Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar 608002, Tamilnadu, India.
Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar 608002, Tamilnadu, India.
Chem Biol Interact. 2015 Mar 5;229:44-54. doi: 10.1016/j.cbi.2015.01.026. Epub 2015 Jan 29.
The present study was designed to evaluate the effects of tyrosol, a phenolic compound, on the activities of key enzymes of carbohydrate metabolism in the control and streptozotocin-induced diabetic rats. Diabetes mellitus was induced in rats by a single intraperitoneal injection of streptozotocin (40 mg/kg body weight). Experimental rats were administered tyrosol 1 ml intra gastrically at the doses of 5, 10 and 20mg/kg body weight and glibenclamide 1 ml at a dose of 600 μg/kg body weight once a day for 45 days. At the end of the experimental period, diabetic control rats exhibited significant (p<0.05) increase in plasma glucose, glycosylated hemoglobin with significant (p<0.05) decrease in plasma insulin, total hemoglobin and body weight. The activities of key enzymes of carbohydrate metabolism such as phosphoenolpyruvate carboxykinase, fructose-1,6-bisphosphatase and glucose-6-phosphatase were significantly (p<0.05) increased and the activities of hexokinase and glucose-6-phosphate dehydrogenase were significantly (p<0.05) decreased in the liver and kidney of diabetic control rats. Further, antioxidants were lowered in diabetic control rats. A significant (p<0.05) decline in glycogen level in the liver and muscle and glycogen synthase activity in the liver and a significant (p<0.05) increase in the activity of liver glycogen phosphorylase were observed in diabetic control rats compared to normal control rats. Oral administration of tyrosol to diabetic rats reversed all the above mentioned biochemical parameters to near normal in a dose dependent manner. Tyrosol at a dose of 20mg/kg body weight showed the highest significant effect than the other two doses. Immunohistochemical staining of pancreas revealed that tyrosol treated diabetic rats showed increased insulin immunoreactive β-cells, which confirmed the biochemical findings. The observed results were compared with glibenclamide, a standard oral hypoglycemic drug. The results of the present study suggest that tyrosol decreases hyperglycemia, by its antioxidant effect.
本研究旨在评估酚类化合物酪醇对正常和链脲佐菌素诱导的糖尿病大鼠糖代谢关键酶活性的影响。糖尿病通过单次腹腔注射链脲佐菌素(40mg/kg 体重)诱导大鼠。实验大鼠每天胃内给予酪醇 1ml,剂量分别为 5、10 和 20mg/kg 体重,给予格列本脲 1ml,剂量为 600μg/kg 体重,共 45 天。在实验期末,糖尿病对照组大鼠的血浆葡萄糖、糖化血红蛋白显著升高(p<0.05),血浆胰岛素、总血红蛋白和体重显著降低(p<0.05)。糖代谢关键酶如磷酸烯醇丙酮酸羧激酶、果糖-1,6-二磷酸酶和葡萄糖-6-磷酸酶的活性显著升高(p<0.05),肝、肾中己糖激酶和葡萄糖-6-磷酸脱氢酶的活性显著降低(p<0.05)。此外,糖尿病对照组大鼠的抗氧化剂水平降低。与正常对照组大鼠相比,糖尿病对照组大鼠肝、肌肉中糖原含量显著降低(p<0.05),肝、肌肉中糖原合酶活性降低(p<0.05),肝糖原磷酸化酶活性显著升高(p<0.05)。与糖尿病对照组大鼠相比,口服酪醇可使上述生化参数在一定剂量范围内接近正常。与其他两种剂量相比,20mg/kg 体重的酪醇剂量显示出最高的显著效果。胰腺免疫组织化学染色显示,酪醇治疗的糖尿病大鼠胰岛素免疫反应性β细胞增加,这证实了生化研究的结果。将观察到的结果与格列本脲(一种标准的口服降糖药物)进行了比较。本研究结果表明,酪醇通过抗氧化作用降低高血糖。