Abstract

There is increasing interest in the potential for metabolic profiling to evaluate the progression of pulmonary hypertension (PH). However, a detailed analysis of the metabolic changes in lungs at the early stage of PH, characterized by increased pulmonary artery pressure but prior to the development of right ventricle hypertrophy and failure, is lacking in a preclinical animal model of PH. Thus, we undertook a study using rats 14 days after exposure to monocrotaline (MCT), to determine whether we could identify early stage metabolic changes prior to the manifestation of developed PH. We observed changes in multiple pathways associated with the development of PH, including activated glycolysis, increased markers of proliferation, disruptions in carnitine homeostasis, increased inflammatory and fibrosis biomarkers, and a reduction in glutathione biosynthesis. Further, our global metabolic profile data compare favorably with prior work carried out in humans with PH. We conclude that despite the MCT-model not recapitulating all the structural changes associated with humans with advanced PH, including endothelial cell proliferation and the formation of plexiform lesions, it is very similar at a metabolic level. Thus, we suggest that despite its limitations it can still serve as a useful preclinical model for the study of PH.

Highlights

  • Pulmonary hypertension (PH) is a disease characterized by increased proliferation of the vascular wall leading to increased pulmonary artery pressure that results in right ventricle hypertrophy and subsequent heart failure

  • The Fulton index (RV/left ventricle and septum (LV+S)) did not identify any signs of right ventricle (RV) hypertrophy 14 days after MCT, while at 28 days there was a significant evidence of RV hypertrophy (Fig 1D)

  • Our data indicate that 14 days after the injection of MCT, but prior to the development of pulmonary hypertension (PH) [16] there is already a switch to glycolysis and a reduction in mitochondrial beta oxidation as reflected in the accumulation of glycolytic intermediates and products and reductions in acyl-carnitine long-chain fatty acid metabolites

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Summary

Introduction

Pulmonary hypertension (PH) is a disease characterized by increased proliferation of the vascular wall leading to increased pulmonary artery pressure that results in right ventricle hypertrophy and subsequent heart failure. The specific roles of these authors are articulated in the 'author contributions' section

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Results
Conclusion

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