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      Unique Effects of Clozapine: A Pharmacological Perspective

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          Abstract

          Schizophrenia is a heterogenous and severe neuropsychiatric disorder that affects nearly 1% of the population worldwide. Antipsychotic drugs are the mainstay of treatment, but not all patients with schizophrenia respond to treatment with these agents. Clozapine, the first atypical antipsychotic, is a highly effective medication for patients with schizophrenia who do not respond to other antipsychotics. Although clozapine tends not to produce extrapyramidal symptoms, other side effects of the drug (e.g., agranulocytosis, myocarditis, seizures) limit its widespread use. This chapter reviews clozapine’s unique clinical effects and unusual pharmacological profile. In addition to its effects in treatment resistant schizophrenia, clozapine has been shown to decrease suicidality, which occurs at an increased rate in patients with schizophrenia. Still preliminary, but consistent data, also suggest that clozapine limits substance use in these patients, an important effect since substance use disorders are common in patients with schizophrenia and are associated with a poor outcome, including an increased risk for suicide and poor response to treatment. We have suggested, from animal studies, that clozapine’s apparent ability to limit substance use may occur through its actions as a weak dopamine D2 receptor antagonist, a potent norepinephrine ɑ-2 receptor antagonist and a norepinephrine reuptake inhibitor. Using animal models, we have built combination of agents toward creation of safer clozapine-like drugs to reduce substance use in these patients. Future research into the mechanisms of action of clozapine toward the development of safe clozapine-like agents is of great public health importance.

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          Author and article information

          Journal
          9015397
          1826
          Adv Pharmacol
          Adv. Pharmacol.
          Advances in pharmacology (San Diego, Calif.)
          1054-3589
          1557-8925
          6 April 2020
          12 January 2018
          2018
          04 May 2020
          : 82
          : 137-162
          Affiliations
          [1 ]Department of Psychiatry, Geisel School of Medicine at Dartmouth
          [2 ]Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth
          [3 ]Dartmouth Clinical and Translational Science Institute, Dartmouth College
          Author notes

          Foreword:

          We are delighted to contribute this article in honor of Solomon H. Snyder. I (Alan I. Green) was the first medical student to work in his laboratory, just fifty years ago, in the early months of 1967. Sol was then, as he has remained, an inspirational figure, encouraging a naïve student, a history major in college, that he had a talent for scientific research. Sol’s many contributions to neuropsychopharmacology, including toward an early understanding of the action of antipsychotic drugs, as noted in the following article, while extraordinary, are at least equaled by his unique ability to launch the careers of dozens of productive scientists. While I have tried over these many years to capture the Snyder gift for inspiration, I have learned that there is only one Sol.

          Send correspondence to: Alan I. Green, MD, Department of Psychiatry, Geisel School of Medicine at Dartmouth, One Medical Center Drive, Lebanon, NH 03756, Tel: 603-650-7549, Fax: 603-650-8415, Alan.I.Green@ 123456dartmouth.edu
          Article
          PMC7197512 PMC7197512 7197512 nihpa1580339
          10.1016/bs.apha.2017.09.009
          7197512
          29413518
          c717fa00-1feb-4cdc-9888-56ea7791d71c
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