Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder

Detalhes bibliográficos
Autor(a) principal: Layden, Brian T.
Data de Publicação: 2003
Outros Autores: Abukhdeir, Abde M., Williams, Nicole, Fonseca, Carla P., Carroll, Laura, Castro, Margarita M. C. A., Geraldes, Carlos F. G. C., Bryant, Fred B., Freitas, Duarte Mota de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/3871
https://doi.org/10.1016/j.bcp.2003.07.001
Resumo: Li+/Mg2+ competition has been implicated in the therapeutic action of Li+ treatment in bipolar illness. We hypothesized that this competition depended on cell-specific properties. To test this hypothesis, we determined the degree of Li+ transport, immobilization, and Li+/Mg2+ competition in lymphoblastomas, neuroblastomas, and erythrocytes. During a 50 mmol/L Li+-loading incubation, Li+ accumulation at 30 min (mmoles Li+/L cells) was the greatest in lymphoblastomas (11.1±0.3), followed by neuroblastomas (9.3±0.5), and then erythrocytes (4.0±0.5). Li+ binding affinities to the plasma membrane in all three cell types were of the same order of magnitude; however, Li+ immobilization in intact cells was greatest in neuroblastomas and least in erythrocytes. When cells were loaded for 30 min in a 50 mmol/L Li+-containing medium, the percentage increase in free intracellular [Mg2+] in neuroblastoma and lymphoblastoma cells (~55 and ~52%, respectively) was similar, but erythrocytes did not exhibit any substantial increase (~6%). With the intracellular [Li+] at 15 mmol/L, the free intracellular [Mg2+] increased by the greatest amount in neuroblastomas (~158%), followed by lymphoblastomas (~75%), and then erythrocytes (~50%). We conclude that Li+ immobilization and transport are related to free intracellular [Mg2+] and to the extent of Li+/Mg2+ competition in a cell-specific manner.
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spelling Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorderFluorescenceAtomic absorptionNeuroblastomaLymphoblastomaLi+/Mg2+ competition has been implicated in the therapeutic action of Li+ treatment in bipolar illness. We hypothesized that this competition depended on cell-specific properties. To test this hypothesis, we determined the degree of Li+ transport, immobilization, and Li+/Mg2+ competition in lymphoblastomas, neuroblastomas, and erythrocytes. During a 50 mmol/L Li+-loading incubation, Li+ accumulation at 30 min (mmoles Li+/L cells) was the greatest in lymphoblastomas (11.1±0.3), followed by neuroblastomas (9.3±0.5), and then erythrocytes (4.0±0.5). Li+ binding affinities to the plasma membrane in all three cell types were of the same order of magnitude; however, Li+ immobilization in intact cells was greatest in neuroblastomas and least in erythrocytes. When cells were loaded for 30 min in a 50 mmol/L Li+-containing medium, the percentage increase in free intracellular [Mg2+] in neuroblastoma and lymphoblastoma cells (~55 and ~52%, respectively) was similar, but erythrocytes did not exhibit any substantial increase (~6%). With the intracellular [Li+] at 15 mmol/L, the free intracellular [Mg2+] increased by the greatest amount in neuroblastomas (~158%), followed by lymphoblastomas (~75%), and then erythrocytes (~50%). We conclude that Li+ immobilization and transport are related to free intracellular [Mg2+] and to the extent of Li+/Mg2+ competition in a cell-specific manner.http://www.sciencedirect.com/science/article/B6T4P-49JHRTX-1/1/a707c6f5021c0af8d926e0ee947843b82003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/3871http://hdl.handle.net/10316/3871https://doi.org/10.1016/j.bcp.2003.07.001engBiochemical Pharmacology. 66:10 (2003) 1915-1924Layden, Brian T.Abukhdeir, Abde M.Williams, NicoleFonseca, Carla P.Carroll, LauraCastro, Margarita M. C. A.Geraldes, Carlos F. G. C.Bryant, Fred B.Freitas, Duarte Mota deinfo: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:RCAAP2021-09-01T08:59:47Zoai:estudogeral.uc.pt:10316/3871Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:42.709430Repositório 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 Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
title Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
spellingShingle Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
Layden, Brian T.
Fluorescence
Atomic absorption
Neuroblastoma
Lymphoblastoma
title_short Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
title_full Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
title_fullStr Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
title_full_unstemmed Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
title_sort Effects of Li+ transport and Li+ immobilization on Li+/Mg2+ competition in cells: implications for bipolar disorder
author Layden, Brian T.
author_facet Layden, Brian T.
Abukhdeir, Abde M.
Williams, Nicole
Fonseca, Carla P.
Carroll, Laura
Castro, Margarita M. C. A.
Geraldes, Carlos F. G. C.
Bryant, Fred B.
Freitas, Duarte Mota de
author_role author
author2 Abukhdeir, Abde M.
Williams, Nicole
Fonseca, Carla P.
Carroll, Laura
Castro, Margarita M. C. A.
Geraldes, Carlos F. G. C.
Bryant, Fred B.
Freitas, Duarte Mota de
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Layden, Brian T.
Abukhdeir, Abde M.
Williams, Nicole
Fonseca, Carla P.
Carroll, Laura
Castro, Margarita M. C. A.
Geraldes, Carlos F. G. C.
Bryant, Fred B.
Freitas, Duarte Mota de
dc.subject.por.fl_str_mv Fluorescence
Atomic absorption
Neuroblastoma
Lymphoblastoma
topic Fluorescence
Atomic absorption
Neuroblastoma
Lymphoblastoma
description Li+/Mg2+ competition has been implicated in the therapeutic action of Li+ treatment in bipolar illness. We hypothesized that this competition depended on cell-specific properties. To test this hypothesis, we determined the degree of Li+ transport, immobilization, and Li+/Mg2+ competition in lymphoblastomas, neuroblastomas, and erythrocytes. During a 50 mmol/L Li+-loading incubation, Li+ accumulation at 30 min (mmoles Li+/L cells) was the greatest in lymphoblastomas (11.1±0.3), followed by neuroblastomas (9.3±0.5), and then erythrocytes (4.0±0.5). Li+ binding affinities to the plasma membrane in all three cell types were of the same order of magnitude; however, Li+ immobilization in intact cells was greatest in neuroblastomas and least in erythrocytes. When cells were loaded for 30 min in a 50 mmol/L Li+-containing medium, the percentage increase in free intracellular [Mg2+] in neuroblastoma and lymphoblastoma cells (~55 and ~52%, respectively) was similar, but erythrocytes did not exhibit any substantial increase (~6%). With the intracellular [Li+] at 15 mmol/L, the free intracellular [Mg2+] increased by the greatest amount in neuroblastomas (~158%), followed by lymphoblastomas (~75%), and then erythrocytes (~50%). We conclude that Li+ immobilization and transport are related to free intracellular [Mg2+] and to the extent of Li+/Mg2+ competition in a cell-specific manner.
publishDate 2003
dc.date.none.fl_str_mv 2003
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/3871
http://hdl.handle.net/10316/3871
https://doi.org/10.1016/j.bcp.2003.07.001
url http://hdl.handle.net/10316/3871
https://doi.org/10.1016/j.bcp.2003.07.001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochemical Pharmacology. 66:10 (2003) 1915-1924
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