Li Chang, Zhou Hai-Meng
School of Life Sciences, Tsinghua University, Beijing 100084, China.
Enzyme Res. 2011;2011:387176. doi: 10.4061/2011/387176. Epub 2011 Oct 3.
Antioxidant enzymes maintain cellular redox homeostasis. Manganese superoxide dismutase (MnSOD), an enzyme located in mitochondria, is the key enzyme that protects the energy-generating mitochondria from oxidative damage. Levels of MnSOD are reduced in many diseases, including cancer, neurodegenerative diseases, and psoriasis. Overexpression of MnSOD in tumor cells can significantly attenuate the malignant phenotype. Past studies have reported that this enzyme has the potential to be used as an anti-inflammatory agent because of its superoxide anion scavenging ability. Superoxide anions have a proinflammatory role in many diseases. Treatment of a rat model of lung pleurisy with the MnSOD mimetic MnTBAP suppressed the inflammatory response in a dose-dependent manner. In this paper, the mechanisms underlying the suppressive effects of MnSOD in inflammatory diseases are studied, and the potential applications of this enzyme and its mimetics as anti-inflammatory agents are discussed.
抗氧化酶维持细胞氧化还原稳态。锰超氧化物歧化酶(MnSOD)是一种位于线粒体中的酶,是保护产生能量的线粒体免受氧化损伤的关键酶。在包括癌症、神经退行性疾病和银屑病在内的许多疾病中,MnSOD水平会降低。肿瘤细胞中MnSOD的过表达可显著减弱恶性表型。过去的研究报道,由于该酶具有超氧阴离子清除能力,它有潜力用作抗炎剂。超氧阴离子在许多疾病中具有促炎作用。用MnSOD模拟物MnTBAP治疗大鼠肺胸膜炎模型,可剂量依赖性地抑制炎症反应。本文研究了MnSOD在炎症性疾病中发挥抑制作用的机制,并讨论了该酶及其模拟物作为抗炎剂的潜在应用。