Lighton John R B, Schilman Pablo E
Department of Biological Sciences, University of Nevada at Las Vegas, Las Vegas, Nevada, United States of America.
PLoS One. 2007 Dec 5;2(12):e1267. doi: 10.1371/journal.pone.0001267.
The deleterious effects of anoxia followed by reperfusion with oxygen in higher animals including mammals are well known. A convenient and genetically well characterized small-animal model that exhibits reproducible, quantifiable oxygen reperfusion damage is currently lacking. Here we describe the dynamics of whole-organism metabolic recovery from anoxia in an insect, Drosophila melanogaster, and report that damage caused by oxygen reperfusion can be quantified in a novel but straightforward way. We monitored CO(2) emission (an index of mitochondrial activity) and water vapor output (an index of neuromuscular control of the spiracles, which are valves between the outside air and the insect's tracheal system) during entry into, and recovery from, rapid-onset anoxia exposure with durations ranging from 7.5 to 120 minutes. Anoxia caused a brief peak of CO(2) output followed by knock-out. Mitochondrial respiration ceased and the spiracle constrictor muscles relaxed, but then re-contracted, presumably powered by anaerobic processes. Reperfusion to sustained normoxia caused a bimodal re-activation of mitochondrial respiration, and in the case of the spiracle constrictor muscles, slow inactivation followed by re-activation. After long anoxia durations, both the bimodality of mitochondrial reactivation and the recovery of spiracular control were impaired. Repeated reperfusion followed by episodes of anoxia depressed mitochondrial respiratory flux rates and damaged the integrity of the spiracular control system in a dose-dependent fashion. This is the first time that physiological evidence of oxygen reperfusion damage has been described in an insect or any invertebrate. We suggest that some of the traditional approaches of insect respiratory biology, such as quantifying respiratory water loss, may facilitate using D. melanogaster as a convenient, well-characterized experimental model for studying the underlying biology and mechanisms of ischemia and reperfusion damage and its possible mitigation.
在包括哺乳动物在内的高等动物中,缺氧后再进行氧灌注的有害影响是众所周知的。目前缺乏一种方便且遗传特征明确的小动物模型,该模型能表现出可重复、可量化的氧再灌注损伤。在此,我们描述了昆虫黑腹果蝇从缺氧状态下全生物体代谢恢复的动态过程,并报告氧再灌注造成的损伤可以通过一种新颖但直接的方式进行量化。我们监测了在快速发作的缺氧暴露(持续时间从7.5分钟到120分钟)期间及恢复过程中的二氧化碳排放(线粒体活性指标)和水汽输出(气门神经肌肉控制指标,气门是外界空气与昆虫气管系统之间的瓣膜)。缺氧导致二氧化碳输出出现短暂峰值,随后停止。线粒体呼吸停止,气门收缩肌松弛,但随后再次收缩,推测是由厌氧过程提供动力。恢复到持续的常氧状态导致线粒体呼吸出现双峰式重新激活,对于气门收缩肌而言,则是缓慢失活后再激活。在长时间缺氧后,线粒体重新激活的双峰现象和气门控制的恢复均受到损害。反复进行再灌注后紧接着缺氧发作会以剂量依赖的方式降低线粒体呼吸通量率,并损害气门控制系统的完整性。这是首次在昆虫或任何无脊椎动物中描述氧再灌注损伤的生理学证据。我们认为,昆虫呼吸生物学的一些传统方法,如量化呼吸水分流失,可能有助于将黑腹果蝇用作研究缺血再灌注损伤的潜在生物学和机制及其可能缓解方法的方便、特征明确的实验模型。