Effects of maternal LPS and developmental exposure to an environmentally relevant phthalate mixture on neuron number in the rat medial prefrontal cortex

被引:0
作者
Riesgo, V. R. [1 ]
Sellinger, E. P. [2 ]
Brinks, A. S. [2 ]
Juraska, J. M. [2 ]
Willing, J. [1 ]
机构
[1] Bowling Green State Univ, Dept Psychol, JP Scott Ctr Neurosci Mind & Behav, Bowling Green, OH 43403 USA
[2] Univ Illinois, Neurosci Program, 603 E Daniel St, Champaign, IL 61820 USA
关键词
Lipopolysaccharide; Prefrontal cortex; Development; Neurotoxicity; Endocrine disruptor; PRENATAL EXPOSURE; FETAL; REPRODUCTION; EXPRESSION; CHEMICALS; PLACENTA; DEATH; MILK;
D O I
10.1016/j.ntt.2024.107370
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The brain is especially vulnerable to environmental influences during the perinatal period. While the effects of environmental factors are usually studied in isolation, it is more typical to be exposed to multiple influences during early development, necessitating study of synergistic actions on the developing brain. Both maternal infection and endocrine disrupting phthalates can decrease cell number in the medial prefrontal cortex (mPFC), a region critical for executive functioning. In the present study, groups of pregnant Long Evans rats were treated with either (1) 100 pg/kg (i.p.) lipopolysaccharide (LPS) on embryonic days 15 and 16 combined with a low-dose (1 mg/kg) phthalate mixture throughout gestation and the neonatal period, (2) LPS alone, (3) phthalates alone, or (4) neither phthalates nor LPS (control). Neurons and glial cells were stereologically quantified in the mPFC. The adult offspring previously exposed to LPS or phthalates alone had reduced mPFC neuron number in exposed males, but not females, while the combination treatment did not produce significant effects. In males, LPS alone also reduced the number of glia in the mPFC. Additionally, the combination of LPS and phthalates resulted in fewer pregnancies to term and decreased litter size. These results provide insight into how common environmental factors can interact to alter the developmental trajectory of the mPFC.
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