Method of reducing neuronal cell damage
A brain damage and purpose technology, applied in extracellular fluid diseases, nervous system diseases, pharmaceutical formulations, etc., can solve the problem that amphetamine will not improve recovery.
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[0052] The neuroprotective efficacy of amphetamines after transient ischemic injury has not been previously investigated. In this study, methamphetamine (MA) was evaluated using in vitro and in vivo models of transient cerebral ischemia. For the in vitro model, rat hippocampal slice cultures were challenged under hypoxia and glucose deficiency. In a second series of experiments, the in vivo neuroprotective efficacy of MA was investigated using a combination of a 5-minute 2-VO occlusion gerbil model and behavioral testing. During this study it was surprisingly found and demonstrated that administration of MA within 16 hours after transient cerebral ischemia is indeed neuroprotective, reducing neuronal cell damage, including death.
[0053] Materials and methods
[0054] 1.1 Animals
[0055] All experimental animal manipulations were approved by the University Institutional Animal Care and Use Committee. Twenty-eight adult male Mongolian gerbils (gerbils) weighing 60-80 gm w...
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