Pharmacodynamic and pharmacokinetic behavior of landiolol during dobutamine challenge in healthy adults
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
PubMed
33239108
PubMed Central
PMC7691079
DOI
10.1186/s40360-020-00462-x
PII: 10.1186/s40360-020-00462-x
Knihovny.cz E-zdroje
- Klíčová slova
- Cardioselective β-blocker, Dobutamine, Landiolol, Pharmacodynamics, Pharmacokinetics,
- MeSH
- beta blokátory aplikace a dávkování farmakokinetika MeSH
- dobutamin aplikace a dávkování farmakokinetika MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- intravenózní infuze MeSH
- kardiotonika aplikace a dávkování farmakokinetika MeSH
- klinické křížové studie MeSH
- krevní tlak účinky léků fyziologie MeSH
- lidé MeSH
- mladý dospělý MeSH
- močovina aplikace a dávkování analogy a deriváty farmakokinetika MeSH
- morfoliny aplikace a dávkování farmakokinetika MeSH
- prospektivní studie MeSH
- srdeční frekvence účinky léků fyziologie MeSH
- zdraví dobrovolníci pro lékařské studie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- beta blokátory MeSH
- dobutamin MeSH
- kardiotonika MeSH
- landiolol MeSH Prohlížeč
- močovina MeSH
- morfoliny MeSH
BACKGROUND: To study the pharmacokinetic and -dynamic behavior of landiolol in the presence of dobutamine in healthy subjects of European ancestry. METHODS: We conducted a single-center, prospective randomized study in 16 healthy subjects each receiving an infusion of dobutamine sufficient to increase heart rate by 30 bpm followed by a 60 min infusion of 10 μg/kg/min landiolol. RESULTS: Dobutamine-induced increases in heart rate were stable for at least 20 min before a 60 min landiolol- infusion was started. The dobutamine effects were rapidly antagonized by landiolol within 16 min. A further slight decrease in heart rate during 20-60 min of the landiolol infusion occurred as well. Upon termination of landiolol infusion, heart rate and blood pressure recovered rapidly in response to the persisting dobutamine infusion but did not return to the maximum values before landiolol infusion. The pharmacokinetic parameters of landiolol in presence of dobutamine showed a short half-life (3.5 min) and a low distribution volume (0.3 l/kg). No serious adverse events were observed. CONCLUSION: Landiolol can antagonize the dobutamine-induced increases in heart rate and blood pressure in a fast way. A rapid bradycardic effect until steady-state plasma levels is followed by a slow heart rate reduction. The latter can be attributed to an early desensitization to dobutamine. Consequently, after termination of landiolol, the heart rate did not achieve maximum pre-landiolol values. The pharmacokinetics of landiolol during dobutamine infusion are similar when compared to short- and long-term data in Caucasian subjects. Landiolol in the given dose can thus serve as an antagonist of dobutamine-induced cardiac effects. TRIAL REGISTRATION: Registration number 2010-023311-34 at the EU Clinical Trials Register, registration date 2010-12-21.
Aixial s r o Brno Czech Republic
AOP Orphan Pharmaceuticals AG Vienna Austria
Center for Pharmacology and Analysis s r o Plzeň Czech Republic
MRN Medical Research Network GmbH Postgasse 11 22 A 1010 Vienna Austria
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