4.4 Article

Cerebrovascular Dysfunction and Blood-Brain Barrier Permeability Induced by Oxidized LDL are Prevented by Apocynin and Magnesium Sulfate in Female Rats

期刊

JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
卷 63, 期 1, 页码 33-39

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FJC.0000000000000021

关键词

blood-brain barrier permeability; oxidized LDL; magnesium sulfate; cerebral arteries; myogenic responses

资金

  1. National Institutes of Health, National Institute of Neurological Disorders and Stroke [RO1 NS045940]
  2. National Institute of Neurological Disorders and Stroke Neural Environment Cluster supplement [RO1 NS045940-06S1]
  3. National Heart Lung and Blood Institute [PO1 HL095488]
  4. Totman Medical Research Trust

向作者/读者索取更多资源

Oxidized low-density lipoprotein (oxLDL) is elevated during several neurologic conditions that involve cerebral edema formation, including severe preeclampsia and eclampsia; however, our understanding of its effect on the cerebral vasculature is limited. We hypothesized that oxLDL induced blood-brain barrier (BBB) disruption and changes in cerebrovascular reactivity occur through NADPH oxidase-derived superoxide. We also investigated the effect of MgSO4 on oxLDL-induced changes in the cerebral vasculature as this is commonly used in preventing cerebral edema formation. Posterior cerebral arteries from female rats were perfused with 5 mu g/mL oxLDL in rat serum with or without 50 mu M apocynin or 16 mM MgSO4 and BBB permeability and vascular reactivity were compared. oxLDL increased BBB permeability and decreased myogenic tone that were prevented by apocynin. oxLDL increased constriction to the nitric oxide synthase inhibitor nitro-L-arginine that was unaffected by apocynin. oxLDL enhanced dilation to the NO donor sodium nitroprusside that was prevented by apocynin. MgSO4 prevented oxLDL-induced BBB permeability without affecting oxLDL-induced changes in myogenic tone. Thus, oxLDL seems to cause BBB disruption and vascular tone dysregulation through NADPH oxidase derived superoxide. These results highlight oxLDL and NADPH oxidase as potentially important therapeutic targets in neurologic conditions that involve elevated oxLDL.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据