CNS Depressant and Analgesic Activities of Thysanolaena maxima Roxb. Available in Bangladesh

N. Hoque, Nusrat Fatemee, Md. Junayet Hossain, Meena Afroze Shanta, M. Asaduzzaman
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Abstract

In Bangladesh, numerous tribal people of Chittagong Hill Tracts have been using different parts of Thysanolaena maxima Roxb. for many years. The present study was designed to investigate CNS depressant and analgesic activities of methanol extract of the aerial parts of the plant in mice models. CNS depressant activity of the crude extract (200 and 400 mg/kg) was evaluated using open field, hole cross and thiopental-induced sleeping time tests using diazepam as the standard. Analgesic activity was determined using acetic acid-induced writhing and hot plate tests using diclofenac sodium as the standard. The extract showed dose dependent suppression of locomotion in open field and hole cross tests and exerted sedative action in thiopental induced sleeping time. In the open field and the hole-cross tests, maximum CNS depressant activity was observed at 90 min after administration of extract and the standard drug. The extract significantly induced the onset of sleep and prolonged the sleeping time in thiopental induced sleeping test compared to the control group. The extract produced significant (p < 0.05) analgesic activity by inhibiting writhing by 41.89% and 60.81%, at doses of 200 and 400 mg/kg body weight, respectively, which was comparable to the inhibition of diclofenac sodium (73.64%). Additionally, in hot plate test, the extract exhibited a significant (p < 0.05) increase in pain threshold in a dose dependent manner. The findings of the study are encouraging and demands further investigation of other bioactivities with isolation of pure compounds. Dhaka Univ. J. Pharm. Sci. 20(2): 227-233, 2021 (December)
百里菊对中枢神经系统的抑制和镇痛作用。孟加拉国有售
在孟加拉国,吉大港山区的许多部落人民一直在使用Thysanolaena maxima Roxb的不同部分。很多年了。本研究旨在研究植物地皮甲醇提取物对小鼠中枢神经系统的抑制和镇痛作用。以地西泮为标准,采用空地试验、孔交叉试验和硫喷妥诱发睡眠时间试验评价粗提物(200和400 mg/kg)的中枢神经系统抑制活性。以双氯芬酸钠为标准品,采用醋酸扭体法和热板法测定镇痛活性。该提取物在野外和孔交叉实验中表现出剂量依赖性的运动抑制作用,并在硫喷妥钠诱导的睡眠时间中表现出镇静作用。在野外和孔交叉试验中,在给药后90 min观察到最大的中枢神经抑制活性。在硫喷妥钠诱导睡眠试验中,与对照组相比,提取物显著诱导睡眠,延长睡眠时间。在200和400 mg/kg体重下,该提取物对扭体的抑制率分别为41.89%和60.81%,与双氯芬酸钠的抑制率(73.64%)相当(p < 0.05)。此外,在热板试验中,提取物表现出显著(p < 0.05)的疼痛阈值增加,且呈剂量依赖性。该研究结果令人鼓舞,并要求进一步研究其他生物活性的分离纯化化合物。达卡大学药学院。科学通报,20(2):227- 233,2021(12月)
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