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Peer-reviewed article

Evaluation of Sedative and Physiological Effects of Intramuscular or Intranasal Ketamine-Midazolam and Ketamine-Dexmedetomidine in Capuchin Monkeys (Sapajus sp.).

Gomes VHiD, Stocco AV, de Resende AV, Farsette ABNiD, da Silva LN, Balthazar DAiD

Journal of medical primatologyOct 1, 2026Brazil0 citationsDOI: 10.1111/jmp.70115

Abstract

<h4>Background</h4>This study evaluated the sedative and physiological effects of intramuscular (IM) or intranasal (IN) ketamine-midazolam and ketamine-dexmedetomidine in capuchin monkeys (Sapajus sp.).<h4>Material and methods</h4>Twenty-four capuchin monkeys were randomly assigned into four groups (6 per group) to be administered ketamine (15 mg/kg) combined with midazolam (0.5 mg/kg) or dexmedetomidine (5 μg/kg) IM (KM<sub>IM</sub> and KD<sub>IM</sub> groups, respectively) or IN (KM<sub>IN</sub> and KD<sub>IN</sub> groups, respectively). Physiological variables, sedation scores, and anesthetic recovery times were evaluated.<h4>Results</h4>All protocols resulted in tachypnea and heart rate values within the range indicated for the species. Blood pressure was significantly higher in KD<sub>IM</sub> compared with KM<sub>IM</sub>. All animals in KM<sub>IM</sub> and KD<sub>IM</sub>, and three animals in KM<sub>IN</sub> and KD<sub>IN</sub>, adopted lateral recumbency. Sedation, muscle relaxation, resistance to dorsal recumbency, and mandible tone scores were higher in KM<sub>IM</sub> and KD<sub>IM</sub> compared to KD<sub>IN</sub>. Posture scores were higher in KM<sub>IM</sub> and KD<sub>IM</sub> compared to KM<sub>IN</sub>. Time to standing was longer in KM<sub>IM</sub> and KD<sub>IM</sub> than in KD<sub>IN</sub>.<h4>Conclusion</h4>All protocols promoted tachypnea and few effects on HR and blood pressure. KM<sub>IM</sub> and KD<sub>IM</sub> result in deep sedation. KM<sub>IN</sub> and KD<sub>IN</sub> result in light sedation. Anesthetic recovery was faster with KD<sub>IN</sub>.

Topics & conditions

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Ketamine

Keywords

SedationAnesthesiaBenzodiazepinesPhysiological VariablesDissociative AnesthesiaAdministration RoutesChemical RestraintNon‐human PrimateAnesthetic RecoveryA2‐adrenergic Agonist

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