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首页> 外文期刊>The Journal of Experimental Biology >Mitochondrial plasticity in the cerebellum of two anoxia-tolerant sharks: contrasting responses to anoxia/re-oxygenation
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Mitochondrial plasticity in the cerebellum of two anoxia-tolerant sharks: contrasting responses to anoxia/re-oxygenation

机译:两种贫砷鲨的小脑中的线粒体可塑性:对缺氧/重氧化的对比反应

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摘要

Exposure to anoxia leads to rapid ATP depletion, alters metabolic pathways and exacerbates succinate accumulation. Upon re-oxygenation, the preferential oxidation of accumulated succinate most often impairs mitochondrial function. Few species can survive prolonged periods of hypoxia and anoxia at tropical temperatures and those that do may rely on mitochondria plasticity in response to disruptions to oxygen availability. Two carpet sharks, the epaulette shark (Hemiscyllium ocellaturn) and the grey carpet shark (Chiloscyllium punctatum) display different adaptive responses to prolonged anoxia: while H. ocellatum enters energy-conserving metabolic depression, C. punctatum temporarily elevates its haematocrit, prolonging oxygen delivery. High-resolution respirometry was used to investigate mitochondrial function in the cerebellum, a highly metabolically active organ that is oxygen sensitive and vulnerable to injury after anoxia/re-oxygenation (AR). Succinate was titrated into cerebellar preparations in vitro, with or without pre-exposure to AR, then the activity of mitochondrial complexes was examined. As in most vertebrates, C. punctatum mitochondria significantly increased succinate oxidation rates, with impaired complex I function post-AR. In contrast, H. ocellatum mitochondria inhibited succinate oxidation rates and both complex I and II capacities were conserved, resulting in preservation of oxidative phosphorylation capacity post-AR. Divergent mitochondrial plasticity elicited by elevated succinate post-AR parallels the inherently divergent physiological adaptations of these animals to prolonged anoxia, namely the absence (C. punctatum) and presence (H. ocellatum) of metabolic depression. As anoxia tolerance in these species also occurs at temperatures close to that for humans. examining their mitochondrial responses to AR could provide insights for novel interventions in clinical settings.
机译:暴露于缺氧导致快速ATP耗尽,改变代谢途径和加剧琥珀酸盐积累。重新氧合时,积累的琥珀酸盐的优先氧化通常损害线粒体功能。在热带温度下,很少有物种可以在热带温度下存活长期的缺氧和缺氧,并且可以依赖于线粒体可塑性的缺氧,以应对氧可用性的破坏。两个地毯鲨鱼,肩骨鲨(乳头葡萄牙)和灰色地毯鲨(Chiloscylium punctatum)显示出不同的适应性反应,延长缺氧:而H. Ocellatum进入节能代谢抑郁症,C.尖尖临时升高其血细胞比容,延长氧气递送。高分辨率呼​​吸测定法用于研究小脑中的线粒体功能,高度代谢的活性器官,其含氧敏感,易受缺氧/再氧化(AR)损伤。琥珀酸盐在体外滴定到小脑制剂中,用或不暴露于AR,然后检查线粒体复合物的活性。如在大多数脊椎动物中,C.尖尖线粒体显着增加琥珀酸氧化率,效果损害了I次效果。相比之下,H. Ocellatum线粒体抑制琥珀酸氧化率,并且保守了复合I和II能力,导致保存氧化磷酸化能力后Ar。通过升高的琥珀酸酯后AR引起的发散线粒体可塑性使这些动物的固有发散的生理适应延长缺氧,即代谢抑郁症的缺失(C.斑态)和存在(H. Ocellatum)。由于这些物种中的贫血性耐受性也发生在接近人类的温度下。检查其对AR的线粒体反应可以为临床环境中的新型干预措施提供见解。

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