Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro
Background. Hypercholesterolemia and disruptions of the blood brain barrier (BBB) have been implicated as underlying mechanisms in the pathogenesis of Alzheimer's disease (AD). Simvastatin therapy may be of benefit in treating AD; however, its mechanism has not been yet fully understood. Object...
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Series: | International Journal of Alzheimer's Disease |
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doaj-598410bc065b402c83e5326ecf318f822020-11-24T23:20:42ZengHindawi LimitedInternational Journal of Alzheimer's Disease2090-80242090-02522012-01-01201210.1155/2012/109324109324Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In VitroXijuan Jiang0Maojuan Guo1Jinling Su2Bin Lu3Dongming Ma4Ruifeng Zhang5Lin Yang6Qiang Wang7Yiwen Ma8Yingchang Fan9Department of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Experimental Teaching, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Experimental Teaching, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Experimental Teaching, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Experimental Teaching, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaDepartment of Pathology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, ChinaBackground. Hypercholesterolemia and disruptions of the blood brain barrier (BBB) have been implicated as underlying mechanisms in the pathogenesis of Alzheimer's disease (AD). Simvastatin therapy may be of benefit in treating AD; however, its mechanism has not been yet fully understood. Objective. To explore whether simvastatin could block disruption of BBB induced by cholesterol both in vivo and in vitro. Methods. New Zealand rabbits were fed cholesterol-enriched diet with or without simvastatin. Total cholesterol of serum and brain was measured. BBB dysfunction was evaluated. To further test the results in vivo, rat brain microvascular endothelial cells (RBMECs) were stimulated with cholesterol in the presence/absence of simvastatin in vitro. BBB disruption was evaluated. Results. Simvastatin blocked cholesterol-rich diet induced leakage of Evan's blue dye. Cholesterol content in the serum was affected by simvastatin, but not brain cholesterol. Simvastatin blocked high-cholesterol medium-induced decrease in TEER and increase in transendothelial FITC-labeled BSA Passage in RBMECs. Conclusions. The present study firstly shows that simvastatin improves disturbed BBB function both in vivo and in vitro. Our data provide that simvastatin may be useful for attenuating disturbed BBB mediated by hypercholesterolemia.http://dx.doi.org/10.1155/2012/109324 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xijuan Jiang Maojuan Guo Jinling Su Bin Lu Dongming Ma Ruifeng Zhang Lin Yang Qiang Wang Yiwen Ma Yingchang Fan |
spellingShingle |
Xijuan Jiang Maojuan Guo Jinling Su Bin Lu Dongming Ma Ruifeng Zhang Lin Yang Qiang Wang Yiwen Ma Yingchang Fan Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro International Journal of Alzheimer's Disease |
author_facet |
Xijuan Jiang Maojuan Guo Jinling Su Bin Lu Dongming Ma Ruifeng Zhang Lin Yang Qiang Wang Yiwen Ma Yingchang Fan |
author_sort |
Xijuan Jiang |
title |
Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro |
title_short |
Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro |
title_full |
Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro |
title_fullStr |
Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro |
title_full_unstemmed |
Simvastatin Blocks Blood-Brain Barrier Disruptions Induced by Elevated Cholesterol Both In Vivo and In Vitro |
title_sort |
simvastatin blocks blood-brain barrier disruptions induced by elevated cholesterol both in vivo and in vitro |
publisher |
Hindawi Limited |
series |
International Journal of Alzheimer's Disease |
issn |
2090-8024 2090-0252 |
publishDate |
2012-01-01 |
description |
Background. Hypercholesterolemia and disruptions of the blood brain barrier (BBB) have been implicated as underlying mechanisms in the pathogenesis of Alzheimer's disease (AD). Simvastatin therapy may be of benefit in treating AD; however, its mechanism has not been yet fully understood. Objective. To explore whether simvastatin could block disruption of BBB induced by cholesterol both in vivo and in vitro. Methods. New Zealand rabbits were fed cholesterol-enriched diet with or without simvastatin. Total cholesterol of serum and brain was measured. BBB dysfunction was evaluated. To further test the results in vivo, rat brain microvascular endothelial cells (RBMECs) were stimulated with cholesterol in the presence/absence of simvastatin in vitro. BBB disruption was evaluated. Results. Simvastatin blocked cholesterol-rich diet induced leakage of Evan's blue dye. Cholesterol content in the serum was affected by simvastatin, but not brain cholesterol. Simvastatin blocked high-cholesterol medium-induced decrease in TEER and increase in transendothelial FITC-labeled BSA Passage in RBMECs. Conclusions. The present study firstly shows that simvastatin improves disturbed BBB function both in vivo and in vitro. Our data provide that simvastatin may be useful for attenuating disturbed BBB mediated by hypercholesterolemia. |
url |
http://dx.doi.org/10.1155/2012/109324 |
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