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代谢组学分析揭示肉鸡肺动脉高压相关的生化途径。

Metabonomics Profiling Reveals Biochemical Pathways Associated with Pulmonary Arterial Hypertension in Broiler Chickens.

机构信息

Department of Veterinary Medicine , Zhejiang University , Hangzhou 310058 , P. R. China.

出版信息

J Proteome Res. 2018 Oct 5;17(10):3445-3453. doi: 10.1021/acs.jproteome.8b00316. Epub 2018 Sep 17.

DOI:10.1021/acs.jproteome.8b00316
PMID:30178671
Abstract

Pulmonary arterial hypertension (PAH) is the major cause of death in fast growing meat-type chickens (broiler chickens). At present, the underlying mechanisms that give rise to PAH are not fully understood. To identify the metabonomics profiles characterizing the process, we conducted a comprehensive gas chromatography-mass spectrometry (GC-MS)-based metabolic profiling of lung tissues from PAH broilers and age-matched controls. PAH was induced by excess salt in drinking water. Medial hypertrophy of pulmonary arteries was present in PAH birds as compared with controls. The metabonomics profiles of lung tissues well distinguished PAH broilers from control subjects. Significant changes in the levels of 41 metabolites were detected in PAH vs normal birds. Aside from the metabolic alterations indicating a status of oxidative stress and inflammation, evidence of reduced cellular uptake of arginine due to increased lysine biosynthesis and of a shift of arginine metabolism to arginase pathway were observed. In addition, PAH birds showed increased biosynthesis of fatty acids, which may be associated with excessive proliferation of vascular cells during pulmonary vascular remodeling. Furthermore, we observed significant changes in pentose phosphate pathway and increased aminomalonic acid in PAH broilers. These results provide additional biochemical insights into the pathogenesis of the PAH. Our data may lead to the development of new strategies to control PAH in broilers.

摘要

肺动脉高压(PAH)是快速生长的肉用型鸡(肉鸡)死亡的主要原因。目前,导致 PAH 的潜在机制尚不完全清楚。为了确定特征性的代谢组学特征,我们对 PAH 肉鸡和年龄匹配的对照组的肺组织进行了全面的气相色谱-质谱(GC-MS)代谢组学分析。PAH 是通过饮用水中过量的盐诱导的。与对照组相比,PAH 鸟类的肺动脉中层肥大。肺组织的代谢组学特征很好地区分了 PAH 肉鸡和对照组。与正常鸟类相比,在 PAH 中检测到 41 种代谢物的水平发生了显著变化。除了表明氧化应激和炎症状态的代谢改变外,还观察到由于赖氨酸生物合成增加和精氨酸代谢向精氨酸酶途径的转变,导致细胞摄取精氨酸减少的证据。此外,PAH 鸟类表现出脂肪酸合成的增加,这可能与肺血管重塑过程中血管细胞的过度增殖有关。此外,我们还观察到 PAH 肉鸡的戊糖磷酸途径和氨基丙二酸显著变化。这些结果为 PAH 的发病机制提供了额外的生化见解。我们的数据可能会导致开发控制肉鸡 PAH 的新策略。

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