Sultan Ramiz Ahmed, Kabir Mohammad Shah Hafez, Uddin Mir Muhammad Nasir, Uddin Mohi, Mahmud Zobaer Al, Raihan Sheikh Zahir, Qais Nazmul
Department of Pharmacy, University of Chittagong, Chittagong.
Department of Pharmacy, International Islamic University Chittagong, Chittagong.
J Basic Clin Physiol Pharmacol. 2017 May 1;28(3):283-291. doi: 10.1515/jbcpp-2016-0066.
In this ethnopharmacological study, methanolic extract of the aerial plant parts of Phragmites karka (Family: Poaceae) and its petroleum ether and carbon tetrachloride fractions were investigated for bioactivities in Swiss-albino mice, namely, analgesic, central nervous system (CNS) depressant, hypoglycemic, and antidiarrheal activity.
The cold methanolic extract of the aerial plant parts of Phragmites karka (MEPK) was first prepared, and it was then further fractionated as petroleum ether (PEFMEPK) and carbon tetrachloride (CTFMEPK) fractions. Analgesic activity was performed employing acidic acid-induced writhing test, central analgesic effect by radiant heat tail-flick method. CNS depressant activity was evaluated by phenobarbitone-induced sleeping time test. Hypoglycemic activity was tested by glucose tolerance test (GTT). Antidiarrheal activity was evaluated by castor oil-induced diarrhea method. For all in vivo tests, doses of 200 and 400 mg/kg body weight were used.
In the mice model, the MEPK, PEFMEPK, and CTFMEPK fractions showed significant peripheral analgesic activity at a dose of 400 mg/kg body weight with percentage of inhibition of acetic acid-induced writhing 77.67 (p<0.001), 33.50 (p<0.001), and 40.29 (p<0.001), respectively, compared to the standard dichlofenac (60.68%, p<0.001) group. The hypoglycemic properties of MEPK, PEFMEPK, and CTFMEPK extracts were evaluated in normoglycemic mice where the reduction of blood glucose level after 30 min of glucose load were 69.85%, 78.91%, and 72.73%, respectively, and for standard glibenclamide, the reduction was 72.85%. All results were significant (p<0.05). In the case of the CNS depressant activity by phenobarbitone-induced sleeping time test, the crude ME significantly reduced sleep latency by 57.14% and increased the duration of sleep by 63.29% compared to the control, which were comparable to that of standard diazepam (65.71% and 77.62%, respectively). Among all the extract and fractions, methanolic extract showed the maximum antidiarrheal effect. The methanolic extract at 200 mg/kg dose induced a significant decrease in the total number of defecation in 4 h (69.05% of inhibition, p<0.001) and at 400 mg/kg dose showed 76.19% of inhibition (p<0.001).
In light of the available literature, these findings represent the first experimental investigation of biological activities of P. karka in the perspective of their traditional use.
在这项民族药理学研究中,对芦苇(禾本科)地上部分的甲醇提取物及其石油醚和四氯化碳馏分在瑞士白化小鼠体内的生物活性进行了研究,即镇痛、中枢神经系统(CNS)抑制、降血糖和抗腹泻活性。
首先制备芦苇地上部分的冷甲醇提取物(MEPK),然后将其进一步分离为石油醚(PEFMEPK)和四氯化碳(CTFMEPK)馏分。采用乙酸诱导扭体试验进行镇痛活性研究,通过辐射热甩尾法研究中枢镇痛作用。通过苯巴比妥诱导的睡眠时间试验评估CNS抑制活性。通过葡萄糖耐量试验(GTT)测试降血糖活性。通过蓖麻油诱导的腹泻法评估抗腹泻活性。对于所有体内试验,使用200和400mg/kg体重的剂量。
在小鼠模型中,MEPK、PEFMEPK和CTFMEPK馏分在400mg/kg体重剂量下显示出显著的外周镇痛活性,与标准双氯芬酸(60.68%,p<0.001)组相比,乙酸诱导扭体的抑制率分别为77.67(p<0.001)、33.50(p<0.001)和40.29(p<0.001)。在血糖正常的小鼠中评估了MEPK、PEFMEPK和CTFMEPK提取物的降血糖特性,葡萄糖负荷30分钟后血糖水平的降低分别为69.85%、78.91%和72.73%,对于标准格列本脲,降低率为72.85%。所有结果均具有显著性(p<0.05)。在苯巴比妥诱导的睡眠时间试验评估CNS抑制活性的情况下,与对照组相比,粗甲醇提取物显著缩短睡眠潜伏期57.14%,并将睡眠时间延长63.29%,这与标准地西泮(分别为65.71%和77.62%)相当。在所有提取物和馏分中,甲醇提取物显示出最大的抗腹泻作用。200mg/kg剂量的甲醇提取物在4小时内排便总数显著减少(抑制率69.05%,p<0.001),400mg/kg剂量时抑制率为76.19%(p<0.001)。
根据现有文献,这些发现代表了从传统用途角度对芦苇生物活性的首次实验研究。