Review of Clinical Pharmacology and Pharmacokinetics – International Edition Volume 38 (2024) – Issue 2

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Ketamine as a treatment of stress-induced maternal depression in mice: effects on offspring behaviour
Taqwa B. Thanoon1,*A green circle with white letters Description automatically generated, Zeina A. Althanoon1A green circle with white letters Description automatically generated
1 Department of Pharmacology and Toxicology, College of Pharmacy, University of Mosul, Mosul, Iraq


*Corresponding author:
Taqwa B. Thanoon, Department of Pharmacology and Toxicology, College of Pharmacy, University of Mosul, Mosul, Iraq; Tel.:+9647714411038
Email: taqwa.23php6@student.uomosul.edu.iq


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Published: 17 June 2024; DOI: 10.61873/XEVC6813

Abstract
Maternal depression during pregnancy adversely affects offspring neurodevelopment and behaviour. Typical antide­pressants like selective serotonin reuptake inhibitors have limitations due to risks of crossing the placenta. Ketamine has emerged as a promising alternative treatment. This research examined ketamine’s effects on offspring of mater­nally stressed mice. Dams were divided into control, maternal adversity, fluoxetine, and ketamine groups. Open field, sucrose preference, elevated plus maze, and forced swim tests assessed offspring anxiety, anhedonia, and despair. Maternal adversity increased anxiety-like behaviours and ketamine or fluoxetine reversed some effects. However, fluoxetine more effectively mitigated despair in forced swim tests. Ketamine moderately alleviated anhedonia versus controls. Further research on dose-response and timing is needed to optimize ketamine treatment. Mitigating maternal depression is crucial for preventing maladaptive offspring neurobehavioral trajectories.

Keywords:
maternal depression, maternal adversity, ketamine, fluoxetine, offspring behaviour, anxiety, anhedonia, despair

Please cite as:
Thanoon T. B. Althanoon Z. A. Ketamine as a treatment of stress-induced maternal depression in mice: effects on offspring behaviour. Rev. Clin. Pharmacol. Pharmacokinet. Int. Ed. 38 (2): 125-132 (2024). DOI: 10.61873/XEVC6813

 

 

 

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