Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells

Detalhes bibliográficos
Autor(a) principal: Rego, Ana Cristina
Data de Publicação: 1998
Outros Autores: Areias, Filipe Miguel, Santos, Maria Sancha, Oliveira, Catarina R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/4857
https://doi.org/10.1006/exnr.1998.6865
Resumo: The relationship between bioenergetics and the glutamate system was analyzed in a neuronal model of retinal cells in culture, submitted to glucose deprivation and exposed to glutamate for 2 h, and compared with exposure to glutamate in the presence of glucose. Under glucose deprivation, a reduction (about 1.1-fold) in the energy charge of the cells occurred, probably as a result of a decrement (by about 75%) in the cellular redox efficacy, as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) test. In the absence of glucose, exposure of retinal cells to 10 [mu]M glutamate potentiated the reduction in the energy charge (by about 1.2-fold) and induced a significant increase in the uptake of45Ca2+by the cells (1.3-fold), although no significant changes were observed in the presence of glucose. Under glucose deprivation, 100 [mu]M glutamate caused an irreversible cell membrane damage, as shown by the significant increase in lactate dehydrogenase (LDH) leakage (about 1.8-fold). A significant increase in membrane depolarization, measured by the reduction of [3H]tetraphenylphosphonium+([3H]TPP+) uptake, was also observed after glutamate exposure in the absence of glucose. In the presence of glucose, high glutamate concentrations (10 mM) induced a major increase in Ca2+entry into the cells and membrane depolarization, without affecting the energy charge or cell survival. In contrast, in the absence of glucose, 10 mM glutamate did not alter Ca2+accumulation by the cells and a smaller decrease in membrane potential occurred, as compared to 100 [mu]M glutamate exposure. Data shown in this study suggest that during a prolonged (2 h) and acute exposure to high glutamate (10 mM), under glucose deprivation conditions, the neuronal systems have "adaptive" mechanisms that allow the survival of cells. These findings may have implications in neuronal degeneration occurring during brain ischemia.
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spelling Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal CellsCa2+uptake; cell injury; energy charge; glucose deprivation; glutamate; membrane potential; retinal cellsThe relationship between bioenergetics and the glutamate system was analyzed in a neuronal model of retinal cells in culture, submitted to glucose deprivation and exposed to glutamate for 2 h, and compared with exposure to glutamate in the presence of glucose. Under glucose deprivation, a reduction (about 1.1-fold) in the energy charge of the cells occurred, probably as a result of a decrement (by about 75%) in the cellular redox efficacy, as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) test. In the absence of glucose, exposure of retinal cells to 10 [mu]M glutamate potentiated the reduction in the energy charge (by about 1.2-fold) and induced a significant increase in the uptake of45Ca2+by the cells (1.3-fold), although no significant changes were observed in the presence of glucose. Under glucose deprivation, 100 [mu]M glutamate caused an irreversible cell membrane damage, as shown by the significant increase in lactate dehydrogenase (LDH) leakage (about 1.8-fold). A significant increase in membrane depolarization, measured by the reduction of [3H]tetraphenylphosphonium+([3H]TPP+) uptake, was also observed after glutamate exposure in the absence of glucose. In the presence of glucose, high glutamate concentrations (10 mM) induced a major increase in Ca2+entry into the cells and membrane depolarization, without affecting the energy charge or cell survival. In contrast, in the absence of glucose, 10 mM glutamate did not alter Ca2+accumulation by the cells and a smaller decrease in membrane potential occurred, as compared to 100 [mu]M glutamate exposure. Data shown in this study suggest that during a prolonged (2 h) and acute exposure to high glutamate (10 mM), under glucose deprivation conditions, the neuronal systems have "adaptive" mechanisms that allow the survival of cells. These findings may have implications in neuronal degeneration occurring during brain ischemia.http://www.sciencedirect.com/science/article/B6WFG-45K0YG1-1F/1/f72f07d2f8f34513657ace7d1febf7ca1998info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/4857http://hdl.handle.net/10316/4857https://doi.org/10.1006/exnr.1998.6865engExperimental Neurology. 153:1 (1998) 128-134Rego, Ana CristinaAreias, Filipe MiguelSantos, Maria SanchaOliveira, Catarina R.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:RCAAP2020-11-06T16:48:38Zoai:estudogeral.uc.pt:10316/4857Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:29.423171Repositório 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 Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
title Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
spellingShingle Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
Rego, Ana Cristina
Ca2+uptake; cell injury; energy charge; glucose deprivation; glutamate; membrane potential; retinal cells
title_short Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
title_full Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
title_fullStr Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
title_full_unstemmed Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
title_sort Effect of Glucose Deprivation and Acute Glutamate Exposure in Cultured Retinal Cells
author Rego, Ana Cristina
author_facet Rego, Ana Cristina
Areias, Filipe Miguel
Santos, Maria Sancha
Oliveira, Catarina R.
author_role author
author2 Areias, Filipe Miguel
Santos, Maria Sancha
Oliveira, Catarina R.
author2_role author
author
author
dc.contributor.author.fl_str_mv Rego, Ana Cristina
Areias, Filipe Miguel
Santos, Maria Sancha
Oliveira, Catarina R.
dc.subject.por.fl_str_mv Ca2+uptake; cell injury; energy charge; glucose deprivation; glutamate; membrane potential; retinal cells
topic Ca2+uptake; cell injury; energy charge; glucose deprivation; glutamate; membrane potential; retinal cells
description The relationship between bioenergetics and the glutamate system was analyzed in a neuronal model of retinal cells in culture, submitted to glucose deprivation and exposed to glutamate for 2 h, and compared with exposure to glutamate in the presence of glucose. Under glucose deprivation, a reduction (about 1.1-fold) in the energy charge of the cells occurred, probably as a result of a decrement (by about 75%) in the cellular redox efficacy, as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) test. In the absence of glucose, exposure of retinal cells to 10 [mu]M glutamate potentiated the reduction in the energy charge (by about 1.2-fold) and induced a significant increase in the uptake of45Ca2+by the cells (1.3-fold), although no significant changes were observed in the presence of glucose. Under glucose deprivation, 100 [mu]M glutamate caused an irreversible cell membrane damage, as shown by the significant increase in lactate dehydrogenase (LDH) leakage (about 1.8-fold). A significant increase in membrane depolarization, measured by the reduction of [3H]tetraphenylphosphonium+([3H]TPP+) uptake, was also observed after glutamate exposure in the absence of glucose. In the presence of glucose, high glutamate concentrations (10 mM) induced a major increase in Ca2+entry into the cells and membrane depolarization, without affecting the energy charge or cell survival. In contrast, in the absence of glucose, 10 mM glutamate did not alter Ca2+accumulation by the cells and a smaller decrease in membrane potential occurred, as compared to 100 [mu]M glutamate exposure. Data shown in this study suggest that during a prolonged (2 h) and acute exposure to high glutamate (10 mM), under glucose deprivation conditions, the neuronal systems have "adaptive" mechanisms that allow the survival of cells. These findings may have implications in neuronal degeneration occurring during brain ischemia.
publishDate 1998
dc.date.none.fl_str_mv 1998
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/4857
http://hdl.handle.net/10316/4857
https://doi.org/10.1006/exnr.1998.6865
url http://hdl.handle.net/10316/4857
https://doi.org/10.1006/exnr.1998.6865
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Experimental Neurology. 153:1 (1998) 128-134
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