Center for Environmental Epigenetics and Development, Department of Biological Sciences, University of Toronto, Scarborough, 1265 Military Trail, Toronto, ON, Canada.
Department of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
J Neuroinflammation. 2020 Apr 15;17(1):116. doi: 10.1186/s12974-020-01798-1.
Maternal obesity as a result of high levels of saturated fat (HFD) consumption leads to significant negative health outcomes in both mother and exposed offspring. Offspring exposed to maternal HFD show sex-specific alterations in metabolic, behavioral, and endocrine function, as well as increased levels of basal neuroinflammation that persists into adulthood. There is evidence that psychosocial stress or exogenous administration of corticosterone (CORT) potentiate inflammatory gene expression; however, the response to acute CORT or immune challenge in adult offspring exposed to maternal HFD during perinatal life is unknown. We hypothesize that adult rat offspring exposed to maternal HFD would show enhanced pro-inflammatory gene expression in response to acute administration of CORT and lipopolysaccharide (LPS) compared to control animals, as a result of elevated basal pro-inflammatory gene expression. To test this, we examined the effects of acute CORT and/or LPS exposure on pro and anti-inflammatory neural gene expression in adult offspring (male and female) with perinatal exposure to a HFD or a control house-chow diet (CHD).
Rat dams consumed HFD or CHD for four weeks prior to mating, during gestation, and throughout lactation. All male and female offspring were weaned on to CHD. In adulthood, offspring were 'challenged' with administration of exogenous CORT and/or LPS, and quantitative PCR was used to measure transcript abundance of glucocorticoid receptors and downstream inflammatory markers in the amygdala, hippocampus, and prefrontal cortex.
In response to CORT alone, male HFD offspring showed increased levels of anti-inflammatory transcripts, whereas in response to LPS alone, female HFD offspring showed increased levels of pro-inflammatory transcripts. In addition, male HFD offspring showed greater pro-inflammatory gene expression and female HFD offspring exhibited increased anti-inflammatory gene expression in response to simultaneous CORT and LPS administration.
These findings suggest that exposure to maternal HFD leads to sex-specific changes that may alter inflammatory responses in the brain, possibly as an adaptive response to basal neuroinflammation.
由于饱和脂肪(HFD)摄入水平高,导致母体肥胖,从而对母亲和暴露的后代产生重大的负面健康后果。暴露于母体 HFD 的后代表现出代谢、行为和内分泌功能的性别特异性改变,以及基础神经炎症水平升高,这种情况持续到成年期。有证据表明,心理社会应激或外源性给予皮质酮(CORT)会增强炎症基因表达;然而,在围产期暴露于母体 HFD 的成年后代对急性 CORT 或免疫挑战的反应尚不清楚。我们假设,与对照动物相比,在围产期暴露于母体 HFD 的成年大鼠后代在急性给予 CORT 和脂多糖(LPS)时,由于基础促炎基因表达升高,会表现出更强的促炎基因表达。为了验证这一点,我们研究了急性 CORT 和/或 LPS 暴露对围产期暴露于 HFD 或对照家庭饲料(CHD)的成年后代(雄性和雌性)的促炎和抗炎神经基因表达的影响。
大鼠母鼠在交配前、妊娠期和哺乳期前四周内食用 HFD 或 CHD。所有雄性和雌性后代均用 CHD 断奶。成年后,用外源性 CORT 和/或 LPS 对后代进行“挑战”,并使用定量 PCR 测量杏仁核、海马体和前额叶皮质中糖皮质激素受体和下游炎症标志物的转录丰度。
仅给予 CORT 时,雄性 HFD 后代的抗炎转录物水平升高,而仅给予 LPS 时,雌性 HFD 后代的促炎转录物水平升高。此外,雄性 HFD 后代在同时给予 CORT 和 LPS 时表现出更强的促炎基因表达,而雌性 HFD 后代表现出增加的抗炎基因表达。
这些发现表明,暴露于母体 HFD 会导致性别特异性变化,可能会改变大脑中的炎症反应,这可能是对基础神经炎症的一种适应性反应。