。方法:通过正交实验{L 9(3)4}检验优化了乙醇提取条件,包括乙醇浓度,提取温度,液固比和设计的pH。通过乙酸扭体反射试验,热板试验,辣椒素诱导的伤害感受试验,甩尾试验和福尔马林诱导的疼痛试验评价提取物对小鼠的抗伤害作用。此外,用纳洛酮(2 mg / kg)对动物进行了预处理,以研究其抗伤害感受作用是否涉及阿片类药物途径。还评估了TA在小鼠中的运动活性。结果:TA的最佳提取条件为:固液比为1:15(w / v),乙醇浓度为80%,pH为9.0,提取温度为70℃。口服TA在小鼠中产生明显的抗伤害感受活性,并且用纳洛酮预处理不能逆转小鼠中TA的抗伤害感受活性。同样,小鼠的运动能力不受TA的影响。此外,TA显着下调了100、200和400 mg / kg剂量的小鼠脊髓背根中COX-2的表达水平。结论:结果表明TA具有显着的抗伤害感受作用,其机制与抑制COX-2的表达密切相关。总体而言,研究结果为使用TA治疗疼痛提供了科学依据。

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