[THE INFLUENCE OF SHORT-TIME CEREBRAL ISCHEMIA ON PIAL VESSELS ADRENOREACTIVITY IN RATS].

Reactivity of pial vessels in response to a brain surface irrigation by norepinephrine solution in rats, subjected to transient global cerebral ischemia (2VO+hypo model), was investigated. Four different groups of rats at 2, 7, 14 or 21 days after ischemia were subjected to microvascular studies using in vivo video microscopy method. The diameter changes of pial arteries and veins in response to norepinephrine were measured.

Intracerebroventricular administration of creatine protects against damage by global cerebral ischemia in rat.

Although a large body of evidence shows that pretreatment of brain tissue with creatine protects against anoxic injury in vitro, only a couple of papers have investigated creatine protection in vivo, and they yielded conflicting results. We attempted to clarify how creatine may be protective in an in vivo model of global cerebral ischemia (GCI). We administered creatine either before of after GCI.

Role of creatine and phosphocreatine in neuronal protection from anoxic and ischemic damage.

Phosphocreatine can to some extent compensate for the lack of ATP synthesis that is caused in the brain by deprivation of oxygen or glucose. Treatment of in vitro rat hippocampal slices with creatine increases the neuronal store of phosphocreatine. In this way it increases the resistance of the tissue to anoxic or ischemic damage.