Butorphanol or a Combination of Ketamine and Xylazine Do Not Interfere With Arrhythmogenic Parameters in Agoutis (Dasyprocta prymnolopha) Obtained Through High-Resolution Electrocardiogram.
Charlys Rhands Coelho de Moura, Hermínio José da Rocha Neto, Regina Lucia Dos Santos Silva, Nayla Maria da Silva Rezende Amorim, José Lindenberg Rocha Sarmento, Miguel Ferreira Cavalcante Filho, Wanderson Gabriel Gomes de Melo, Dayseanny de Oliveira Bezerra, Maria Acelina Martins Carvalho, Napoleão Martins Argolo Neto
Journal of experimental zoology. Part A, Ecological and integrative physiology July 1, 2025 DOI: 10.1002/jez.2922 (opens in new tab) via PubMed
Summary
AI-generated from the abstractIn non-sedated agoutis, a medium-sized wild rodent, the QRS duration measured by high-resolution electrocardiography was 93.25 ± 9.51 ms. Sedation with ketamine-xylazine decreased QRS duration, while butorphanol increased it. Neither sedation protocol altered the late potentials (LAS < 40 μV) or root-mean-square voltage (RMS). The spatial QRS-T angle (sQRST) in non-sedated animals was 54.20° ± 43.63; ketamine-xylazine increased it to 102.87° ± 53.57, whereas butorphanol caused no change. Both sedation protocols mildly and similarly reduced systolic, diastolic, and mean arterial pressures compared to physical restraint. The sedation protocols did not interfere with high-resolution electrocardiogram values and produced only minimal changes in vectorcardiographic data and blood pressure.
Study at a glance
| Characteristics | Observational study Peer reviewed |
|---|---|
| Sample size | 8 |
| Population | Agoutis (medium-sized wild rodents) |
| Interventions | ketamine-xylazine butorphanol |
| Keywords | Cardiology Wild animals Rodent physiology Veterinary medicine Wildlife research |
| Key finding | Ketamine-xylazine and butorphanol sedation minimally affect high-resolution electrocardiogram and vectorcardiogram parameters in agoutis, though ketamine-xylazine increases the spatial QRS-T angle. |
Abstract
Agoutis is a medium-sized wild rodent with potential for use as an experimental model. This study aimed to evaluate physiological parameters of arrhythmogenesis in this species, by HR-ECG and VCG techniques, under physical and pharmacological containment (ketamine-xylazine and butorphanol). Eight agouti in which the physiological parameters of arrhythmogenesis were evaluated by HR-ECG and VCG techniques, under physical and pharmacological containment. We evaluated cardiac and pulmonary foci sounds, made femoral pulse inspection, body score analysis, gestational evaluation, echocardiographic examination, blood pressure measurement, and conventional electrocardiography. The non-sedated agoutis exhibited QRS duration of 93.25 ± 9.51, LAS < 40 μV of 28.50 ± 4.65 and RMS of 93.50 ± 29.75. The value of QRS duration decreased in animals treated with ketamine-xylazine and increased in those receiving butorphanol. The non-sedated agoutis exhibited QRS duration of 93.25 ± 9.51, LAS < 40 μV of 28.50 ± 4.65 and RMS of 93.50 ± 29.75. The value of QRS duration decreased in animals treated with ketamine-xylazine and increased in those receiving butorphanol. The sedation protocols did not cause alterations for LAS < 40 μV and RMS. The sQRST value in non-sedated animals was 54.20° ± 43.63 and the administration of ketamine-xylazine increased this index to 102.87° ± 53.57, while butorphanol did not induce alteration. The mean systolic, diastolic, and mean arterial pressures differed between physical and pharmacological restraints. Both pharmacological constraints reduced the blood pressure of the agoutis, analogously and mildly. The adoption of sedation protocols using the ketamine-xylazine association and butorphanol did not interfere with HR-ECG values and exhibited minimal VCG data and blood pressure changes.