J 2015

Long-term haloperidol treatment prolongs QT interval and increases expression of sigma 1 and IP3 receptors in guinea pig hearts

STRAČINA, Tibor, Iva SLANINOVÁ, Hana POLANSKÁ, Martina AXMANOVÁ, Veronika OLEJNÍČKOVÁ et. al.

Základní údaje

Originální název

Long-term haloperidol treatment prolongs QT interval and increases expression of sigma 1 and IP3 receptors in guinea pig hearts

Autoři

STRAČINA, Tibor (703 Slovensko, garant, domácí), Iva SLANINOVÁ (203 Česká republika, domácí), Hana POLANSKÁ (203 Česká republika, domácí), Martina AXMANOVÁ (203 Česká republika, domácí), Veronika OLEJNÍČKOVÁ (203 Česká republika, domácí), Petr KONEČNÝ (203 Česká republika, domácí), Michal MASAŘÍK (203 Česká republika, domácí), Olga KRIZANOVA (703 Slovensko) a Marie NOVÁKOVÁ (203 Česká republika)

Vydání

Tohoku Journal of Experimental Medicine, Miyagi, Tohoku University Medical Press, 2015, 0040-8727

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30105 Physiology

Stát vydavatele

Japonsko

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 1.287

Kód RIV

RIV/00216224:14110/15:00083475

Organizační jednotka

Lékařská fakulta

UT WoS

000358823400006

Klíčová slova anglicky

Guinea pig; Haloperidol; Heart; QT prolongation; Sigma 1 receptor

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 28. 4. 2016 13:46, Ing. Mgr. Věra Pospíšilíková

Anotace

V originále

Find fulltext at Masaryk University(opens in a new window)|View at Publisher| Export | Download | More... Tohoku Journal of Experimental Medicine Volume 236, Issue 3, 19 June 2015, Pages 199-207 Long-term haloperidol treatment prolongs QT interval and increases expression of sigma 1 and IP3 receptors in guinea pig hearts (Article) Stracina, T.a, Slaninova, I.b, Polanska, H.c, Axmanova, M.c, Olejnickova, V.a, Konecny, P.d, Masarik, M.c, Krizanova, O.e, Novakova, M.af a Department of Physiology, Masaryk University, Brno, Czech Republic b Department of Biology, Masaryk University, Brno, Czech Republic c Department of Pathological Physiology, Masaryk University, Brno, Czech Republic d Department of Physiotherapy and Rehabilitation, Masaryk University, Brno, Czech Republic e Center for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovakia f International Clinical Research Center, Animal Center, St. Anne’s Faculty Hospital, Brno, Czech Republic View additional affiliations View references (47) Abstract Haloperidol is a neuroleptic drug used for a medication of various psychoses and deliria. Its administration is frequently accompanied by cardiovascular side effects, expressed as QT interval prolongation and occurrence of even lethal arrhythmias. Despite these side effects, haloperidol is still prescribed in Europe in clinical practice. Haloperidol binds to sigma receptors that are coupled with inositol 1,4,5-trisphosphate (IP3) receptors. Sigma receptors are expressed in various tissues, including heart muscle, and they modulate potassium channels. Together with IP3 receptors, sigma receptors are also involved in calcium handling in various tissues. Therefore, the present work aimed to study the effects of long-term haloperidol administration on the cardiac function. Haloperidol (2 mg/kg once a day) or vehiculum was administered by intraperitoneal injection to guinea pigs for 21 consecutive days. We measured the responsiveness of the hearts isolated from the haloperidol-treated animals to additional application of haloperidol. Expression of the sigma 1 receptor and IP3 receptors was studied by real time-PCR and immunohistochemical analyses. Haloperidol treatment caused the significant decrease in the relative heart rate and the prolongation of QT interval of the isolated hearts from the haloperidol-treated animals, compared to the hearts isolated from control animals. The expression of sigma 1 and IP3 type 1 and type 2 receptors was increased in both atria of the haloperidol-treated animals but not in ventricles. The modulation of sigma 1 and IP3 receptors may lead to altered calcium handling in cardiomyocytes and thus contribute to changed sensitivity of cardiac cells to arrhythmias.

Návaznosti

MUNI/A/1326/2014, interní kód MU
Název: Kardiovaskulární systém od buňky k lůžku pacienta (Akronym: KASBUNPAC)
Investor: Masarykova univerzita, Kardiovaskulární systém od buňky k lůžku pacienta, DO R. 2020_Kategorie A - Specifický výzkum - Studentské výzkumné projekty