Pwaniyibo Samson Faith, Teru Patrick Ambrose, Samuel Nadro Margret, Jahng Wan Jin
Department of Biochemistry, School of Life Sciences, Modibbo Adama University of Technology, Adamawa State, Yola, Nigeria.
Retina Proteomics Laboratory, Department of Petroleum Chemistry, American University of Nigeria, Adamawa State, Yola, Nigeria.
J Diabetes Metab Disord. 2020 Apr 14;19(1):605-616. doi: 10.1007/s40200-020-00524-1. eCollection 2020 Jun.
The current study aimed to determine the antidiabetic effects of leaf extract of in streptozotocin-induced diabetic rats.
A total of ninety-five (95) adult rats were used for the experiment. The whole study protocol was divided into three sets of individual experiments. The animals were divided randomly into seven groups of five rats each. The rats were given a diet supplemented with 50 g high fat to 50 g vital feeds for two weeks. The study lasted 28 days with daily administration and weekly blood glucose and body weight check. At the end of the experiment protocol, the rats were fasted overnight and were anesthetized. Blood was collected via cardiac puncture from each animal for biochemical analysis. Metglim 3.38 mg/kg bodyweight was used as positive control. Diabetes was induced using streptozotocin (35 mg/kg in 0.1 M phosphate-buffered saline) intraperitoneally for 5 days. Phytochemicals were analyzed in both extract and fractions.
Phytochemical screening revealed the presence of alkaloids, saponins, flavonoids, glycosides, tannins, carotenoids, terpenes, and steroids in both extract and fractions. Proteins, carbohydrates, and fats were detected by systematic molecular analysis. Fraction 1 of plant extracts prevented glucose-induced hyperglycaemia 30 min' post glucose load in all rats. Streptozotocin treatment caused a significant increase (p˂0.05) in blood sugar, total cholesterol, triacylglycerol, low-density lipoproteins and a significant (p˂0.05) decrease in food intake, body weight and high-density lipoproteins in diabetic rats.
Treatment with the extract significantly improved the derangements caused by streptozotocin. These results suggest that the leaf extracts of could serve as a potential treatment for diabetes therapy.
本研究旨在确定[植物名称]叶提取物对链脲佐菌素诱导的糖尿病大鼠的抗糖尿病作用。
总共95只成年大鼠用于实验。整个研究方案分为三组独立实验。将动物随机分为七组,每组五只大鼠。给大鼠喂食添加了50克高脂肪饲料和50克重要饲料的食物,持续两周。研究持续28天,每天给药,并每周检查血糖和体重。在实验方案结束时,大鼠禁食过夜并麻醉。通过心脏穿刺从每只动物采集血液进行生化分析。以3.38毫克/千克体重的美格列奈作为阳性对照。使用链脲佐菌素(35毫克/千克,溶于0.1 M磷酸盐缓冲盐水中)腹腔注射诱导糖尿病,持续5天。对提取物和馏分进行植物化学分析。
植物化学筛选显示提取物和馏分中均存在生物碱、皂苷、黄酮类化合物、糖苷、单宁、类胡萝卜素、萜类化合物和甾体。通过系统分子分析检测到蛋白质、碳水化合物和脂肪。植物提取物的馏分1在所有大鼠葡萄糖负荷后30分钟可预防葡萄糖诱导的高血糖。链脲佐菌素治疗导致糖尿病大鼠血糖、总胆固醇、三酰甘油、低密度脂蛋白显著升高(p˂0.05),食物摄入量、体重和高密度脂蛋白显著降低(p˂0.05)。
提取物治疗显著改善了链脲佐菌素引起的紊乱。这些结果表明,[植物名称]叶提取物可作为糖尿病治疗的潜在疗法。