Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/8323
DC FieldValueLanguage
dc.contributor.authorFerreira, Fernanda M.-
dc.contributor.authorPalmeira, Carlos M.-
dc.contributor.authorSeiça, Raquel-
dc.contributor.authorMoreno, António J.-
dc.contributor.authorSantos, Maria S.-
dc.date.accessioned2009-02-09T14:33:57Z-
dc.date.available2009-02-09T14:33:57Z-
dc.date.issued2003en_US
dc.identifier.citationJournal of Biochemical and Molecular Toxicology. 17:4 (2003) 214-222en_US
dc.identifier.urihttps://hdl.handle.net/10316/8323-
dc.description.abstractSeveral studies have been carried out to evaluate the alterations in mitochondrial functions of diabetic rats. However, some of the results reported are controversial, since experimental conditions, such as aging, and/or strain of animals used were different. The purpose of this study was to evaluate the metabolic changes in liver mitochondria, both in the presence of severe hyperglycaemia (STZ-treated rats) and mild hyperglycaemia (Goto-Kakizaki (GK) rats). Moreover, metabolic alterations were evaluated both at initial and at advanced states of the disease.We observed that both models of type 1 and type 2 diabetes presented alterations on respiratory chain activity. Because of continual severe hyperglycaemia, 9 weeks after the induction of diabetes, the respiratory function declined in STZ-treated rats, as observed by membrane potential and respiratory ratios (RCR, P/O, and FCCP-stimulated respiration) assessment. In contrast, GK rats of 6 months age presented increased respiratory ratios.To localize which respiratory complexes are affected by diabetes, enzymatic respiratory chain activities were evaluated. We observed that succinate dehydrogenase and cytochrome c oxidase activities were significantly augmented both in STZ-treated rats and GK rats of 6 months age. Moreover, H+-ATPase activity was also significantly increased in STZ-treated rats with 3 weeks of diabetes and in GK rats of 6 months age as compared to controls. Therefore, these results clearly suggest that both animal models of diabetes present some metabolic adjustments in order to circumvent the deleterious effects promoted by the high glucose levels typical of the disease. © 2003 Wiley Periodicals, Inc. J Biochem Mol Toxicol 17:214-222, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.10081en_US
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleDiabetes and mitochondrial bioenergetics: Alterations with ageen_US
dc.typearticleen_US
dc.identifier.doi10.1002/8485jbt.10081en_US
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.deptFaculty of Sciences and Technology-
crisitem.author.parentdeptUniversity of Coimbra-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitMARE - Marine and Environmental Sciences Centre-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-2639-7697-
crisitem.author.orcid0000-0002-8378-0895-
crisitem.author.orcid0000-0003-3575-7604-
crisitem.author.orcid0000-0002-6881-9392-
Appears in Collections:FCTUC Ciências da Vida - Artigos em Revistas Internacionais
Files in This Item:
File Description SizeFormat
Diabetes and mitochondrial bioenergetics.pdf153.17 kBAdobe PDFView/Open
Show simple item record

Page view(s)

298
checked on Apr 23, 2024

Download(s)

374
checked on Apr 23, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.