A maternal ketogenic diet alters oviduct fluid nutrients and embryo histone acetylation in mice

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY Reproduction Pub Date : 2024-04-01 DOI:10.1530/rep-24-0026
Emma G Whatley, Alexandra J Harvey, David K Gardner
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Abstract

A ketogenic diet elevates blood β-hydroxybutyrate to concentrations that perturb the development, metabolism, histone acetylation (H3K27ac) and viability of preimplantation mouse embryos in vitro. However, whether a ketogenic diet alters β-hydroxybutyrate concentrations within female reproductive fluid is unknown. This study aimed to quantify glucose and β-hydroxybutyrate within mouse blood and oviduct fluid following standard diet and ketogenic diet consumption and to assess whether a maternal periconceptional ketogenic diet impacts in vivo embryo development and blastocyst H3K27ac. Female C57BL/6 x CBA mice were fed a standard or ketogenic diet (n=24 each) for 24-27 days. Glucose and β-hydroxybutyrate were quantified in blood via an electronic monitoring system, and in oviduct fluid via ultramicrofluorescence. The developmental grade of flushed blastocysts was recorded, and blastocyst cell number and H3K27ac was assessed via immunofluorescence. A maternal ketogenic diet elevated β-hydroxybutyrate in day 24 blood (P<0.001) and oviduct fluid (P<0.05) compared with a standard diet, whereas glucose was unchanged. A periconceptional ketogenic diet did not impact blastocyst cell number, however, significantly delayed blastocyst development (P<0.05) and reduced trophectoderm-specific H3K27ac (P<0.05) compared with standard diet-derived embryos. Maternal ketogenic diet consumption is therefore associated with reproductive tract nutrient changes and altered embryonic development and epigenetics in vivo. Future studies to assess whether periconceptional/gestational ketogenic diet consumption impacts human preimplantation, fetal, and long-term offspring development and health are warranted.

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母体生酮饮食改变小鼠输卵管液营养成分和胚胎组蛋白乙酰化
生酮饮食会使血液中的β-羟丁酸浓度升高,从而扰乱植入前小鼠胚胎的体外发育、代谢、组蛋白乙酰化(H3K27ac)和存活率。然而,生酮饮食是否会改变雌性生殖液中的β-羟丁酸浓度尚不清楚。本研究旨在对食用标准饮食和生酮饮食后小鼠血液和输卵管液中的葡萄糖和β-羟丁酸进行定量分析,并评估母体围孕期生酮饮食是否会影响体内胚胎发育和囊胚H3K27ac。雌性 C57BL/6 x CBA 小鼠喂食标准饮食或生酮饮食(各 24 只)24-27 天。通过电子监测系统对血液中的葡萄糖和β-羟丁酸进行定量,并通过超微荧光法对输卵管液中的葡萄糖和β-羟丁酸进行定量。记录冲洗囊胚的发育等级,并通过免疫荧光评估囊胚细胞数量和 H3K27ac。与标准饮食相比,母体生酮饮食使第 24 天血液(P<0.001)和输卵管液(P<0.05)中的β-羟丁酸升高,而葡萄糖没有变化。围孕期生酮饮食不会影响囊胚细胞数量,但与标准饮食衍生的胚胎相比,生酮饮食会显著延迟囊胚发育(P<0.05)并减少滋养层特异性 H3K27ac(P<0.05)。因此,母体摄入生酮饮食与生殖道营养物质的变化以及体内胚胎发育和表观遗传学的改变有关。今后有必要开展研究,评估围孕期/妊娠期摄入生酮饮食是否会影响人类胚胎植入前、胎儿以及后代的长期发育和健康。
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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
期刊最新文献
IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: A contemporary review of machine learning to predict adverse pregnancy outcomes from pharmaceuticals, including DDIs. O-GlcNAc participates in the meiosis of aging oocytes by mediating mitochondrial function. REPRODUCTIVE HEALTH IN TRANS AND GENDER-DIVERSE PATIENTS: Trauma-informed reproductive care for transgender and nonbinary people. SON controls mouse early embryonic development by regulating RNA splicing and histone methylation. IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: Systemic and ovarian impacts of heat stress in the porcine model.
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