Neuronal and astroglial alterations in the hippocampus of a mouse model for type 1 diabetes

The influence of diabetes mellitus on brain pathology is increasingly recognized. Previous contributions of our laboratory demonstrated in models of type 1 diabetes (nonobese diabetic and streptozotocin (STZ)-treated mice), a marked astrogliosis and neurogenesis deficit in hippocampus and increased...

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Autor principal: Revsin, Y.
Otros Autores: Saravia, F., Roig, P., Lima, A., De Kloet, E.R, Homo-Delarche, F., De Nicola, A.F
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier 2005
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024 7 |2 cas  |a reduced nicotinamide adenine dinucleotide phosphate dehydrogenase, 9001-68-7; streptozocin, 18883-66-4 
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100 1 |a Revsin, Y. 
245 1 0 |a Neuronal and astroglial alterations in the hippocampus of a mouse model for type 1 diabetes 
260 |b Elsevier  |c 2005 
270 1 0 |m De Nicola, A.F.; Lab. of Neuroendocrine Biochemistry, Inst. de Biol. Y Med. Experimental, Obligado 2490, 1428, Buenos Aires, Argentina; email: denicola@dna.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a The influence of diabetes mellitus on brain pathology is increasingly recognized. Previous contributions of our laboratory demonstrated in models of type 1 diabetes (nonobese diabetic and streptozotocin (STZ)-treated mice), a marked astrogliosis and neurogenesis deficit in hippocampus and increased expression of hypothalamic neuropeptides. In the present investigation, we further analyzed alterations of astroglia and neurons in the hippocampus of mice 1 month after STZ-induced diabetes. Results showed that these STZ-diabetic mice presented: (a) increased number of astrocytes positive for apolipoprotein-E (Apo-E), a marker of ongoing neuronal dysfunction; (b) abnormal expression of early gene products associated with neuronal activation, including a high number of Jun + neurons in CA1 and CA3 layers and dentate gyrus, and of Fos-expressing neurons in CA3 layer; (c) augmented activity of NADPH-diaphorase, linked to oxidative stress, in CA3 region. These data support the concept that uncontrolled diabetes leads to hippocampal pathology, which adjoin to changes in other brain structures such as hypothalamus and cerebral cortex. © 2005 Elsevier B.V. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires, M011, TM048, M094 
536 |a Detalles de la financiación: Ministerio de Salud de la Nación, MSAL 
536 |a Detalles de la financiación: WB 88-252 
536 |a Detalles de la financiación: Fundación Antorchas 
536 |a Detalles de la financiación: This study was supported by an International agreement between CONICET-INSERM, NWO-WOTRO Grant (WB 88-252), University of Buenos Aires (TM048, M011 and M094), Antorchas Foundation and Beca Carrillo-Oñativia, Ministerio de Salud, Argentina. Appendix A 
593 |a Lab. of Neuroendocrine Biochemistry, Inst. of Biol. and Exp. Medicine, Obligado 2490, (1428) Buenos Aires, Argentina 
593 |a Department of Human Biochemistry, Faculty of Medicine, University of Buenos Aires, Argentina 
593 |a Department of Medical Pharmacology, Leiden University, Netherlands 
593 |a CNRS UMR 7059, University Paris 7/D. Diderot, Paris, France 
593 |a Lab. of Neuroendocrine Biochemistry, Inst. de Biol. Y Med. Experimental, Obligado 2490, 1428, Buenos Aires, Argentina 
690 1 0 |a APOLIPOPROTEIN-E, FOS, JUN, NADPH-DIAPHORASE 
690 1 0 |a ASTROCYTES 
690 1 0 |a DIABETES MELLITUS 
690 1 0 |a HIPPOCAMPUS 
690 1 0 |a NEURODEGENERATION 
690 1 0 |a NEURONS 
690 1 0 |a STREPTOZOTOCIN 
690 1 0 |a APOLIPOPROTEIN E 
690 1 0 |a GENE PRODUCT 
690 1 0 |a MOLECULAR MARKER 
690 1 0 |a PROTEIN C FOS 
690 1 0 |a PROTEIN C JUN 
690 1 0 |a REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE DEHYDROGENASE 
690 1 0 |a STREPTOZOCIN 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a BRAIN CORTEX 
690 1 0 |a BRAIN REGION 
690 1 0 |a CELL ACTIVATION 
690 1 0 |a CELL COUNT 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DENTATE GYRUS 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a FEMALE 
690 1 0 |a GENE EXPRESSION 
690 1 0 |a GENE MUTATION 
690 1 0 |a GENETIC ANALYSIS 
690 1 0 |a GENETIC LINKAGE 
690 1 0 |a HIPPOCAMPUS 
690 1 0 |a INSULIN DEPENDENT DIABETES MELLITUS 
690 1 0 |a MACROGLIA 
690 1 0 |a MOUSE 
690 1 0 |a NERVE CELL LESION 
690 1 0 |a NONHUMAN 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a STREPTOZOCIN DIABETES 
700 1 |a Saravia, F. 
700 1 |a Roig, P. 
700 1 |a Lima, A. 
700 1 |a De Kloet, E.R. 
700 1 |a Homo-Delarche, F. 
700 1 |a De Nicola, A.F. 
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