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Oxidative stress and adrenocortical insufficiency

机译:氧化应激和肾上腺皮质功能不全

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摘要

Maintenance of redox balance is essential for normal cellular functions. Any perturbation in this balance due to increased reactive oxygen species (ROS) leads to oxidative stress and may lead to cell dysfunction/damage/death. Mitochondria are responsible for the majority of cellular ROS production secondary to electron leakage as a consequence of respiration. Furthermore, electron leakage by the cytochrome P450 enzymes may render steroidogenic tissues acutely vulnerable to redox imbalance. The adrenal cortex, in particular, is well supplied with both enzymatic (glutathione peroxidases and peroxiredoxins) and non-enzymatic (vitamins A, C and E) antioxidants to cope with this increased production of ROS due to steroidogenesis. Nonetheless oxidative stress is implicated in several potentially lethal adrenal disorders including X-linked adrenoleukodystrophy, triple A syndrome and most recently familial glucocorticoid deficiency. The finding of mutations in antioxidant defence genes in the latter two conditions highlights how disturbances in redox homeostasis may have an effect on adrenal steroidogenesis.
机译:维持氧化还原平衡对于正常的细胞功能至关重要。由于增加的活性氧(ROS)而导致的这种平衡中的任何干扰都会导致氧化应激,并可能导致细胞功能障碍/损伤/死亡。由于呼吸作用,线粒体是继电子泄漏后继发于细胞的大部分ROS产生的原因。此外,细胞色素P450酶的电子泄漏可能使类固醇生成组织严重易受氧化还原失衡的影响。尤其是,肾上腺皮质会同时提供酶促(谷胱甘肽过氧化物酶和过氧化物酶)和非酶促(维生素A,C和E)抗氧化剂,以应对由于类固醇生成而增加的ROS产生。然而,氧化应激与几种潜在的致死性肾上腺疾病有关,包括X连锁性肾上腺皮质营养不良,三重A综合征和最近家族性糖皮质激素缺乏症。在后两种情况下,抗氧化剂防御基因突变的发现凸显了氧化还原稳态的紊乱可能如何影响肾上腺类固醇生成。

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