Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model

Detalhes bibliográficos
Autor(a) principal: Ferreira, Fernanda M.
Data de Publicação: 2006
Outros Autores: Moreno, António J., Seiça, Raquel, Santos, Maria S., Palmeira, Carlos M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8996
https://doi.org/10.1080/15376520600616925
Resumo: In the present study we investigated the changes in the oxidative phosphorylation system of liver mitochondria, isolated from diabetic Goto-Kakizaki (GK) and Wistar (control) rats with different ages (6, 12, 26, and 52 weeks). We used a kinetic approach known as “top-down” analysis, which conceptually divides the oxidative phosphorylation system into two subsystems: one producing the protonmotive force (Δp) and another that consumes Δp. The overall response of the Δp generators to Δp was obtained from an uncoupler titration of respiration rate versus Δp, while the overall response of Δp consumers to Δp was obtained from an inhibitor titration of respiration rate versus Δp. Our results showed that GK liver mitochondrial preparations presented an increase in Δp production and phosphorylative subsystems (using succinate as respiratory substrate). The alterations observed may suggest the existence of biochemical compensatory mechanisms to type 2 diabetes mellitus in GK rats during their first year of life, in order to reduce the injury associated with the disease. Furthermore, we observed that liver metabolic efficiency of mitochondrial respiration declined with age, this decrease in respiratory activity being visible both in control and diabetic rats.
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spelling Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a ModelIn the present study we investigated the changes in the oxidative phosphorylation system of liver mitochondria, isolated from diabetic Goto-Kakizaki (GK) and Wistar (control) rats with different ages (6, 12, 26, and 52 weeks). We used a kinetic approach known as “top-down” analysis, which conceptually divides the oxidative phosphorylation system into two subsystems: one producing the protonmotive force (Δp) and another that consumes Δp. The overall response of the Δp generators to Δp was obtained from an uncoupler titration of respiration rate versus Δp, while the overall response of Δp consumers to Δp was obtained from an inhibitor titration of respiration rate versus Δp. Our results showed that GK liver mitochondrial preparations presented an increase in Δp production and phosphorylative subsystems (using succinate as respiratory substrate). The alterations observed may suggest the existence of biochemical compensatory mechanisms to type 2 diabetes mellitus in GK rats during their first year of life, in order to reduce the injury associated with the disease. Furthermore, we observed that liver metabolic efficiency of mitochondrial respiration declined with age, this decrease in respiratory activity being visible both in control and diabetic rats.http://www.informaworld.com/10.1080/153765206006169252006info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8996http://hdl.handle.net/10316/8996https://doi.org/10.1080/15376520600616925engToxicology Mechanisms and Methods - Informa Healthcare. 16:6 (2006) 323-330Ferreira, Fernanda M.Moreno, António J.Seiça, RaquelSantos, Maria S.Palmeira, Carlos M.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-10-07T10:32:21Zoai:estudogeral.uc.pt:10316/8996Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:32.425721Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
title Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
spellingShingle Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
Ferreira, Fernanda M.
title_short Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
title_full Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
title_fullStr Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
title_full_unstemmed Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
title_sort Mitochondrial Bioenergetics, Diabetes, and Aging: Top-Down Analysis Using the Diabetic Goto-Kakizaki (GK) Rat as a Model
author Ferreira, Fernanda M.
author_facet Ferreira, Fernanda M.
Moreno, António J.
Seiça, Raquel
Santos, Maria S.
Palmeira, Carlos M.
author_role author
author2 Moreno, António J.
Seiça, Raquel
Santos, Maria S.
Palmeira, Carlos M.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ferreira, Fernanda M.
Moreno, António J.
Seiça, Raquel
Santos, Maria S.
Palmeira, Carlos M.
description In the present study we investigated the changes in the oxidative phosphorylation system of liver mitochondria, isolated from diabetic Goto-Kakizaki (GK) and Wistar (control) rats with different ages (6, 12, 26, and 52 weeks). We used a kinetic approach known as “top-down” analysis, which conceptually divides the oxidative phosphorylation system into two subsystems: one producing the protonmotive force (Δp) and another that consumes Δp. The overall response of the Δp generators to Δp was obtained from an uncoupler titration of respiration rate versus Δp, while the overall response of Δp consumers to Δp was obtained from an inhibitor titration of respiration rate versus Δp. Our results showed that GK liver mitochondrial preparations presented an increase in Δp production and phosphorylative subsystems (using succinate as respiratory substrate). The alterations observed may suggest the existence of biochemical compensatory mechanisms to type 2 diabetes mellitus in GK rats during their first year of life, in order to reduce the injury associated with the disease. Furthermore, we observed that liver metabolic efficiency of mitochondrial respiration declined with age, this decrease in respiratory activity being visible both in control and diabetic rats.
publishDate 2006
dc.date.none.fl_str_mv 2006
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8996
http://hdl.handle.net/10316/8996
https://doi.org/10.1080/15376520600616925
url http://hdl.handle.net/10316/8996
https://doi.org/10.1080/15376520600616925
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dc.relation.none.fl_str_mv Toxicology Mechanisms and Methods - Informa Healthcare. 16:6 (2006) 323-330
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