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(Stroke. 1996;27:498-503.)
© 1996 American Heart Association, Inc.
Articles |
From the Departments of Neurology (K.L., N.F., L.C.W., D.Z.W.) and Biochemistry and Molecular Biology (N.F.), Medical College of Ohio, Toledo; Department of Biostatistics and Medical Epidemiology, Henry Ford Hospital, Detroit, Mich (L.R.S.); and Department of Neurology, Creighton University School of Medicine, Omaha, Neb (J.S.T.).
Correspondence to Nancy Futrell, MD, Department of Neurology, Medical College of Ohio, 3000 Arlington Ave, PO Box 10008, Toledo, OH 43614-0008.
Background and Purpose The inflammatory response within cerebral infarcts may have an influence on tissue damage. Since old animals with an impaired immune response have decreased inflammation after experimental cerebral infarction, we postulated that female animals with an increased immune response will have an increased inflammatory response after cerebral infarction.
Methods Embolic cerebral infarcts were produced by photochemical irradiation of the right carotid artery in 12 female Fischer rats. The inflammatory response within 4-day-old infarcts was quantitated by histology with the use of computer-assisted image analysis and compared with that in 12 male rats from a previous series.
Results Severe infarcts had the most pronounced inflammatory response. Female rats had an increased inflammatory response in infarcts of all severity, which was statistically significant in severe cerebral infarcts even after adjustment for infarct size. Severe infarcts in males were significantly larger than those in females.
Conclusions Gender influences the outcome of embolic cerebral infarcts after photochemical damage to the carotid artery, both in terms of the magnitude of the inflammatory response and infarct size. There are numerous gender-related differences in neurochemicals, cytokine production, and drug metabolism that may influence tissue damage after stroke and responsiveness to therapeutic intervention. The preponderance of male animals in stroke research may produce results not applicable to female stroke patients. The use of female animals will be required to provide adequate models for the study of stroke in women.
Key Words: cerebral infarction gender immunology inflammation rats
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