Evidence map›Paper›PMID 27371498›Full record

ReviewJournal of psychopharmacology (Oxford, England)2016

Antipsychotic-induced sensitization and tolerance: Behavioral characteristics, developmental impacts, and neurobiological mechanisms.

Ming Li

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of psychopharmacology (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
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  16. The Effects of Antipsychotics on the Synaptic Plasticity GeneInternational journal of molecular sciences · 2020
    Article
  17. Article
  18. Review
  19. Article
  20. 5-HTPharmacology, biochemistry, and behavior · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Ming LiDepartment of Psychology, University of Nebraska-Lincoln, Lincoln, NE, USA mli@unl.edu.
University of Nebraska–Lincoln · US

Funding

Behavioral mechanisms of antipsychotic actionR01MH085635 · NIMH · UNIVERSITY OF NEBRASKA LINCOLN · PI LI, MING · 2010 to 2014
$1.4M
Adolescence neurogenesis mechanisms of antipsychotic sensitization and toleranceR03HD079870 · NICHD · UNIVERSITY OF NEBRASKA LINCOLN · PI LI, MING · 2015 to 2016
$157k
NICHD NIH HHS R03 HD079870NIMH NIH HHS R01 MH085635
6 · The paper itself

Abstract

Antipsychotic sensitization and tolerance refer to the increased and decreased drug effects due to past drug use, respectively. Both effects reflect the long-term impacts of antipsychotic treatment on the brain and result from the brain's adaptive response to the foreign property of the drug. In this review, clinical evidence of the behavioral aspect of antipsychotic sensitization and tolerance is selectively reviewed, followed by an overview of preclinical literature that examines these behavioral characteristics and the related pharmacological and nonpharmacological factors. Next, recent work on the developmental impacts of adolescent antipsychotic sensitization and tolerance is presented and recent research that delineates the neurobiological mechanisms of antipsychotic sensitization and tolerance is summarized. A theoretical framework based on "drug learning and memory" principles is proposed to account for the phenomena of antipsychotic sensitization and tolerance. It is maintained that antipsychotic sensitization and tolerance follow basic principles of learning or acquisition ("induction") and memory ("expression"). The induction and expression of both effects reflect the consequences of associative and nonassociative processing and are strongly influenced by various pharmacological, environmental, and behavioral factors. Drug-induced neuroplasticity, such as functional changes of striatal dopamine D2 and prefrontal serotonin (5-HT)2A receptors and their mediated signaling pathways, in principle, is responsible for antipsychotic sensitization and tolerance. Understanding the behavioral characteristics and neurobiological underpinnings of antipsychotic sensitization and tolerance has greatly enhanced our understanding of mechanisms of antipsychotic action, and may have important implications for future drug discovery and clinical practice.

Indexed as

AdolescentAnimalsAntipsychotic AgentsBrainDrug ToleranceHumansNeuronal PlasticityReceptors, Dopamine D2Receptor, Serotonin, 5-HT2ASignal TransductionAntipsychotic AgentsReceptors, Dopamine D2Receptor, Serotonin, 5-HT2Aadolescent ratsAntipsychotic drugsdopamine D2GSK3 βpsychosissensitizationserotonin 2Atolerance

Identifiers

PMID27371498
PMCPMC4944179
OpenAlexW2469567703

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.