Why the study?
Do antipsychotic agents (haloperidol, risperidone, clozapine) affect heart rate variability in male WKY rats?
Do antipsychotic agents (haloperidol, risperidone, clozapine) affect heart rate variability in male WKY rats?
In a rat model, clozapine significantly suppresses cardiac autonomic function and increases heart rate compared to haloperidol and risperidone, suggesting haloperidol may have a better cardiovascular safety profile.
Rat data suggest clozapine impairs cardiac autonomic balance more than haloperidol or risperidone; hypothesis-generating for human cardiovascular effects.
BACKGROUND: Sudden cardiac death is higher among schizophrenic patients and is associated with parasympathetic hypoactivity. Antipsychotic agents are highly suspected to be a precipitating factor. Thus, we aimed to test if the antipsychotics haloperidol, risperidone and clozapine affect cardiac autonomic function, excluding the confounding effect of altered sleep structure by the drugs. METHODS: In this study, haloperidol, risperidone and clozapine were given separately by intraperitoneal injection to male Wistar-Kyoto rats for 5 days. Electroencephalogram (EEG), electromyogram (EMG) and electrocardiographic signals were recorded at baseline and 5 days after drug treatments. Sleep scoring was based on EEG and EMG signals. Cardiac autonomic function was assessed using heart rate variability analysis. RESULTS: Clozapine increased heart rate and suppressed cardiac sympathetic and parasympathetic activity. Cardiac acceleration was more severe during sleep. Haloperidol tended to decrease heart rate while risperidone mildly increased heart rate; however, their effects were less obvious than those of clozapine. There was a significant drug-by-stage interaction on several heart rate variability measures. CONCLUSION: Taking this evidence as a whole, we conclude that haloperidol has a better level of cardiovascular safety than either risperidone or clozapine. Application of this approach to other psychotropic agents in the future will be a useful and helpful way to evaluate the cardiovascular safety of the various psychotropic medications that are in clinical use.
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Wang et al. (2012) studied this question.
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