J 2022

Efficacy and safety of higher oral doses of azaperone to achieve sedation in pigs

SVOBODA, Martin, Jana BLAHOVA, Martin HOSTOVSKY, Jiří JARKOVSKÝ, Jakub NETOLICKY et. al.

Basic information

Original name

Efficacy and safety of higher oral doses of azaperone to achieve sedation in pigs

Authors

SVOBODA, Martin (203 Czech Republic, guarantor), Jana BLAHOVA (203 Czech Republic), Martin HOSTOVSKY (203 Czech Republic), Jiří JARKOVSKÝ (203 Czech Republic, belonging to the institution), Jakub NETOLICKY (203 Czech Republic), Patrik PREDNY (203 Czech Republic), Ivana SIMKOVA (203 Czech Republic), Jonas VANHARA (203 Czech Republic) and Jan VASEK (203 Czech Republic)

Edition

Veterinarni Medicina, Praha, Czech Academy of Agricultural Sciences, 2022, 0375-8427

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

40301 Veterinary science

Country of publisher

Czech Republic

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 0.700

RIV identification code

RIV/00216224:14110/22:00128412

Organization unit

Faculty of Medicine

UT WoS

000868736000001

Keywords in English

behaviour; biochemical indicators; pharmacodynamics

Tags

Tags

International impact, Reviewed
Změněno: 20/2/2023 14:07, Mgr. Tereza Miškechová

Abstract

V originále

The aim of this study is to evaluate the possibility of achieving more effective and prolonged sedation in pigs by the oral administration of increased doses of azaperone and to evaluate its safety. This was performed through a prospective randomised and double blinded study. A total of 32 weaned piglets were divided into 4 groups (8 in each group). Group A was given 1 ml of saline orally and served as the control group. Group B received azaperone orally at a dose of 4 mg/kg b.w. Group C received azaperone orally at a dose of 8 mg/kg b.w. Group D was given azaperone orally at a dose of 12 mg/kg b.w. The response to the defined stimulus, movement level, degree of salivation, body temperature, respiratory frequency, blood plasma azaperone concentration and biochemical variables were included in the trial. We found that by increasing the dose of the orally administered azaperone, the onset of the sedation is faster, the end of the sedation starts later and the sedation time is longer. However, the use of higher doses of oral azaperone is not suitable for piglets because the doses negatively affect the respiratory rate, body temperature, some biochemical parameters and cause the immobility of the piglets.