Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?

Detalhes bibliográficos
Autor(a) principal: Baierle, Marília
Data de Publicação: 2014
Outros Autores: Charão, Mariele Feiffer, Göethel, Gabriela, Barth, Anelise, Fracasso, Rafael, Bubols, Guilherme Borges, Sauer, Elisa, Campanharo, Sarah Chagas, Rocha, Rafael Christian Chávez, Saint'Pierre, Tatiana Dillenburg, Bordignon, Suelen, Zibetti, Murilo Ricardo, Trentini, Clarissa Marceli, Ávila, Daiana Silva de, Gioda, Adriana, Garcia, Solange Cristina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/140110
Resumo: Aging is often accompanied by cognitive impairments and influenced by oxidative status and chemical imbalances. Thus, this study was conducted to examinewhether age-related cognitive deficit is associated with oxidative damage, especially with inhibition of the enzyme delta-aminolevulinate dehydratase (ALA-D), as well as to verify the influence of some metals in the enzyme activity and cognitive performance. Blood ALA-D activity, essential (Fe, Zn, Cu, Se) and non-essential metals (Pb, Cd, Hg, As, Cr, Ni, V) were measured in 50 elderly and 20 healthy young subjects. Cognitive function was assessed by tests from Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) battery and other. The elderly group presented decreased ALA-D activity compared to the young group. The index of ALA-D reactivation was similar to both study groups, but negatively associated with metals. The mean levels of essential metals were within the reference values, while the most toxic metals were above them in both groups. Cognitive function impairments were observed in elderly group and were associated with decreased ALA-D activity, with lower levels of Se and higher levels of toxic metals (Hg and V). Results suggest that the reduced ALA-D activity in elderly can be an additional factor involved in cognitive decline, since its inhibition throughout life could lead to accumulation of the neurotoxic compound ALA. Toxic metals were found to contribute to cognitive decline and also to influence ALA-D reactivation.
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spelling Baierle, MaríliaCharão, Mariele FeifferGöethel, GabrielaBarth, AneliseFracasso, RafaelBubols, Guilherme BorgesSauer, ElisaCampanharo, Sarah ChagasRocha, Rafael Christian ChávezSaint'Pierre, Tatiana DillenburgBordignon, SuelenZibetti, Murilo RicardoTrentini, Clarissa MarceliÁvila, Daiana Silva deGioda, AdrianaGarcia, Solange Cristina2016-05-04T02:07:10Z20141660-4601http://hdl.handle.net/10183/140110000978148Aging is often accompanied by cognitive impairments and influenced by oxidative status and chemical imbalances. Thus, this study was conducted to examinewhether age-related cognitive deficit is associated with oxidative damage, especially with inhibition of the enzyme delta-aminolevulinate dehydratase (ALA-D), as well as to verify the influence of some metals in the enzyme activity and cognitive performance. Blood ALA-D activity, essential (Fe, Zn, Cu, Se) and non-essential metals (Pb, Cd, Hg, As, Cr, Ni, V) were measured in 50 elderly and 20 healthy young subjects. Cognitive function was assessed by tests from Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) battery and other. The elderly group presented decreased ALA-D activity compared to the young group. The index of ALA-D reactivation was similar to both study groups, but negatively associated with metals. The mean levels of essential metals were within the reference values, while the most toxic metals were above them in both groups. Cognitive function impairments were observed in elderly group and were associated with decreased ALA-D activity, with lower levels of Se and higher levels of toxic metals (Hg and V). Results suggest that the reduced ALA-D activity in elderly can be an additional factor involved in cognitive decline, since its inhibition throughout life could lead to accumulation of the neurotoxic compound ALA. Toxic metals were found to contribute to cognitive decline and also to influence ALA-D reactivation.application/pdfengInternational Journal of Environmental Research and Public Health. Beijing. Vol. 11, no.10 (2014), p. 10851-10867FarmáciaALA-DCognitive declineCognitive assessmentToxic metalsEssential metalsAre delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?Estrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000978148.pdf000978148.pdfTexto completo (inglês)application/pdf743406http://www.lume.ufrgs.br/bitstream/10183/140110/1/000978148.pdf6faee3fae4cacbbca93de1cb37f7ae09MD51TEXT000978148.pdf.txt000978148.pdf.txtExtracted Texttext/plain50417http://www.lume.ufrgs.br/bitstream/10183/140110/2/000978148.pdf.txt119467230658e332d9aac2c894e0c383MD52THUMBNAIL000978148.pdf.jpg000978148.pdf.jpgGenerated Thumbnailimage/jpeg2146http://www.lume.ufrgs.br/bitstream/10183/140110/3/000978148.pdf.jpg44be029c6d233992a1b4acfe6d9c30c4MD5310183/1401102021-09-18 04:36:30.594265oai:www.lume.ufrgs.br:10183/140110Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:36:30Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
title Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
spellingShingle Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
Baierle, Marília
Farmácia
ALA-D
Cognitive decline
Cognitive assessment
Toxic metals
Essential metals
title_short Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
title_full Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
title_fullStr Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
title_full_unstemmed Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
title_sort Are delta-aminolevulinate dehydratase inhibition and metal concentrations additional factors for the age-related cognitive decline?
author Baierle, Marília
author_facet Baierle, Marília
Charão, Mariele Feiffer
Göethel, Gabriela
Barth, Anelise
Fracasso, Rafael
Bubols, Guilherme Borges
Sauer, Elisa
Campanharo, Sarah Chagas
Rocha, Rafael Christian Chávez
Saint'Pierre, Tatiana Dillenburg
Bordignon, Suelen
Zibetti, Murilo Ricardo
Trentini, Clarissa Marceli
Ávila, Daiana Silva de
Gioda, Adriana
Garcia, Solange Cristina
author_role author
author2 Charão, Mariele Feiffer
Göethel, Gabriela
Barth, Anelise
Fracasso, Rafael
Bubols, Guilherme Borges
Sauer, Elisa
Campanharo, Sarah Chagas
Rocha, Rafael Christian Chávez
Saint'Pierre, Tatiana Dillenburg
Bordignon, Suelen
Zibetti, Murilo Ricardo
Trentini, Clarissa Marceli
Ávila, Daiana Silva de
Gioda, Adriana
Garcia, Solange Cristina
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Baierle, Marília
Charão, Mariele Feiffer
Göethel, Gabriela
Barth, Anelise
Fracasso, Rafael
Bubols, Guilherme Borges
Sauer, Elisa
Campanharo, Sarah Chagas
Rocha, Rafael Christian Chávez
Saint'Pierre, Tatiana Dillenburg
Bordignon, Suelen
Zibetti, Murilo Ricardo
Trentini, Clarissa Marceli
Ávila, Daiana Silva de
Gioda, Adriana
Garcia, Solange Cristina
dc.subject.por.fl_str_mv Farmácia
topic Farmácia
ALA-D
Cognitive decline
Cognitive assessment
Toxic metals
Essential metals
dc.subject.eng.fl_str_mv ALA-D
Cognitive decline
Cognitive assessment
Toxic metals
Essential metals
description Aging is often accompanied by cognitive impairments and influenced by oxidative status and chemical imbalances. Thus, this study was conducted to examinewhether age-related cognitive deficit is associated with oxidative damage, especially with inhibition of the enzyme delta-aminolevulinate dehydratase (ALA-D), as well as to verify the influence of some metals in the enzyme activity and cognitive performance. Blood ALA-D activity, essential (Fe, Zn, Cu, Se) and non-essential metals (Pb, Cd, Hg, As, Cr, Ni, V) were measured in 50 elderly and 20 healthy young subjects. Cognitive function was assessed by tests from Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) battery and other. The elderly group presented decreased ALA-D activity compared to the young group. The index of ALA-D reactivation was similar to both study groups, but negatively associated with metals. The mean levels of essential metals were within the reference values, while the most toxic metals were above them in both groups. Cognitive function impairments were observed in elderly group and were associated with decreased ALA-D activity, with lower levels of Se and higher levels of toxic metals (Hg and V). Results suggest that the reduced ALA-D activity in elderly can be an additional factor involved in cognitive decline, since its inhibition throughout life could lead to accumulation of the neurotoxic compound ALA. Toxic metals were found to contribute to cognitive decline and also to influence ALA-D reactivation.
publishDate 2014
dc.date.issued.fl_str_mv 2014
dc.date.accessioned.fl_str_mv 2016-05-04T02:07:10Z
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dc.identifier.issn.pt_BR.fl_str_mv 1660-4601
dc.identifier.nrb.pt_BR.fl_str_mv 000978148
identifier_str_mv 1660-4601
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url http://hdl.handle.net/10183/140110
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv International Journal of Environmental Research and Public Health. Beijing. Vol. 11, no.10 (2014), p. 10851-10867
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