Pathophysiology and pathogenic mechanisms of pulmonary hypertension: role of membrane receptors, ion channels, and Ca2+ signaling

A Balistrieri, A Makino, JXJ Yuan - Physiological reviews, 2023 - journals.physiology.org
The pulmonary circulation is a low-resistance, low-pressure, and high-compliance system
that allows the lungs to receive the entire cardiac output. Pulmonary arterial pressure is a …

Role of resveratrol in inhibiting pathological cardiac remodeling

S Fan, Y Hu, Y You, W Xue, R Chai, X Zhang… - Frontiers in …, 2022 - frontiersin.org
Cardiovascular disease is a group of diseases with high mortality in clinic, including
hypertension, coronary heart disease, cardiomyopathy, heart valve disease, heart failure, to …

IL-11 system participates in pulmonary artery remodeling and hypertension in pulmonary fibrosis

J Milara, I Roger, P Montero, E Artigues, J Escrivá… - Respiratory …, 2022 - Springer
Background Pulmonary hypertension (PH) associated to idiopathic pulmonary fibrosis (IPF)
portends a poor prognosis. IL-11 has been implicated in fibrotic diseases, but their role on …

Interleukin-6 and pulmonary hypertension: from physiopathology to therapy

WJ Xu, Q Wu, WN He, S Wang, YL Zhao… - Frontiers in …, 2023 - frontiersin.org
Pulmonary hypertension (PH) is a progressive, pulmonary vascular disease with high
morbidity and mortality. Unfortunately, the pathogenesis of PH is complex and remains …

Mechanosensitive channel Piezo1 is required for pulmonary artery smooth muscle cell proliferation

J Chen, M Rodriguez, J Miao, J Liao… - … of Physiology-Lung …, 2022 - journals.physiology.org
Concentric pulmonary vascular wall thickening due partially to increased pulmonary artery
(PA) smooth muscle cell (PASMC) proliferation contributes to elevating pulmonary vascular …

[HTML][HTML] Targeting IL-11 system as a treatment of pulmonary arterial hypertension

J Milara, I Roger, P Montero, E Artigues, J Escrivá… - Pharmacological …, 2023 - Elsevier
IL-11 is linked to fibrotic diseases, but its role in pulmonary hypertension is unclear. We
examined IL-11's involvement in idiopathic pulmonary arterial hypertension (iPAH). Using …

Notopterol attenuates monocrotaline-induced pulmonary arterial hypertension in rat

L Huang, H Li, S Huang, S Wang, Q Liu… - Frontiers in …, 2022 - frontiersin.org
Introduction Current targeted pulmonary arterial hypertension (PAH) therapies have
improved lung hemodynamics, cardiac function, and quality of life; however, none of these …

mTOR signaling network in cell biology and human disease

JJ Yu, EA Goncharova - International journal of molecular sciences, 2022 - mdpi.com
The mechanistic target of rapamycin (mTOR) is a serine/threonine protein kinase that
regulates multiple processes, including gene transcription, protein synthesis, ribosome …

CircItgb5 promotes synthetic phenotype of pulmonary artery smooth muscle cells via interacting with miR-96-5p and Uba1 in monocrotaline-induced pulmonary …

H Su, H Zhu, S Wang, Y Li, C Yan, J Wang, K Ying - Respiratory Research, 2023 - Springer
Background Pulmonary arterial hypertension (PAH) is a rare but fatal cardiopulmonary
disease mainly characterized by pulmonary vascular remodeling. Aberrant expression of …

Integrated bioinformatic analysis reveals TXNRD1 as a novel biomarker and potential therapeutic target in idiopathic pulmonary arterial hypertension

W Lin, Y Tang, M Zhang, B Liang, M Wang… - Frontiers in …, 2022 - frontiersin.org
Idiopathic pulmonary arterial hypertension (IPAH) is a life-threatening cardiopulmonary
disease lacking specific diagnostic markers and targeted therapy, and its mechanism of …