使用代谢组学和脂质组学评估怀孕期间重复剂量碘化钾摄入对雄性和雌性大鼠后代的影响。

Clément Rosique, Dalila Lebsir, Philippe Lestaevel, Sheherazade Benatia, Pierre Guigon, François Caire-Maurisier, Marc Benderitter, Djawed Bennouna, Maâmar Souidi, Jean-Charles Martin
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引用次数: 16

摘要

应对核事故的准备工作包括采取干预措施,保护孕妇不长期接触放射性碘。本研究的目的是研究一种新的设计,包括在妊娠后期第9-16天(GD9-GD16)大鼠重复给药碘化钾(KI, 1 mg/kg) 8天。这种早期碘甲状腺阻断(ITB)策略在后代出生后两个月进行了评估。雌雄大鼠的功能行为测试(包括强迫游泳测试(FST)和旋转杆测试(RRT))显示,ki处理的雌性大鼠FST表现较低,ki处理的雄性大鼠RRT表现较低。这种表现下降与皮质代谢紊乱有关,包括氨基酸代谢、酪氨酸代谢、二十二碳六烯酸(DHA)脂质和信号脂质。除了这些与行为相关的代谢变化外,在断奶后大鼠的皮质和血浆中,一部分捕获的代谢组(17-25%)和脂质组(3.7-7.35%)对子宫内KI预防治疗仍然敏感,存在一些与性别相关的差异。这些紊乱只有一部分归因于较低的TSH和T4水平(仅限男性)。ki诱导的代谢变化涉及广泛的功能,包括代谢和细胞稳态以及细胞信号功能。无论性别和组织如何,KI的主要作用是影响神经递质、氨基酸代谢和omega-3 DHA代谢。综上所述,数据表明,在妊娠后期连续8天每天以1mg /kg/天的剂量重复给药并不能保护母亲和胎儿免受核事故辐射的伤害。CV-ANOVA:方差交叉验证分析;DHA:二十二碳六烯酸;FST:强迫游泳测试;FT3:血浆游离三碘甲状腺原氨酸;FT4:血浆游离甲状腺素;GD:妊娠日;ITB:碘甲状腺阻断;KI:碘化钾;LC/MS:液相色谱-质谱联用;MTBE:甲基叔丁基醚;M /z:质荷比;PLS-DA:偏最小二乘判别分析;PRIODAC:意外放射性释放中反复稳定碘预防RRT: Rotarod测试;TSH:促甲状腺激素;VIP:在投影中不同的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of the effects of repeated doses of potassium iodide intake during pregnancy on male and female rat offspring using metabolomics and lipidomics.

Preparedness for nuclear accident responsiveness includes interventions to protect pregnancies against prolonged exposure to radioactive iodine. The aim of this study was to investigate a new design consisting of repeated administration of potassium iodide (KI, 1 mg/kg) for 8 days in late pregnancy gestational day 9-16 (GD9-GD16) in rats. The later-life effects of this early-life iodine thyroid blocking (ITB) strategy were assessed in offspring two months afterbirth. Functional behavioral tests including forced swimming test (FST) and rotarod test (RRT) in rats of both genders showed lower FST performance in KI-treated females and lower RRT performance in KI-treated male pups. This performance decline was associated with metabolic disruptions in cortex involving amino acid metabolism, tyrosine metabolism, as well as docosahexaenoic acid (DHA) lipids and signaling lipids in males and females. Beyond these behavior-associated metabolic changes, a portion of the captured metabolome (17-25%) and lipidome (3.7-7.35%) remained sensitive to in utero KI prophylactic treatment in both cortex and plasma of post-weaning rats, with some gender-related variance. Only part of these disruptions was attributed to lower levels of TSH and T4 (males only). The KI-induced metabolic shifts involved a broad spectrum of functions encompassing metabolic and cell homeostasis and cell signaling functions. Irrespective Regardless of gender and tissues, the predominant effects of KI affected neurotransmitters, amino acid metabolism, and omega-3 DHA metabolism. Taken together, data demonstrated that repeated daily KI administration at 1 mg/kg/day for 8 days during late pregnancy failed to protect the mother-fetus against nuclear accident radiation. Abbreviations: CV-ANOVA: Cross-validation analysis of variance; DHA: Docosahexaenoic acid; FST: Forced swimming test; FT3: plasma free triiodothyronine; FT4: plasma free thyroxine; GD: Gestational day; ITB: Iodine thyroid blocking; KI: potassium iodide; LC/MS: Liquid chromatography coupled with mass spectrometry; MTBE: Methyl tert-butyl ether; m/z: mass-to-charge ratio; PLS-DA: Partial least squares-discriminant analysis; PRIODAC: Repeated stable iodide prophylaxis in accidental radioactive releases; RRT: Rotarod test; TSH: Thyroid-stimulating hormone; VIP: Variable importance in projection.

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