Eckert G P, Kirsch C, Mueller W E
Department of Pharmacology, Biocenter Niederursel, University of Frankfurt, Germany.
Neuroreport. 2001 Apr 17;12(5):883-7. doi: 10.1097/00001756-200104170-00003.
Growing evidence indicates that membrane cholesterol is involved in the development of Alzheimer's disease. Therefore, the availability of pharmacological strategies to modify brain cholesterol is of increasing importance. Accordingly, we investigated the effects of the HMG-CoA reductase inhibitor lovastatin on brain cholesterol levels in vivo. Brain cholesterol was significantly decreased by lovastatin treatment (100 mg/kg/day) in 1- and 12-month-old C57BL/6J mice. Reduced brain cholesterol was associated with decreased pyrene-excimer fluorescence, indicating altered membrane function. Lovastatin had no effect on brain cholesterol ApoE-/- mice. Peripheral cholesterol levels were not affected by lovastatin in all three groups of mice. We demonstrate for the first time that lovastatin represents a valid pharmacological tool to significantly modulate brain cholesterol levels.
越来越多的证据表明,膜胆固醇与阿尔茨海默病的发展有关。因此,采用药理学策略调节脑胆固醇水平变得越来越重要。相应地,我们研究了HMG-CoA还原酶抑制剂洛伐他汀对体内脑胆固醇水平的影响。在1月龄和12月龄的C57BL/6J小鼠中,洛伐他汀治疗(100 mg/kg/天)可显著降低脑胆固醇水平。脑胆固醇的降低与芘激基缔合物荧光的降低有关,表明膜功能发生了改变。洛伐他汀对脑胆固醇ApoE-/-小鼠没有影响。在所有三组小鼠中,外周胆固醇水平均不受洛伐他汀的影响。我们首次证明,洛伐他汀是一种有效调节脑胆固醇水平的药理学工具。