The Antioxidant Potential of Azadirachta indica Ameliorates Cardioprotection Following Diabetic Mellitus-Induced Microangiopathy

被引:12
作者
Gupta, Naveen Kumar [1 ,2 ]
Srivastva, Nidhi [2 ]
Bubber, Parvesh [3 ]
Puri, Sanjeev [1 ]
机构
[1] Panjab Univ, Univ Inst Engn & Technol, Dept Biotechnol, Chandigarh 160014, India
[2] Banasthali Univ, Dept Biotechnol, Banasthali, Rajasthan, India
[3] IGNOU, Dept Biochem, New Delhi, India
关键词
Antioxidants; Azadirachta indica; diabetes mellitus; lipid peroxidation; MEDICINAL-PLANTS; REACTIVE OXYGEN; RATS; STREPTOZOTOCIN; MECHANISMS; DAMAGE; CONSEQUENCES; PREVALENCE; DEFICIENCY; MANAGEMENT;
D O I
10.4103/0973-1296.185772
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Cardiac complications associated with diabetes mellitus have become major cause of concern. Antidiabetic drugs, with varied mode of action, are although available, apprehensions exist for their limited action or side effects upon prolonged use. Efforts are therefore inclined toward finding other alternatives. The present study was, thus, undertaken to evaluate the cardioprotective effect of Azadirachta indica (AI) on microangiopathic changes in rat model of diabetes. Materials and Methods: Diabetes was induced in male rats by single intraperitoneal injection of streptozotocin (60 mg/kg body weight). Seven days after glucose levels are stabilized, aqueous leaf extract of AI (ALE) (600 mg/kg(1) body weight) was administered orally to diabetic animals every day for 7 days. Results: High blood glucose characterizing diabetes in these animals was found to show increased lipid peroxidation (LPO), altered antioxidant biomarkers together with microangiopathic alterations. The treatment of diabetic rats with ALE reduced the levels of blood glucose, LPO, and restored the activities of antioxidant enzyme. Light and transmission electron microscopic analysis revealed reduced necrotic areas and inflammation in tissue architecture of ALE treated heart in comparison to untreated diabetic group. Conclusion: AI provides cardioprotection by ameliorating oxidative stress in rat model of diabetic mellitus.
引用
收藏
页码:S371 / S378
页数:8
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