Haemodynamic unloading reverses occlusive vascular lesions in severe pulmonary hypertension.

Abstract

AIMS An important pathogenic mechanism in the development of idiopathic pulmonary arterial hypertension is hypothesized to be a cancer-like cellular proliferation independent of haemodynamics. However, because the vascular lesions are inseparably coupled with haemodynamic stress, the fate of the lesions is unknown when haemodynamic stress is eliminated. METHODS AND RESULTS We applied left pulmonary artery banding to a rat model with advanced pulmonary hypertension to investigate the effects of decreased haemodynamic stress on occlusive vascular lesions. Rats were given an injection of the VEGF blocker Sugen5416 and exposed to 3 weeks of hypoxia plus an additional 7 weeks of normoxia (total 10 weeks) (SU/Hx/Nx rats). The banding surgery to reduce haemodynamic stress to the left lung was done at 1 week prior to (preventive) or 5 weeks after (reversal) the SU5416 injection. All SU/Hx/Nx-exposed rats developed severe pulmonary hypertension and right ventricular hypertrophy. Histological analyses showed that the non-banded right lungs developed occlusive lesions including plexiform lesions with marked perivascular cell accumulation. In contrast, banding the left pulmonary artery not only prevented the development of but also reversed the established occlusive lesions as well as perivascular inflammation in the left lungs. CONCLUSION Our results indicate that haemodynamic stress is prerequisite to the development and progression of occlusive neointimal lesions in this rat model of severe pulmonary hypertension. We conclude that perivascular inflammation and occlusive neointimal arteriopathy are driven by haemodynamic stress.

DOI: 10.1093/cvr/cvw070

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@article{Abe2016HaemodynamicUR, title={Haemodynamic unloading reverses occlusive vascular lesions in severe pulmonary hypertension.}, author={Kohtaro Abe and Masako Shinoda and Mariko Tanaka and Yukimitsu Kuwabara and Keimei Yoshida and Yoshitaka Hirooka and Ivan F. McMurtry and Masahiko Oka and Kenji Sunagawa}, journal={Cardiovascular research}, year={2016}, volume={111 1}, pages={16-25} }