1 May Institute for Medical Research of the Jewish Hospital of Cincinnati and Department of Pathology, University of Cincinnati, College of Medicine, Cincinnati, Ohio 45229
The left carotid artery of arteriosclerotic and nonarteriosclerotic male and female rats was surgically ligated to induce a state of cerebral ischemia. The animals promptly developed signs of cerebral impairment and were sacrificed 2, 4, 6, 8, 10, 12, 24, and 48 hours later to determine what dynamic pathophysiological changes attend acute cerebral ischemia. Several of the arteriosclerotic animals developed myocardial infarcts concomitant with the cerebral edema, hemorrhage, necrosis, and leptomeningitis observed in general. All of the experimental animals manifested necrosis and fatty infiltration of the liver, and their adrenal glands were hypertrophied, hemorrhagic, and depleted of lipid. Serum creatine phosphokinase and glutamic oxalacetic transaminase rose abruptly after 24 hours of cerebral ischemia. Triglycerides, free fatty acids, and cholesterol alterations were in keeping with intense lipid mobilization, dissolution of peripheral adipose tissue sites, and fatty metamorphosis of the liver. The animals also showed marked hyperglycemia and increased secretion of corticosterone. These investigations indicate that acute cerebral ischemia is a severe stress and will elicit dynamic alterations in serum parameters such as enzymes, lipids, glucose, and the adrenocortical stress hormones. Animals with pre-existing arteriosclerosis manifest more untoward effects and greater excursion in serum metabolic parameters than nonarteriosclerotic subjects.
© 1970 American Heart Association, Inc.
Metabolic Changes in Response to Acute Cerebral Ischemia Following Unilateral Carotid Artery Ligation in Arteriosclerotic Versus Nonarteriosclerotic Rats
Key Words: carotid artery ligation cerebral ischemia arteriosclerotic breeder rats myocardial infarction hepatic necrosis fatty liver cerebral edema CPK SGOT triglycerides free fatty acids total cholesterol glucose Cmpd. B
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