桄榔子叶提取物对四氧嘧啶诱导的糖尿病大鼠的抗糖尿病活性。

Mukesh S Sikarwar, M B Patil
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引用次数: 65

摘要

研究了桄榔子叶提取物对四氧嘧啶诱导的糖尿病白化大鼠的抗糖尿病作用。比较了桄榔子不同提取物与已知抗糖尿病药物格列本脲(600 μg/kg b. wt.)的作用。同时对实验性糖尿病大鼠进行口服糖耐量试验(OGTT)。采用简单浸渍法得到石首菜的石油醚、氯仿、醇和水提物,并采用生药学和植物化学筛选方法进行标准化。剂量选择是根据急性口服毒性研究(50- 5000mg /kg体重)根据经合组织指南进行的。桄榔子醇提物(PPEE)和水提物(PPAE)的抗糖尿病活性显著(P < 0.001)。在四氧嘧啶诱导模型中,与糖尿病对照组(413.50±4.752mg/dl)和氯仿提取物(210.83±14.912mg/dl)相比,四氧嘧啶诱导模型第7天的血糖水平分别为155.83±11.211mg/dl (PPEE)和132.00±4.955mg/dl (PPAE)。在葡萄糖负荷大鼠中,PPEE在30分钟和90分钟后的血糖水平分别为164.50±6.350mg/dl和156.50±4.089mg/dl,而PPAE处理的动物在30分钟和90分钟后的血糖水平分别为176±3.724mg/dl和110.33±6.687mg/dl。这些提取物还可以防止糖尿病大鼠的体重减轻。这种药物有可能成为一种抗糖尿病药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antidiabetic activity of Pongamia pinnata leaf extracts in alloxan-induced diabetic rats.

Antidiabetic activity of Pongamia pinnata leaf extracts in alloxan-induced diabetic rats.

Antidiabetic activity of Pongamia pinnata leaf extracts in alloxan-induced diabetic rats.

Antidiabetic activity of Pongamia pinnata leaf extracts in alloxan-induced diabetic rats.

The antidiabetic activity of Pongamia pinnata ( Family: Leguminosae) leaf extracts was investigated in alloxan-induced diabetic albino rats. A comparison was made between the action of different extracts of P. pinnata and a known antidiabetic drug glibenclamide (600 μg/kg b. wt.). An oral glucose tolerance test (OGTT) was also performed in experimental diabetic rats. The petroleum ether, chloroform, alcohol and aqueous extracts of P. pinnata were obtained by simple maceration method and were subjected to standardization using pharmacognostical and phytochemical screening methods. Dose selection was made on the basis of acute oral toxicity study (50-5000 mg/kg b. w.) as per OECD guidelines. P. pinnata ethanolic extract (PPEE) and aqueous extract (PPAE) showed significant (P < 0.001) antidiabetic activity. In alloxan-induced model, blood glucose levels of these extracts on 7th day of the study were 155.83 ± 11.211mg/dl (PPEE) and 132.00 ± 4.955mg/dl (PPAE) in comparison of diabetic control (413.50 ± 4.752mg/dl) and chloroform extract (210.83 ± 14.912mg/dl). In glucose loaded rats, PPEE exhibited glucose level of 164.50 ± 6.350mg/dl after 30 min and 156.50 ± 4.089mg/dl after 90 min, whereas the levels in PPAE treated animals were 176 ± 3.724mg/dl after 30 min and 110.33 ± 6.687mg/dl after 90 min. These extracts also prevented body weight loss in diabetic rats. The drug has the potential to act as an antidiabetic drug.

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