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Prepulse Inhibition During Withdrawal from an Escalating Dosage Schedule of Amphetamine View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by RERO DOC Digital Library Psychopharmacology (2003) 169:340–353 DOI 10.1007/s00213-002-1254-4 ORIGINAL INVESTIGATION Holger Russig · Carol A. Murphy · Joram Feldon Prepulse inhibition during withdrawal from an escalating dosage schedule of amphetamine Received: 6 March 2002 / Accepted: 21 August 2002 / Published online: 12 November 2002 Springer-Verlag 2002 Abstract Rationale: Psychomotor stimulants can induce Keywords Startle · Schizophrenia · Latent inhibition · psychotic states in humans that closely resemble those Sensitization · Rat observed in patients with idiopathic schizophrenia. At- tentional and sensorimotor gating impairments are ob- served in schizophrenic patients using the latent inhibition Introduction (LI) and prepulse inhibition (PPI) behavioral assays, respectively. Our previous studies demonstrated that after Administration of amphetamine (AMPH) can induce 4 days of withdrawal from a period of amphetamine symptoms of psychosis in humans. This outcome is most (AMPH) administration, animals exhibited disrupted LI frequently associated with a chronic high-dose escalating but normal PPI. Objective: The aim of the present study pattern of stimulant abuse (Davis and Schlemmer 1980; was to test PPI in AMPH-withdrawn rats under experi- Angrist 1994). Given that stimulant-induced psychosis in mental conditions similar to those used to best demon- humans closely resembles the psychosis observed in strate locomotor sensitization following AMPH patients with idiopathic schizophrenia (Ellinwood 1967; withdrawal. Methods: We examined the effects on PPI Griffith et al. 1972; Snyder 1973), it has been suggested of (1) pairing drug injections with PPI test-associated that similar neural adaptations could be responsible for cues, (2) administration of a low-dose dopamine agonist the development of these two phenomena. It is well challenge and (3) testing following longer withdrawal known that repeated exposure to psychostimulants, like periods (23, 30, 60 days). Results: Although none of these AMPH or cocaine, induces psychomotor sensitization in conditions revealed a disruption of PPI in AMPH- experimental animals. This phenomenon is indicated by a withdrawn rats, we did observe that the acoustic startle progressive behavioral augmentation of responses (in- response was reduced during a restricted time period creased locomotion, stereotypies) to drug challenge, as following AMPH withdrawal. Similar to our previous well as an enhanced release of nucleus accumbens findings, AMPH-withdrawn animals showed disrupted LI dopamine (DA) following challenge AMPH administra- on day 16 of withdrawal and locomotor sensitization to a tion (Robinson and Becker 1986; Segal and Kuczenski challenge injection of AMPH after 62 days of withdrawal. 1994). It has therefore been proposed that studies of the Conclusion: We conclude that the effects of repeated neural bases of psychomotor stimulant sensitization might AMPH on PPI are not modulated by the same experi- yield insights into the biological mechanisms responsible mental parameters known to be important for eliciting for the onset of schizophrenia (Kokkinidis and Anismann locomotor sensitization and that withdrawal from the 1980; Robinson and Becker 1986; Lieberman et al. 1990). schedule of AMPH administration used in this study Specifically, Lieberman and colleagues have suggested models only specific cognitive dysfunctions linked to that a process of endogenous sensitization, in which schizophrenic symptoms, since LI was disrupted but PPI schizophrenic patients exhibit enhanced DA release in was not affected. response to AMPH challenge, is a key element in the pathology of the disease (Lieberman et al. 1990; Lieber- man et al. 1997). Recent positron emission tomography H. Russig · C.A. Murphy · J. Feldon ()) (PET) imaging studies examining competition for recep- Laboratory of Behavioural Neurobiology, tor occupancy between endogenously released DA and Swiss Federal Institute of Technology (ETH Zurich), D2 receptor radioligand binding have established that not Postfach Schorenstrasse 16, 8603 Schwerzenbach, Switzerland only do schizophrenic patients show enhanced striatal DA e-mail: [email protected] release in response to AMPH administration (i.e., a Tel.: +41-1-6557448 sensitized response) but the DA response is positively Fax: +41-1-6557203 341 correlated with the severity of their positive symptoms day 4 of withdrawal (Murphy et al. 2001b). Given the (reviewed in Laruelle 2000). Thus, there is convincing similarities in brain areas and cognitive functions impli- evidence for the involvement of sensitization processes in cated in LI and PPI (Weiner and Feldon 1997; Swerdlow the expression of the schizophrenic phenotype. A number et al. 2000) and the clear disruptive effects of withdrawal of studies have also established that, during the acute from this escalating dose AMPH schedule on LI, it is phase of withdrawal from high-dose AMPH, animals somewhat surprising that AMPH withdrawal does not also often exhibit depressive-like symptoms – in particular, affect PPI. The purpose of the present investigation was to anhedonia as it is indexed by decreased sensitivity to further explore this issue of PPI disruptibility during rewarding brain stimulation (Lin et al. 1999; Koob and Le AMPH withdrawal, by specifically examining the effects Moal 2001). However, the state of anhedonia during on PPI of experimental conditions that are known to AMPH withdrawal is typically very transient, persisting maximize locomotor sensitization effects. for up to only 3–5 days following the last administration. The role of contextual cues in psychostimulant-related In comparison, behavioral sensitization can persist even behavior has been extensively studied in sensitization after prolonged periods of abstinence, a time course experiments (Robinson et al. 1998; Ohmori et al. 2000). It which is perhaps more consistent with the long-term has been shown that under certain experimental circum- adaptations typically associated with chronic mental stances, sensitization to psychostimulants is only detected illness. when repeated drug administrations were previously Two animal models believed to reflect cognitive/ paired with specific contextual cues (Hinson and Poulos attentional deficits typical of schizophrenic patients are 1981; Drew and Glick 1988; Badiani et al. 1995; latent inhibition (LI) of classically conditioned respond- Robinson et al. 1998). There is also direct evidence that ing and prepulse inhibition (PPI) of the startle response drug-conditioned cues disrupt sensorimotor gating. A (Weiner and Feldon 1997; Swerdlow et al. 2000). Both LI study with abstinent smokers indicated that a presentation and PPI are disrupted in schizophrenic patients, and these of smoking-associated stimuli reduced PPI (Hutchison et deficits can be restored by neuroleptic treatment (Baruch al. 1999). Moreover, other studies have shown that PPI et al. 1988; Gray et al. 1992, 1995; Weiner and Feldon was reduced during withdrawal from repeated DA agonist 1997; Braff et al. 2001). LI refers to the observation that treatment when drug administrations were repeatedly repeated exposure to a stimulus without consequence paired with PPI testing (Zhang et al. 1998; Martin-Iverson comes to impede the formation of subsequent associations 1999) whereas repeated psychostimulant treatment that with that stimulus (Lubow 1973). Our previous studies was not paired with PPI testing failed to result in PPI have shown that LI is disrupted in rats pretreated with reduction (Mansbach et al. 1988; Druhan et al. 1998; escalating doses of AMPH during the first two weeks of Martinez et al. 1999; Byrnes et al. 2000; Adams et al. withdrawal (Murphy et al. 2001b). Moreover, the anti- 2001). These studies suggest that PPI reduction following psychotic drugs haloperidol and clozapine restored LI in repeated psychostimulant administration may, like loco- AMPH-withdrawn rats (Russig et al. 2002). Thus, the LI motor sensitization, be context dependent such that results during AMPH withdrawal are consistent with the AMPH withdrawal-induced deficits in the PPI paradigm hypothesis, based on neuroimaging studies, that sensitized might only be detected if a drug-related cue were present levels of DA are associated with an animal model of during test. This hypothesis was tested in the present schizophrenic deficits. study by measuring PPI in AMPH-withdrawn animals that PPI is the phenomenon whereby moderate-intensity previously received drug injections paired with an prepulse stimuli attenuate startle responses to subsequent environment similar to that experienced during PPI intense stimulation (Graham 1975; Braff et al. 1978; testing. Hoffman and Ison 1980). This phenomenon is thought to Locomotor sensitization is always measured following result from the activation of central inhibitory mecha- the administration of a DA agonist challenge. Swerdlow nisms that gate behavioral responses to ensuing stimuli et al. (1995) previously demonstrated PPI disruption in (Swerdlow et al. 1992; Taylor et al. 1995). Acute rats with lesions of the hippocampus and prefrontal cortex administration of psychomotor stimulants such as AMPH, following the administration of very low doses of the apomorphine (APO) or selective D2 DA agonists disrupts direct DA agonist APO, whereas lesioned animals PPI, such that startle responses are less influenced by the receiving vehicle injections
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