Related Experiment Video
Updated: May 31, 2026

Acquisition of Resting-State Functional Magnetic Resonance Imaging Data in the Rat
Published on: August 28, 2021
Acepromazine does not enhance sedation or reduce propofol requirements when combined with dexmedetomidine in dogs
Luã Borges Iepsen1, Leonardo Bergmann Griebeler2, Iara Catarina Alves de Almeida3
1Department of Veterinary Medicine, Federal University of Paraná, Curitiba, Paraná, Brazil.
Abstract:
This study aimed to evaluate the sedative effects of acepromazine and dexmedetomidine in dogs and their influence on propofol requirements for anesthetic induction, electrocardiographic findings, heart rate and arterial blood pressure. Twenty-one healthy mixed-breed dogs were included in the study. Dogs were randomly assigned to one of 3 protocols (n = 7): dexmedetomidine (2 µg/kg IM) (GD); dexmedetomidine (2 µg/kg IM) and acepromazine (0.02 mg/kg IM) (GAD); or acepromazine (0.02 mg/kg IM) followed 15 minutes later by dexmedetomidine (2 µg/kg IM) (GAD15). Sedation scores and cardiorespiratory variables were recorded at baseline (T0), 15 minutes after the first drug administration (T15), and 15 minutes after the second drug administration (T30). Propofol induction dose was recorded. All protocols produced moderate sedation, with no significant differences among groups. Heart rate decreased significantly at T30 compared with T0 in GD but not in GAD or GAD15. SAP decreased significantly at T30 compared with T0 in GAD15. Propofol induction doses (mean ± SD) were 3.8 ± 1.1 mg/kg (GD), 3.6 ± 0.5 mg/kg (GAD), and 3.1 ± 0.5 mg/kg (GAD15), with no significant differences. Retching occurred in 2 dogs (GD and GAD), and none in GAD15. The combination of acepromazine and dexmedetomidine provided mild to moderate sedation but did not reduce propofol requirements compared with dexmedetomidine alone.
Related Concept Videos
Parenteral Anesthetics: Overview
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists
Phenothiazines, such as prochlorperazine...
Drugs Affecting GI Tract Motility: Dopamine Receptor Antagonists
Skeletal Muscle Relaxants: Adverse Effects
Unlike...
Sedatives and Hypnotics Drugs: Benzodiazepines
Benzodiazepines work by enhancing the effects of the inhibitory neurotransmitter GABA. They bind to the GABAA receptor, increasing its affinity for GABA, which opens chloride...