Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA.
Curr Neuropharmacol. 2011 Dec;9(4):662-73. doi: 10.2174/157015911798376244.
The brain is a highly metabolically active organ producing large amounts of reactive oxygen species (ROS). These ROS are kept in check by an elaborate network of antioxidants. Although ROS are necessary for signaling and synaptic plasticity, their uncontrolled levels cause oxidation of essential macromolecules such as membrane lipids, nucleic acids, enzymes and cytoskeletal proteins. Indeed, overproduction of ROS and/or failure of the antioxidant network lead to neuronal oxidative stress, a condition associated with not only aging but also Alzheimer's disease (AD). However, the specific source of excessive ROS production has not yet been identified. On one hand, amyloid beta (Aβ) has been extensively shown to act as an oxidant molecule. On the other hand, oxidative stress has been shown to precede and exacerbate Aβ pathology. This review will address the involvement of oxidative stress in the context of neuronal as well as vascular dysfunction associated with AD.
大脑是一个高度代谢活跃的器官,会产生大量的活性氧(ROS)。这些 ROS 通过一个复杂的抗氧化剂网络来控制。虽然 ROS 对于信号转导和突触可塑性是必要的,但它们不受控制的水平会导致膜脂质、核酸、酶和细胞骨架蛋白等必需大分子的氧化。事实上,ROS 的过度产生和/或抗氧化网络的失效会导致神经元氧化应激,这种情况不仅与衰老有关,也与阿尔茨海默病(AD)有关。然而,过量 ROS 产生的具体来源尚未确定。一方面,淀粉样蛋白β(Aβ)已被广泛证明是一种氧化分子。另一方面,氧化应激已被证明先于并加剧 Aβ 病理。这篇综述将讨论氧化应激在 AD 相关神经元和血管功能障碍中的作用。