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Neonatal phencyclidine administration and post-weaning social isolation as a dual-hit model of ‘schizophrenia-like’ behaviour in the rat

Rationale Schizophrenia is a debilitating disorder comprising positive, negative and cognitive deficits with a poorly defined neurobiological aetiology; therefore, animal models with greater translational reliability are essential to develop improved therapies. Objectives This study combines two dev...

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Published in:Psychopharmacology 2014-06, Vol.231 (12), p.2533-2545
Main Authors: Gaskin, Philip LR, Alexander, Stephen PH, Fone, Kevin CF
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description Rationale Schizophrenia is a debilitating disorder comprising positive, negative and cognitive deficits with a poorly defined neurobiological aetiology; therefore, animal models with greater translational reliability are essential to develop improved therapies. Objectives This study combines two developmental challenges in rats, neonatal phencyclidine (PCP) injection and subsequent rearing in social isolation from weaning, to attempt to produce more robust behavioural deficits with greater translational relevance to schizophrenia than either challenge alone. Methods Forty-two male Lister-hooded rat pups received the N -methyl- d -aspartate (NMDA) receptor antagonist, phencyclidine (PCP, 10 mg/kg, s.c.), or vehicle on post-natal day (PND) 7, 9 and 11 and were weaned on PND 23 into group housing (saline-treated n  = 11 or PCP-treated n  = 10) or isolation (saline n  = 10 or PCP n  = 11). Six weeks post-weaning, novelty- and PCP-induced (3.2 mg/kg) locomotor activity, novel object discrimination, prepulse inhibition of acoustic startle and contextual memory in a conditioned emotion response (CER) were recorded. Results Isolation rearing alone significantly elevated baseline locomotor activity and induced visual recognition memory impairment in novel object discrimination. Neonatal PCP treatment did not induce locomotor sensitisation to a subsequent acute PCP injection, but it impaired prepulse inhibition when combined with isolation rearing. CER freezing behaviour was significantly reduced by isolation rearing but an even greater effect occurred when combined with neonatal PCP treatment. Conclusions Neonatal PCP and isolation rearing both produce behavioural deficits in adult rats, but combined treatment caused a wider range of more severe cognitive impairments, providing a more comprehensive preclinical model to determine the neurobiological aetiology of schizophrenia than either treatment alone.
doi_str_mv 10.1007/s00213-013-3424-y
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Objectives This study combines two developmental challenges in rats, neonatal phencyclidine (PCP) injection and subsequent rearing in social isolation from weaning, to attempt to produce more robust behavioural deficits with greater translational relevance to schizophrenia than either challenge alone. Methods Forty-two male Lister-hooded rat pups received the N -methyl- d -aspartate (NMDA) receptor antagonist, phencyclidine (PCP, 10 mg/kg, s.c.), or vehicle on post-natal day (PND) 7, 9 and 11 and were weaned on PND 23 into group housing (saline-treated n  = 11 or PCP-treated n  = 10) or isolation (saline n  = 10 or PCP n  = 11). Six weeks post-weaning, novelty- and PCP-induced (3.2 mg/kg) locomotor activity, novel object discrimination, prepulse inhibition of acoustic startle and contextual memory in a conditioned emotion response (CER) were recorded. Results Isolation rearing alone significantly elevated baseline locomotor activity and induced visual recognition memory impairment in novel object discrimination. Neonatal PCP treatment did not induce locomotor sensitisation to a subsequent acute PCP injection, but it impaired prepulse inhibition when combined with isolation rearing. CER freezing behaviour was significantly reduced by isolation rearing but an even greater effect occurred when combined with neonatal PCP treatment. Conclusions Neonatal PCP and isolation rearing both produce behavioural deficits in adult rats, but combined treatment caused a wider range of more severe cognitive impairments, providing a more comprehensive preclinical model to determine the neurobiological aetiology of schizophrenia than either treatment alone.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-013-3424-y</identifier><identifier>PMID: 24402141</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acoustic Stimulation ; Animal behavior ; Animals ; Animals, Newborn ; Biomedical and Life Sciences ; Biomedicine ; Complications and side effects ; Conditioning (Psychology) ; Disease Models, Animal ; Dosage and administration ; Drug therapy ; Emotions ; Excitatory Amino Acid Antagonists - administration &amp; dosage ; Freezing Reaction, Cataleptic ; Male ; Memory ; Motor Activity - drug effects ; Neuropsychological Tests ; Neurosciences ; Original Investigation ; Pattern Recognition, Visual ; Pharmacology/Toxicology ; Phencyclidine ; Phencyclidine - administration &amp; dosage ; Prepulse Inhibition ; Psychiatry ; Psychopharmacology ; Rats ; Rodents ; Schizophrenia ; Schizophrenia - physiopathology ; Social Isolation</subject><ispartof>Psychopharmacology, 2014-06, Vol.231 (12), p.2533-2545</ispartof><rights>Springer-Verlag Berlin Heidelberg 2014</rights><rights>COPYRIGHT 2014 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-649c07b7a24c8e9cc6556ee351e9e1290f9c263e07c1f286e8647d7c184275473</citedby><cites>FETCH-LOGICAL-c472t-649c07b7a24c8e9cc6556ee351e9e1290f9c263e07c1f286e8647d7c184275473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24402141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gaskin, Philip LR</creatorcontrib><creatorcontrib>Alexander, Stephen PH</creatorcontrib><creatorcontrib>Fone, Kevin CF</creatorcontrib><title>Neonatal phencyclidine administration and post-weaning social isolation as a dual-hit model of ‘schizophrenia-like’ behaviour in the rat</title><title>Psychopharmacology</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Rationale Schizophrenia is a debilitating disorder comprising positive, negative and cognitive deficits with a poorly defined neurobiological aetiology; therefore, animal models with greater translational reliability are essential to develop improved therapies. Objectives This study combines two developmental challenges in rats, neonatal phencyclidine (PCP) injection and subsequent rearing in social isolation from weaning, to attempt to produce more robust behavioural deficits with greater translational relevance to schizophrenia than either challenge alone. Methods Forty-two male Lister-hooded rat pups received the N -methyl- d -aspartate (NMDA) receptor antagonist, phencyclidine (PCP, 10 mg/kg, s.c.), or vehicle on post-natal day (PND) 7, 9 and 11 and were weaned on PND 23 into group housing (saline-treated n  = 11 or PCP-treated n  = 10) or isolation (saline n  = 10 or PCP n  = 11). Six weeks post-weaning, novelty- and PCP-induced (3.2 mg/kg) locomotor activity, novel object discrimination, prepulse inhibition of acoustic startle and contextual memory in a conditioned emotion response (CER) were recorded. Results Isolation rearing alone significantly elevated baseline locomotor activity and induced visual recognition memory impairment in novel object discrimination. Neonatal PCP treatment did not induce locomotor sensitisation to a subsequent acute PCP injection, but it impaired prepulse inhibition when combined with isolation rearing. CER freezing behaviour was significantly reduced by isolation rearing but an even greater effect occurred when combined with neonatal PCP treatment. 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Objectives This study combines two developmental challenges in rats, neonatal phencyclidine (PCP) injection and subsequent rearing in social isolation from weaning, to attempt to produce more robust behavioural deficits with greater translational relevance to schizophrenia than either challenge alone. Methods Forty-two male Lister-hooded rat pups received the N -methyl- d -aspartate (NMDA) receptor antagonist, phencyclidine (PCP, 10 mg/kg, s.c.), or vehicle on post-natal day (PND) 7, 9 and 11 and were weaned on PND 23 into group housing (saline-treated n  = 11 or PCP-treated n  = 10) or isolation (saline n  = 10 or PCP n  = 11). Six weeks post-weaning, novelty- and PCP-induced (3.2 mg/kg) locomotor activity, novel object discrimination, prepulse inhibition of acoustic startle and contextual memory in a conditioned emotion response (CER) were recorded. Results Isolation rearing alone significantly elevated baseline locomotor activity and induced visual recognition memory impairment in novel object discrimination. Neonatal PCP treatment did not induce locomotor sensitisation to a subsequent acute PCP injection, but it impaired prepulse inhibition when combined with isolation rearing. CER freezing behaviour was significantly reduced by isolation rearing but an even greater effect occurred when combined with neonatal PCP treatment. Conclusions Neonatal PCP and isolation rearing both produce behavioural deficits in adult rats, but combined treatment caused a wider range of more severe cognitive impairments, providing a more comprehensive preclinical model to determine the neurobiological aetiology of schizophrenia than either treatment alone.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>24402141</pmid><doi>10.1007/s00213-013-3424-y</doi><tpages>13</tpages></addata></record>
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source SPORTDiscus; Springer Link
subjects Acoustic Stimulation
Animal behavior
Animals
Animals, Newborn
Biomedical and Life Sciences
Biomedicine
Complications and side effects
Conditioning (Psychology)
Disease Models, Animal
Dosage and administration
Drug therapy
Emotions
Excitatory Amino Acid Antagonists - administration & dosage
Freezing Reaction, Cataleptic
Male
Memory
Motor Activity - drug effects
Neuropsychological Tests
Neurosciences
Original Investigation
Pattern Recognition, Visual
Pharmacology/Toxicology
Phencyclidine
Phencyclidine - administration & dosage
Prepulse Inhibition
Psychiatry
Psychopharmacology
Rats
Rodents
Schizophrenia
Schizophrenia - physiopathology
Social Isolation
title Neonatal phencyclidine administration and post-weaning social isolation as a dual-hit model of ‘schizophrenia-like’ behaviour in the rat
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