
doi: 10.1159/000436974
pmid: 26228694
<b><i>Background/Aims:</i></b> To this date, the only available drugs for treating Alzheimer's disease are cognitive enhancers, which may improve the cognitive function of patients for a few years while the disease continues to progress. As such, there are intense investigations to develop disease-modifying drugs to suppress progressive neurodegeneration. <b><i>Methods:</i></b> In this study, a range of procognitive compounds are tested in a primary neuronal culture to determine their relative potential for promoting neuritogenesis. <b><i>Results:</i></b> We report that donepezil, memantine, dimebon, Pre-084 and 4-IBP are neuritogenic while tacrine, rosemarinic acid, memoquin and a BACE1 inhibitor suppress neurite outgrowth of neurons. <b><i>Conclusions:</i></b> The results of this study indicate that some procognitive compounds may possess a disease-modifying potential.
Neurons, Neurogenesis, Primary Cell Culture, Neurites, Animals, Nootropic Agents, Rats
Neurons, Neurogenesis, Primary Cell Culture, Neurites, Animals, Nootropic Agents, Rats
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 16 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
