401. Excess salt exacerbates blood-brain barrier disruption via a p38/MAPK/SGK1-dependent pathway in permanent cerebral ischemia.
- Author
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Zhang T, Fang S, Wan C, Kong Q, Wang G, Wang S, Zhang H, Zou H, Sun B, Sun W, Zhang Y, Mu L, Wang J, Wang J, Zhang H, Wang D, and Li H
- Subjects
- Adult, Aged, Animals, Blood-Brain Barrier pathology, Brain drug effects, Brain metabolism, Brain pathology, Brain Ischemia diagnosis, Brain Ischemia genetics, Brain Ischemia immunology, Disease Models, Animal, Endothelial Cells drug effects, Endothelial Cells metabolism, Female, Gene Expression, Gene Expression Regulation drug effects, Humans, Lymphocytes immunology, Lymphocytes metabolism, Lymphocytes pathology, Macrophages immunology, Macrophages metabolism, Macrophages pathology, Male, Mice, Middle Aged, Occludin genetics, Occludin metabolism, Permeability, Sodium urine, Stroke genetics, Stroke immunology, Stroke metabolism, Stroke pathology, Tight Junction Proteins genetics, Tight Junction Proteins metabolism, Zonula Occludens-1 Protein genetics, Zonula Occludens-1 Protein metabolism, Blood-Brain Barrier metabolism, Brain Ischemia metabolism, Immediate-Early Proteins metabolism, Mitogen-Activated Protein Kinases metabolism, Protein Serine-Threonine Kinases metabolism, Signal Transduction drug effects, Sodium Chloride, Dietary administration & dosage, p38 Mitogen-Activated Protein Kinases metabolism
- Abstract
High salt diet (HSD) is one of the most important risk factors that contribute to many vascular diseases including ischemic stroke. One proposed mechanism underlying the disruption of blood-brain barrier (BBB) mediated by HSD is indirectly through enhancing blood pressure. The direct role of HSD on BBB integrity is unclear. Our purpose is to determine whether and how HSD might be involved in BBB breakdown during ischemia. To test that, we induced model of cerebral ischemia by permanent middle cerebral artery ligation (pMCAL) in either normal diet or HSD fed mice. We observed that HSD significantly enhanced ischemic brain damage which was associated with enhanced BBB disruption, increased leukocytes infiltration and loss of tight junction (TJ) proteins expression without apparently altering blood pressure. Our in vitro experiment also revealed that sodium chloride (NaCl) treatment down-regulated TJ protein expression by endothelial cells and substantially increased BBB permeability during starvation. Inhibition of p38/MAPK/SGK1 pathway eliminated the effect of NaCl on BBB permeability in vitro. In addition, we noticed a positive correlation between urinary sodium levels and ischemic lesion size in stroke patients. Together, our study demonstrates a hypertension-independent role of HSD during ischemia and provides rationale for post cerebral ischemic attack management.
- Published
- 2015
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