中文摘要：

目的：探讨新型糖原磷酸化酶抑制剂山楂酸（MA）对高血糖大鼠脑缺血/再灌损伤的作用。方法：通过高脂饮食（HFD）合并低剂量链脲佐菌素（STZ）注射,制作II型糖尿病大鼠模型。不同剂量MA（10,5和2.5mg·kg？1·d？1）灌胃2周。双侧颈总结扎诱导建立大鼠脑缺血模型,评价MA对脑缺血/再灌II型糖尿病大鼠神经保护作用。结果：MA可显著降低II型糖尿病大鼠的空腹血糖（GLU）、血浆甘油三酯（TG）和总胆固醇（TC）水平。脑缺血II型糖尿病大鼠脑组织中丙二醛（MDA）含量显著增高,超氧化物歧化酶（SOD）活性显著下降;缺血3d后海马CA1区可观察到显著神经元损伤。MA显著减轻脑缺血损伤,并呈剂量依赖性。此外,MA可显著降低皮层和海马区MDA含量,减轻脑组织的脂质过氧化反应,提高缺血再灌大鼠脑组织的SOD活性。结论：MA预作用对II型糖尿病合并脑缺血诱导的损伤具有良好的保护作用。

英文摘要：

AIM：To investigate the effects of maslinic acid（MA）,a novel glycogen phosphorylase inhibitor in hyperglycemic rats after cerebral ischemia/reperfusion injury.METHODS：Rats were fed with high fat diet（HFD） followed by low-dose streptozotocin（STZ） injection to induce metabolic syndrome.Three doses of MA（10,5 and 2.5 mg·kg？1·d？1） were administered once daily by i.g.for 2 weeks.Neurological outcomes were compared in vehicle and MA treated HFD/STZ rats with cerebral ischemia/reperfusion injury induced by bilateral common carotid artery occlusion.RESULTS：The elevation of plasma fasting glucose（GLU）,serum plasma triglyceride（TG） and plasma total cholesterol（TC） was antagonized by MA significantly.Cerebral ischemia with pre-existing hyperglycemia and hyperlipemia caused prominent elevation in MDA levels and decrease in SOD activity.Extensive neuronal death occurred in the CA1 area of hippocampus at day 3 after forebrain ischemia.MA significantly attenuated ischemia-induced neuronal death in a dose-dependent manner.Moreover,MA caused a significant reduction in MDA levels and elevation in SOD activity in both cortex and hippocampus.CONCLUSION：Results suggested the prophylaxis of MA may also show beneficial effects in reducing cerebral damage after stroke for patients with type 2 diabetes.