Zhou J, Fu Y, Tang X C
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 294 Tai-yuan Road, 200031, Shanghai, People's Republic of China.
Neurosci Lett. 2001 Jun 22;306(1-2):53-6. doi: 10.1016/s0304-3940(01)01855-9.
Huperzine A (HupA) and donepezil, two novel selective acetylcholinesterase inhibitors available for Alzheimer's disease, were tested for their ability to alleviate injury from oxygen-glucose deprivation (OGD) in the rat pheochromocytoma line PC12 cells. OGD for 30 min triggered death in more than 50% of cells, along with major changes in morphology and biochemistry including elevated levels of lipid peroxide, superoxide disamutase activity and lactate. Cells pretreated for 2 h with HupA or donepezil showed improved survival and reduced biochemical and morphologic signs of toxicity (statistically significant over the range from 10 microM down to 1.0 and 0.1 microM, respectively). Our results indicated that HupA and donepezil protected PC12 cells against OGD-induced toxicity, most likely by alleviating disturbances of oxidative and energy metabolism.
石杉碱甲(HupA)和多奈哌齐是两种可用于治疗阿尔茨海默病的新型选择性乙酰胆碱酯酶抑制剂,本研究检测了它们减轻大鼠嗜铬细胞瘤PC12细胞氧糖剥夺(OGD)损伤的能力。30分钟的OGD导致超过50%的细胞死亡,同时细胞形态和生化指标发生重大变化,包括脂质过氧化物水平升高、超氧化物歧化酶活性增强和乳酸水平升高。用HupA或多奈哌齐预处理2小时的细胞存活率提高,毒性的生化和形态学指标降低(在10微摩尔至1.0微摩尔和0.1微摩尔范围内分别具有统计学意义)。我们的结果表明,HupA和多奈哌齐可保护PC12细胞免受OGD诱导的毒性,最可能的机制是减轻氧化和能量代谢紊乱。