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dc.contributor.author Ádám, Veronika
dc.contributor.author Tretter, László
dc.date.accessioned 2016-07-21T12:11:22Z
dc.date.available 2016-07-21T12:11:22Z
dc.date.issued 2013
dc.identifier 84875719244
dc.identifier.citation pagination=757-763; journalVolume=62; journalIssueNumber=5; journalTitle=NEUROCHEMISTRY INTERNATIONAL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1018
dc.identifier.uri doi:10.1016/j.neuint.2013.01.012
dc.description.abstract In addition to complexes in the respiratory chain, few dehydrogenases playing key roles in the physiological metabolism in neurons, are able to generate reactive oxygen species (ROS) in mitochondria. One of them is the Krebs cycle enzyme, α-ketoglutarate dehydrogenase (α-KGDH), which is capable of producing superoxide and hydrogen peroxide by the E3 subunit of the enzyme regulated by changes in the NADH/NAD+ ratio. Mutations in the E3 subunit known to be related to diseases in humans were shown to have increased ROS-forming ability. α-Glycerophosphate dehydrogenase (α-GPDH) located on the outer surface of the inner membrane can also generate ROS, which is stimulated by Ca2+. ROS production by α-GPDH is unique as it does not require Ca2+ uptake and it is observed in respiring as well as damaged, bioenergetically incompetent mitochondria. The possible role of ROS generation by these dehydrogenases in brain pathology is discussed in this review. © 2013 Elsevier Ltd. All rights reserved.
dc.relation.ispartof urn:issn:0197-0186
dc.title The role of mitochondrial dehydrogenases in the generation of oxidative stress
dc.type Journal Article
dc.date.updated 2015-01-13T11:23:07Z
dc.language.rfc3066 en
dc.identifier.mtmt 2227476
dc.identifier.wos 000317873900025
dc.identifier.pubmed 23357482
dc.contributor.department SE/AOK/I/Orvosi Biokémiai Intézet
dc.contributor.department SE/AOK/I/OBI/MTA-SE Neurobiokémiai Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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