Effect of ketamine enantiomers and maternal deprivation on depressive-like behavior and plasma concentration of BDNF in rats
G. Beanes, Beatriz A. Carneiro, G. Marques, Pedro Guilherme B. de S. Nazaré, Israel N. Matos, G. C. D. Carvalho, C. Schitine, Alex Cleber Improta-Caria, R. S. Costa, Rejane Conceição Santana
Research, Society and Development July 15, 2024 DOI: 10.33448/rsd-v13i7.46352 via Semantic Scholar
Summary
AI-generated from the abstractIn a study of male rats, maternal deprivation did not induce depressive-like behavior, and a single dose of ketamine, esketamine, or arketamine did not alter depressive-like behavior, anhedonic-like behavior, or locomotor activity. Plasma brain-derived neurotrophic factor levels also remained unchanged across all groups. The findings suggest that neither the maternal deprivation model nor the ketamine enantiomers produced measurable antidepressant-like effects in this experimental setup.
Study at a glance
| Characteristics | Randomized controlled trial Peer reviewed |
|---|---|
| Sample size | 71 |
| Population | Male rats |
| Interventions | ketamine esketamine arketamine |
| Keywords | Medicine |
| Key finding | Maternal deprivation did not induce depressive-like behavior, and ketamine enantiomers did not alter depressive-like behavior or plasma BDNF levels. |
Abstract
Background: Low doses of different ketamine enantiomers have demonstrated rapid behavioural and biological actions in animals with depressive-like behavior. However, some authors report different effects depending on model of depression and ketamine isomer used. Objective: Our primary aim was to evaluate the effect of ketamine enantiomers on depressive-like behavior, anhedonic-like behavior and locomotor activity of rats subjected to maternal deprivation (MD). Secondarily, we investigated the Brain-derived neurotrophic factor plasma concentration between experimental groups. Methods: Male rats (n=71) were randomized into seven experimental groups: one non-deprived with placebo and other six deprived split into control and intervention groups. Rats were treated with a single intraperitoneal dose of ketamine, esketamine, or arketamine. One hour after drug application, we performed experimental tests to evaluate the antidepressant-like behavior and locomotor activity. Furthermore, blood was collected to measure plasmatic BDNF levels. Results: We did not observe induction of depressive-like in rats subjected to MD. Furthermore, there was no change in BDNF (F (6,64) = 0.9664, p=0.455) between all experimental groups. Conclusion: Neither MD nor the different ketamine isomers were able to change depressive-like behavior or plasma BDNF levels.