Fang Fang, Liu Gengtao
Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Basic Clin Pharmacol Toxicol. 2007 Dec;101(6):447-54. doi: 10.1111/j.1742-7843.2007.00138.x. Epub 2007 Oct 25.
The aim of the present study was to access the protective effect of a novel synthesized squamosamide cyclic analogue, compound FLZ, on memory impairment in artificially senescent mice induced by chronic injection of D-galactose and sodium nitrite (NaNO(2)). Artificially senescent mouse model was induced by consecutive injection of D-galactose (120 mg/kg) and NaNO(2) (90 mg/kg) once daily for 60 days. Compound FLZ (75 and 150 mg/kg) was orally administered once daily for 30 days after D-galactose and NaNO(2) injection for 30 days. The water maze test was used to evaluate the learning and memory function of mice. The content of malondialdehyde (MDA) and the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in serum were determined using different biochemical kits. The alterations in hippocampus morphology were assessed by light and electronic microscope. Immunoreactive cells of Bcl-2 in the hippocampus were counted by immunohistochemical staining, and Bcl-2 protein expression was analysed by Western blot method. The results indicate that injection of D-galactose and NaNO(2) induces memory impairment and neuronal damage in hippocampus of mice. In addition, serum SOD and GSH-Px activities decreased, while MDA level increased. Bcl-2-positive neurons and Bcl-2 protein expression in the hippocampus decreased remarkably. Oral administration of FLZ for 30 days significantly improved the cognitive deficits and the biochemical markers mentioned above, and also reduced the pathological alterations in mouse hippocampus. The results suggest that FLZ ameliorates memory deficits and pathological injury in artificially senescent mice induced by chronic injection of D-galactose and NaNO(2), indicating that FLZ is worth further studies for fighting antisenescence and dementia.
本研究的目的是评估一种新合成的鳞状酰胺环类似物化合物FLZ对慢性注射D-半乳糖和亚硝酸钠(NaNO₂)诱导的人工衰老小鼠记忆损伤的保护作用。通过每天连续注射D-半乳糖(120 mg/kg)和NaNO₂(90 mg/kg),持续60天来诱导人工衰老小鼠模型。在注射D-半乳糖和NaNO₂ 30天后,每天口服给予化合物FLZ(75和150 mg/kg),持续30天。采用水迷宫试验评估小鼠的学习和记忆功能。使用不同的生化试剂盒测定血清中丙二醛(MDA)的含量以及超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的活性。通过光学显微镜和电子显微镜评估海马体形态的变化。通过免疫组织化学染色对海马体中Bcl-2的免疫反应细胞进行计数,并通过蛋白质印迹法分析Bcl-2蛋白的表达。结果表明,注射D-半乳糖和NaNO₂会诱导小鼠海马体的记忆损伤和神经元损伤。此外,血清SOD和GSH-Px活性降低,而MDA水平升高。海马体中Bcl-2阳性神经元和Bcl-2蛋白表达显著降低。口服FLZ 30天可显著改善上述认知缺陷和生化指标,还可减轻小鼠海马体的病理改变。结果表明,FLZ可改善慢性注射D-半乳糖和NaNO₂诱导的人工衰老小鼠的记忆缺陷和病理损伤,表明FLZ在抗衰老和抗痴呆方面值得进一步研究。