Goodchild Christopher G, DuRant Sarah E
Physiol Biochem Zool. 2020 Mar/Apr;93(2):129-139. doi: 10.1086/707920.
Oxidative stress is generally understood to be an important mediator of life-history traits, yet the specific relationships between oxidative stress and life-history traits have been difficult to describe because there is often a lack of covariation among biomarkers of oxidative stress. For instance, although oxidative damage to red blood cell (RBC) membranes can lead to pathological conditions (i.e., anemia), in some cases there is not a clear relationship between lipid oxidation and RBC membrane resistance to pro-oxidants. Alternatively, oxidative damage to hemoglobin may be an indirect mechanism contributing to RBC membrane damage. To better understand the mechanisms contributing to oxidative damage and probe new approaches to measuring oxidative stress, we used a series of in vitro and in vivo procedures in zebra finches () to explore (1) whether avian RBCs exposed to a pro-oxidant generate fluorescent heme degradation products (HDPs), (2) whether HDPs interact with RBC membranes, and (3) whether HDPs are linked to impaired RBC integrity. We found that finch RBCs exposed in vitro to hydrogen peroxide produced fluorescent HDPs and HDPs associated with RBC membranes. Exposure to hydrogen peroxide also caused a reduction in hemoglobin and an increase in percent methemoglobin (a hemoglobin oxidation product), further indicating hemoglobin degradation. Moreover, HDP fluorescence correlated with impaired membrane integrity and erythrocyte osmotic fragility in vivo. This study suggests that reactive oxygen species may indirectly impair RBC membrane integrity via hemoglobin degradation products that associate with RBC membranes and that HDPs may be an inexpensive and logistically simple tool for measuring oxidative stress.
氧化应激通常被认为是生活史特征的重要调节因子,然而氧化应激与生活史特征之间的具体关系一直难以描述,因为氧化应激生物标志物之间往往缺乏协变关系。例如,虽然红细胞(RBC)膜的氧化损伤会导致病理状况(即贫血),但在某些情况下,脂质氧化与RBC膜对促氧化剂的抗性之间并没有明确的关系。另外,血红蛋白的氧化损伤可能是导致RBC膜损伤的间接机制。为了更好地理解导致氧化损伤的机制并探索测量氧化应激的新方法,我们在斑胸草雀()中使用了一系列体外和体内实验程序,以探究:(1)暴露于促氧化剂的鸟类RBC是否会产生荧光血红素降解产物(HDPs);(2)HDPs是否与RBC膜相互作用;(3)HDPs是否与RBC完整性受损有关。我们发现,体外暴露于过氧化氢的雀科鸟类RBC产生了荧光HDPs以及与RBC膜相关的HDPs。暴露于过氧化氢还导致血红蛋白减少,高铁血红蛋白(一种血红蛋白氧化产物)百分比增加,进一步表明血红蛋白降解。此外,HDP荧光与体内膜完整性受损和红细胞渗透脆性相关。这项研究表明,活性氧可能通过与RBC膜相关的血红蛋白降解产物间接损害RBC膜完整性,并且HDPs可能是一种测量氧化应激的廉价且操作简便的工具。