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首页> 外文期刊>Behavioural Brain Research: An International Journal >Maternal manipulation during late gestation (GDs 17-20) enhances ethanol consumption and promotes changes and opioid mRNA expression in infant rats
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Maternal manipulation during late gestation (GDs 17-20) enhances ethanol consumption and promotes changes and opioid mRNA expression in infant rats

机译:晚期妊娠期间的产妇操作(GDS 17-20)增强乙醇消耗,促进婴儿大鼠的变化和阿片类药物mRNA表达

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Fetal ethanol experience generates learning and memories capable to increase ethanol consummatory behaviors during infancy. Opioid system seems to be involved in mediating those alcohol-related behaviors. In this work, we proposed to study the impact of prenatal exposure to a moderate ethanol dose, upon ingestion of the drug and possible ethanol-induced molecular changes on opioid precursor peptides (POMC, Pro-enk and Pro-DYN) and receptors (MOR, DOR and KOR) mRNA expression, in hypothalamus. Pregnant rats received during gestational days (GDs) 17-20, a daily intragastric (i.g.) administration with 2g/kg ethanol or water. A third group of dams was left undisturbed during pregnancy (Unmanipulated group). Intake test was conducted at postnatal days (PDs) 14-15. Three groups of pups were performed: control (no intake test), water (vehicle) and 5% ethanol. At the end of intake test blood samples were taken to quantify blood ethanol concentrations (BECs) and hypothalamus sections were obtained to perform qRT-PRC assessment of opioid precursor peptides and receptors. The analysis of the consummatory responses (% of consumption) and pharmacokinetic profiles (BECs) suggested that maternal manipulation induced by i.g. intubations, during the last four days of gestation (whenever ethanol or water), are sufficient to induce infantile ethanol intake during infancy. Gene expression from the hypothalamus of unmanipulated group revealed that infantile ingestive experiences with ethanol can down-regulate expression of mRNA Pro-Dyn and up-regulate mRNA expression of MOR and KOR. Finally, MOR mRNA expression was attenuated by prenatal i.g. manipulation in pups exposed to 5% ethanol.
机译:胎儿乙醇体验产生了学习和记忆能够在婴儿期间增加乙醇污染行为。阿片类药系统似乎参与了调解这些与酗酒相关的行为。在这项工作中,我们提出研究产前暴露于中度乙醇剂量的影响,以摄入药物和可能的乙醇诱导的阿片类药物前体肽(POMC,Pro-ENK和Pro-Dyn)和受体(Mor ,dor和kor)mRNA表达,在下丘脑中。在妊娠期(GDS)17-20期间收到的孕大鼠,每日胃内(即)用2g / kg乙醇或水施用。在怀孕期间,第三组水坝被干扰(非法集团)。进气试验在后期(PDS)14-15进行。进行三组幼崽:对照(无摄入试验),水(载体)和5%乙醇。在摄入量结束时,试验血液样品被取量血液乙醇浓度(BECS),并获得下丘脑部分以进行阿片类药物前体肽和受体的QRT-PRC评估。分析综合反应(占消费量的百分比)和药代动力学谱(BECS)表明I.G的母体操纵诱导。在妊娠的最后四天(每当乙醇或水时),插管就足以在婴儿期间诱导幼儿乙醇摄入量。非甲基丘脑的基因表达揭示了乙醇的婴儿摄取经验可以下调mRNA pro-dyn的表达及Mor和Kor的上调mRNA表达。最后,MoraTAl I.G的MormRNA表达衰减。在暴露于5%乙醇的幼崽中操纵。

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