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[Role of 15-lipoxygenase/15-hydroxyeicosatetraenoic acid in hypoxic pulmonary arterial hypertension].
Yu, Hang; Ma, Cui; Zhu, Da-Ling.
Afiliação
  • Yu H; Branch Campus of Daqing, Harbin Medical University, Daqing 163311, China.
  • Ma C; Branch Campus of Daqing, Harbin Medical University, Daqing 163311, China.
  • Zhu DL; Branch Campus of Daqing, Harbin Medical University, Daqing 163311, China.
Sheng Li Xue Bao ; 73(4): 646-656, 2021 Aug 25.
Article em Zh | MEDLINE | ID: mdl-34405220
Pulmonary arterial hypertension (PAH) is a rare disease with a complex aetiology characterized by elevated pulmonary artery resistance, which leads to progressive right ventricular failure and ultimately death. The aberrant metabolism of arachidonic acid in the pulmonary vasculature plays a central role in the pathogenesis of PAH. The levels of 15-lipoxygenase (15-LO) and 15-hydroxyeicosatetraenoic acid (15-HETE) are elevated in the pulmonary arterial endothelial cells (PAECs), pulmonary smooth muscle cells (PASMCs) and fibroblasts of PAH patients. Under hypoxia condition, 15-LO/15-HETE induces pulmonary artery contraction, promotes the proliferation of PAECs and PASMCs, inhibits apoptosis of PASMCs, promotes fibrosis of pulmonary vessels, and then leads to the occurrence of PAH. Here, we review the research progress on the relationship between 15-LO/15-HETE and hypoxic PAH, in order to clarify the significance of 15-LO/15-HETE in hypoxic PAH.
Assuntos
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Base de dados: MEDLINE Assunto principal: Araquidonato 15-Lipoxigenase / Hipertensão Arterial Pulmonar Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Araquidonato 15-Lipoxigenase / Hipertensão Arterial Pulmonar Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article