Literature DB >> 30178671

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

Feng-Jin Shao1, Yi-Tian Ying1, Xun Tan1, Qiao-Yan Zhang1, Wen-Ting Liao1.   

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.

Entities:  

Keywords:  broiler chicken; fatty acid; inflammation; lung; metabonomics; nitric oxide; oxidative stress; pentose phosphate pathway; pulmonary arterial hypertension

Mesh:

Year:  2018        PMID: 30178671     DOI: 10.1021/acs.jproteome.8b00316

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  3 in total

1.  Potential contribution of early endothelial progenitor cell (eEPC)-to-macrophage switching in the development of pulmonary plexogenic lesion.

Authors:  Feng-Jin Shao; Xiao-Ling Guo; Jia-Xue Xu; Rui Liu; Dan-Yue Li; Qing-Hao Li; Ting Zhou; Cun Fang; Xun Tan
Journal:  Respir Res       Date:  2022-10-23

2.  Metabolic Reprogramming of the Right Ventricle and Pulmonary Arteries in a Flow-Associated Pulmonary Arterial Hypertension Rat Model.

Authors:  Dongli Liu; Suyuan Qin; Danyan Su; Kai Wang; Yanyun Huang; Yuqin Huang; Yusheng Pang
Journal:  ACS Omega       Date:  2021-12-27

3.  MSC Transplantation Attenuates Inflammation, Prevents Endothelial Damage and Enhances the Angiogenic Potency of Endogenous MSCs in a Model of Pulmonary Arterial Hypertension.

Authors:  Fengjin Shao; Rui Liu; Xun Tan; Qiaoyan Zhang; Lujie Ye; Bingxuan Yan; Ying Zhuang; Jiaxue Xu
Journal:  J Inflamm Res       Date:  2022-03-30
  3 in total

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