Hasan Md Mahedi, Hossain Amir, Shamim Abdullah, Rahman Md Mustafizur
Pharmacy Discipline, Life Science School, Khulna University, Khulna, 9208, Bangladesh.
Department of Pharmacy, Dhaka International University, Satarkul, Badda, Dhaka, Bangladesh.
BMC Complement Altern Med. 2017 Nov 22;17(1):496. doi: 10.1186/s12906-017-2010-y.
The current study was conducted to evaluate the antioxidant, analgesic, antihyperglycemic, neuropharmacological and antidiarrheal activities of ethanolic extract of Lepisanthes rubiginosa L. leaves in different experimental models.
Quantitative and qualitative analysis were done by TLC (thin layer chromatography) and DPPH (1,1-diphenyl-2-picrylhydrazyl) free radical scavenging assay. Analgesic, antihyperglycemic and antidiarrheal activities were evaluated using acetic acid induced writhing in mice, oral glucose tolerance test and castor oil induced diarrhea, respectively. Neuropharmacological activity was investigated in mice using both Open Field and Hole Board methods.
TLC analysis indicated the presence of antioxidant compounds in the extract we used. The extract showed IC value was 31.62 μg/mL whereas the standard ascorbic acid showed 12.02 μg/mL. In acetic acid induced writhing assay, the extract showed 46.07% and 58.43% writhing inhibition at the doses of 250 mg/kg and 500 mg/kg body weight, respectively whereas standard diclofenac-Na (25 mg/kg) showed 86.52% writhing inhibition. The plant extract showed significant (p < 0.05) antihyperglycemic activity on mice as compared to control groups. In neuropharmacological activity assay the experimental animal showed a noticeable decrease in locomotion by showing a decrease in number of square crossed and head dipping at both doses (250 mg/kg & 500 mg/kg). In antidiarrheal activity test, the plant extract at the doses of 250 mg/kg and 500 mg/kg showed percent inhibition of defecation 57.89 and 77.19 respectively, whereas standard loperamide (3 mg/kg) showed percent inhibition of defecation 88.59.
The results demonstrated that the extract has potential antioxidant, analgesic, antihyperglycemic, neuropharmacological and antidiarrheal activity.
本研究旨在评估红毛丹叶乙醇提取物在不同实验模型中的抗氧化、镇痛、抗高血糖、神经药理和止泻活性。
通过薄层色谱法(TLC)和1,1-二苯基-2-苦基肼自由基清除试验(DPPH)进行定量和定性分析。分别采用乙酸诱导小鼠扭体法、口服葡萄糖耐量试验和蓖麻油诱导腹泻法评估镇痛、抗高血糖和止泻活性。使用旷场试验和洞板试验对小鼠的神经药理活性进行研究。
TLC分析表明我们使用的提取物中存在抗氧化化合物。提取物的IC值为31.62μg/mL,而标准抗坏血酸的IC值为12.02μg/mL。在乙酸诱导的扭体试验中,提取物在250mg/kg和500mg/kg体重剂量下分别显示出46.07%和58.43%的扭体抑制率,而标准双氯芬酸钠(25mg/kg)显示出86.52%的扭体抑制率。与对照组相比,该植物提取物对小鼠具有显著的(p<0.05)抗高血糖活性。在神经药理活性试验中,实验动物在两个剂量(250mg/kg和500mg/kg)下均表现出明显的运动减少,即穿过的方格数和头部下探次数减少。在止泻活性试验中,250mg/kg和500mg/kg剂量的植物提取物分别显示出57.89%和77.19%的排便抑制率,而标准洛哌丁胺(3mg/kg)显示出88.59%的排便抑制率。
结果表明该提取物具有潜在的抗氧化、镇痛、抗高血糖、神经药理和止泻活性。