MDPV (3,4-methylenedioxypyrovalerone) administered to mice during development of the central nervous system produces persistent learning and memory impairments

• Published in: Pharmacological reports 2024-06, Vol.76 (3), p.519-534
• Main Authors: Kuczyńska, Katarzyna, Bartkowska, Katarzyna, Djavadian, Ruzanna, Zwierzyńska, Ewa, Wojcieszak, Jakub
• Format: Article
• Language: English
• Subjects: Animals; Benzodioxoles - administration & dosage; Benzodioxoles - pharmacology; Central Nervous System - drug effects; Central Nervous System - metabolism; Drug Safety and Pharmacovigilance; Female; Hippocampus - drug effects; Hippocampus - metabolism; Male; Maze Learning - drug effects; Medicine; Memory - drug effects; Memory Disorders - chemically induced; Mice; Mice, Inbred C57BL; Pharmacotherapy; Pharmacy; Pyrrolidines - administration & dosage; Pyrrolidines - pharmacology; Synthetic Cathinone
• ISSN: 1734-1140; 2299-5684; 2299-5684
• DOI: 10.1007/s43440-024-00599-0

Background Synthetic cathinones (SC) constitute the second most frequently abused class of new psychoactive substances. They serve as an alternative to classic psychostimulatory drugs of abuse, such as methamphetamine, cocaine, or 3,4-methylenedioxymethamphetamine (MDMA). Despite the worldwide prevalence of SC, little is known about their long-term impact on the central nervous system. Here, we examined the effects of repeated exposure of mice during infancy, to 3,4-methylenedioxypyrovalerone (MDPV), a SC potently enhancing dopaminergic neurotransmission, on learning and memory in young adult mice. Methods All experiments were performed on C57BL/6J male and female mice. Animals were injected with MDPV (10 or 20 mg/kg) and BrdU (bromodeoxyuridine, 25 mg/kg) during postnatal days 11–20, which is a crucial period for the development of their hippocampus. At the age of 12 weeks, mice underwent an assessment of various types of memory using a battery of behavioral tests. Afterward, their brains were removed for detection of BrdU-positive cells in the dentate gyrus of the hippocampal formation with immunohistochemistry, and for measurement of the expression of synaptic proteins, such as synaptophysin and PSD95, in the hippocampus using Western blot. Results Exposure to MDPV resulted in impairment of spatial working memory assessed with Y-maze spontaneous alternation test, and of object recognition memory. However, no deficits in hippocampus-dependent spatial learning and memory were found using the Morris water maze paradigm. Consistently, hippocampal neurogenesis and synaptogenesis were not interrupted. All observed MDPV effects were sex-independent. Conclusions MDPV administered repeatedly to mice during infancy causes learning and memory deficits that persist into adulthood but are not related to aberrant hippocampal development.