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妊娠引起的氧化应激和炎症与母体神经元活动或记忆功能受损无关。

Pregnancy-induced oxidative stress and inflammation are not associated with impaired maternal neuronal activity or memory function.

机构信息

Department of Pharmaceutical Sciences, University of North Texas Health Science Center, Fort Worth, Texas, United States.

Department of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, Texas, United States.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2024 Jul 1;327(1):R35-R45. doi: 10.1152/ajpregu.00026.2024. Epub 2024 May 6.

Abstract

Pregnancy is associated with neural and behavioral plasticity, systemic inflammation, and oxidative stress, yet the impact of inflammation and oxidative stress on maternal neural and behavioral plasticity during pregnancy is unclear. We hypothesized that healthy pregnancy transiently reduces learning and memory and these deficits are associated with pregnancy-induced elevations in inflammation and oxidative stress. Cognitive performance was tested with novel object recognition (recollective memory), Morris water maze (spatial memory), and open field (anxiety-like) behavior tasks in female Sprague-Dawley rats of varying reproductive states [nonpregnant (nulliparous), pregnant (near term), and 1-2 mo after pregnancy (primiparous); = 7 or 8/group]. Plasma and CA1 proinflammatory cytokines were measured with a MILLIPLEX magnetic bead assay. Plasma oxidative stress was measured via advanced oxidation protein products (AOPP) assay. CA1 markers of oxidative stress, neuronal activity, and apoptosis were quantified via Western blot analysis. Our results demonstrate that CA1 oxidative stress-associated markers were elevated in pregnant compared with nulliparous rats ( ≤ 0.017) but there were equivalent levels in pregnant and primiparous rats. In contrast, reproductive state did not impact CA1 inflammatory cytokines, neuronal activity, or apoptosis. Likewise, there was no effect of reproductive state on recollective or spatial memory. Even so, spatial learning was impaired ( ≤ 0.007) whereas anxiety-like behavior ( ≤ 0.034) was reduced in primiparous rats. Overall, our data suggest that maternal hippocampal CA1 is protected from systemic inflammation but vulnerable to peripartum oxidative stress. Peripartum oxidative stress elevations, such as in pregnancy complications, may contribute to peripartum neural and behavioral plasticity. Healthy pregnancy is associated with elevated maternal systemic and brain oxidative stress. During postpregnancy, brain oxidative stress remains elevated whereas systemic oxidative stress is resolved. This sustained maternal brain oxidative stress is associated with learning impairments and decreased anxiety-like behavior during the postpregnancy period.

摘要

妊娠与神经和行为可塑性、全身炎症和氧化应激有关,但炎症和氧化应激对妊娠期间母体神经和行为可塑性的影响尚不清楚。我们假设健康妊娠会短暂降低学习和记忆能力,而这些缺陷与妊娠引起的炎症和氧化应激升高有关。我们在不同生殖状态的雌性 Sprague-Dawley 大鼠(未怀孕(初产)、怀孕(接近足月)和怀孕后 1-2 个月(经产);每组 7 或 8 只)中用新物体识别(回忆记忆)、Morris 水迷宫(空间记忆)和旷场(焦虑样)行为任务测试认知表现。通过 MILLIPLEX 磁珠分析测量血浆和 CA1 前炎症细胞因子。通过先进氧化蛋白产物(AOPP)测定法测量血浆氧化应激。通过 Western blot 分析定量 CA1 氧化应激相关标志物、神经元活性和细胞凋亡。我们的研究结果表明,与初产大鼠相比,怀孕大鼠 CA1 氧化应激相关标志物升高(≤0.017),但怀孕和经产大鼠的水平相当。相比之下,生殖状态不影响 CA1 中的炎症细胞因子、神经元活性或细胞凋亡。同样,生殖状态对回忆或空间记忆也没有影响。尽管如此,空间学习能力受损(≤0.007),而经产大鼠的焦虑样行为(≤0.034)减少。总体而言,我们的数据表明,母体海马 CA1 免受全身炎症的影响,但易受围产期氧化应激的影响。围产期氧化应激升高,如在妊娠并发症中,可能导致围产期神经和行为可塑性改变。健康妊娠与母体全身和大脑氧化应激升高有关。在产后期间,大脑氧化应激仍然升高,而全身氧化应激得到解决。这种持续的母体大脑氧化应激与产后期间的学习障碍和焦虑样行为减少有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d27/11381002/ce0b2931000d/ajpregu.00026.2024_f001.jpg

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