首页> 外文期刊>Experimental Gerontology >Roles of the lipid peroxidation product 4-hydroxynonenal in obesity, the metabolic syndrome, and associated vascular and neurodegenerative disorders.
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Roles of the lipid peroxidation product 4-hydroxynonenal in obesity, the metabolic syndrome, and associated vascular and neurodegenerative disorders.

机译:脂质过氧化产物4-羟基壬烯醛在肥胖,代谢综合征以及相关血管和神经退行性疾病中的作用。

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A rising tide of obesity and type 2 diabetes has resulted from the development of technologies that have made inexpensive high calorie foods readily available and exercise unnecessary for many people. Obesity and the metabolic syndrome (insulin resistance, visceral adiposity and dyslipidemia) wreak havoc on cells throughout the body thereby promoting cardiovascular and kidney disease, and degenerative diseases of the brain and body. Obesity and insulin resistance promote disease by increasing oxidative damage to proteins, lipids and DNA as the result of a combination of increased free radical production and an impaired ability of cells to detoxify the radicals and repair damaged molecules. By covalently modifying membrane-associated proteins, the membrane lipid peroxidation product 4-hydroxynonenal (HNE) may play particularly sinister roles in the metabolic syndrome and associated disease processes. HNE can damage pancreatic beta cells and can impair the ability of muscle and liver cells to respond to insulin. HNE may promote atherosclerosis by modifying lipoproteins and can cause cardiac cell damage by impairing metabolic enzymes. An adverse role for HNE in the brain in obesity and the metabolic syndrome is suggested by studies showing that HNE levels are increased in brain cells with aging and Alzheimer's disease. HNE can cause the dysfunction and degeneration of neurons by modifying membrane-associated glucose and glutamate transporters, ion-motive ATPases, enzymes involved in amyloid metabolism, and cytoskeletal proteins. Exercise and dietary energy restriction reduce HNE production and may also increase cellular systems for HNE detoxification including glutathione and oxidoreductases. The recent development of low molecular weight molecules that scavenge HNE suggests that HNE can be targeted in the design of drugs for the treatment of obesity, the metabolic syndrome, and associated disorders.
机译:肥胖和2型糖尿病的兴起源于技术的发展,这些技术已使廉价的高卡路里食物容易获得,并且许多人不需要运动。肥胖和代谢综合征(胰岛素抵抗,内脏脂肪异常和血脂异常)严重破坏了整个身体的细胞,从而促进了心血管和肾脏疾病以及脑和身体的退行性疾病。肥胖和胰岛素抵抗是由于增加的自由基产生和受损的细胞对自由基进行解毒和修复受损分子的能力结合而导致的对蛋白质,脂质和DNA的氧化损伤,从而加剧疾病。通过共价修饰膜相关蛋白,膜脂质过氧化产物4-hydroxynonenal(HNE)在代谢综合征和相关疾病过程中可能起特别危险的作用。 HNE会损害胰腺β细胞,并削弱肌肉和肝细胞对胰岛素的反应能力。 HNE可能通过修饰脂蛋白促进动脉粥样硬化,并可能通过损害代谢酶而引起心脏细胞损伤。研究表明,随着年龄增长和阿尔茨海默氏病,脑细胞中的HNE水平升高,这表明HNE在肥胖症和代谢综合征中对大脑的不利作用。 HNE可通过修饰膜相关的葡萄糖和谷氨酸转运蛋白,离子动力ATP酶,参与淀粉样蛋白代谢的酶和细胞骨架蛋白来引起神经元功能障碍和变性。运动和饮食能量的限制会减少HNE的产生,还可能增加用于HNE解毒的细胞系统,包括谷胱甘肽和氧化还原酶。清除HNE的低分子量分子的最新发展表明,HNE可以靶向用于治疗肥胖症,代谢综合征和相关疾病的药物设计。

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