Abstract
The goal of this study was to compare the neuroprotective properties of the l-type Ca2+ 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 (1-100μM) 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 5h but not at longer OGD exposures. Nifedipine (1-100μM), 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 100μM 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.
| Original language | English |
|---|---|
| Pages (from-to) | 465-469 |
| Number of pages | 5 |
| Journal | International Journal of Developmental Neuroscience |
| Volume | 30 |
| Issue number | 6 |
| DOIs | |
| State | Published - Oct 2012 |
Keywords
- Analysis of Variance
- Animals
- Calcium/metabolism
- Caspase 3/metabolism
- Catecholamines/metabolism
- Cell Differentiation/drug effects
- Cell Hypoxia/drug effects
- Glucose/deficiency
- Hippocampus/drug effects
- In Vitro Techniques
- L-Lactate Dehydrogenase/metabolism
- Nerve Growth Factor/metabolism
- Neuroprotective Agents/pharmacology
- Nifedipine/pharmacology
- Nimodipine/pharmacology
- PC12 Cells/drug effects
- Rats
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