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Título : The maintenance of hippocampal pyramidal neuron populations is dependent on the modulation of specific cell cycle regulators by thyroid hormones
Creador: Alva Sánchez C
Nivel de acceso: Open access
Palabras clave : Antitiroideos - farmacologia - ratas
Ciclo Celular - genética - ratas
Proteínas de Ciclo Celular - genética - ratas
Proteínas de Ciclo Celular - metabolismo - ratas
Proliferación de la Célula - genética - ratas
Supervivencia Celular - genética - ratas
Ciclina D1 - genética - ratas
Ciclina D1 - metabolismo - ratas
Inhibidor p21 de las Quinasas Dependientes de la Ciclina - genética - ratas
Inhibidor p21 de las Quinasas Dependientes de la Ciclina - metabolismo - ratas
Hipocampo - citología - ratas
Hipocampo - metabolismo - ratas
Hipotiroidismo - inducido químicamentea - ratas
Hipotiroidismo - metabolismo - ratas
Hipotiroidismo - fisiopatologia - ratas
Metimazol - farmacologia - ratas
Antígeno Nuclear de Célula en Proliferación - genética - ratas
Antígeno Nuclear de Célula en Proliferación - metabolismo - ratas
Proteínas Proto-Oncogénicas c-bcl-2 - genética - ratas
Proteínas Proto-Oncogénicas c-bcl-2 - metabolismo - ratas
Células Piramidales - citología - ratas
Células Piramidales - metabolismo - ratas
Ratas Wistar
Glándula Tiroides - efectos de drogas - ratas
Glándula Tiroides - metabolismo - ratas
Glándula Tiroides - fisiopatologia - ratas
Hormonas Tiroideas - metabolismo - ratas
Hormonas Tiroideas - farmacologia - ratas
Proteína p53 Supresora de Tumor - genética - ratas
Proteína p53 Supresora de Tumor - metabolismo - ratas
Proteína X Asociada a bcl-2 - genética - ratas
Proteína X Asociada a bcl-2 - metabolismo - ratas
Antithyroid Agents - pharmacology - rats
Cell Cycle - genetics - rats
Cell Cycle Proteins - genetics - rats
Cell Cycle Proteins - metabolism - rats
Cell Proliferation - genetics - rats
Cell Survival - genetics - rats
Cyclin D1 - genetics - rats
Cyclin D1 - metabolism - rats
Cyclin-Dependent Kinase Inhibitor p21 - genetics - rats
Cyclin-Dependent Kinase Inhibitor p21 - metabolism - rats
Hippocampus - cytology - rats
Hippocampus - metabolism - rats
Hypothyroidism - chemically induced - rats
Hypothyroidism - metabolism - rats
Hypothyroidism - physiopathology - rats
Methimazole - pharmacology - rats
Proliferating Cell Nuclear Antigen - genetics - rats
Proliferating Cell Nuclear Antigen - metabolism - rats
Proto-Oncogene Proteins c-bcl-2 - genetics - rats
Proto-Oncogene Proteins c-bcl-2 - metabolism - rats
Pyramidal Cells - cytology - rats
Pyramidal Cells - metabolism - rats
Rats, Wistar
Thyroid Gland - drug effects - rats
Thyroid Gland - metabolism - rats
Thyroid Gland - physiopathology - rats
Thyroid Hormones - metabolism - rats
Thyroid Hormones - pharmacology - rats
Tumor Suppressor Protein p53 - genetics - rats
Tumor Suppressor Protein p53 - metabolism - rats
bcl-2-Associated X Protein - genetics - rats
bcl-2-Associated X Protein/metabolism - rats
Apoptosis, Ciclina D1, PCNA, Bax/Bcl-2, Hipotiroidismo
Apoptosis Cycline D1 PCNA Bax/Bcl-2 Hypothyroidism
Descripción : The onset of adult hypothyroidism causes neuronal damage in the CA3 hippocampal region, which is attenuated by T(4) administration. We analyzed the expression of molecular proliferation markers (Cyclin D1 and PCNA), cellular damage-arrest (p53 and p21), and apoptosis (Bax/Bcl-2 index) in the hippocampus of hypothyroid (methimazole; 60 mg/kg) or thyroid replaced (T(4), 20 microg/kg; MMI+T(4) or T(3), 20 microg/kg; MMI+T(3)) adult male rats. Histological analysis showed that hypothyroid animals exhibit significant neuronal damage in all regions of the hippocampus accompanied by the triggering of the apoptotic pathway (increases in p53, p21 and the Bax/Bcl-2 index) and no changes in proliferation (Cyclin D1 and PCNA). MMI+T(4) replaced animals were completely protected with no changes in molecular markers. In contrast, MMI+T(3) replaced animals showed partial protection in which, although pro-apoptotic effects remained (increase in the Bax/Bcl-2), proliferative mechanisms were triggered (increase in p53, Cyclin D1 and PCNA expression). Our results indicate that thyroid hormones participate in the maintenance of the hippocampal neuronal population even in adulthood, suggesting that THs have different physiological roles as neuronal survival factors: T(4) prevents the activation of apoptotic pathways, whereas T(3) activates cell differentiation and proliferation mechanisms
Colaborador(es) u otros Autores: Sánchez-Huerta K
Arroyo-Helguera O
Anguiano B
Aceves C
Pacheco-Rosado J
Fecha de publicación : 2009
Tipo de publicación: Artículo
Formato: pdf
Identificador del Recurso : 10.1016/j.brainres.2009.02.043
Fuente: Brain Res 1271():27-35
URI : http://repositorio.pediatria.gob.mx:8180/handle/20.500.12103/2885
Idioma: eng
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