Developmental exposure of bisphenol A induces spatial memory deficits by weakening the excitatory neural circuits of CA3-CA1 and EC-CA1 in mice

• Published in: Toxicology and applied pharmacology 2021-09, Vol.426, p.115641, Article 115641
• Main Authors: Bi, Nanxi, Ding, Jinjun, Zou, Rongxin, Gu, Xiaozhen, Liu, Zhi-Hua, Wang, Hui-Li
• Format: Article
• Language: English
• Subjects: Animals; Benzhydryl Compounds - toxicity; Bisphenol A; Endocrine Disruptors - toxicity; Female; Hippocampus; Hippocampus - drug effects; Hippocampus - physiology; Male; Maze Learning - drug effects; Memory Disorders - chemically induced; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neural circuit; Neurons - drug effects; Neurotoxicity; Phenols - toxicity; Spatial memory; Spatial Memory - drug effects; Synapses - drug effects; Virus tracing
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2021.115641

Bisphenol-A (BPA) is an environmental endocrine disruptor and impairs learning and memory. However, the direct evidence for BPA exposure affecting neural circuits has been limited. In this study, a virus tracing assay has been established to explore the brain's neural circuits. Thy1-Cre mice were used to investigate the effects of BPA on the neural projection of glutamatergic pyramidal neurons in hippocampal CA1 based on Thy1 promoter. These transgenic mice were orally exposed to BPA (0, 0.5 mg/kg/day) from postnatal day (PND) 0 to PND60 and then subjected to behavioral tests. Morris water maze(MWM)and Barnes maze's showed that the spatial memory was seriously impaired in BPA exposed Thy1-Cre mice. Virus tracing assay indicated that CA1 pyramidal neurons mainly received neural inputs from hippocampal CA3, entorhinal cortex (EC), and medial septum (MS). The analysis showed that BPA reduced the number of RV+ neurons in CA3 and EC but not MS. The immunohistochemistry experiment displayed that BPA decreased the percentage of CaMKIIRV+ cells in CA3 and EC. The results demonstrated that the synaptic connection of upstream glutamatergic neurons and CA1 pyramidal cells was weakened by BPA exposure. These point to potentially detrimental effects of BPA exposure on the excitatory neural circuit of CA3-CA1 and EC-CA1 in memory formation. Thus, our findings revealed that the decrease in excitatory neural circuits of CA3-CA1 and EC-CA1 contribute to the BPA-induced spatial memory deficits in Thy1-Cre mice.