Blood–Brain Barrier Breakdown in Reduced Uterine Perfusion Pressure: A Possible Model of Posterior Reversible Encephalopathy Syndrome

Background Posterior reversible encephalopathy syndrome (PRES) is a clinical entity characterized by headaches, altered mental status, seizures, and visual disturbances and is associated with white matter vasogenic edema. There are no experimental models to study PRES brain changes. Methods Twenty-e...

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Veröffentlicht in:Journal of stroke and cerebrovascular diseases 2014-09, Vol.23 (8), p.2075-2079
Hauptverfasser: Porcello Marrone, Luiz Carlos, MD, Gadonski, Giovani, MD, PhD, de Oliveira Laguna, Gabriela, MD, Poli-de-Figueiredo, Carlos Eduardo, MD, PhD, Pinheiro da Costa, Bartira Ercilia, MD, PhD, Lopes, Maria Francisca Torres, MD, Brunelli, João Pedro Farina, MD, Diogo, Luciano Passamani, MD, PhD, Huf Marrone, Antônio Carlos, MD, PhD, Da Costa, Jaderson Costa, MD, PhD
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Sprache:eng
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Zusammenfassung:Background Posterior reversible encephalopathy syndrome (PRES) is a clinical entity characterized by headaches, altered mental status, seizures, and visual disturbances and is associated with white matter vasogenic edema. There are no experimental models to study PRES brain changes. Methods Twenty-eight pregnant Wistar rats were divided into 4 groups of 7: (1) pregnant-control; (2) reduced uterine perfusion pressure (RUPP); (3) invasive blood pressure (IBP); and (4) reduced uterine perfusion pressure plus invasive blood pressure (RUPP-IBP). The RUPP and RUPP-IBP groups were submitted to a reduction of uterine perfusion pressure at pregnancy days 13 to 15. The invasive mean arterial pressure of the IBP and RUPP-IBP groups was measured on day 20. The blood–brain barriers (BBBs) of all groups were analyzed using 2% Evans Blue dye on day 21. Results RUPP rats had higher blood pressures and increased BBB permeability to Evans Blue dye compared with the control animals. Brain staining occurred in 11 of 14 RUPP rats and in none of the control groups ( P  
ISSN:1052-3057
1532-8511
DOI:10.1016/j.jstrokecerebrovasdis.2014.03.012