Abstract
Intracerebral serum proteins in rats with altered blood-brain barrier (BBB) function were examined by a new method of electrophoretography. The rats were divided into 7 groups: controls (n =5), 6 hr of bilateral common carotid artery ligation (n =10), 6 hr of bilateral common carotid and right vertebral artery occlusion (n =7), 6 and 24 hr after cold injury (n = 6 and n = 6) and 6 and 24 hr after intracarotid injection of hypertonic solution (3 M urea) (n = 7 and n = 6).
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