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Effects of repeated phencyclidine administration on adult hippocampal neurogenesis in the rat
Author(s) -
Liu Juan,
Suzuki Toshihito,
Seki Tatsunori,
Namba Takashi,
Tanimura Atsushi,
Arai Heii
Publication year - 2006
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.20275
Subject(s) - dentate gyrus , neurogenesis , hippocampal formation , subgranular zone , phencyclidine , neuroscience , hippocampus , granule cell , pharmacology , medicine , endocrinology , psychology , neural stem cell , nmda receptor , biology , stem cell , microbiology and biotechnology , receptor , subventricular zone
Dysfunctional maturation of neural networks, particularly hippocampus‐prefrontal networks, may be of particular interest in determining the pathophysiology of schizophrenia. Phencyclidine (PCP)‐induced symptoms in humans appear to offer a more complete model of schizophrenia than do amphetamine‐induced symptoms. This study investigated the effects of intermittent i.p. injections of PCP (7.5 mg/kg) on cell proliferation and survival of granule cells in the dentate gyrus of the rat brain using quantitative immunohistochemical techniques for 5‐bromo‐2′‐deoxyuridine (BrdU)‐positive cells. After repeated PCP injection for 14 days, mean scores for stereotyped behavior increased with the number of injections, while scores for ataxia and backpedaling as serotonergic behaviors gradually decreased. The number of BrdU‐positive cells decreased by 23% in the subgranular zone of the dentate gyrus by 24 h after repeated injections. However, decreased levels of BrdU‐positive cells returned to control levels within 1 week. Differentiation of newly formed cells was not influenced. Repeated PCP administration after BrdU injection did not exert any effects on survival of newly generated cells. These findings suggest that transient disturbances of cell proliferation in the dentate gyrus occur under PCP‐related behavioral abnormalities. Whether disturbed cell proliferation would thus be closely implicated in the development of behavioral sensitization induced by PCP administration is unclear, but this would possibly result from adaptation to new pharmacological conditions under behavioral sensitization or stressful conditions of PCP‐related abnormal behaviors. Further studies are required to elucidate the biological significance of hippocampal neurogenesis in the mechanisms underlying the development of cognitive dysfunctions and the psychosis of schizophrenia. Synapse 60:56–68, 2006. © 2006 Wiley‐Liss, Inc.