Stading Rachel, Chu Chun, Couroucli Xanthi, Lingappan Krithika, Moorthy Bhagavatula
Section of Neonatology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX.
Curr Opin Toxicol. 2020 Apr-Jun;20-21:77-84. doi: 10.1016/j.cotox.2020.07.001. Epub 2020 Jul 24.
Cytochrome P4501A (CYP1A) enzymes play important roles in xenobiotic and endobiotic metabolism. Due to uncoupling reactions during the enzymatic cycle, CYP1A enzymes can release reactive oxidative species (ROS) in the form of superoxide radical, hydrogen peroxide, hydroxyl radical etc. An imbalance between production of free radicals and the ability of antioxidants to detoxify the free radicals can lead to accumulation of ROS, which in turn can lead to oxidative stress. Oxidative stress can lead to inflammation and toxicity, which in turn can cause human diseases such as bronchopulmonary disease (BPD), ARDS, renal hypertension, etc. CYP1A enzymes, depending on the organ system, they either contribute or protect against oxidative injury. Thus, they have dual roles in regard to oxidative stress. This review presents an overview of the mechanistic relationship between CYP1A enzymes and oxidative stress in relation to various diseases in different organs (e.g., liver, lungs, heart, kidneys, and reproductive organs).
细胞色素P4501A(CYP1A)酶在异生物质和内生物质代谢中发挥着重要作用。由于酶促循环中的解偶联反应,CYP1A酶可以以超氧自由基、过氧化氢、羟基自由基等形式释放活性氧化物质(ROS)。自由基产生与抗氧化剂清除自由基能力之间的失衡会导致ROS积累,进而导致氧化应激。氧化应激可导致炎症和毒性,进而引发人类疾病,如支气管肺疾病(BPD)、急性呼吸窘迫综合征(ARDS)、肾性高血压等。根据器官系统的不同,CYP1A酶既可能促成氧化损伤,也可能起到保护作用以抵御氧化损伤。因此,它们在氧化应激方面具有双重作用。本综述概述了CYP1A酶与氧化应激之间的机制关系,以及其与不同器官(如肝脏、肺、心脏、肾脏和生殖器官)的各种疾病的关系。