Woo Taeseon, Ahmed Nick I, Appenteng Michael K, King Candice, Li Runting, Fritsche Kevin L, Sun Grace Y, Cui Jiankun, Will Matthew J, Maurer Sara V, Stevens Hanna E, Beversdorf David Q, Greenlief C Michael
Interdisciplinary Neuroscience Program, University of Missouri, Columbia, MO 65211, USA.
Department of Psychological Sciences, University of Missouri, Columbia, MO 65211, USA.
Int J Mol Sci. 2025 Jul 14;26(14):6730. doi: 10.3390/ijms26146730.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restricted social communication and repetitive behaviors. Prenatal stress is critical in neurodevelopment and increases risk for ASD, particularly in those with greater genetic susceptibility to stress. Docosahexaenoic acid (DHA) is one of the most abundant ω-3 fatty acids in the membrane phospholipids of the mammalian brain, and dietary DHA plays an important role in brain development and maintenance of brain structure. In this study, we investigated whether peri-natal supplementation of DHA can alleviate autistic-like behaviors in a genetic risk/stress mouse model and how it alters lipid peroxidation activity and GABAergic system gene expression in the forebrain. Pregnant heterozygous serotonin transporter knockout (SERT-KO) and wild-type (WT) dams were placed in either non-stressed control conditions or chronic variable stress (CVS) conditions and fed either a control diet or a DHA-rich (1% by weight) diet. Offspring of each group were assessed for anxiety and autism-associated behavior at post-natal day 60 using an open field test, elevated plus maze test, repetitive behavior, and the 3-chamber social approach test. A liquid chromatography-mass spectrometry (LC-MS)-based method was used to follow changes in levels of lipid peroxidation products in the cerebral cortex. Male offspring of prenatally stressed SERT-het KO dams exhibited decreased social preference behaviors and increased repetitive grooming behaviors compared to WT control offspring. Moreover, DHA supplementation in male SERT-het mice decreased frequency of grooming behaviors albeit showing no associated effects on social behaviors. Regardless of stress conditions, supplementation of DHA to the WT mice did not result in alterations in grooming nor social interaction in the offspring. Furthermore, no apparent changes were observed in the lipid peroxidation products comparing the stressed and non-stressed brains. was downregulated in the cortex of female offspring of prenatally stressed SERT-KO dams, and this change appeared to be rescued by DHA supplementation in offspring. was upregulated in the striatum of male offspring of prenatally stressed SERT-KO dams, but DHA did not significantly alter the expression compared to the control diet condition.
自闭症谱系障碍(ASD)是一种神经发育障碍,其特征为社交沟通受限和重复行为。产前应激在神经发育中至关重要,并会增加患ASD的风险,尤其是在那些对压力具有更高遗传易感性的个体中。二十二碳六烯酸(DHA)是哺乳动物大脑膜磷脂中最丰富的ω-3脂肪酸之一,饮食中的DHA在大脑发育和脑结构维持中起着重要作用。在本研究中,我们调查了围产期补充DHA是否可以减轻遗传风险/应激小鼠模型中的类自闭症行为,以及它如何改变前脑的脂质过氧化活性和γ-氨基丁酸能系统基因表达。将怀孕的杂合子血清素转运体敲除(SERT-KO)和野生型(WT)母鼠置于非应激对照条件或慢性可变应激(CVS)条件下,并分别喂食对照饮食或富含DHA(重量比1%)的饮食。在出生后第60天,使用旷场试验、高架十字迷宫试验、重复行为和三室社交接近试验对每组后代的焦虑和自闭症相关行为进行评估。使用基于液相色谱-质谱(LC-MS)的方法追踪大脑皮层中脂质过氧化产物水平的变化。与WT对照后代相比,产前应激的SERT-het KO母鼠的雄性后代表现出社交偏好行为减少和重复梳理行为增加。此外,雄性SERT-het小鼠补充DHA可降低梳理行为的频率,尽管对社交行为没有相关影响。无论应激条件如何,给WT小鼠补充DHA均未导致后代梳理行为和社交互动的改变。此外,在比较应激和非应激大脑时,脂质过氧化产物未观察到明显变化。产前应激的SERT-KO母鼠的雌性后代皮层中 被下调,而这种变化似乎通过后代补充DHA得以挽救。产前应激的SERT-KO母鼠的雄性后代纹状体中 被上调,但与对照饮食条件相比,DHA并未显著改变其表达。