Ali Mohammad Shawkat, Dash Pritesh Ranjan, Nasrin Mahmuda
Department of Pharmacy, BRAC University, 41, Pacific Tower, Mohakhali, Dhaka, Bangladesh.
Department of Pharmacy, Jahangirnagar University, Savar, Dhaka, Bangladesh.
BMC Complement Altern Med. 2015 May 27;15:158. doi: 10.1186/s12906-015-0670-z.
Kaempferia galanga is an important medicinal plant and has been traditionally used to help restlessness, stress, anxiety, depression etc. in tropics and subtropics of Asia including Bangladesh, India, China, Japan and Indochina. Literature survey revealed that there are very less reports on neuropharmacological activity of this plant. Therefore, the present study investigated the sedative activity of different extracts of rhizome and leaf of Kaempferia galanga.
The sedative activity was evaluated by using thiopental sodium induced sleeping time, hole cross and open field tests in Swiss albino mice at the doses of 100 and 200 mg/kg body weight per oral (p.o). The acetone extract of rhizome (ACR), as well as petroleum ether fraction (PEF), chloroform fraction (CHF), methanol fraction (MEF) and acetone extract of leaf (ACL) were examined for sedative activity.
In the sedative activity study, all the extracts exhibited significant (p < 0.05 and p < 0.001) reduction of onset and duration of thiopental sodium induced sleeping time, reduction of locomotor and exploratory activities in the hole cross and open field tests. In thiopental sodium induced sleeping time test, the chloroform extract of rhizome (200 mg/kg) showed maximum 358.55 % effect in duration of loss of righting reflex, whereas the standard drug Diazepam (2 mg/kg) produced 231.42 % effect. In hole cross and open field tests, maximum 95.09 % and 95.58 % suppression of locomotor activity were observed with the acetonic leaf extract (200 mg/kg) whereas suppression of locomotor activity of the standard drug Diazepam were 71.70 % and 70.58 % respectively.
The present study indicates that the acetone extracts of rhizome and leaf of Kaempferia galanga including fractions possess central nervous system (CNS) depressant properties which supports its use in traditional medicine. So, the plant may be further investigated to find out for its pharmacological active natural products.
山柰是一种重要的药用植物,在亚洲热带和亚热带地区,包括孟加拉国、印度、中国、日本和印度支那,传统上一直被用于缓解烦躁、压力、焦虑、抑郁等症状。文献调查显示,关于这种植物神经药理活性的报道非常少。因此,本研究调查了山柰根茎和叶子不同提取物的镇静活性。
通过戊巴比妥钠诱导睡眠时间、穿洞试验和旷场试验,以100和200毫克/千克体重的口服剂量对瑞士白化小鼠的镇静活性进行评估。对根茎的丙酮提取物(ACR)以及石油醚馏分(PEF)、氯仿馏分(CHF)、甲醇馏分(MEF)和叶子的丙酮提取物(ACL)进行镇静活性检测。
在镇静活性研究中,所有提取物在戊巴比妥钠诱导睡眠时间试验中均显著(p < 0.05和p < 0.001)降低了诱导睡眠时间的起始时间和持续时间,在穿洞试验和旷场试验中降低了运动和探索活动。在戊巴比妥钠诱导睡眠时间试验中,根茎的氯仿提取物(200毫克/千克)在翻正反射消失持续时间方面显示出最大358.55%的效果,而标准药物地西泮(2毫克/千克)产生了231.42%的效果。在穿洞试验和旷场试验中,丙酮叶提取物(200毫克/千克)对运动活性的最大抑制率分别为95.09%和95.58%,而标准药物地西泮对运动活性的抑制率分别为71.70%和70.58%。
本研究表明,山柰根茎和叶子的丙酮提取物及其馏分具有中枢神经系统(CNS)抑制特性,这支持了其在传统医学中的应用。因此,该植物可进一步研究以找出其具有药理活性的天然产物。