Ischemic stroke is one of the leading causes of mortality, hence search for the clinically successful compounds and its neuroprotective activity exploration are necessary. Aim of the research was to assess effect of ischemic damage on bioelectric brain activity of rats in model of global ischemia.\r\nBefore ischemic stroke (IS) modeling, long-term electrodes were implanted into rat brain structures — striatum, cortex, hypothalamus, and hippocampus, and a week after implantation background EEG was recorded. IS simulation was performed in rats (n = 17) via occlusion of both carotid arteries.Then, EEG was recorded in freely-moving rats at 1, 2, 3, 5, 7, 14, 21 and 28 day after IS modeling.\r\nAt 1st day after IS modelling EEG amplitude decreased in all frequency ranges relative to the background recording. Animal’s survival after IS was accompanied by decrease in % of delta activity power relative to the background values and it’s increase from 2nd to 7th day of the post-stroke period. In the opposite case of incease delta waves at the 1st day and decease from 2nd to 7th day after IS, animals usually died after 7 days from IS modeling. And degree of delta activity reduction from 2nd day after IS correlated with the severity of the neurological deficit. The second prognostic sign of decrease in the neurological deficit and survival of animals was the increase of theta activity in the range of 6-8 Hz after 14 days of ischemia modeling. \r\nSo an increase in delta and theta activity from the 2nd day of post-stroke period can be predictive indicator of animal survival and decrease of nevrological deficite in the model of ishemic stroke.\r\n\r\n