Early maternal deprivation retards neurodevelopment in Wistar rats

References

• Adler LE, Pachtman E, Franks RD, Pecevich M, Waldo MC, Freedman R. Neurophysiological evidence for a defect in neuronal mechanisms involved in sensory gating in schizophrenia. Biol Psychiatry 1982; 17649–17654
   Google Scholar
• Agid O, Shapira B, Zislin J, Ritsner M, Hanin B, Murad H, Troudart T, Bloch M, Heresco LU, Lerer B. Environment and vulnerability to major psychiatric illness: A case control study of early parental loss in major depression, bipolar disorder and schizophrenia. Mol Psychiatry 1999; 4(2)163–172
   PubMed Web of Science ®Google Scholar
• Barbeau D, Liang JJ, Robitalille Y, Quirion R, Srivastava LK. Decreased expression of the embryonic form of the neural cell adhesion molecule in schizophrenic brains. Proc Natl Acad Sci USA 1995; 92(7)2785–2789
   PubMedGoogle Scholar
• Baso ACZ, Goulart FC, Teodorov E, Felicio LF, Bernardi MM. Effects of maternal exposure to picrotoxin during lactation on physical and reflex development, square crossing and sexual behaviour of rat offspring. Pharmacol Biochem Behav 2003; 75(4)733–740
   PubMedGoogle Scholar
• Boksa P. Animal models of obstetric complications in relation to schizophrenia. Brain Res Rev 2004a; 45(1)1–17
   PubMedGoogle Scholar
• Boksa P. Animal models of obstetric complications in relation to schizophrenia. Brain Res Rev 2004b; 45(1)1–17
   PubMedGoogle Scholar
• Boksa P. Lasting effects of birth insult on dopamine function in animal models: Implications for schizophrenia and other disorders. Int J Neuropsychopharm 2004c; 7S76
   Google Scholar
• Bortolozzi AA, Duffard RO, de Duffard ME. Behavioral alterations induced in rats by a pre- and postnatal exposure to 2,4-dichlorophenoxyacetic acid. Neurotoxicol Teratol 1999; 21(4)451–465
   PubMed Web of Science ®Google Scholar
• Braff D, Stone C, Callaway E, Geyer MA, Glick ID, Bali L. Prestimulus effects of human startle reflex in normals and schizophrenics. Psychophysiology 1978; 15339–15343
   Google Scholar
• Braff DL, Grillon C, Geyer MA. Gating and habituation of the startle reflex in schizophrenic patients. Arch Gen Psychiatry 1992; 49(3)206–215
   PubMed Web of Science ®Google Scholar
• Broekkamp CL, Pijnenburg AJ, Cools AR, van RJ. The effect of microinjections of amphetamine into the neostriatum and the nucleus accumbens on self-stimulation behaviour. Psychopharmacologia 1975; 42(2)179–183
   PubMedGoogle Scholar
• Cannon M, Caspi A, Moffitt TE, Harrington H, Taylor A, Murray RM, Poulton R. Evidence for early-childhood, pan-developmental impairment specific to schizophreniform disorder—results from a longitudinal birth cohort. Arch Gen Psychiatry 2002; 59(5)449–456
   PubMed Web of Science ®Google Scholar
• Coleman CN, Mason T, Hooker EP, Robinson SE. Developmental effects of intermittent prenatal exposure to 1,1,1-trichloroethane in the rat. Neurotoxicol Teratol 1999; 21(6)699–708
   PubMedGoogle Scholar
• Coulter CL, Happe HK, Murrin LC. Postnatal development of the dopamine transporter: A quantitative autoradiographic study. Dev Brain Res 1996; 92172–92181
   Google Scholar
• Daenen EWPM, Wolterink G, Van der Heyden JA, Kruse CG, Van Ree JM. Neonatal lesions in the amygdala or ventral hippocampus disrupt prepulse inhibition of the acoustic startle response; implications for an animal model of neurodevelopmental disorders like schizophrenia. Eur Neuropsychopharmacol 2003; 13(3)187–197
   PubMedGoogle Scholar
• Degen SB, Ellenbroek BA, Wiegant VM, Cools AR. The development of various somatic markers is retarded in an animal model for schizophrenia, namely apomorphine-susceptible rats. Behav Brain Res 2005; 157(2)369–377
   PubMedGoogle Scholar
• Eilam D, Golani I. The ontogeny of exploratory-behavior in the house rat (Rattus-Rattus)—The mobility gradient. Dev Psychobiol 1988; 21(7)679–710
   PubMed Web of Science ®Google Scholar
• Ellenbroek BA, Cools AR. Maternal separation reduces latent inhibition in the conditioned taste aversion paradigm. Neurosci Res Comm 1995; 17(1)27–33
   Google Scholar
• Ellenbroek BA, Cools AR. The neurodevelopmental hypothesis of schizophrenia: Clinical evidence and animal models. Neurosci Res Comm 1998; 22(3)127–136
   Google Scholar
• Ellenbroek BA, Cools AR. The long-term effects of maternal deprivation depend on the genetic background. Neuropsychopharmacology 2000; 23(1)99–106
   PubMed Web of Science ®Google Scholar
• Ellenbroek BA, Cools AR. Animal models for schizophrenia. Textbook of biological psychiatry, H D'Haenen, JA den Boer, H Westenberg, P Willner. John Wiley & Sons, Chichester 2002a; 567–580
   Google Scholar
• Ellenbroek BA, Cools AR. Early maternal deprivation and prepulse inhibition—The role of the postdeprivation environment. Pharmacol Biochem Behav 2002b; 73(1)177–184
   PubMedGoogle Scholar
• Ellenbroek BA, de Bruin NMWJ, van Den Kroonenburg PT, van Luijtelaar ELJM, Cools AR. The effects of early maternal deprivation on auditory information processing in adult Wistar rats. Biol Psychiatry 2004; 55(7)701–707
   PubMedGoogle Scholar
• Ellenbroek BA, Riva MA. Early maternal deprivation as an animal model for schizophrenia. Clin Neurosci Res 2003; 3(4–5)297–302
   Google Scholar
• Ellenbroek BA. Simulation models for schizophrenia. Atypical antipsychotics, BA Ellenbroek, AR Cools. Birkhauser Verlag, Basel 2000; 121–142
   Google Scholar
• Ellenbroek BA, van den Kroonenberg PTJM, Cools AR. The effects of an early stressful life event on sensorimotor gating in adult rats. Schizophr Res 1998; 30(2)251–260
   PubMedGoogle Scholar
• Ferguson SA, Paule MG, Holson RR. Neonatal dexamethasone on day 7 in rats causes behavioral alterations reflective of hippocampal, but not cerebellar, deficits. Neurotoxicol Teratol 2001; 23(1)57–69
   PubMedGoogle Scholar
• Foley A, Ellenbroek B, Lubbers L, Cools A, Regan C. Role of NCAM polysialylation in the developmental emergence of learning mechanisms. Behav Pharmacol 2000; 11(3)337
   Google Scholar
• Frederiksen SO, Ekman R, Gottfries CG, Widerlov EJ, Jonsson S. Reduced concentrations of galanin, arginine vasopressin, neuropeptide Y and peptide YY in the temporal cortex but not in the hypothalamus of brains from schizophrenics. Acta Psychiatr Scand 1991; 83(4)273–277
   PubMed Web of Science ®Google Scholar
• Galineau L, Kodas E, Guilloteau D, Vilar MP, Chalon S. Ontogeny of the dopamine and serotonin transporters in the rat brain: An autoradiographic study. Neurosci Lett 2004; 363(3)266–271
   PubMedGoogle Scholar
• Gould E, Tanapat P. Stress and hippocampal neurogenesis. Biol Psychiatry 1999; 461472–461479
   Google Scholar
• Gramsbergen A, Mulder EJH. The influence of betamethasone and dexamethasone on motor development in young rats. Pediatr Res 1998; 44(1)105–110
   PubMedGoogle Scholar
• Hannigan JH. Effects of prenatal exposure to alcohol plus caffeine in rats—pregnancy outcome and early offspring development. Alcoholism-Clinical and Experimental Research 1995; 19(1)238–246
   PubMedGoogle Scholar
• Harris Harrison PJ, Law AJ, Eastwood SL. Glutamate receptors and transporters in the hippocampus in schizophrenia. 2003
   Google Scholar
• Husum H, Termeer E, Mathe AA, Bolwig TG, Ellenbroek BA. Early maternal deprivation alters hippocampal levels of neuropeptide Y and calcitonin-gene related peptide in adult rats. Neuropharmacology 2002; 42(6)798–806
   PubMedGoogle Scholar
• Ikonomidou Isohanni M, Jones P, Kemppainen L, Croudace T, Isohanni I, Veijola J, Rasanen S, Wahlberg KE, Tienari P, Rantakallio P. Childhood and adolescent predictors of schizophrenia in the Northern Finland 1966 Birth Cohort—A descriptive life-span model. Eur Arch Psychiatry Clin Neurosci 2000; 250(6)311–319
   PubMedGoogle Scholar
• Jones P. The early origins of schizophrenia. Br Med Bull 1997; 53(1)135–155
   PubMed Web of Science ®Google Scholar
• Jones P, Rodgers B, Murray R, Marmot M. Child development risk factors for adult schizophrenia in the British 1946 birth cohort. Lancet 1994; 344(8934)1398–1402
   PubMed Web of Science ®Google Scholar
• Jung AB, Bennett JP. Development of striatal dopaminergic function. I. Pre- and postnatal development of mRNA and binding sites for striatal D1 (D1a) and D2 (D2a) receptors. Dev Brain Res 1996; 109–120
   PubMedGoogle Scholar
• Koenig JI, Elmer GI, Shepard PD, Lee PR, Mayo C, Joy B, Hercher E, Brady DL. Prenatal exposure to a repeated variable stress paradigm elicits behavioral and neuroendocrinological changes in the adult offspring: Potential relevance to schizophrenia. Behav Brain Res 2005; 156(2)251–261
   PubMed Web of Science ®Google Scholar
• Kreider JC, Blumberg MS. Geotaxis in 2-week-old Norway rats (Rattus norvegicus): A reevaluation. Dev Psychobiol 1999; 35(1)35–42
   PubMedGoogle Scholar
• Kuczenski R, Segal DS. In vivo measures of monoamines during amphetamine-induced behaviors in rats. Prog Neuropsychopharmacol Biol Psychiatr 1990, 14 Suppl-50
   PubMedGoogle Scholar
• Kuwagata M, Nagao T. Behavior and reproductive function of rat male offspring treated prenatally with 5-bromo-2′-deoxyuridine. Reprod Toxicol 1998; 12(5)541–549
   PubMedGoogle Scholar
• Lammers C-H, Garcia-Borreguero D, Schmider J, Gotthardt U, Dettling M, Holsboer F, Heuser IJE. Combined dexamethasone/corticotropin-releasing hormone test in patients with schizophrenia and in normal controls II. Biol Psychiatr 1995; 38803–38807
   Google Scholar
• Levine S, Huchton DM, Wiener SG, Rosenfeld P. Time course of the effect of maternal deprivation on the hypothalamic-pituitary-adrenal axis in the infant rat. Dev Psychobiol 1991; 24(8)547–558
   PubMed Web of Science ®Google Scholar
• Lieberman JA, Kane JM, Alvir J. Provocative tests with psychostimulant drugs in schizophrenia. Psychopharmacology 1987; 91415–91533
   Google Scholar
• Lipska BK, Jaskiw GE, Weinberger DR. Postpubertal emergence of hyperresponsiveness to stress and to amphetamine after neonatal excitotoxic hippocampal damage: A potential animal model of schizophrenia. Neuropsychopharmacology 1993; 967–975
   Google Scholar
• Lubics A, Reglodi D, Tamas A, Kiss P, Szalai M, Szalontay L, Lengvari I. Neurological reflexes and early motor behaviour in rats subjected to neonatal hypoxic-ischemic injury. Behav Brain Res 2005; 157(1)157–165
   PubMedGoogle Scholar
• McCartney MA, Scinto PL, Wang SS, Altan S. Developmental effects of phenytoin may differ depending on sex of offspring. Neurotoxicol Teratol 1999; 21(2)119–128
   PubMedGoogle Scholar
• Meador-Woodruff J, Beneyto M, Kristiansen LV, McCullumsmith RE, Scarr E, Dean B. NMDA receptor subunit and associated PSD protein transcripts in hippocampus in schizophrenia and bipolar disorder. Schizophr Bull 2005; 31(2)291
   Google Scholar
• Meaney MJ, Brake W, Gratton A. Environmental regulation of the development of mesolimbic dopamine systems: A neurobiological mechanism for vulnerability to drug abuse?. Psychoneuroendocrinology 2002; 27(1–2)127–138
   PubMed Web of Science ®Google Scholar
• Mednick SA. Breakdown in individuals at high risk for schizophrenia: Possible predispositional perinatal factors. Mental Hygiene 1970; 5450–5463
   Google Scholar
• Park HJ, Lim S, Lee HS, Lee HJ, Yoo YM, Lee HJ, Kim SA, Yin CS, Seo JC, Chung JH. Acupuncture enhances cell proliferation in dentate gyrus of maternally-separated rats. Neurosci Lett 2002; 319(3)153–156
   PubMedGoogle Scholar
• Patin V, Vincent A, Lordi B, Caston J. Does prenatal stress affect the motoric development of rat pups?. Brain Res Dev Brain Res 2004; 149(2)85–92
   PubMedGoogle Scholar
• Penke Z, Felszeghy K, Fernette B, Sage D, Nyakas C, Burlet A. Postnatal maternal deprivation produces long-lasting modifications of the stress response, feeding and stress-related behaviour in the rat. Eur J Neurosci 2001; 14747–14755
   Google Scholar
• Pilowsky LS, Kerwin RW, Murray RM. Schizophrenia: A neurodevelopmental perspective. Neuropsychopharmacology 1993; 9(1)83–91
   PubMedGoogle Scholar
• Roceri M, Hendriks W, Racagni G, Ellenbroek BA, Riva MA. Early maternal deprivation reduces the expression of BDNF and NMDA receptor subunits in rat hippocampus. Mol Psychiatry 2002; 7(6)609–616
   PubMedGoogle Scholar
• Rots NY, de JJ, Workel JO, Levine S, Cools AR, de KE. Neonatal maternally deprived rats have as adults elevated basal pituitary-adrenal activity and enhanced susceptibility to apomorphine. J Neuroendocrinol 1996; 8(7)501–506
   PubMed Web of Science ®Google Scholar
• Schwabe K, Enkel T, Klein S, Schutte M, Koch M. Effects of neonatal lesions of the medial prefrontal cortex on adult rat behaviour. Behav Brain Res 2004; 153(1)21–34
   PubMed Web of Science ®Google Scholar
• Suchecki D, Mozaffarian D, Gross G, Rosenfeld P, Levine S. Effects of maternal deprivation on the ACTH stress response in the infant rat. Neuroendocrinology 1993; 57(2)204–212
   PubMed Web of Science ®Google Scholar
• Sulzer D, Sonders MS, Poulsen NW, Galli A. Mechanisms of neurotransmitter release by amphetamines: A review. Prog Neurobiol 2005; 75406–75433
   Google Scholar
• Tsuchida K, Akiyama K, Sakai K, Ujike H, Li X, Kuroda S. Ontogeny of striatal dopamine relase in rats after acutre administration of methamphetamine. Pharmacol Biochem Behav 1998; 53(3)575–580
   Google Scholar
• Walker EF, Savoie T, Davis D. Neuromotor precursors of schizophrenia. Schizophr Bull 1994; 20(3)441–451
   PubMedGoogle Scholar
• Weinberger DR. Implications of normal brain development for the pathogenesis of schizophrenia. Arch Gen Psychiatry 1987; 44(7)660–669
   PubMed Web of Science ®Google Scholar
• Weinberger DR. Cell biology of the hippocampal formation in schizophrenia. Biol Psychiatry 1999; 45(4)395–402
   PubMedGoogle Scholar
• Workel JO, Oitzl MS, Ledeboer A, de KE. The Brown Norway rat displays enhanced stress-induced ACTH reactivity at day 18 after 24 h maternal deprivation at day 3. Brain Res Dev Brain Res 1997; 103(2)199–203
   PubMedGoogle Scholar
• Zhang LX, Levine S, Dent G, Zhan YT, Xing GQ, Okimoto D, Gordon MK, Post RM, Smith MA. Maternal deprivation increases cell death in the infant rat brain. Developmental Brain Research 2002; 133(1)1–11
   PubMedGoogle Scholar
• Zimmerberg B, Shartrand AM. Temperature-dependent effects of maternal separation on growth, activity, and amphetamine sensitivity in the rat. Dev Psychobiol 1992; 25(3)213–226
   PubMedGoogle Scholar