母体免疫激活模型中产前和产后环境的相互作用。

Anna Gundacker, Laura Cuenca Rico, Peter Stoehrmann, Katharina E Tillmann, Ulrike Weber-Stadlbauer, Daniela D Pollak
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引用次数: 0

摘要

怀孕期间的不利影响与发育中的后代的一系列不利结果有关。母亲的社会心理压力、暴露于感染和营养失衡是已知的神经发育紊乱的危险因素,并在后代以后的生活中出现精神和神经方面的表现。在此背景下,母体免疫激活(MIA)模型已被广泛用于临床前研究,以研究妊娠期间母体免疫系统的刺激如何详细说明胎儿神经发育的紧密协调序列。MIA对后代大脑结构和功能的影响主要表现在行为和认知异常,表现在青春期和成年期。这些观察结果在“双重打击假说”的框架内得到了解释,该假说认为,神经发育障碍的风险升高是由于个体在生命的不同时期受到两种不利环境的影响,共同导致病理的出现。在产后早期,父母是新生儿环境的主要决定因素,构成了对外部刺激的脆弱性窗口。考虑到MIA不仅影响发育中的胎儿,还会影响母亲的大脑,而母亲的大脑在怀孕期间处于高度可塑状态,因此MIA对母亲产后大脑功能和行为的影响可能是对其后代不利影响的重要因素。在这里,我们回顾了目前关于产前和产后母亲环境在调节后代发育中的相互作用及其与MIA模型病理生理学的相关性的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction of the pre- and postnatal environment in the maternal immune activation model.

Adverse influences during pregnancy are associated with a range of unfavorable outcomes for the developing offspring. Maternal psychosocial stress, exposure to infections and nutritional imbalances are known risk factors for neurodevelopmental derangements and according psychiatric and neurological manifestations later in offspring life. In this context, the maternal immune activation (MIA) model has been extensively used in preclinical research to study how stimulation of the maternal immune system during gestation derails the tightly coordinated sequence of fetal neurodevelopment. The ensuing consequence of MIA for offspring brain structure and function are majorly manifested in behavioral and cognitive abnormalities, phenotypically presenting during the periods of adolescence and adulthood. These observations have been interpreted within the framework of the "double-hit-hypothesis" suggesting that an elevated risk for neurodevelopmental disorders results from an individual being subjected to two adverse environmental influences at distinct periods of life, jointly leading to the emergence of pathology. The early postnatal period, during which the caregiving parent is the major determinant of the newborn´s environment, constitutes a window of vulnerability to external stimuli. Considering that MIA not only affects the developing fetus, but also impinges on the mother´s brain, which is in a state of heightened malleability during pregnancy, the impact of MIA on maternal brain function and behavior postpartum may importantly contribute to the detrimental consequences for her progeny. Here we review current information on the interaction between the prenatal and postnatal maternal environments in the modulation of offspring development and their relevance for the pathophysiology of the MIA model.

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