Parental cardiorespiratory fitness influences early life energetics and metabolic health.

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Physiological genomics Pub Date : 2024-02-01 Epub Date: 2023-11-27 DOI:10.1152/physiolgenomics.00045.2023
Daniel G Sadler, Lillie Treas, Taylor Ross, James D Sikes, Steven L Britton, Lauren G Koch, Brian D Piccolo, Elisabet Børsheim, Craig Porter
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引用次数: 0

Abstract

High cardiorespiratory fitness (CRF) is associated with a reduced risk of metabolic disease and is linked to superior mitochondrial respiratory function. This study investigated how intrinsic CRF affects bioenergetics and metabolic health in adulthood and early life. Adult rats selectively bred for low and high running capacity [low capacity runners (LCR) and high capacity runners (HCR), respectively] underwent metabolic phenotyping before mating. Weanlings were evaluated at 4-6 wk of age, and whole body energetics and behavior were assessed using metabolic cages. Mitochondrial respiratory function was assessed in permeabilized tissues through high-resolution respirometry. Proteomic signatures of adult and weanling tissues were determined using mass spectrometry. The adult HCR group exhibited lower body mass, improved glucose tolerance, and greater physical activity compared with the LCR group. The adult HCR group demonstrated higher mitochondrial respiratory capacities in the soleus and heart compared with the adult LCR group, which coincided with a greater abundance of proteins involved in lipid catabolism. HCR and LCR weanlings had similar body mass, but HCR weanlings displayed reduced adiposity. In addition, HCR weanlings exhibited better glucose tolerance and higher physical activity levels than LCR weanlings. Higher respiratory capacities were observed in the soleus, heart, and liver tissues of HCR weanlings compared with LCR weanlings, which were not owed to greater mitochondrial content. Proteomic analyses indicated a greater potential for lipid oxidation in the contractile muscles of HCR weanlings. In conclusion, offspring born to parents with high CRF possess an enhanced capacity for lipid catabolism and oxidative phosphorylation, thereby influencing metabolic health. These findings highlight that intrinsic CRF shapes the bioenergetic phenotype with implications for metabolic resilience in early life.NEW & NOTEWORTHY Inherited cardiorespiratory fitness (CRF) influences early life bioenergetics and metabolic health. Higher intrinsic CRF was associated with reduced adiposity and improved glucose tolerance in early life. This metabolic phenotype was accompanied by greater mitochondrial respiratory capacity in skeletal muscle, heart, and liver tissue. Proteomic profiling of these three tissues further revealed potential mechanisms linking inherited CRF to early life metabolism.

父母心肺健康影响生命早期能量学和代谢健康。
背景:高心肺适能(CRF)与降低代谢性疾病的风险相关,并与优越的线粒体呼吸功能有关。本研究探讨了内在CRF如何影响成年期和早期生命的生物能量学和代谢健康。方法:选择低(LCR)和高(HCR)跑步能力的成年大鼠在交配前进行代谢表型分析。在4-6周龄时对断奶仔猪进行评估,并在代谢笼中评估全身能量学和行为。通过高分辨率呼吸仪评估透性组织的线粒体呼吸功能。用质谱法测定成体和断奶组织的蛋白质组学特征。结果:与LCR相比,成人HCR表现出较低的体重,改善的葡萄糖耐量和更多的身体活动。与成年LCR相比,成年HCR在比目鱼和心脏表现出更高的线粒体呼吸能力,这与参与脂质分解代谢的蛋白质更丰富相吻合。HCR断奶仔猪和LCR断奶仔猪的体重相似,但HCR断奶仔猪的肥胖程度有所降低。此外,与LCR断奶仔猪相比,HCR断奶仔猪表现出更好的葡萄糖耐量和更高的身体活动量。与LCR断奶仔猪相比,HCR断奶仔猪的比目鱼、心脏和肝脏组织的呼吸能力更高,这不是由于线粒体含量更高。蛋白质组学分析表明,HCR断奶仔猪收缩肌肉中脂质氧化的可能性更大。结论:高CRF后代的脂质分解代谢和氧化磷酸化能力增强,从而影响代谢健康。这些发现强调,内在的CRF塑造了生命早期代谢弹性的生物能量表型。
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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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