母体遗传和饮食调节后代的维生素 A 平衡,并影响小鼠成年后的肥胖易感性。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM American journal of physiology. Endocrinology and metabolism Pub Date : 2024-09-01 Epub Date: 2024-07-17 DOI:10.1152/ajpendo.00116.2024
Ramkumar Srinivasagan, Sebastià Galmés, Denitsa Vasileva, Paula Rubí, Andreu Palou, Jaume Amengual, Joan Ribot, Johannes von Lintig, M Luisa Bonet
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引用次数: 0

摘要

围产期营养对成年后的代谢健康有着深远的影响。本研究旨在探讨增加母体维生素 A(VA)供应量是否会导致后代出现有益的代谢表型。研究人员利用缺乏肠特异性同源框(ISX)转录因子的小鼠进行研究,这种小鼠通过饮食中的β-胡萝卜素(BC)增加了肠道维生素A视黄醇的生成。在妊娠最后一周和整个哺乳期,给 ISX 缺乏的母鼠喂食 VA 充足或 BC 丰富的食物。饲喂BC的母鼠的后代(BC后代)在乳汁和断奶肝脏中的总视黄醇水平高出2到2.5倍,这表明在妊娠后期和哺乳期VA供应量增加。自断奶起饲喂标准或高脂饮食(HFD)13周后,对相应的VAS和BC后代(雄性和雌性)在断奶和成年时的情况进行了比较。高脂饮食引起的脂肪堆积质量和脂肪细胞直径等脂肪指标的增加在雄性动物中比雌性动物更明显,而在BC后代中则有所减弱或抑制。值得注意的是,BC 后代对 HFD 引起的循环三酰甘油水平升高和肝脏脂肪变性具有保护作用。这些保护作用与 BC 后代食物效率降低、脂肪组织产热和线粒体氧化代谢能力增强以及脂肪细胞增生而非肥大有关。总之,受遗传影响的母体VA营养可能会给后代带来代谢方面的益处,在妊娠晚期和哺乳期轻度增加VA营养可防止成年后肥胖和代谢失调。
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Maternal genetics and diet modulate vitamin A homeostasis of the offspring and affect the susceptibility to obesity in adulthood in mice.

Perinatal nutrition exerts a profound influence on adult metabolic health. This study aimed to investigate whether increased maternal vitamin A (VA) supply can lead to beneficial metabolic phenotypes in the offspring. The researchers utilized mice deficient in the intestine-specific homeobox (ISX) transcription factor, which exhibits increased intestinal VA retinoid production from dietary β-carotene (BC). ISX-deficient dams were fed a VA-sufficient or a BC-enriched diet during the last week of gestation and the whole lactation period. Total retinol levels in milk and weanling livers were 2- to 2.5-fold higher in the offspring of BC-fed dams (BC offspring), indicating increased VA supplies during late gestation and lactation. The corresponding VA-sufficient and BC offspring (males and females) were compared at weaning and adulthood after being fed either a standard or high-fat diet (HFD) with regular VA content for 13 weeks from weaning. HFD-induced increases in adiposity metrics, such as fat depot mass and adipocyte diameter, were more pronounced in males than females and were attenuated or suppressed in the BC offspring. Notably, the BC offspring were protected from HFD-induced increases in circulating triacylglycerol levels and hepatic steatosis. These protective effects were associated with reduced food efficiency, enhanced capacity for thermogenesis and mitochondrial oxidative metabolism in adipose tissues, and increased adipocyte hyperplasia rather than hypertrophy in the BC offspring. In conclusion, maternal VA nutrition influenced by genetics may confer metabolic benefits to the offspring, with mild increases in late gestation and lactation protecting against obesity and metabolic dysregulation in adulthood.NEW & NOTEWORTHY A genetic mouse model, deficient in intestine-specific homeobox (ISX) transcription factor, is used to show that a mildly increased maternal vitamin A supply from β-carotene feeding during late gestation and lactation programs energy and lipid metabolism in tissues and protects the offspring from diet-induced hypertrophic obesity and hepatic steatosis. This knowledge may have implications for human populations where polymorphisms in ISX and ISX target genes involved in vitamin A homeostasis are prevalent.

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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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