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Título : 24-hour rhythm in gene expression of redox pathway enzymes in rat hypothalamus : effect of melatonin treatment
Autor : Jiménez Ortega, Vanesa 
Cano Barquilla, Pilar 
Cardinali, Daniel Pedro 
Esquifino, Ana I. 
Palabras clave : MELATONINARITMO CIRCADIANOHIPOTALAMO MEDIOEXPRESION DE GENESCATALASAOXIDO NITRICO SINTASA
Fecha de publicación : 2009
Editorial : Taylor & Francis
Cita : Jiménez-Ortega, V., et al. 24-hour rhythm in gene expression of redox pathway enzymes in rat hypothalamus : effect of melatonin treatment [en línea]. Redox Report 2009, 14 (3). doi:10.1179/135100009X392548. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/1626
Resumen : Abstract: The 24-h changes in medial basal hypothalamic (MBH) gene expression of redox pathway enzymes nitric oxide synthase (NOS)-1 and NOS-2, heme oxygenase (HO)-1 and HO-2, Cu/Znand Mn-superoxide dismutases (SOD) and catalase were examined in adult male Wistar rats. Half of the animals received melatonin (ca. 60 μg/day) in the drinking water. After 1 month, rats were killed at six different time intervals, throughout a 24-h cycle. MBH mRNA levels were measured by real-time PCR analysis. In controls NOS-1 mRNA expression did not exhibit 24-h variations while NOS-2 gene expression peaked at the early light phase of cycle. MBH mRNA for both the inducible (HO-1) and constitutive (HO-2) isoforms of HO showed a significant 24 h pattern with a maximum at the middle of the dark phase or at the early light phase, respectively. None of mRNAs encoding Cu/Zn-SOD, Mn-SOD and catalase exhibited significant 24-h variations in rat MBH under control conditions. Chronic melatonin administration in the drinking water decreased significantly mRNAs for NOS-1, NOS-2, HO-1 and HO-2 as well as changed their 24-h profile. Melatonin augmented gene expression of the antioxidant enzymes Cu/Zn-SOD, Mn-SOD or catalase at certain time intervals only
URI : https://repositorio.uca.edu.ar/handle/123456789/1626
ISSN : 1351-0002 (impreso)
1743-2928 (online)
Disciplina: MEDICINA
DOI: 10.1179/135100009X392548
Derechos: Acceso Abierto
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