Oxidative stress and adrenocortical insufficiency
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 s...
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Veröffentlicht in: | Journal of endocrinology 2014-06, Vol.221 (3), p.R63-R73 |
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container_issue | 3 |
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container_title | Journal of endocrinology |
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creator | Prasad, R Kowalczyk, J C Meimaridou, E Storr, H L Metherell, L A |
description | 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. |
doi_str_mv | 10.1530/JOE-13-0346 |
format | Article |
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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.</description><subject>Adrenal Insufficiency - metabolism</subject><subject>Antioxidants - metabolism</subject><subject>Humans</subject><subject>Mitochondria - metabolism</subject><subject>Models, Biological</subject><subject>Oxidation-Reduction</subject><subject>Oxidative Stress</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Review</subject><issn>0022-0795</issn><issn>1479-6805</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQQC0EoqUwsaOMSChwF8f5WJBQVb5UqUt3y3ZsMErjYicV_fckaqlgYbrhnt6dHiGXCLfIKNy9LmYx0hhomh2RMaZ5GWcFsGMyBkiSGPKSjchZCB8AyDCnp2SUpFlC8zIfE1x82Uq0dqOj0HodQiSaKhKV141TzrdWiTqyTeiMscrqRm3PyYkRddAX-zkhy8fZcvoczxdPL9OHeSwZxTbOczBUG0WzEik1WWGUVkkOspC0BCmUVKVCgQJEJZlWygCTFAqDhmJS0Am532nXnVzpSumm9aLma29Xwm-5E5b_3TT2nb-5DU8hZQkOguu9wLvPToeWr2xQuq5Fo10XOLKUJgUAZD16s0OVdyF4bQ5nEPjQmPeNOVI-NO7pq9-fHdifqD2AO0BaF4Zore3jiX-l36FKiOA</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Prasad, R</creator><creator>Kowalczyk, J C</creator><creator>Meimaridou, E</creator><creator>Storr, H L</creator><creator>Metherell, L A</creator><general>Bioscientifica Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140601</creationdate><title>Oxidative stress and adrenocortical insufficiency</title><author>Prasad, R ; Kowalczyk, J C ; Meimaridou, E ; Storr, H L ; Metherell, L A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b531t-770f3efc369133f68fcec270b8b390bacbc9c1a1a0adb5eccf05b308f1f31283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adrenal Insufficiency - metabolism</topic><topic>Antioxidants - metabolism</topic><topic>Humans</topic><topic>Mitochondria - metabolism</topic><topic>Models, Biological</topic><topic>Oxidation-Reduction</topic><topic>Oxidative Stress</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prasad, R</creatorcontrib><creatorcontrib>Kowalczyk, J C</creatorcontrib><creatorcontrib>Meimaridou, E</creatorcontrib><creatorcontrib>Storr, H L</creatorcontrib><creatorcontrib>Metherell, L A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prasad, R</au><au>Kowalczyk, J C</au><au>Meimaridou, E</au><au>Storr, H L</au><au>Metherell, L A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxidative stress and adrenocortical insufficiency</atitle><jtitle>Journal of endocrinology</jtitle><addtitle>J Endocrinol</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>221</volume><issue>3</issue><spage>R63</spage><epage>R73</epage><pages>R63-R73</pages><issn>0022-0795</issn><eissn>1479-6805</eissn><abstract>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.</abstract><cop>England</cop><pub>Bioscientifica Ltd</pub><pmid>24623797</pmid><doi>10.1530/JOE-13-0346</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal Insufficiency - metabolism Antioxidants - metabolism Humans Mitochondria - metabolism Models, Biological Oxidation-Reduction Oxidative Stress Reactive Oxygen Species - metabolism Review |
title | Oxidative stress and adrenocortical insufficiency |
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