Molecular mechanism of Copper Albumin Complex on NDEA induced brain vascular damage via promoting VEGF expression.

L. Taha, Zainab M. Maher, Ahmed E. Nassar, Mohamed-Cherif Abdallah, H. Embark, M. Youssef, A. Abdeen, Rofida F. Moftah, H. Madhyastha, Obeid Shanab
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引用次数: 1

Abstract

source Abstract Nitrosodiethylamine (NDEA) is a potent oxidant induces neurodegeneration via (reactive oxygen species) ROS. Copper is an important metal essential for scavenging free radicals, development of central nervous system (CNS) and redox angiogenesis signaling. Vascular endothelial growth factor (VEGF) is well known as efficacious and long-term signal that stimulates angiogenesis, where its expression is copper dependent. We examined the copper protective effect against brain vascular damage initiated by NDEA. NDEA induces brain vascular wall damage, necrosis with interstitial hemorrhage and diminishes VEGF expression. Histopathological examination showing a great improvement of brain tissue in copper treated mice with significant increase in VEGF expression. Higher levels of intracellular copper can stimulate angiogenesis and exhibited a significant protection against NDEA induced brain vascular damage, confirming its ability to enhance antioxidant activity and angiogenesis initiation. Our report presents first evidence that inducible VEGF expression in brain is sensitive to copper; moreover, copper-based therapeutics represents a novel approach to reduce brain vascular damage induced by NDEA generated ROS.
铜白蛋白复合物通过促进VEGF表达对NDEA诱导的脑血管损伤的分子机制。
来源摘要亚硝基二乙胺(NDEA)是一种通过活性氧诱导神经退行性变的强效氧化剂。铜是清除自由基、中枢神经系统(CNS)发育和氧化还原血管生成信号传导所必需的重要金属。众所周知,血管内皮生长因子(VEGF)是刺激血管生成的有效和长期信号,其表达是铜依赖性的。我们检测了铜对NDEA引发的脑血管损伤的保护作用。NDEA可诱导脑血管壁损伤、坏死和间质出血,并降低VEGF的表达。组织病理学检查显示铜处理小鼠的脑组织有很大改善,VEGF表达显著增加。较高水平的细胞内铜可以刺激血管生成,并对NDEA诱导的脑血管损伤表现出显著的保护作用,证实了其增强抗氧化活性和血管生成起始的能力。我们的报告首次提出了大脑中诱导型VEGF表达对铜敏感的证据;此外,铜基疗法代表了一种减少NDEA产生的ROS诱导的脑血管损伤的新方法。
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