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Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood

K. Akillioglu, M. Karadepe

Clinical Psychopharmacology and Neuroscience February 28, 2021 DOI: 10.9758/cpn.2021.19.1.93 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Controlled experimental animal study Peer reviewed
Population Male Balb/c and C57BL/6 mice exposed to ketamine on postnatal day 7 and tested in adulthood
Intervention Ketamine
Dose single dose 10 or 20 mg/kg; repeated doses 10 or 20 mg/kg every 240 minutes, three times
Topics Anxiety Esketamine Ketamine
Key findings In C57BL/6 mice, single and repeated 20 mg/kg neonatal ketamine doses and repeated 10 mg/kg doses increased anxiety-like behaviour and decreased exploratory behaviour in the elevated plus maze and open field, while Balb/c mice showed no significant behavioural effects at any dose. The authors conclude that hereditary factors may influence the behavioural response to neonatal ketamine.

Abstract

Objective: In this study, we evaluated the effect of neonatal ketamine exposure on anxiety-like and exploratory behaviours in adult the Balb/c and C57BL/6 strains of mice which anxiety responses are different.

Methods: Ketamine was administered at two different doses single dose (10, 20 mg/kg, 0.1 ml/10 g body weight, intraperitoneally) and repeated doses (10, 20 mg/kg every 240 minutes; thrice times) on the 7th postnatal day to male Balb/c and C57BL/6 mice. In adulthood, open-field (OF) and elevated plus maze (EPM) apparatuses were used to evaluate exploratory and anxiety-like behaviour.

Results: In the C57BL/6 mice, the 20 mg/kg single dose decreased open-arm time and total-arm entries in EPM and increased time of central latency and decreased distance travelled in OF. Both the 10 and 20 mg/kg repetitive doses increased time of central latency and decreased time spent in the centre, frequency of rearing and centre crossing in OF and decreased open-arm time, total-arm entries, number of open-arm entries in EPM. The 20 mg/kg repetitive dose decreased number of head dipping behaviours in EPM. In the Balb/c mice, both the single and repetitive 10−20 mg/kg doses had no significant effect on anxiety-like and exploratory behaviours.

Conclusion: There were no significant differences in anxiety-like and exploratory behaviour in different strains by the single 10 mg/kg dose. However, in the C57BL/6 mice, both the single and repetitive 20 mg/kg doses and the 10 mg/kg repetitive dose increased anxiety-like behaviour and decreased exploratory behaviour in EPM and OF. In conclusion, hereditary factors may be effective on the effect of neonatal ketamine treatment on anxiety-like and exploratory behaviour.

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