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Influence of Hypercholesterolemia and Hypertension on the Integrity of the Blood–Brain Barrier in Rats

内分泌学 内科学 胆固醇 血脑屏障 封堵器 丙二醛 化学 内皮功能障碍 血管紧张素II 一氧化氮 医学 紧密连接 氧化应激 中枢神经系统 血压 生物化学
作者
Rivaze Kalaycı,Mehmet Kaya,Hafize Uzun,Bilge Bılgıç,Bülent Ahıshalı,Nadir Arıcan,İmdat Elmas,Mutlu Küçük
出处
期刊:International Journal of Neuroscience [Taylor & Francis]
卷期号:119 (10): 1881-1904 被引量:37
标识
DOI:10.1080/14647270802336650
摘要

Hypercholesterolemia and/or hypertension impair endothelial function in peripheral vasculature; however, their impact on endothelial cells of brain microvessels is unclear. We investigated the effects of hypercholesterolemia on the integrity of the blood–brain barrier (BBB) and the activity of astrocytes during Nω-nitro-L-arginine methyl ester (L-NAME) hypertension followed by angiotensin (ANG) II. We found significant decreases in superoxide dismutase levels with all treatments except ANG II and L-NAME plus ANG II, and in catalase concentrations except ANG II and cholesterol plus L-NAME. Nitric oxide (NO) concentrations were significantly decreased by L-NAME but significantly increased by cholesterol. L-NAME-stimulated plasma malondialdehyde (MDA), Ox-LDL, and cholesterol levels were significantly augmented by cholesterol. Glutathione (GSH) levels significantly decreased, while MDA, TNF-α, and Ox-LDL levels significantly increased in cholesterol and/or L-NAME. The increase in BBB permeability by acute hypertension in hypercholesterolemic hypertensive animals was less than that observed in chronically hypertensive animals. Brain vessels of L-NAME-treated animals showed a considerable loss of immunoreactivity for tight junction proteins, occludin, and ZO-1. Immunoreactivity for occludin and ZO-1 increased in cholesterol plus L-NAME and decreased in cholesterol. Glial fibrillary acidic protein (GFAP) immunoreactivity was seen in few astrocytes in the brain sections of L-NAME-treated animals, but increased in cholesterol plus L-NAME. Positive immunoreactivity for vascular endothelial growth factor (VEGF) was observed in cholesterol and cholesterol plus L-NAME plus ANG II. We suggest that hypercholesterolemia may affect BBB integrity through increasing the expression of tight junction proteins and GFAP and leading to the production of VEGF, at least partly, via increased NO, TNF-α, and catalase in hypertensive conditions.
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