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首页> 外文期刊>Translational psychiatry. >Elevated paternal glucocorticoid exposure alters the small noncoding RNA profile in sperm and modifies anxiety and depressive phenotypes in the offspring
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Elevated paternal glucocorticoid exposure alters the small noncoding RNA profile in sperm and modifies anxiety and depressive phenotypes in the offspring

机译:高态糖皮质激淋暴露在精子中改变了小型非编码RNA谱,并在后代修饰焦虑和抑郁表型

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Recent studies have suggested that physiological and behavioral traits may be transgenerationally inherited through the paternal lineage, possibly via non-genomic signals derived from the sperm. To investigate how paternal stress might influence offspring behavioral phenotypes, a model of hypothalamic–pituitary–adrenal (HPA) axis dysregulation was used. Male breeders were administered water supplemented with corticosterone (CORT) for 4 weeks before mating with untreated female mice. Female, but not male, F1 offspring of CORT-treated fathers displayed altered fear extinction at 2 weeks of age. Only male F1 offspring exhibited altered patterns of ultrasonic vocalization at postnatal day 3 and, as adults, showed decreased time in open on the elevated-plus maze and time in light on the light–dark apparatus, suggesting a hyperanxiety-like behavioral phenotype due to paternal CORT treatment. Interestingly, expression of the paternally imprinted gene Igf2 was increased in the hippocampus of F1 male offspring but downregulated in female offspring. Male and female F2 offspring displayed increased time spent in the open arm of the elevated-plus maze, suggesting lower levels of anxiety compared with control animals. Only male F2 offspring showed increased immobility time on the forced-swim test and increased latency to feed on the novelty-supressed feeding test, suggesting a depression-like phenotype in these animals. Collectively, these data provide evidence that paternal CORT treatment alters anxiety and depression-related behaviors across multiple generations. Analysis of the small RNA profile in sperm from CORT-treated males revealed marked effects on the expression of small noncoding RNAs. Sperm from CORT-treated males contained elevated levels of three microRNAs, miR-98, miR-144 and miR-190b, which are predicted to interact with multiple growth factors, including Igf2 and Bdnf . Sustained elevation of glucocorticoids is therefore involved in the transmission of paternal stress-induced traits across generations in a process involving small noncoding RNA signals transmitted by the male germline.
机译:最近的研究表明,通过父系谱系,可以通过源于精子的非基因组信号进行生理和行为特征。为了探讨父权应力如何影响后代行为表型,使用丘脑 - 垂体肾上腺(HPA)轴缺剂的模型。在与未经处理的雌性小鼠交配前4周给予雄性饲养剂,施用皮质酮(皮质)4周。女性,但不是男性,CORT治疗的父亲的F1后代显示出现改变的恐惧灭绝在2周龄。只有雄性F1后代在后期3天,在后期第3天表现出改变的超声波发作模式,并且作为成人,在升高的加迷宫和光暗仪器上的光线上的时间内显示出降低的时间,表明由于父亲皮层治疗。有趣的是,在F1雄性后代的海马中增加了患者印迹基因IGF2的表达,但在女性后代下调。男性和女性F2后代显示在升高的加迷宫的开放式臂上的增加时间,表明与对照动物相比的焦虑水平较低。只有雄性F2后代在强制游泳试验中显示出不可动脉的时间增加,并增加了新型 - 压制喂养试验的潜水时间,表明这些动物中的抑郁状表型。统称,这些数据提供了证据表明父系皮甲治疗改变了多个代代症的焦虑和抑郁相关行为。从皮质处理的雄性中分析精子中的小RNA谱揭示了对小型非编码RNA的表达的标记作用。来自皮质处理的雄性的精子含有升高的三个微小RORNA,miR-98,miR-144和miR-190b,其预测预测与多种生长因子相互作用,包括IGF2和BDNF。因此,在涉及由雄性系丝传递的小型非分量RNA信号的过程中,血糖皮质激素的持续升高涉及跨越父胁迫诱导的特性的映射。

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