Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Tiago B.
Data de Publicação: 2005
Outros Autores: Gray, Heather L., Benito, Marina, Garrido, Susana, Sierra, Alejandra, Geraldes, Carlos F., Ballesteros, Paloma, Cerdán, Sebastián
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8127
https://doi.org/10.1002/jnr.20308
Resumo: We report a novel (13C, 2H) nuclear magnetic resonance (NMR) procedure to investigate lactate recycling through the monocarboxylate transporter of the plasma membrane of cells in culture. C6 glioma cells were incubated with [3-13C]lactate in Krebs-Henseleit Buffer containing 50% 2H2O (vol/vol) for up to 30 hr. 13C NMR analysis of aliquots progressively taken from the medium, showed: (1) a linearly decreasing singlet at sim20.85 parts per million (ppm; -0.119 mumol/mg protein/hr) derived from the methyl carbon of [3-13C]lactate; and (2) an exponentially increasing shifted singlet at sim20.74 ppm (0.227 mumol/ mg protein/hr) from the methyl carbon of [3-13C, 2-2H]lactate. The shifted singlet appears because during its transit through the cytosol, [3-13C]lactate generates [3-13C, 2-2H]lactate in the lactate dehydrogenase (LDH) equilibrium, which may return to the incubation medium through the reversible monocarboxylate carrier. The methyl group of [3-13C, 2-2H]lactate is shifted -0.11 ppm with respect to that of [3-13C]lactate, making it possible to distinguish between both molecules by 13C NMR. During incubations with 2.5 mM [1-13C]glucose and 3.98 mM [U-13C3]lactate or with 2.5 mM [1-13C]glucose and 3.93 mM [2-13C]pyruvate, C2-deuterated lactate was produced only from [1-13C]glucose or [U-13C3]lactate, revealing that this deuteration process is redox sensitive. When [1-13C]glucose and [U-13C3]lactate were used as substrates, no significant [3-13C]lactate production from [1-13C]glucose was detected, suggesting that glycolytic lactate production may be stopped under the high lactate concentrations prevailing under mild hypoxic or ischemic episodes or during cerebral activation. © 2004 Wiley-Liss, Inc.
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spelling Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMRWe report a novel (13C, 2H) nuclear magnetic resonance (NMR) procedure to investigate lactate recycling through the monocarboxylate transporter of the plasma membrane of cells in culture. C6 glioma cells were incubated with [3-13C]lactate in Krebs-Henseleit Buffer containing 50% 2H2O (vol/vol) for up to 30 hr. 13C NMR analysis of aliquots progressively taken from the medium, showed: (1) a linearly decreasing singlet at sim20.85 parts per million (ppm; -0.119 mumol/mg protein/hr) derived from the methyl carbon of [3-13C]lactate; and (2) an exponentially increasing shifted singlet at sim20.74 ppm (0.227 mumol/ mg protein/hr) from the methyl carbon of [3-13C, 2-2H]lactate. The shifted singlet appears because during its transit through the cytosol, [3-13C]lactate generates [3-13C, 2-2H]lactate in the lactate dehydrogenase (LDH) equilibrium, which may return to the incubation medium through the reversible monocarboxylate carrier. The methyl group of [3-13C, 2-2H]lactate is shifted -0.11 ppm with respect to that of [3-13C]lactate, making it possible to distinguish between both molecules by 13C NMR. During incubations with 2.5 mM [1-13C]glucose and 3.98 mM [U-13C3]lactate or with 2.5 mM [1-13C]glucose and 3.93 mM [2-13C]pyruvate, C2-deuterated lactate was produced only from [1-13C]glucose or [U-13C3]lactate, revealing that this deuteration process is redox sensitive. When [1-13C]glucose and [U-13C3]lactate were used as substrates, no significant [3-13C]lactate production from [1-13C]glucose was detected, suggesting that glycolytic lactate production may be stopped under the high lactate concentrations prevailing under mild hypoxic or ischemic episodes or during cerebral activation. © 2004 Wiley-Liss, Inc.2005info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8127http://hdl.handle.net/10316/8127https://doi.org/10.1002/jnr.20308engJournal of Neuroscience Research. 79:1-2 (2005) 119-127Rodrigues, Tiago B.Gray, Heather L.Benito, MarinaGarrido, SusanaSierra, AlejandraGeraldes, Carlos F.Ballesteros, PalomaCerdán, Sebastiáninfo: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:RCAAP2022-05-25T03:18:47Zoai:estudogeral.uc.pt:10316/8127Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:44.413815Repositório 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 Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
title Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
spellingShingle Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
Rodrigues, Tiago B.
title_short Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
title_full Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
title_fullStr Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
title_full_unstemmed Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
title_sort Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR
author Rodrigues, Tiago B.
author_facet Rodrigues, Tiago B.
Gray, Heather L.
Benito, Marina
Garrido, Susana
Sierra, Alejandra
Geraldes, Carlos F.
Ballesteros, Paloma
Cerdán, Sebastián
author_role author
author2 Gray, Heather L.
Benito, Marina
Garrido, Susana
Sierra, Alejandra
Geraldes, Carlos F.
Ballesteros, Paloma
Cerdán, Sebastián
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Tiago B.
Gray, Heather L.
Benito, Marina
Garrido, Susana
Sierra, Alejandra
Geraldes, Carlos F.
Ballesteros, Paloma
Cerdán, Sebastián
description We report a novel (13C, 2H) nuclear magnetic resonance (NMR) procedure to investigate lactate recycling through the monocarboxylate transporter of the plasma membrane of cells in culture. C6 glioma cells were incubated with [3-13C]lactate in Krebs-Henseleit Buffer containing 50% 2H2O (vol/vol) for up to 30 hr. 13C NMR analysis of aliquots progressively taken from the medium, showed: (1) a linearly decreasing singlet at sim20.85 parts per million (ppm; -0.119 mumol/mg protein/hr) derived from the methyl carbon of [3-13C]lactate; and (2) an exponentially increasing shifted singlet at sim20.74 ppm (0.227 mumol/ mg protein/hr) from the methyl carbon of [3-13C, 2-2H]lactate. The shifted singlet appears because during its transit through the cytosol, [3-13C]lactate generates [3-13C, 2-2H]lactate in the lactate dehydrogenase (LDH) equilibrium, which may return to the incubation medium through the reversible monocarboxylate carrier. The methyl group of [3-13C, 2-2H]lactate is shifted -0.11 ppm with respect to that of [3-13C]lactate, making it possible to distinguish between both molecules by 13C NMR. During incubations with 2.5 mM [1-13C]glucose and 3.98 mM [U-13C3]lactate or with 2.5 mM [1-13C]glucose and 3.93 mM [2-13C]pyruvate, C2-deuterated lactate was produced only from [1-13C]glucose or [U-13C3]lactate, revealing that this deuteration process is redox sensitive. When [1-13C]glucose and [U-13C3]lactate were used as substrates, no significant [3-13C]lactate production from [1-13C]glucose was detected, suggesting that glycolytic lactate production may be stopped under the high lactate concentrations prevailing under mild hypoxic or ischemic episodes or during cerebral activation. © 2004 Wiley-Liss, Inc.
publishDate 2005
dc.date.none.fl_str_mv 2005
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8127
http://hdl.handle.net/10316/8127
https://doi.org/10.1002/jnr.20308
url http://hdl.handle.net/10316/8127
https://doi.org/10.1002/jnr.20308
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dc.relation.none.fl_str_mv Journal of Neuroscience Research. 79:1-2 (2005) 119-127
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