Key result
Acute administration of a sublethal dose of Clozapine in rats significantly reduced arterial blood pressure by 12% and peripheral blood flow by 48% compared to control, accompanied by morphological signs of myocardial damage.
Why the study?
The study evaluated the influence of a sublethal dose of clozapine on the functional and morphological parameters of the cardiovascular system in rats.
Effect estimate: 12% reduction
Absolute Event Rate: 109% vs 124%
p-value: p=<0.05
Acute sublethal clozapine poisoning in a rat model induces significant arterial hypotension, decreased peripheral blood flow, and morphological myocardial damage.
Alerts to possible clozapine cardiotoxicity; leaves open human translation and requires clinical study.
Purpose of the study. To evaluate the influence of sublethal dose of Clozapine on the functional and morphological parameters of the cardiovascular system in rats 4 hrs. after the drug administration. Materials and methods. The experiments were carried out on male Wistar rats weighing 200–250g ( n =14). Group I received 0.9% NaCl solution administered via enteral feeding tubing under general anesthesia using Sevoflurane; group II — Clozapine dosed at 150 mg/kg in 0.9% NaCl solution; group III — Clozapine dosed at 150 mg/kg in 40% ethyl alcohol solution. 4 hrs. after drug administration, arterial blood pressure (ABP), heart rate (HR), microcirculation in the skin using laser Doppler flowmetry (LSF), fluorescence intensity of coenzymes NADH and FAD were evaluated. After euthanasia, autopsy including withdrawal of the internal organs of rats for morphological analysis was performed. Thereafter, paraffin sections of hearts were made and subsequently stained with hematoxylin and eosin, which were later examined with the help of light microscope Nikon Eclipse Ni-U. Results. In both Clozapine groups, ABP and blood flow in the skin were lower than in the control group: ABP — by 12% in group I and by 15% in group II; blood flow — by 48% and 37%, respectively. No significant difference between the groups was observed in respect of the microcirculation indices studied. Increased fluorescence intensity of coenzyme NADH in the skin was found in the Clozapine groups compared to the control group (2.3-fold in group I and 1.9-fold in group II). Histological analysis of the hearts of animals that received Clozapine established uneven blood filling, erythrocyte sludges, fine-focal hemorrhaging, endotheliocyte nuclei oriented perpendicular to the basal membrane, uneven staining of myocardium with hypereosinophilic segments, fragmentation and undulating deformity of muscle fibers. Conclusion. During acute Clozapine poisoning, morphological signs of disturbed circulation and myocardium damage are found in the heart, which are accompanied with development of myocardium dysfunction with arterial hypotension and decreased peripheral blood flow, also disturbed oxidative metabolism in peripheral tissues.
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Babkina et al. (2019) studied Acute Clozapine poisoning (n=14). Clozapine vs. 0.9% NaCl solution was evaluated on Mean arterial blood pressure (ABP) (12% reduction, p=<0.05). Acute administration of a sublethal dose of Clozapine in rats significantly reduced arterial blood pressure by 12% and peripheral blood flow by 48% compared to control, accompanied by morphological signs of myocardial damage.
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