Pharmacology Division, Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Post Box: 38, Hisar, 125001, India.
Cardiovasc Diabetol. 2012 Aug 10;11:95. doi: 10.1186/1475-2840-11-95.
This study was made to investigate the antidiabetic, antioxidant and hypolipidemic potential of Cinnamomum tamala, (Buch.-Ham.) Nees & Eberm (Tejpat) oil (CTO) in streptozotocin (STZ) induced diabetes in rats along with evaluation of chemical constituents.
The GC-MS (Gas chromatography-mass spectrometry) analysis of the oil showed 31 constituents of which cinnamaldehyde was found the major component (44.898%). CTO and cinnamaldehyde was orally administered to diabetic rats to study its effect in both acute and chronic antihyperglycemic models. The body weight, oral glucose tolerance test and biochemical parameters viz. glucose level, insulin level, liver glycogen content, glycosylated hemoglobin, total plasma cholesterol, triglyceride and antioxidant parameters were estimated for all treated groups and compared against diabetic control group.
CTO (100 mg/kg and 200 mg/kg), cinnamaldehyde (20 mg/kg) and glibenclamide (0.6 mg/kg) in respective groups of diabetic animals administered for 28 days reduced the blood glucose level in streptozotocin induced diabetic rats. There was significant increase in body weight, liver glycogen content, plasma insulin level and decrease in the blood glucose, glycosylated hemoglobin and total plasma cholesterol in test groups as compared to control group. The results of CTO and cinnamaldehyde were found comparable with standard drug glibenclamide. In vitro antioxidant studies on CTO using various models showed significant antioxidant activity. In vivo antioxidant studies on STZ induced diabetic rats revealed decreased malondialdehyde (MDA) and increased reduced glutathione (GSH).
Thus the investigation results that CTO has significant antidiabetic, antioxidant and hypolipidemic activity.
本研究旨在探讨肉桂(Buch.-Ham.)Nees & Eberm(Tejpat)油(CTO)在链脲佐菌素(STZ)诱导的糖尿病大鼠中的降血糖、抗氧化和降血脂作用,并评估其化学成分。
油的 GC-MS(气相色谱-质谱)分析显示 31 种成分,其中肉桂醛是主要成分(44.898%)。CTO 和肉桂醛口服给予糖尿病大鼠,以研究其在急性和慢性抗高血糖模型中的作用。所有治疗组均测量体重、口服葡萄糖耐量试验和生化参数(血糖水平、胰岛素水平、肝糖原含量、糖化血红蛋白、总血浆胆固醇、甘油三酯和抗氧化参数),并与糖尿病对照组进行比较。
CTO(100mg/kg 和 200mg/kg)、肉桂醛(20mg/kg)和格列本脲(0.6mg/kg)在分别给予糖尿病动物 28 天的各组中降低了链脲佐菌素诱导的糖尿病大鼠的血糖水平。与对照组相比,试验组的体重、肝糖原含量、血浆胰岛素水平显著增加,血糖、糖化血红蛋白和总血浆胆固醇水平显著降低。CTO 和肉桂醛的结果与标准药物格列本脲相当。使用各种模型对 CTO 的体外抗氧化研究显示出显著的抗氧化活性。STZ 诱导的糖尿病大鼠体内抗氧化研究显示,丙二醛(MDA)减少,还原型谷胱甘肽(GSH)增加。
因此,研究结果表明 CTO 具有显著的降血糖、抗氧化和降血脂作用。