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在小鼠胚胎植入前培养过程中,胰岛素和支链氨基酸的消耗会导致出生后早期体重增加和血压升高。

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

机构信息

Biological Sciences, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, UK; School of Natural and Environmental Sciences, Newcastle University, Newcastle Upon Tyne NE1 7RU, UK.

Biological Sciences, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, UK.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2018 Feb;1864(2):590-600. doi: 10.1016/j.bbadis.2017.11.020. Epub 2017 Nov 28.

Abstract

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.

摘要

在着床前发育阶段(胚胎着床前),仅用低蛋白饮食喂养母鼠足以改变后代的生长和心血管功能障碍。在这里,我们使用了一种体外模型,包括在胰岛素和支链氨基酸(BCAA)缺乏的培养基中进行着床前培养,这两种物质是胚胎着床前低蛋白饮食研究中提出的两种胚胎编程诱导因子,以研究其对囊胚组织的影响,以及胚胎移植(ET)后,后代疾病起源的影响。将二细胞胚胎在补充有胰岛素和 BCAA 浓度的四种组合的 KSOM 培养基中培养至囊胚阶段。对照培养基含有在母体饮食模型中(N-insulin+N-bcaa)从对照母鼠的血清胰岛素和子宫腔液氨基酸浓度(包括 BCAA)中发现的胰岛素和 BCAA。实验培养基(三组)含有 50%的胰岛素和/或 BCAA 减少(L-insulin+N-bcaa、N-insulin+L-bcaa 和 L-insulin+N-bcaa)。处理后,胚胎培养过程中胰岛素和 BCAA 的联合耗竭不会影响囊胚的谱系特异性细胞数量。ET 后,胚胎培养期间胰岛素和 BCAA 的联合耗竭会导致出生体重增加和出生后早期体重增加增加,且无性别特异性。此外,雄性后代表现出相对高血压,而雌性后代则表现出心脏/体重降低,这是胚胎着床前低蛋白饮食后代的特征。代谢物的联合耗竭还导致体重和葡萄糖代谢之间存在强烈的正相关,而在对照组中则不存在这种相关性。我们的结果支持这样一种观点,即着床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,这表明两种重要的营养介质参与了诱导机制。我们的数据还对人类辅助生殖治疗(ART)实践具有启示意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73e/5764225/81c334a8265f/gr1.jpg

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