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Insulin and branched-chain amino acid depletion during mouse preimplantation embryo culture programmes body weight gain and raised blood pressure during early postnatal life

机译:小鼠胚胎植入前胚胎培养过程中胰岛素和支链氨基酸的消耗会在出生后早期阶段增加体重并提高血压

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摘要

Mouse maternal low protein diet exclusively during preimplantation development (Emb-LPD) is sufficient to programme altered growth and cardiovascular dysfunction in offspring. Here, we use an in vitro model comprising preimplantation culture in medium depleted in insulin and branched-chain amino acids (BCAA), two proposed embryo programming inductive factors from Emb-LPD studies, to examine the consequences for blastocyst organisation and, after embryo transfer (ET), postnatal disease origin. Two-cell embryos were cultured to blastocyst stage in defined KSOM medium supplemented with four combinations of insulin and BCAA concentrations. Control medium contained serum insulin and uterine luminal fluid amino acid concentrations (including BCAA) found in control mothers from the maternal diet model (N-insulin + N-bcaa). Experimental medium (three groups) contained 50% reduction in insulin and/or BCAA (L-insulin + N-bcaa, N-insulin + L-bcaa, and L-insulin + N-bcaa). Lineage-specific cell numbers of resultant blastocysts were not affected by treatment. Following ET, a combined depletion of insulin and BCAA during embryo culture induced a non sex-specific increase in birth weight and weight gain during early postnatal life. Furthermore, male offspring displayed relative hypertension and female offspring reduced heart/body weight, both characteristics of Emb-LPD offspring. Combined depletion of metabolites also resulted in a strong positive correlation between body weight and glucose metabolism that was absent in the control group. Our results support the notion that composition of preimplantation culture medium can programme development and associate with disease origin affecting postnatal growth and cardiovascular phenotypes and implicate two important nutritional mediators in the inductive mechanism. Our data also have implications for human assisted reproductive treatment (ART) practice.
机译:仅在植入前发育期间(Emb-LPD)进行的小鼠母体低蛋白饮食足以控制后代生长的改变和心血管功能障碍。在这里,我们使用体外模型,包括在胰岛素和支链氨基酸(BCAA)贫乏的培养基中进行植入前培养,这是从Emb-LPD研究中提出的两个拟议的胚胎编程诱导因子,以检查对胚泡组织的影响,以及在胚胎移植后(ET),产后疾病的起源。在限定的KSOM培养基中,将两种细胞的胚胎培养到胚泡期,并补充四种胰岛素和BCAA浓度组合。对照培养基含有从母体饮食模型(N-胰岛素+ N-bcaa)中发现的对照母亲的血清胰岛素和子宫腔液氨基酸浓度(包括BCAA)。实验培养基(三组)的胰岛素和/或BCAA含量降低了50%(L-胰岛素+ N-bcaa,N-胰岛素+ L-bcaa和L-胰岛素+ N-bcaa)。所得胚泡的谱系特异性细胞数不受治疗影响。 ET后,胚胎培养过程中胰岛素和BCAA的联合消耗导致出生后早期出生体重和体重增加非性别特异性增加。此外,雄性后代表现出相对的高血压,而雌性后代降低了心脏/体重,这都是Emb-LPD后代的两​​个特征。代谢物的综合耗竭还导致体重和葡萄糖代谢之间的强正相关,而对照组则没有。我们的结果支持这样的观点,即植入前培养基的组成可以编程发育并与影响出生后生长和心血管表型的疾病起源相关,并且在诱导机制中涉及两个重要的营养介质。我们的数据也对人类辅助生殖治疗(ART)的实践有影响。

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