Department of Endocrinology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China.
Department of Physiology and Neurobiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Aging (Albany NY). 2021 Jul 28;13(14):18287-18297. doi: 10.18632/aging.203274.
To explore the effect of albiflorin (AL) on streptozotocin (STZ)-induced Alzheimer's disease (AD) in rats.
A mouse model of diabetic encephalopathy was established by intraperitoneal injection of 1%STZ. Step down test and water maze test were used to test the cognitive function of rats. Congo Red Staining was used to detect the distribution of Aβ plaques in the hippocampus of rats. Cytokine levels in serum and hippocampus were measured using ELISA. Serum insulin, oral glucose tolerance (OGTT), serum superoxide dismutase (SOD) activity and malondialdehyde (MDA) content were measured by commercial kits. And the content of Nrf-2/HO-1/HMGB1/NF-kB in the hippocampus of diabetic rats were detected by western blot.
Compared with the STZ model group, the average escape latency of rats in the AL group in the Morris water maze test was significantly shortened, and the average number of platform crossings and the ratio of distance/total swimming distance in the target quadrant were increased significantly. Staining of tissue sections and ELISA showed a decrease in Aβ plaque density in the hippocampus of rats in the AL group. And serum insulin levels of rats in the ALgroup were significantly reduced and OGTT was improved. In addition, AL could also regulate the Nrf-2/HO-1/HMGB1/NF-kB signal pathway in the hippocampus. Therefore, AL may ameliorate STZ-induced cognitive impairment in rats by regulating oxidative stress and inflammation in the brain.
探讨白芍总苷(AL)对链脲佐菌素(STZ)致阿尔茨海默病(AD)大鼠的作用。
腹腔注射 1%STZ 建立糖尿病脑病小鼠模型。采用跳台实验和水迷宫实验检测大鼠的认知功能。刚果红染色检测大鼠海马区 Aβ斑块的分布。采用 ELISA 法检测血清和海马组织细胞因子水平。采用试剂盒检测血清胰岛素、口服葡萄糖耐量(OGTT)、血清超氧化物歧化酶(SOD)活性和丙二醛(MDA)含量。采用 Western blot 法检测糖尿病大鼠海马组织中 Nrf-2/HO-1/HMGB1/NF-kB 的含量。
与 STZ 模型组比较,AL 组大鼠在 Morris 水迷宫实验中的平均逃避潜伏期明显缩短,平台穿越次数和目标象限距离/总游泳距离比值明显增加。组织切片染色和 ELISA 结果显示,AL 组大鼠海马区 Aβ斑块密度降低。同时,AL 组大鼠血清胰岛素水平降低,OGTT 改善。此外,AL 还可以调节大鼠海马组织中的 Nrf-2/HO-1/HMGB1/NF-kB 信号通路。综上所述,AL 可能通过调节脑内氧化应激和炎症反应改善 STZ 诱导的大鼠认知功能障碍。