Behavioral and hippocampal changes after prenatal invasive interventions with possible relevance to schizophrenia

Behavioural Brain Research

Volumn 172, Issue 2, 2006, Pages 179-186

  Sprick, Ulrich ^a   von Wilmsdorff, Martina ^a   Bouvier, Marie Luise ^a   Schulz, Daniela ^a   Gaebel, Wolfgang ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Animal model; CA3; Fear; Hippocampus; Neurodevelopmental; Perseveration; Schizophrenia; Social interaction

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BEHAVIOR CHANGE; BRAIN; COGNITION; CONTROLLED STUDY; FEMALE; HIPPOCAMPUS; ILLUMINATION; LATENT PERIOD; LOCOMOTION; MALE; MAZE TEST; MORPHOLOGY; NEUROLOGIC DISEASE; NONHUMAN; PRENATAL CARE; PRIORITY JOURNAL; PROGENY; PYRAMIDAL NERVE CELL; RAT; RAT STRAIN; SCHIZOPHRENIA; SOCIAL BEHAVIOR; SOCIAL INTERACTION; TASK PERFORMANCE; WEIGHT GAIN;

AGE FACTORS; ANALYSIS OF VARIANCE; ANIMALS; CELL SIZE; DISCRIMINATION LEARNING; DISEASE MODELS, ANIMAL; EXPLORATORY BEHAVIOR; FEMALE; HIPPOCAMPUS; INJECTIONS, INTRAVENTRICULAR; KAINIC ACID; MALE; MOTOR ACTIVITY; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RATS; RATS, INBRED F344; REACTION TIME; RISK FACTORS; SCHIZOPHRENIA; SOCIAL BEHAVIOR;

EID: 33746642144     PISSN: 01664328     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbr.2006.03.014     Document Type: Article

References (39)

1. Akbarian S., Bunney Jr. W.E., Potkin S.G., Wigal S.B., Hagman J.O., Sandman C.A., et al. Altered distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase cells in frontal lobe of schizophrenics implies disturbances of cortical development. Arch Gen Psychiatry 50 (1993) 169-177
2. Akbarian S., Vinuela A., Kim J.J., Potkin S.G., Bunney Jr. W.E., and Jones E.G. Distorted distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase neurons in temporal lobe of schizophrenics implies anomalous cortical development. Arch Gen Psychiatry 50 (1993) 178-187
3. Akdag S.J., Nestor P.G., O'Donnell B.F., Niznikiewicz M.A., Shenton M.E., and McCarley R.W. The startle reflex in schizophrenia: habituation and personality correlates. Schizophr Res 64 (2003) 165-173
4. Arango C., Kirkpatrick B., and Koenig J. At issue: stress, hippocampal neuronal turnover and neuropsychiatric disorders. Schizophr Bull 27 (2001) 477-480
5. Arnold S.E., Franz B.R., Gur R.C., Gur R.E., Shapiro R.M., Moberg P.J., et al. Smaller neuron size in schizophrenia in hippocampal subfields that mediate cortical-hippocampal interactions. Am J Psychiatry 152 (1995) 738-748
6. Becker A., Grecksch G., Bernstein H.-G., Höllt V., and Bogerts B. Social behaviour in rats lesioned with ibotenic acid in the hippocampus: quantitative and qualitative analysis. Psychopharmacology 144 (1999) 333-338
7. Benes F.M., Sorensen I., and Bird E.D. Reduced neuronal size in posterior hippocampus of schizophrenic patients. Schizophr Bull 17 (1991) 597-608
8. Berger M.A., Barros V.G., Sarchi M.I., Tarazi F.I., and Antonelli M.C. Long-term effects of prenatal stress on dopamine and glutamate receptors in adult rat brain. Neurochem Res 27 (2002) 1525-1533
9. Boksa P., and El-Khodor B.F. Birth insult interacts with stress at adulthood to alter dopaminergic function in animal models: possible implications for schizophrenia and other disorders. Neurosci Biobehav Rev 27 (2003) 91-101
10. Borrell J., Vela J.M., Arevalo-Martin A., Molina-Holgado E., and Guaza C. Prenatal immune challenge disrupts sensorimotor gating in adult rats: implications for the etiopathogenesis of schizophrenia. Neuropsychopharmacology 26 (2002) 204-215
11. Bracha H.S., Torrey E.F., Gottesman I.I., Bigelow L.B., and Cunniff C. Second-trimester markers of fetal size in schizophrenia: a study of monozygotic twins. Am J Psychiatry 149 (1992) 1355-1361
12. Chambers R.A., Moore J., McEvoy J.P., and Levin E.D. Cognitive effects of neonatal hippocampal lesions in a rat model of schizophrenia. Neuropsychopharmacology 15 (1996) 587-594
13. Chapillon P., Patin V., Roy V., Vincent A., and Caston J. Effects of pre- and postnatal stimulation on developmental, emotional, and cognitive aspects in rodents: a review. Dev Psychobiol 41 (2002) 373-387
14. Csernansky J.G., Wang L., Jones D., Rastogi-Cruz D., Posener J.A., Heydebrand G., et al. Hippocampal deformities in schizophrenia characterized by high dimensional brain mapping. Am J Psychiatry 159 (2002) 2000-2006
15. Daenen E.W., Wolterink G., Gerrits M.A., and Van Ree J.M. Amygdala or ventral hippocampal lesions at two early stages of life differentially affect open field behaviour later in life; an animal model of neurodevelopmental psychopathological disorders. Behav Brain Res 131 (2002) 67-78
16. Daenen E.W., Wolterink G., Gerrits M.A., and Van Ree J.M. The effects of neonatal lesions in the amygdala or ventral hippocampus on social behaviour later in life. Behav Brain Res 136 (2002) 571-582
17. Dickerson F.B., Boronow J.J., Stallings C., Origoni A.E., Ruslanova I., and Yolken R.H. Association of serum antibodies to herpes simplex virus I with cognitive deficits in individuals with schizophrenia. Arch Gen Psychiatry 60 (2003) 466-472
18. El-Khodor B., and Boksa P. Cesarean section birth produces long term changes in dopamine D1 receptors and in stress-induced regulation of D3 and D4 receptors in the rat brain. Neuropsychopharmacology 5 (2001) 423-439
19. Gressens P., Muaku S.M., Besse L., Nsegbe E., Gallego J., Delpech B., et al. Maternal protein restriction early in rat pregnancy alters brain development in the progeny. Brain Res Dev Brain Res 103 (1997) 21-35
20. Jonsson S.A., Luts A., Guldberg-Kjaer N., and Brun A. Hippocampal pyramidal cell disarray correlates negatively to cell number: implications for the pathogenesis of schizophrenia. Eur Arch Psychiatry Clin Neurosci 47 (1997) 120-127
21. Kim S.H., Lee J.-M., Kim H.-P., Jang D.P., Shin Y.-W., Ha T.H., et al. Asymmetry analysis of deformable hippocampal model using the principal component in schizophrenia. Hum Brain Mapp 25 (2005) 361-369
22. Lebain P., Vabret A., Freymuth F., Brazo P., Chabot B., Dollfus S., et al. Borna disease virus and psychiatric disorders. Schizophr Res 7 (2002) 303-305
23. LePen G., Grottick A.J., Higgins G.A., Martin J.R., Jenck F., and Moreau J.-L. Spatial and associative learning deficits induced by neonatal excitotoxic hippocampal damage in rats: Further evaluation of an animal model of schizophrenia. Behav Pharmacol 11 (2000) 257-268
24. Limosin F., Rouillon F., Payan C., Cohen J.M., and Strub N. Prenatal exposure to influenza as a risk for adult schizophrenia. Acta Psychiatr Scand 107 (2003) 331-335
25. Lipska B.K., Jaskiw G.E., and Weinberger D.R. Postpubertal emergence of hyperresponsiveness to stress and to amphetamine after neonatal excitotoxic hippocampal damage: a potential animal model of schizophrenia. Neuropsychopharmacology 9 (1993) 67-75
26. Lipska B.K., Swerdlow N.R., Geyer M.A., Jaskiw G.E., Braff D.L., and Weinberger D.R. Neonatal excitotoxic hippocampal damage in rats causes post-pubertal changes in prepulse inhibition of startle and its disruption by apomorphine. Psychopharmacology 122 (1995) 35-43
27. Lipska B.K., Halim N.D., Segal P.N., and Weinberger D.R. Effects of reversible inactivation of the neonatal ventral hippocampus on behavior in the adult rat. J Neurosci 22 (2002) 2835-2842
28. Luebke J., St John J., and Galler J.R. Prenatal protein malnutrition results in increased frequency of miniature inhibitory synaptic currents in rat CA1 pyramidal cells. Synapse 37 (2000) 23-31
29. Palmer A.A., Printz D.J., Butler P.D., Dulawa S.C., and Printz M.P. Prenatal protein deprivation in rats induces changes in prepulse inhibition and NMDA receptor binding. Brain Res 996 (2004) 193-201
30. Pearce B.D. Schizophrenia and viral infection during neurodevelopment: a focus on mechanisms. Mol Psychiatry 6 (2001) 634-646
31. Pellegrino L.J., Pellegrino A.S., and Cushman A.J. A stereotaxic atlas of the rat brain (1979), Plenum Press, New York
32. Sams-Dodd F., Lipska B.K., and Weinberger D.R. Neonatal lesions of the rat ventral hippocampus result in hyperlocomotion and deficits in social behaviour in adulthood. Psychopharmacology 132 (1997) 303-310
33. Sheline Y.I., Wang P.W., Gado M.H., and Csernansky J.G. Hippocampal atrophy in recurrent major depression. Proc Natl Acad Sci USA 93 (1996) 3908-3913
34. Sprick U. Transient and long-lasting beneficial behavioral effects of grafts in the damaged hippocampus of rat. Behav Brain Res 42 (1991) 187-199
35. Starkman M.N., Gebarski S.S., Berent S., and Schteingart D.E. Hippocampal formation volume, memory dysfunction, and cortisol levels in patients with Cushing's syndrome. Biol Psychiatry 32 (1992) 756-765
36. Urakubo A., Jarskog L.F., Lieberman J.A., and Gilmore J.H. Prenatal exposure to maternal infection alters cytokine expression in the placenta, amniotic fluid and fetal brain. Schizophr Res 47 (2001) 27-36
37. Wahlbeck K., Forsen T., Osmond C., Barker D.J.P., and Eriksson J.G. Association of schizophrenia with low maternal body mass index, small size at birth, and thinness during childhood. Arch Gen Psychiatry 58 (2001) 48-52
38. Westergaard T., Mortensen P.B., Pedersen C.B., Wohlfahrt J., and Melbye M. Exposure to prenatal and childhood infections and the risk of schizophrenia: suggestions from a study of sibship characteristics and influenza prevalence. Arch Gen Psychiatry 56 (1999) 993-998
39. Wood S.J., Yucel M., Velakoulis D., Phillips L.J., Yung A.R., Brewer W., et al. Hippocampal and anterior cingulated morphology in subjects at ultra-high-risk psychosis: The role of family history of psychotic illness. Schizophr Res 75 (2005) 295-301