Prenatal diesel exhaust exposure alters hippocampal synaptic plasticity in offspring

• Published in: Aging (Albany, NY.) NY.), 2024-03, Vol.16 (5), p.4348-4362
• Main Authors: Yu, Shali, Zhang, Ziyang, Qin, Ziyu, Liu, Meijun, Zhao, Xiaoye, Cheng, Yulan, Xue, Peng, Wang, Xiaoke, Chen, Lin, Wu, Qiyun, Ju, Linling, Tang, Juan
• Format: Article
• Language: English
• Subjects: Animals; Female; Hippocampus - metabolism; Humans; Male; Maze Learning; Mice; Mice, Inbred C57BL; Neuronal Plasticity; Pregnancy; Prenatal Exposure Delayed Effects - metabolism; Receptors, N-Methyl-D-Aspartate - metabolism; Research Paper; RNA-Binding Proteins - metabolism; Vehicle Emissions - toxicity
• ISSN: 1945-4589; 1945-4589
• DOI: 10.18632/aging.205592

Diesel exhaust particles (DEPs) are major air pollutants emitted from automobile engines. Prenatal exposure to DEPs has been linked to neurodevelopmental and neurodegenerative diseases associated with aging. However, the specific mechanism by DEPs impair the hippocampal synaptic plasticity in the offspring remains unclear. Pregnant C57BL/6 mice were administered DEPs solution via the tail vein every other day for a total of 10 injections, then the male offsprings were studied to assess learning and memory by the Morris water maze. Additionally, protein expression in the hippocampus, including CPEB3, NMDAR (NR1, NR2A, NR2B), PKA, SYP, PSD95, and p-CREB was analyzed using Western blotting and immunohistochemistry. The alterations in the histomorphology of the hippocampus were observed in male offspring on postnatal day 7 following prenatal exposure to DEPs. Furthermore, 8-week-old male offspring exposed to DEPs during prenatal development exhibited impairments in the Morris water maze test, indicating deficits in learning and memory. Mechanistically, the findings from our study indicate that exposure to DEPs during pregnancy may alter the expression of CPEB3, SYP, PSD95, NMDAR (NR1, NR2A, and NR2B), PKA, and p-CREB in the hippocampus of both immature and mature male offspring. The results offer evidence for the role of the NMDAR/PKA/CREB and CPEB3 signaling pathway in mediating the learning and memory toxicity of DEPs in male offspring mice. The alterations in signaling pathways may contribute to the observed damage to synaptic structure and transmission function plasticity caused by DEPs. The findings hold potential for informing future safety assessments of DEPs.