Abstract: The peripheral alpha2-adrenoceptor antagonist vatinoxan attenuated the side effects of alpha2-adrenergic sedatives in experimental studies in horses. This clinical study investigated the effects of vatinoxan in horses sedated for gastroscopy with detomidine and butorphanol. Client-owned horses were randomly allocated to receive one of the following two intravenous treatments: detomidine hydrochloride (HCl) (12μg/kg) + butorphanol tartrate (12μg/kg) (DB; n=11) or DB + vatinoxan HCl (200μg/kg) (DBV; n=11). Borborygmi score and heart rate were recorded by auscultation. Sedation level was evaluated and blood samples were collected before drug administration and up to 240minutes thereafter. Gastroscopy was performed within 30minutes of sedation. Glucose concentration was measured immediately with a portable glucometer. Serum insulin and triglyceride concentrations were analysed from frozen samples. Sedation level was adequate in all horses for gastroscopy. Overall heart rate decreased significantly more with DB than with DBV. In general, audible borborygmi, blood insulin, and glucose concentrations remained closer to baseline values with DBV compared DB. In conclusion, vatinoxan improved borborygmi and alleviated the decreased heart rate in horses sedated with detomidine and butorphanol for gastroscopy. The detomidine-induced inhibition to insulin secretion and thus the increase in blood glucose concentration were attenuated by vatinoxan. Vatinoxan may be a beneficial addition to equine sedation protocols in clinical settings.
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Overview
This study evaluated how the drug vatinoxan affects sedation outcomes and side effects in horses sedated with detomidine and butorphanol for gastroscopy.
The research specifically examined heart rate, digestive sounds, blood glucose, and insulin levels to assess whether vatinoxan reduces negative side effects associated with alpha2-adrenergic sedatives.
Background and Purpose
Alpha2-adrenergic sedatives like detomidine are commonly used in horses for procedures such as gastroscopy but can cause side effects including decreased heart rate (bradycardia), reduced gastrointestinal motility (reflected by decreased borborygmi), and altered glucose and insulin levels.
Vatinoxan is a peripheral alpha2-adrenoceptor antagonist shown in experimental studies to reduce some of these side effects by blocking peripheral receptors while presumably maintaining sedation centrally.
The study aimed to investigate if adding vatinoxan to a standard sedative regimen (detomidine and butorphanol) would improve side effect profiles in clinical, client-owned horses.
Study Design and Methods
The study was a randomized clinical trial involving 22 client-owned horses undergoing gastroscopy.
DBV group: Same as DB plus vatinoxan hydrochloride (200 μg/kg IV), n=11 horses.
Data collection included:
Heart rate and borborygmi (gut sounds) scored by auscultation before and up to 240 minutes post drug administration.
Assessment of sedation level to ensure adequate sedation for gastroscopy.
Blood sampling for glucose measurements (via portable glucometer immediately) and serum insulin and triglyceride analysis from frozen samples.
Gastroscopy performed within 30 minutes after sedation was initiated.
Key Findings
All horses in both groups achieved adequate sedation for performing gastroscopy.
Heart rate:
The DB group experienced a more notable decrease in heart rate compared to the DBV group.
Vatinoxan attenuated the bradycardia caused by detomidine and butorphanol sedation.
Borborygmi:
The horses receiving vatinoxan (DBV group) maintained gut sounds closer to baseline, indicating better preservation of gastrointestinal motility.
In the DB group without vatinoxan, borborygmi decreased more significantly.
Glucose and Insulin:
Detomidine typically inhibits insulin secretion, resulting in increased blood glucose.
In the DBV group, the rise in blood glucose and the suppression of insulin secretion were less pronounced than in the DB group.
This suggests vatinoxan helps moderate metabolic side effects related to insulin and glucose.
Conclusions and Implications
Vatinoxan improved the side effect profile of detomidine and butorphanol sedation in horses without compromising sedative efficacy.
Specifically, it helped prevent excessive heart rate reduction and preserved gastrointestinal motility.
It also attenuated detomidine’s negative impact on insulin secretion and prevented significant hyperglycemia.
These findings suggest that adding vatinoxan may be beneficial in clinical equine sedation protocols, enhancing cardiovascular and metabolic safety during procedures like gastroscopy.
Further research could explore optimal dosing and assess potential benefits in other veterinary sedation settings.
Cite This Article
APA
Jantunen N, Raekallio M, Karikoski N.
(2026).
Effects of vatinoxan in horses sedated with detomidine and butorphanol for gastroscopy: a randomized clinical study.
Vet J, 106680.
https://doi.org/10.1016/j.tvjl.2026.106680
University of Helsinki Faculty of Veterinary Medicine. Electronic address: noora.m.jantunen@helsinki.fi.
Raekallio, Marja
University of Helsinki Faculty of Veterinary Medicine.
Karikoski, Ninja
University of Helsinki Faculty of Veterinary Medicine. Electronic address: ninja.karikoski@helsinki.fi.
Conflict of Interest Statement
Conflict of interest statement One of the authors, Marja Raekallio, is named as one of the inventors in a patent concerning vatinoxan. The other authors declare no conflict of interest. Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests. Noora Jantunen reports financial support was provided by Suomen Hippos ry. Marja Raekallio reports financial support was provided by Vetcare Ltd., Finland. Noora Jantunen reports financial support was provided by the Finnish Foundation of Veterinary Research. Marja Raekallio has patent licensed to. One of the authors, Marja Raekallio, is named as one of the inventors in a patent concerning vatinoxan. Patent holder is Vetcare Ltd. The other authors declare no conflict of interest. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.