神经保护
尼莫地平
药理学
硝苯地平
神经生长因子
化学
医学
内科学
受体
钙
作者
Shimon Lecht,Elena Rotfeld,Hadar Arien‐Zakay,Rinat Tabakman,Henry Matzner,Rami Yaka,Peter I. Lelkes,Philip Lazarovici
标识
DOI:10.1016/j.ijdevneu.2012.05.007
摘要
Abstract The goal of this study was to compare the neuroprotective properties of the l ‐type Ca 2+ channel blockers, nimodipine and nifedipine, using nerve growth factor (NGF)‐differentiated PC12 neuronal cultures exposed to oxygen‐glucose deprivation (OGD) and trophic withdrawal‐induced cell death. Nimodipine (1–100 μM) conferred 65 ± 13% neuroprotection upon exposure to OGD and 35 ± 6% neuroprotection towards different trophic withdrawal‐induced cell death measured by lactate dehydrogenase and caspase 3 activities. The time window of nimodipine conferred neuroprotection was detected during the first 5 h but not at longer OGD exposures. Nifedipine (1–100 μM), to a lower potency than nimodipine, conferred 30–55 ± 8% neuroprotection towards OGD in PC12 cells and 29 ± 5% in rat hypocampal slices, and 10 ± 3% neuroprotection at 100 μM towards trophic withdrawal‐induced PC12 cell death. The ability to demonstrate that nimodipine conferred neuroprotection in a narrow therapeutic time‐window indicates that the OGD PC12 model mimics the in vivo models and therefore suitable for neuroprotective drug discovery and development.
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