dc.creatorOliveira S.A.
dc.creatorFontanelli B.A.F.
dc.creatorStefanini M.A.
dc.creatorChuffa L.G.A.
dc.creatorTeixeira G.R.
dc.creatorLizarte F.S.N.
dc.creatorTirapelli L.F.
dc.creatorQuitete V.H.A.
dc.creatorMatheus S.M.M.
dc.creatorPadovani C.R.
dc.creatorMartinez M.
dc.creatorMartinez F.E.
dc.date2014
dc.date2015-06-25T17:56:46Z
dc.date2015-11-26T14:46:14Z
dc.date2015-06-25T17:56:46Z
dc.date2015-11-26T14:46:14Z
dc.date.accessioned2018-03-28T21:55:50Z
dc.date.available2018-03-28T21:55:50Z
dc.identifier
dc.identifierMicroscopy Research And Technique. , v. 77, n. 1, p. 44 - 51, 2014.
dc.identifier1059910X
dc.identifier10.1002/jemt.22311
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84890430046&partnerID=40&md5=281f86bbedf5d7233b03a219fc81d81b
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/87112
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/87112
dc.identifier2-s2.0-84890430046
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1252760
dc.descriptionMaternal care is the main source of signals and stimuli for proper development, growth, and production of adjustment responses to stressful factors. Adverse experiences in childhood are associated with a vulnerability to developing abusive ethanol ingestion via alterations of the response of the hypothalamic-pituitary-adrenal axis. Alcoholism causes global brain abnormalities, with the cerebellum being one of the most susceptible areas. We evaluated the effect of maternal separation on the cerebellum structure of male UCh rats. Adult male UChA (low 10% ethanol consumption) and UChB (high 10% ethanol consumption) rats were divided in to four experimental groups: (1) UChA, (2) UChA maternal separation (MS), (3) UChB, and (4) UChB MS. The MS occurred between the 4th and 14th days of age, for 240 min day-1. Euthanasia was performed at 120 days of age. An image analysis system was used to measure cerebellar cortical height and Purkinje cellular area and height in five rats from each group. The cerebellar sections were stained with antibodies against IGFR-I. MS did not alter the ethanol consumption of UChA and UChB rats. Corticosterone level was significantly higher in UChA MS and UChB MS rats than in UChA and UChB rats. The Purkinje cellular area and height were higher in UChA MS rats. IGFR-I expression was observed in the cortical glomerular area of UChA MS and UChB MS rats. MS altered the Purkinje cells in the cerebella of male UCh rats. Microsc. Res. Tech. 77:44-51, 2014. © 2013 Wiley Periodicals, Inc.
dc.description77
dc.description1
dc.description44
dc.description51
dc.descriptionAmorim, J.P., Chuffa, L.G., Teixeira, G.R., Mendes, L.O., Fioruci, B.A., Martins, O.A., Mello Jr, W., Martinez, F.E., Variations in maternal care alter corticosterone and 17beta-estradiol levels, estrous cycle and folliculogenesis and stimulate the expression of estrogen receptors alpha and beta in the ovaries of UCh rats (2011) Reprod Biol Endocrinol, 9, p. 160
dc.descriptionApfel, M.I., Esberard, C.A., Rodrigues, F.K., Bahamad Jr, F.M., Sillero, R.O., Stereologic study of the cerebellar Purkinje cells submitted to alcoholic intoxication in Wistar rats (2002) Arq Neuropsiquiatr, 60, pp. 258-263
dc.descriptionBanzatto, A.D., Kronka, S.N., (1989) Experimentação agrícola, p. 247. , Jaboticabal: Funep
dc.descriptionBasavarajappa, B.S., Saito, M., Cooper, T.B., Hungund, B.L., Stimulation of cannabinoid receptor agonist 2-arachidonylglycerol by chronic ethanol and its modulation by specific neuromodulators in cerebellar granule neurons (2000) Biochim Biophys Acta, 1535, pp. 78-86
dc.descriptionBjorntorp, P., Rosmond, R., Obesity and cortisol (2000) Nutrition, 16, pp. 924-936
dc.descriptionBondy, C.A., Tansiente IGF-I gene expression during the maturation of functionally related central projection neurons (1991) J Neurosci, 11, pp. 3442-3455
dc.descriptionBonthius, D.J., West, J.R., Alcohol induced neuronal loss in developing rats: Increased brain damage with binge exposure (1990) Alcohol Clin Exp Res, 14, pp. 107-118
dc.descriptionButler, T.R., Prendergast, M.A., Neuroadaptarions in adenosine receptor signaling following long-term ethanol exposure and withdrawal (2012) Alcohol Clin Exp Res, 36, pp. 4-13
dc.descriptionCaldji, C., Tannenbaum, B., Sharma, S., Francis, D., Plotsky, P.M., Meaney, M.J., Maternal care during infancy regulates the development of neural systems mediating the expression of fearfulness in the rat (1998) Proc Natl Acad Sci USA, 95, pp. 5335-5340
dc.descriptionCharness, M.E., Simon, R.P., Greenberg, D.A., Ethanol and the nervous system (1989) N Engl J Med, 321, pp. 442-454
dc.descriptionChocyk, A., Dudys, D., Przyborowska, A., Majcher, I., Mackowiak, M., Wedzony, K., Maternal separation affects the number, proliferation and apoptosis of glia cells in the substantia nigra and ventral tegmental area of juvenile rats (2011) Neuroscience, 173, pp. 1-18
dc.descriptionChuffa, L.G., Amorim, J.P., Teixeira, G.R., Mendes, L.O., Fioruci, B.A., Pinheiro, P.F.F., Seiva, F.R.F., Martinez, F.E., Long-term exogenous melatonin treatment modulates overall feed efficiency and protects ovarian tissue against injuries caused by ethanol-induced oxidative stress in adult UChB rats (2011) Alcohol Clin Exp Res, 35, pp. 1498-1508
dc.descriptionChung, Y.H., Shin, C.M., Joo, K.M., Kim, M.J., Cha, C.I., Region-specific alterations in insulin-like growth factor receptor type I in the cerebral cortex and hippocampus of aged rats (2002) Brain Res, 946, pp. 307-313
dc.descriptionDe LA Monte, S.M., Tong, M., Cohen, A.C., Sheedy, D., Harper, C., Wands, J.R., Insulin and insulin-like growth factor resistance in alcoholic neurodegeneration (2008) Alcohol Clin Exp Res, 32, pp. 1630-1644
dc.descriptionEmanuele, M.A., Emanuele, N., Alcohol and the male reproductive system (2001) Alcohol Res Health, 25, pp. 234-245
dc.descriptionFrancis, D.D., Kuhar, M.J., Frequency of maternal licking and grooming correlates negatively with vulnerability to cocaine and alcohol use in rats (2008) Pharmacol Biochem Behav, 90, pp. 497-500
dc.descriptionFrancis, D.D., Champagne, F.A., Liu, D., Meaney, M.J., Maternal care, gene expression, and the development of individual differences in stress reactivity (1999) Ann N Y Acad Sci, 896, pp. 66-84
dc.descriptionFrancis, D.D., Diorio, J., Liu, D., Meaney, M.J., Nongenomic transmission across generations of maternal behavior and stress responses in the rat (1999) Science, 286, pp. 1155-1158
dc.descriptionGluckman, P.D., Hanson, M.A., Spencer, H.G., Bateson, P., Environmental influences during development and their later consequences for health and disease: Implications for the interpretation of empirical studies (2005) Proc R Soc B, 272, pp. 671-677
dc.descriptionGoodlett, C.R., Marcassen, B.L., West, J.R., A single day of alcohol exposure during the brain spurt induces microcephaly and cerebellar Purkinje cell loss (1990) Alcohol, 7, pp. 107-114
dc.descriptionGordon, H.W., Early environmental stress and biological vulnerability to drug abuse (2002) Psychoneuroendocrinology, 27, pp. 115-126
dc.descriptionGustafsson, L., Nylander, I., Time-dependent alterations in ethanol intake in male Wistar rats exposed to short and prolonged daily maternal separation in a 4-bottle free-choice paradigm (2006) Alcohol Clin Exp Res, 30, pp. 2008-2016
dc.descriptionHamre, K.M., West, J.R., The effects of the timing of ethanol exposure during the brain growth spurt on the number of cerebellar Purkinje and granule cell nuclear profiles (1993) Alcohol Clin Exp Res, 17, pp. 610-622
dc.descriptionHwang, I.K., Yoo, K.Y., Park, S.K., An, S.J., Lee, J.Y., Choi, S.Y., Kang, J.H., Won, M.H., Expression and changes of endogenous insulin-like growth factor-1 in neurons and glia in the gerbil hippocampus and dentate gyrus after ischemic insult (2004) Neurochem Int, 45, pp. 149-156
dc.descriptionIdrus, N.M., Napper, R.M.A., Acute and long-term Purkinje cell loss following a single ethanol binge during the early third trimester equivalent in the rat (2012) Alcohol Clin Exp Res, 36, pp. 1365-1373
dc.descriptionKarhunen, P.J., Erkinjuntti, T., Laippala, P., Moderate alcohol consumption and loss of cerebellar Purkinje cells (1994) Br Med J, 308, pp. 1663-1667
dc.descriptionKozlov, A.P., Nizhnikov, M.E., Varlinskaya, E.I., Spear, N.E., The role of social isolation in ethanol effects on the preweanling rat (2012) Behav Brain Res, 227, pp. 43-57
dc.descriptionKremer, R., (2007) Efeitos da separação maternal e do alcoolismo no testículo de ratos UChA e UChB (bebedores voluntários de etanol a 10%), , dissertação Botucatu: Instituto de Biociências, Universidade Estadual Paulista
dc.descriptionLan, N., Hellemans, K.G.C., Ellis, L., Viau, V., Weinberg, J., Role of testosterone in mediating prenatal ethanol effects on hypothalamic-pituitary-adrenal activity in male rats (2009) Psychoneuroendocrinology, 34, pp. 1314-1328
dc.descriptionLangeland, W., Draijer, N., Van Den Brink, W., Psychiatric comorbidity in treatment-seeking alcoholics: The role of childhood trauma and perceived parental dysfunction (2004) Alcohol Clin Exp Res, 28, pp. 441-447
dc.descriptionLee, K.Y., Miki, T., Yokoyama, T., Ueki, M., Warita, K., Suzuki, S., Ohta, A.I., Takeuchi, Y., Neonatal repetitive maternal separation causes long-lasting alterations in various neurotrophic factor expression in the cerebral cortex of rats (2012) Life Sci, 90, pp. 578-584
dc.descriptionLehmann, J., Russig, H., Feldon, J., Pryce, C.R., Effect of a single maternal separation at different pup ages on the corticosterone stress response in adult and aged rats (2002) Pharmacol Biochem Behav, 73, pp. 141-145
dc.descriptionLevine, S., Primary social relationships influence the development of the hypothalamicpituitary-adrena axis in the rat (2001) Physiol Behav, 73, pp. 255-260
dc.descriptionLiu, D., Diorio, J., Tannenbaum, B., Caldji, C., Francis, D., Freedman, A., Sharma, S., Meaney, M.J., Maternal care, hippocampal glucocorticoid receptors, and hypothalamic-pituitary-adrenal responses to stress (1997) Science, 277, pp. 1659-1662
dc.descriptionLlorente, R., Gallardo, M.L., Berzal, A.L., Prada, C., Garcia-Segura, L.M., Early maternal deprivation in rats induces gender-dependent effects on developing hippocampal and cerebellar cells (2009) Int J Dev Neurosci, 27, pp. 233-241
dc.descriptionLuo, J., Mechanisms of ethanol-induced death of cerebellar granule cells (2012) Cerebellum, 11, pp. 145-154
dc.descriptionMardones, J., Segovia-Riquelme, N., Thirty-two years of selection of rats by ethanol preference: UChA and UChB strains (1983) Neurobehav Toxicol Teratol, 5, pp. 171-178
dc.descriptionMarks, J.L., Porte Jr, D., Baskin, D.G., Localization of type I insulin-like growth factor receptor messenger RNA in the adult rat brain by in situ hybridization (1991) Mol Endocrinol, 5, pp. 1158-1168
dc.descriptionMartins, O.A., (2007) Estresse, alcoolismo e vitamina E: Avaliação de parâmetros bioquímicos e morfofisiologia prostática, , tese. Botucatu: Instituto de Biociências, Universidade Estadual Paulista
dc.descriptionMatos, A.F.G., Moreira, R.O., Guedes, R.P., Aspectos neuroendócrinos da síndrome metabólica (2003) Arq Bras Endocrinol Metab, 47, pp. 410-421
dc.descriptionMeijer, O.C., Understanding stress through the genome (2006) Stress, 9, pp. 61-67
dc.descriptionMhatre, M.C., Pena, G., Sieghart, W., Ticku, M.K., Antibodies specific for GABAA receptor alpha subunits reveal that chronic alcohol treatment down-regulates alpha-subunit expression in rat brain regions (1993) J Neurochem, 61, pp. 1620-1625
dc.descriptionMiki, T., Harris, S., Wilce, P., Takeuchi, Y., Bedi, K.S., The effect of the timing of ethanol exposure during early postnatal life on total number of Purkinje cells in rat cerebellum (1999) J Anat, 194, pp. 423-431
dc.descriptionMiles, M.F., Diaz, J.E., DeGuzman, V.S., Mechanisms of neuronal adaptation to ethanol. Ethanol induces Hsc70 gene transcription in NG108-15 neuroblastoma x glioma cells (1991) J Biol Chem, 266, pp. 2409-2414
dc.descriptionNemeroff, D.C., Neurobiological consequences of childhood trauma (2004) J Clin Psychiatry, 65, pp. 18-28
dc.descriptionOreland, S., Raudkivi, K., Oreland, L., Harro, J., Arborelius, L., Nylander, I., Ethanol-induced effects on the dopamine and serotonin systems in adult Wistar rats are dependent on early-life experiences (2011) Brain Res, 1405, pp. 57-68
dc.descriptionPauli, J., Wilce, P., Bedi, K.S., Acute exposure to alcohol during early postnatal life causes a deficit in the total number of cerebellar Purkinje cells in the rat (1995) J Comp Neurol, 360, pp. 506-512
dc.descriptionPautassi, R.M., Camarini, R., Quadros, I.M., Miczek, K.A., Israel, Y., Genetic and environmental influences on ethanol consumption: Perspectives from preclinical research (2010) Alcohol Clin Exp Res, 34, pp. 976-987
dc.descriptionPentney, R.J., Dlugos, C.A., Cerebellar Purkinje neurons with altered terminal dendritic segments are present in all lobules of the cerebella vermis of ageing, ethanol-treated F344 rats (2000) Alcohol Alcohol, 1, pp. 35-43
dc.descriptionPierce, D.R., Hayar, A., Williams, D.K., Light, K.E., Olivary climbing fiber alterations in PN40 rat cerebellum following postnatal ethanol exposure (2011) Brain Res, 1378, pp. 54-65
dc.descriptionPinheiro, P.F.F., Segatelli, T.M., Almeida Francia, C.C.D., Martinez, M., Padovani, C.R., Franchi, M.R., Martinez, F.E., Morphologic changes in the urethral epithelium in an ethanol-drinking rat strain (UChA and UChB) (2007) Micron, 38, pp. 734-746
dc.descriptionQuintanilla, M.E., Israel, Y., Sapag, A., Tampier, L., The UChA and UChB rat lines: Metabolic and genetic differences influencing ethanol intake (2006) Addict Biol, 11, pp. 310-323
dc.descriptionRamezani, A., Goudarzi, I., Lashkarboluki, T., Ghorbanian, M.T., Abrari, K., Salmani, M.E., Role of oxidative stress in ethanol-induced neurotoxicity in the developing cerebellum (2012) Iran J Basic Med Sci, 15, p. 965
dc.descriptionSchmidt, M., Enthoven, L., Van Woezik, J.H., Levine, S., de Kloet, E.R., Oitzl, M.S., The dynamics of the hypothalamic-pituitary-adrenal axis during maternal deprivation (2004) J Neuroendocrinol, 16, pp. 52-57
dc.descriptionSmith, M.A., Kim, S., Van Oers, H.J.J., Levine, S., Maternal deprivation and stress induce immediate early genes in the infant rat brain (1997) Endocrinology, 138, pp. 4622-4628
dc.descriptionSonntag, W.E., Lynch, C.D., Bennett, S.A., Khan, A.S., Thornton, P.L., Cooney, P.T., Ingram, R.L., Brunso-Bechtold, J.K., Alterations in insuline-like growth factor receptors in the brains of ageing rats (1999) Neuroscience, 88, pp. 269-279
dc.descriptionSpencer, R.L., McEwen, B.S., Adaptation of the hypothalamic-pituitary-adrenal axis to chronic ethanol stress (1990) Neuroendocrinoly, 52, pp. 481-489
dc.descriptionSzyf, M., Weaver, I.C., Champagne, F.A., Diorio, J., Meaney, M.J., Maternal programming of steroid receptor expression and phenotype through DNA methylation in the rat (2005) Front Neuroendocrinol, 26, pp. 139-162
dc.descriptionTampier, L., Quintanilla, M.E., Mardones, J., Acute tolerance, alcohol sensivity and drinking pattern in the F2 generation of UChA and UChB rats (2000) J Stud Alcohol, 61, pp. 647-651
dc.descriptionWest, J.R., Hamre, K.M., Pierce, D.R., Delay in brain development induced by alcohol in artificially reared rat pups (1984) Alcohol, 1, pp. 213-222
dc.descriptionYeomans, M.R., Effects of alcohol on food and energy intake in human subjects: Evidence for passive and active over-consumption of energy (2004) Br J Nutr, 92, pp. 531-534
dc.descriptionZhang, J., Qin, L., Zhao, H., Early repeated maternal separation induces alterations of hippocampus reelin expression in rats (2013) J Biosci, 38, pp. 27-33
dc.descriptionZhang, L.X., Levine, S., Dent, G., Zhan, Y., Xing, G., Okimoto, D., Gordon, M.K., Smith, M.A., Maternal deprivation increases cell death in the infant rat brain (2002) Dev Brain Res, 131, pp. 1-11
dc.languageen
dc.publisher
dc.relationMicroscopy Research and Technique
dc.rightsfechado
dc.sourceScopus
dc.titleInteraction Of Maternal Separation On The Uch Rat Cerebellum
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución