Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice
The aim of this work was to evaluate if the intraperitoneal administration of the natural compound hesperidin, in a sedative dose, and neo-hesperidin, a hesperidin structural analog that exerts minor sedative effect, were able to induce changes in intracellular signaling cascades in different areas...
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todo:paper_00913057_v92_n2_p291_Martinez2023-10-03T14:54:59Z Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice Martínez, M.C. Fernandez, S.P. Loscalzo, L.M. Wasowski, C. Paladini, A.C. Marder, M. Medina, J.H. Viola, H. Hesperidin Mouse pαCaMKII pERK 1/2 Sedation calcium calmodulin dependent protein kinase calcium calmodulin dependent protein kinase ii alpha drug vehicle flavonoid glycoside hesperidin mitogen activated protein kinase 1 mitogen activated protein kinase 3 neohesperidin unclassified drug animal cell animal experiment animal model animal tissue article brain cortex cerebellum controlled study depression drug efficacy enzyme inactivation enzyme phosphorylation intracellular transport locomotion male mouse nonhuman priority journal sedation Animals Behavior, Animal Brain Hesperidin Hypnotics and Sedatives Male Mice Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 Phosphorylation Signal Transduction Mus The aim of this work was to evaluate if the intraperitoneal administration of the natural compound hesperidin, in a sedative dose, and neo-hesperidin, a hesperidin structural analog that exerts minor sedative effect, were able to induce changes in intracellular signaling cascades in different areas of the brain. The systemic administration of hesperidin produced a marked reduction in the phosphorylation state of extracellular signal-regulated kinases 1/2 (ERK 1/2), but not of Ca+2/calmodulin-dependent protein kinase II α subunit (αCaMKII), in the cerebral cortex, cerebellum and hippocampus. In contrast, neo-hesperidin did not markedly affect the activity of ERK 1/2 in both the cortex and the cerebellum. Taken together, these results demonstrated that intracellular signalling involving a selective decrease in ERK1/2 activation accompanied the depressant action of hesperidin. Even more, the low sedative action of neo-hesperidin correlates with a negligible decrease in phosphorylation state of ERK 1/2 (pERK 1/2), suggesting that low levels of pERK 1/2 in CNS could be a marker of sedative efficacy of flavonoids. © 2008 Elsevier Inc. All rights reserved. Fil:Martínez, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Viola, H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00913057_v92_n2_p291_Martinez |
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Universidad de Buenos Aires |
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I-28 |
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R-134 |
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Hesperidin Mouse pαCaMKII pERK 1/2 Sedation calcium calmodulin dependent protein kinase calcium calmodulin dependent protein kinase ii alpha drug vehicle flavonoid glycoside hesperidin mitogen activated protein kinase 1 mitogen activated protein kinase 3 neohesperidin unclassified drug animal cell animal experiment animal model animal tissue article brain cortex cerebellum controlled study depression drug efficacy enzyme inactivation enzyme phosphorylation intracellular transport locomotion male mouse nonhuman priority journal sedation Animals Behavior, Animal Brain Hesperidin Hypnotics and Sedatives Male Mice Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 Phosphorylation Signal Transduction Mus |
spellingShingle |
Hesperidin Mouse pαCaMKII pERK 1/2 Sedation calcium calmodulin dependent protein kinase calcium calmodulin dependent protein kinase ii alpha drug vehicle flavonoid glycoside hesperidin mitogen activated protein kinase 1 mitogen activated protein kinase 3 neohesperidin unclassified drug animal cell animal experiment animal model animal tissue article brain cortex cerebellum controlled study depression drug efficacy enzyme inactivation enzyme phosphorylation intracellular transport locomotion male mouse nonhuman priority journal sedation Animals Behavior, Animal Brain Hesperidin Hypnotics and Sedatives Male Mice Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 Phosphorylation Signal Transduction Mus Martínez, M.C. Fernandez, S.P. Loscalzo, L.M. Wasowski, C. Paladini, A.C. Marder, M. Medina, J.H. Viola, H. Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
topic_facet |
Hesperidin Mouse pαCaMKII pERK 1/2 Sedation calcium calmodulin dependent protein kinase calcium calmodulin dependent protein kinase ii alpha drug vehicle flavonoid glycoside hesperidin mitogen activated protein kinase 1 mitogen activated protein kinase 3 neohesperidin unclassified drug animal cell animal experiment animal model animal tissue article brain cortex cerebellum controlled study depression drug efficacy enzyme inactivation enzyme phosphorylation intracellular transport locomotion male mouse nonhuman priority journal sedation Animals Behavior, Animal Brain Hesperidin Hypnotics and Sedatives Male Mice Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 Phosphorylation Signal Transduction Mus |
description |
The aim of this work was to evaluate if the intraperitoneal administration of the natural compound hesperidin, in a sedative dose, and neo-hesperidin, a hesperidin structural analog that exerts minor sedative effect, were able to induce changes in intracellular signaling cascades in different areas of the brain. The systemic administration of hesperidin produced a marked reduction in the phosphorylation state of extracellular signal-regulated kinases 1/2 (ERK 1/2), but not of Ca+2/calmodulin-dependent protein kinase II α subunit (αCaMKII), in the cerebral cortex, cerebellum and hippocampus. In contrast, neo-hesperidin did not markedly affect the activity of ERK 1/2 in both the cortex and the cerebellum. Taken together, these results demonstrated that intracellular signalling involving a selective decrease in ERK1/2 activation accompanied the depressant action of hesperidin. Even more, the low sedative action of neo-hesperidin correlates with a negligible decrease in phosphorylation state of ERK 1/2 (pERK 1/2), suggesting that low levels of pERK 1/2 in CNS could be a marker of sedative efficacy of flavonoids. © 2008 Elsevier Inc. All rights reserved. |
format |
JOUR |
author |
Martínez, M.C. Fernandez, S.P. Loscalzo, L.M. Wasowski, C. Paladini, A.C. Marder, M. Medina, J.H. Viola, H. |
author_facet |
Martínez, M.C. Fernandez, S.P. Loscalzo, L.M. Wasowski, C. Paladini, A.C. Marder, M. Medina, J.H. Viola, H. |
author_sort |
Martínez, M.C. |
title |
Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
title_short |
Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
title_full |
Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
title_fullStr |
Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
title_full_unstemmed |
Hesperidin, a flavonoid glycoside with sedative effect, decreases brain pERK1/2 levels in mice |
title_sort |
hesperidin, a flavonoid glycoside with sedative effect, decreases brain perk1/2 levels in mice |
url |
http://hdl.handle.net/20.500.12110/paper_00913057_v92_n2_p291_Martinez |
work_keys_str_mv |
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