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Metabolomics analysis reveals that bile acids and phospholipids contribute to variable responses to low-temperature-induced ascites syndrome

机译:代谢组学分析表明,胆汁酸和磷脂有助于对低温诱发的腹水综合征做出不同的反应

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摘要

Ascites is a major problem for both human health and animal production, due to its association with high rates of morbidity and mortality, low efficiency of nutrient utilization, and permanent adverse effects on performance. Although it is one of the three major metabolic diseases in poultry production, the underlying mechanisms are largely unknown. In this study, six ascites syndrome (AS) chickens and six normal chickens were obtained from each group (108 chickens) at 21 and 35 days. A liver metabolomics method based on ultra-performance liquid chromatography/quadruple time-of-flight mass spectrometry (UPLC/Q-TOF/MS) was used to explore the metabolic pattern of low molecular mass metabolites in chickens with low-temperature-induced AS. Coupled with blood biochemistry and histopathology results, the significant difference in metabolic profiling between the AS group and the control group, as determined through pattern recognition analysis, indicated changes in global tissue metabolites. The results showed that a primary bile acid synthesis disorder and inflammation had occurred by 21 days and that lysophospholipid metabolism was disrupted by 35 days with the continuation of low temperatures. Several metabolites, including taurodeoxycholic acid, cholic acid glucuronide, glycocholic acid, LysoPC(15:0) and taurocholic acid, were identified as the potential and proper biomarkers of AS. These biochemical changes in tissue metabolites are related to perturbations of lipid metabolism, which may be helpful to further understand the AS mechanisms. This work shows that the metabolomics is a valuable tool for studying metabolic diseases.
机译:腹水是人类健康和动物生产的主要问题,因为它与高发病率和高死亡率,低养分利用效率以及对性能的长期不利影响有关。尽管它是家禽生产中的三大主要代谢疾病之一,但其潜在机制在很大程度上尚不清楚。在这项研究中,在第21天和第35天从每组(108只鸡)中获得了6只腹水综合征(AS)鸡和6只正常鸡。基于超高效液相色谱/四倍飞行时间质谱(UPLC / Q-TOF / MS)的肝脏代谢组学方法探讨了低温诱导AS鸡中低分子量代谢物的代谢模式。结合血液生化和组织病理学结果,通过模式识别分析确定,AS组和对照组之间代谢谱的显着差异表明整体组织代谢物发生了变化。结果表明,由于持续低温,到21天时发生了原发性胆汁酸合成异常和炎症,而到35天时溶血磷脂代谢被破坏。几种代谢物,包括牛磺脱氧胆酸,胆酸葡糖醛酸,糖胆酸,LysoPC(15:0)和牛磺胆酸被确定为AS的潜在和适当的生物标志物。组织代谢物中的这些生化变化与脂质代谢的紊乱有关,这可能有助于进一步了解AS机制。这项工作表明,代谢组学是研究代谢性疾病的宝贵工具。

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  • 来源
    《Molecular BioSystems》 |2014年第6期|1557-1567|共11页
  • 作者单位

    Poultry Institute, Chinese Academy of Agricultural Sciences, Yangzhou, Jiangsu 225125, China;

    Poultry Institute, Chinese Academy of Agricultural Sciences, Yangzhou, Jiangsu 225125, China,State Key Laboratory of Animal Nutrition, Department of Animal Science and Technology, China Agricultural University, Beijing 100093, China;

    Poultry Institute, Chinese Academy of Agricultural Sciences, Yangzhou, Jiangsu 225125, China;

    State Key Laboratory of Animal Nutrition, Department of Animal Science and Technology, China Agricultural University, Beijing 100093, China;

    Poultry Institute, Chinese Academy of Agricultural Sciences, Yangzhou, Jiangsu 225125, China;

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