Comparing the effects of intravenous injection and intranasal atomisation of detomidine in sheep. Issue 1 (8th December 2022)

• Record Type: Journal Article
• Authors: Tahmasbi, Touran; Raisi, Abbas; Zakian, Amir; Khaldari, Majid
• Is Part Of: Veterinary medicine and science. Volume 9:Issue 1(2023)
• Page Start: 353
• Page End: 362
• Publication Date: 2022-12-08
• Subjects: atomiser -- cardiopulmonary -- detomidine -- intravenous -- sedation; Veterinary medicine -- Periodicals; Animal Diseases; Veterinary medicine; Periodicals; Periodicals; 636.08905
• DOI: 10.1002/vms3.1023
• Languages: English
• ISSNs: 2053-1095

Abstract

Abstract: Background: Detomidine is an α‐2 agonist sedative drug which reduces the release of norepinephrine in nerves. Administering this drug through intranasal (IN) route could cause direct transmission to the central nervous system. Therefore, IN administration of detomidine would decrease the side effects and the onset of sedation. Objectives: In this study, IN administration of detomidine in sheep through an atomiser was compared to its IV administration. Methods: Fifteen mature female sheep with an approximate weight of 49.53 ± 1.72 kg were used. They were randomly divided into three groups: (1) atomising 10 μg/kg (IND10 ); (2) IV 10 μg/kg (IVD) and (3) atomising 30 μg/kg (IND30 ). Following administration, vital signs, electrocardiographic components, sedative score and biochemistry profile were measured after 15, 30 and 60 min, which were compared with the baseline measures. Results: Bradycardia and the percentage of reduction from the baseline value in the respiratory rate were lower in the IND10 group compared to those in the IVD group. There was no significant difference in terms of the temperature and blood oxygen saturation (SpO2 ) among all the groups ( p > 0.05). The level of cortisol declined in all the groups, and in the IND30 (60 min), it was significantly different with the baseline value. The level of glucose increased in all the groups compared to the baseline, which was not significant. Insulin concentration was reduced in all the groups, and in the IND30 group, it changed significantly 60 min after the drug administration. Sedation onset time was faster in the IV group. However, sedation scores between the two administration methods were not different, and only a dose‐dependent increase was found in the sedation score in the atomisation group. Conclusions: Our findings revealed that IN atomisation of detomidine triggers similar sedation as its IV administration, which could be used as an alternative method. Abstract : This paper compares the intravenous and intranasal routs of Detomidine administration in sheep.