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Volume 100, Issue 1, Pages 86-96 (March 2008)


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An initial animal proof-of-concept study for central administration of clozapine to schizophrenia patients

Daniel J. Abramsa, Lijun Zhenga, Kevin S. Chooa, Jun J. Yangb, Wei Weid, Thomas J. Anchordoquyb, Nasser H. Zawiad, Karen E. StevensacCorresponding Author Informationemail address

Received 16 July 2007; received in revised form 19 October 2007; accepted 24 October 2007. published online 07 January 2008.

Abstract 

While clozapine is the acknowledged superior pharmacotherapeutic for the treatment of schizophrenia, the side effect profile, which includes potentially fatal complications, limits its usefulness. Central administration of clozapine directly into the brain could circumvent many of the side effect issues due to the dramatic reduction in dose and the limitation of the drug primarily to the CNS. The present study demonstrates that clozapine can be formulated as a stable solution at physiological pH, which does not have in vitro neurotoxic effects at concentrations which may be effective at treating symptoms. Acute central administration improved auditory gating deficits in a mouse model of schizophrenia-like deficits. Assessment of behavioral alterations in rats receiving chronic central infusions of clozapine via osmotic minipump was performed with the open field and elevated plus mazes. Neither paradigm revealed any detrimental effects of the infusion. While these data represent only an initial investigation, they none-the-less suggest that central administration of clozapine may be a viable alternate therapeutic approach for schizophrenia patients which may be effective in symptom reduction without causing behavioral or neurotoxic effects.

a Department of Psychiatry, University of Colorado at Denver and Health Sciences Center, Aurora, CO 80045, United States

b School of Pharmacy, University of Colorado at Denver and Health Sciences Center, Aurora, CO 80045, United States

c Medical Research, Veterans Affairs Medical Center, Denver CO, United States

d Department of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, RI, United States

Corresponding Author InformationCorresponding author. Department of Psychiatry, MS 8344, University of Colorado at Denver and Health Sciences Center, PO Box 5611, Aurora, CO 80045, United States. Tel.: +1 303 724 4423; fax: +1 303 724 4425.

PII: S0920-9964(07)00470-7

doi:10.1016/j.schres.2007.10.012


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