Ko Chih-Yuan, Xu Jian-Hua, Lo Yangming Martin, Tu Rong-Syuan, Wu James Swi-Bea, Huang Wen-Chung, Shen Szu-Chuan
Department of Clinical Nutrition, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Department of Respiratory and Critical Care Medicine, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Front Aging Neurosci. 2021 Nov 12;13:774477. doi: 10.3389/fnagi.2021.774477. eCollection 2021.
The intricate relationship between type 2 diabetes mellitus (T2DM) and Alzheimer's disease (AD) suggests that insulin is involved in modulating AD-related proteins. Alpha-lipoic acid (ALA) can improve insulin resistance (IR) in diabetic rats. However, the role of ALA in alleviating the cognitive decline of T2DM is not yet clear. This study examined the ameliorative effect of ALA on cognitive impairment, cerebral IR, and synaptic plasticity abnormalities in high-fat diet (HFD) plus streptozotocin (STZ) induced diabetic rats. The HFD/STZ-induced T2DM male Wistar rats were orally administered with ALA (50, 100, or 200 mg/kg BW) once a day for 13 weeks. Abilities of cognition were measured with a passive avoidance test and Morris water maze. Specimens of blood and brain were collected for biochemical analysis after the rats were sacrificed. Western blotting was used to determine protein expressions in the hippocampus and cortex in the insulin signaling pathways, long-term potentiation (LTP), and synaptic plasticity-related protein expressions. Alpha-lipoic acid improved hyperinsulinemia and the higher levels of free fatty acids of the T2DM rats. Behavioral experiments showed that the administration of ALA improved cognitive impairment in HFD/STZ-induced T2DM rats. ALA ameliorated insulin-related pathway proteins [phosphoinositide 3-kinase (PI3K), phospho-protein kinase B (pAkt)/Akt, and insulin-degrading enzyme (IDE)] and the LTP pathway, as well as synaptic plasticity proteins (calmodulin-dependent protein kinase II, cyclic AMP response element-binding protein, and postsynaptic density protein-95) of the cerebral cortex or hippocampus in HFD/STZ-induced T2DM rats. Our findings suggested that ALA may ameliorate cognition impairment alleviating cerebral IR improvement and cerebral synaptic plasticity in diabetic rats.
2型糖尿病(T2DM)与阿尔茨海默病(AD)之间的复杂关系表明,胰岛素参与调节与AD相关的蛋白质。α-硫辛酸(ALA)可改善糖尿病大鼠的胰岛素抵抗(IR)。然而,ALA在减轻T2DM认知功能下降方面的作用尚不清楚。本研究考察了ALA对高脂饮食(HFD)加链脲佐菌素(STZ)诱导的糖尿病大鼠认知障碍、脑IR和突触可塑性异常的改善作用。将HFD/STZ诱导的T2DM雄性Wistar大鼠每天口服ALA(50、100或200mg/kg体重),持续13周。通过被动回避试验和莫里斯水迷宫测量认知能力。大鼠处死后,采集血液和脑标本进行生化分析。采用蛋白质免疫印迹法检测胰岛素信号通路、长时程增强(LTP)及海马和皮质中与突触可塑性相关的蛋白质表达。α-硫辛酸改善了T2DM大鼠的高胰岛素血症和较高的游离脂肪酸水平。行为学实验表明,给予ALA可改善HFD/STZ诱导的T2DM大鼠的认知障碍。ALA改善了HFD/STZ诱导的T2DM大鼠大脑皮质或海马中胰岛素相关通路蛋白[磷脂酰肌醇3激酶(PI3K)、磷酸化蛋白激酶B(pAkt)/Akt和胰岛素降解酶(IDE)]以及LTP通路和突触可塑性蛋白(钙调蛋白依赖性蛋白激酶II、环磷酸腺苷反应元件结合蛋白和突触后致密蛋白95)。我们的研究结果表明,ALA可能通过减轻脑IR改善和脑突触可塑性来改善糖尿病大鼠的认知障碍。