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Treatment mechanisms: traditional and new antipsychotic drugs

The first generation of antipsychotic drugs was discovered in the 1960s and 1970s, These agents were effective in treating psychosis, but were accompanied by significant side effects, including severe parkinsonism and akathisia. Second-generation antipsychotics were introduced in the 1990s, These dr...

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Autor principal: Tamminga, Carol A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181604/
https://www.ncbi.nlm.nih.gov/pubmed/22033640
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author Tamminga, Carol A.
author_facet Tamminga, Carol A.
author_sort Tamminga, Carol A.
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description The first generation of antipsychotic drugs was discovered in the 1960s and 1970s, These agents were effective in treating psychosis, but were accompanied by significant side effects, including severe parkinsonism and akathisia. Second-generation antipsychotics were introduced in the 1990s, These drugs have at least equal efficacy to their predecessors, but far fewer side effects. Some data suggest a broader efficacy profile. Clozapine remains the only superior antipsychotic in terms of the magnitude of psychotic symptom reduction. Clinical and animal studies are consistent in suggesting that the antipsychotic component of antidopaminergic treatments is initiated by dopamine receptor blockade in the striatum and that the signal is transmitted to the neocortex through the established basal ganglia-thalamo-cortical neuronal circuits. Other neurotransmitter actions (eg, antiserotonergic) can be exerted locally, in the neocortex. Defining tissue targets of drug action may suggest additional strategies for developing new antipsychotic drugs.
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spelling pubmed-31816042011-10-27 Treatment mechanisms: traditional and new antipsychotic drugs Tamminga, Carol A. Dialogues Clin Neurosci Pharmacological Aspects The first generation of antipsychotic drugs was discovered in the 1960s and 1970s, These agents were effective in treating psychosis, but were accompanied by significant side effects, including severe parkinsonism and akathisia. Second-generation antipsychotics were introduced in the 1990s, These drugs have at least equal efficacy to their predecessors, but far fewer side effects. Some data suggest a broader efficacy profile. Clozapine remains the only superior antipsychotic in terms of the magnitude of psychotic symptom reduction. Clinical and animal studies are consistent in suggesting that the antipsychotic component of antidopaminergic treatments is initiated by dopamine receptor blockade in the striatum and that the signal is transmitted to the neocortex through the established basal ganglia-thalamo-cortical neuronal circuits. Other neurotransmitter actions (eg, antiserotonergic) can be exerted locally, in the neocortex. Defining tissue targets of drug action may suggest additional strategies for developing new antipsychotic drugs. Les Laboratoires Servier 2000-09 /pmc/articles/PMC3181604/ /pubmed/22033640 Text en Copyright: © 2000 LLS http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmacological Aspects
Tamminga, Carol A.
Treatment mechanisms: traditional and new antipsychotic drugs
title Treatment mechanisms: traditional and new antipsychotic drugs
title_full Treatment mechanisms: traditional and new antipsychotic drugs
title_fullStr Treatment mechanisms: traditional and new antipsychotic drugs
title_full_unstemmed Treatment mechanisms: traditional and new antipsychotic drugs
title_short Treatment mechanisms: traditional and new antipsychotic drugs
title_sort treatment mechanisms: traditional and new antipsychotic drugs
topic Pharmacological Aspects
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181604/
https://www.ncbi.nlm.nih.gov/pubmed/22033640
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