Classics in Chemical Neuroscience: Risperidone

被引:76
作者
Chopko, Trevor C. [1 ]
Lindsley, Craig W. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Sch Med, Vanderbilt Ctr Neurosci Drug Discovery, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pharmacol, Sch Med, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Dept Chem, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
关键词
Risperidone; Risperdal; schizophrenia; atypical; dopamine; serotonin; adrenergic; histamine; D-2; 5-HT2A; ATYPICAL ANTIPSYCHOTICS; RECEPTOR OCCUPANCY; DOPAMINE HYPOTHESIS; P-GLYCOPROTEIN; SCHIZOPHRENIA; DRUGS; PHARMACOGENETICS; MECHANISM; BINDING; PHARMACOKINETICS;
D O I
10.1021/acschemneuro.8b00159
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
After the identification of the influence of serotonergic receptors in ameliorating the negative symptoms associated with schizophrenia, atypical antipsychotics were developed by incorporating dopamine and serotonin antagonism. Risperidone, sold under the trade name Risperdal, was the second atypical antipsychotic developed following clozapine but quickly became a first-line treatment for acute and chronic schizophrenia because of its preferential side effect profile. Despite initial Food and Drug Administration approval 25 years ago, risperidone continues to be a fundamental treatment for Risperidone (Risperdal) schizophrenia, bipolar I disorder, and autism-related irritability. It is on the World Health Organization's List of Essential Medicines for its balance of efficacy, safety, tolerability, and cost-effectiveness. In this review, we highlight the history and importance of risperidone as an atypical antipsychotic, in addition to its chemical synthesis, manufacturing, drug metabolism and pharmacokinetics, pharmacology, structure-activity relationship, indications, and adverse effects.
引用
收藏
页码:1520 / 1529
页数:19
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