Sex-Specific Neuropsychiatric Effects of Subanesthetic Ketamine Exposure in Pregnant Mice and Their Offspring.
Wei-Sheng Lin, Pei-Yu Wang, Sheng-Rong Yeh, Zoe Lai, Andrew Chengyu Lee, Shou-Zen Fan
Cellular and molecular neurobiology July 19, 2025 DOI: 10.1007/s10571-025-01582-w (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Randomized controlled trial Peer reviewed |
|---|---|
| Population | Pregnant C57BL/6 mice and their offspring |
| Intervention | Ketamine |
| Dose | 10 mg/kg/day intraperitoneal |
| Duration | Gestation day 15 to 17 |
| Topics | Anxiety Depression Ketamine Esketamine |
| Keywords | N-methyl-d-aspartate receptor Prenatal influences Stress resilience Neurodevelopmental effects hippocampus Unique developmental impact Shape emotional well-being Sex-dependent manner Male offspring Male embryonic brains Pregnant mothers |
| Key findings | Prenatal subanesthetic ketamine exposure reduced depression- and anxiety-like behaviors in male offspring and increased dendritic spine density in the dentate gyrus, with sex-dependent NMDA receptor expression in embryos. |
Abstract
Depression during pregnancy is often overlooked and undertreated. Ketamine has been shown to exert prompt and sustained antidepressant effects in patients with depression, although concerns of potential neurotoxicity prohibit its use in pregnant women. Here, we aim to investigate the neurobehavioral effects of subanesthetic ketamine on pregnant mice and their offspring. We found that pregnant C57BL/6 mice receiving ketamine (10 mg/kg/day intraperitoneal) from gestation day 15 to 17 exhibited less depression-like behaviors. Prenatal ketamine treatment induced male-specific reduction in depression- and anxiety-like behaviors in adult offspring, without alterations in social and memory performance. These behavioral outcomes were associated with a male-specific increase in dendritic spine density of dentate gyrus granule cells, while neither dendritic architecture nor hippocampal neurogenesis was affected. N-methyl-D-aspartate receptor subunits GluN2A and GluN3A were expressed at significantly higher levels in the hippocampus of male as compared to female mouse embryos, suggesting sex-dependent actions of ketamine on developing brain. Overall, our study showed that prenatal exposure to subanesthetic ketamine could exert long-lasting neurobehavioral effects in a sex-dependent manner, with male offspring being more resilient to stress. These findings may have implications concerning ketamine use during pregnancy, and also provide clues about the developmental origins of emotional problems.