Detailed Information on Publication Record
2008
Acute effects of sigma receptor ligand haloperidol in rat and guinea pig isolated hearts
NOGOVÁ, Kateřina and Marie NOVÁKOVÁBasic information
Original name
Acute effects of sigma receptor ligand haloperidol in rat and guinea pig isolated hearts
Name in Czech
Akutní účinky ligandu sigma receptorů haloperidolu u izolovaných srdcí potkana a morčete
Authors
Edition
8. vyd. Kraków, Polsko, New Frontiers in Cardiovascular Research, p. 82-83, 1 pp. 2008
Publisher
Polish Academy of Arts
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
30105 Physiology
Country of publisher
Poland
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Medicine
Keywords in English
isolated heart;rat;guinea pig;sigma receptor;haloperidol;arrhythmias
Tags
International impact, Reviewed
Změněno: 28/1/2009 11:21, prof. MUDr. Marie Nováková, Ph.D.
V originále
Sigma receptor ligands, mostly antipsychotics, can as an unwanted effect trigger episodes of cardiac arrhythmias - ventricular tachycardia, ventricular fibrillation, torsade de pointes, which occasionally culminate in sudden death. Mechanisms of these life-threatening side effects are not fully understood. Therefore we explored the role of typical sigma ligand haloperidol in susceptibility to develop arrhythmias on 3-D electrogram. Eleven adult male rats and eleven adult male guinea pigs were sacrificed under deep ether anesthesia. The hearts were perfused according to Langendorff with Krebs-Henseleit solution at constant pressure (85mmHg) and 37C (CaCl2, 1.2 mM). The experiment consists of four 30min periods: control, 10nM haloperidol, washout, 10nM haloperidol. Ten successive RR intervals were averaged at the end of control (steady state). This value was used for normalization of heart rate during the rest of experiment. Similarly, QT intervals were examined to determine L-QT. The incidence of arrhythmias was assessed according to Lambeth Conventions. Heart rate and QT interval showed similar changes in both models. Normalized heart rate declines in haloperidol applications and restores in washout. Almost all hearts exhibit L-QT. In guinea pig hearts, typical life-threatening arrhythmias occur; rat hearts show only premature ventricular beats in both haloperidol periods. This effect was attenuated in the next haloperidol phase. In conclusion, lengthened QT observed in our experimental models can explain the occurrence of arrhythmias. Unchanged QT interval in guinea pig hearts in the second haloperidol period can be reasoned by down-regulation of cardiac sigma receptors.
In Czech
Sigma receptor ligands, mostly antipsychotics, can as an unwanted effect trigger episodes of cardiac arrhythmias - ventricular tachycardia, ventricular fibrillation, torsade de pointes, which occasionally culminate in sudden death. Mechanisms of these life-threatening side effects are not fully understood. Therefore we explored the role of typical sigma ligand haloperidol in susceptibility to develop arrhythmias on 3-D electrogram. Eleven adult male rats and eleven adult male guinea pigs were sacrificed under deep ether anesthesia. The hearts were perfused according to Langendorff with Krebs-Henseleit solution at constant pressure (85mmHg) and 37C (CaCl2, 1.2 mM). The experiment consists of four 30min periods: control, 10nM haloperidol, washout, 10nM haloperidol. Ten successive RR intervals were averaged at the end of control (steady state). This value was used for normalization of heart rate during the rest of experiment. Similarly, QT intervals were examined to determine L-QT. The incidence of arrhythmias was assessed according to Lambeth Conventions. Heart rate and QT interval showed similar changes in both models. Normalized heart rate declines in haloperidol applications and restores in washout. Almost all hearts exhibit L-QT. In guinea pig hearts, typical life-threatening arrhythmias occur; rat hearts show only premature ventricular beats in both haloperidol periods. This effect was attenuated in the next haloperidol phase. In conclusion, lengthened QT observed in our experimental models can explain the occurrence of arrhythmias. Unchanged QT interval in guinea pig hearts in the second haloperidol period can be reasoned by down-regulation of cardiac sigma receptors.
Links
| GA102/07/1473, research and development project |
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| MSM0021622402, plan (intention) |
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