In vivo Evaluation of Different Anesthetic Effects in a Rabbit Model

Abdullah Al Sad

Department of Surgery and Theriogenology, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Raf Ana Rabbi Shawon

Laboratory of Wildlife Resources, Gifu University, Gifu 501-1193, Japan.

Md. Tanvir Rahman Sadiq

Faculty of Veterinary, Animal and Biomedical Sciences, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Mamun Islam

Faculty of Veterinary, Animal and Biomedical Sciences, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Nazia Tabassum Nodi

Department of Anatomy and Histology, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Sanowar Ul Islam

Department of Livestock Production and Management, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Md. Masud Pervej

Department of Anatomy and Histology, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Md. Mahfuzul Haque *

Department of Surgery and Theriogenology, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

Md. Matiur Rahman *

Department of Medicine, Sylhet Agricultural University, Sylhet-3100, Bangladesh.

*Author to whom correspondence should be addressed.


Abstract

Background: Injectable anaesthetics are widely used in rabbits in routine veterinary practice. However, selecting an anaesthetic combination that provides rapid induction, adequate surgical anaesthesia, smooth recovery, and minimal physiological disturbances remains an important clinical consideration in Bangladesh.

Objective: This study aimed to compare the efficacy and effects of atropine–xylazine–ketamine (AXK), xylazine–ketamine (XK), and atropine–ketamine (AK) combinations in New Zealand White rabbits.

Methods: Eighteen clinically healthy New Zealand White rabbits (9 male and 9 female) were randomly assigned to three anaesthetic treatment groups (n = 6 per group): AK (atropine 0.04 mg/kg + ketamine 30 mg/kg), AXK (atropine 0.04 mg/kg + xylazine 3 mg/kg + ketamine 30 mg/kg), and XK (xylazine 3 mg/kg + ketamine 30 mg/kg). Drugs were administered intramuscularly, with ketamine injected 5 minutes after premedication. Heart rate, respiratory rate, and rectal temperature were recorded at baseline (0 min) and at 15-minute intervals thereafter, up to 75 minutes post-administration. Physiological reflexes were evaluated over time, followed by assessment of serum biochemical parameters and histopathological changes in major organs. Data were analysed using two-way ANOVA followed by Tukey's post hoc test (p < 0.05).

Results: The results showed that the AXK group produced the shortest induction time (5.58 ± 0.24 min), significantly longer loss of ear pinch (37.42 ± 0.66 min) and pedal withdrawal reflexes (35.17 ± 0.70 min), and an intermediate recovery period (51.00 ± 0.58 min). On the other hand, the XK group required the longest recovery time (67.50 ± 0.43 min) despite a longer induction time (8.00 ± 0.29 min). The AK group showed the longest induction period (12.00 ± 0.29 min) with only brief anaesthetic depth, as reflected by the shortest duration of reflex loss (approximately 5 min). Importantly, the physiological variables differed significantly among the three groups throughout the observation period, with XK showing a progressive decline in heart rate, whereas AXK and AK exhibited transient increases before stabilisation (p < 0.05). Respiratory rate and rectal temperature also varied significantly over time (p < 0.05). Serum biochemical values remained largely within normal reference ranges, except for inorganic phosphate, which exceeded the published reference interval. Histopathological examination of the brain, liver, tongue, spleen, testes, and ovaries revealed normal tissue architecture without detectable anaesthetic-induced lesions.

Conclusion: The AXK combination provided the most balanced anaesthetic profile by producing rapid induction, prolonged surgical anaesthesia, acceptable recovery, and no apparent adverse histopathological effects. The findings suggest that the AXK protocol may be the most suitable injectable anaesthetic regimen among those evaluated for short surgical procedures in New Zealand White rabbits. Future studies incorporating larger sample sizes, multiple dosing regimens, extended monitoring, and controlled environmental conditions would strengthen the translational relevance of these findings to clinical veterinary practice.

Keywords: Anaesthesia, ketamine, xylazine, atropine, physiological parameters, histopathology, New Zealand White rabbit


How to Cite

Sad, Abdullah Al, Raf Ana Rabbi Shawon, Md. Tanvir Rahman Sadiq, Mamun Islam, Nazia Tabassum Nodi, Sanowar Ul Islam, Md. Masud Pervej, Md. Mahfuzul Haque, and Md. Matiur Rahman. 2026. “In Vivo Evaluation of Different Anesthetic Effects in a Rabbit Model”. Asian Journal of Research in Animal and Veterinary Sciences 9 (3):520-34. https://doi.org/10.9734/ajravs/2026/v9i3433.

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