Assessment of right ventricular function in the research setting: knowledge gaps and pathways forward. An Official American Thoracic Society Research Statement

T Lahm, IS Douglas, SL Archer, HJ Bogaard… - American journal of …, 2018 - atsjournals.org
Background: Right ventricular (RV) adaptation to acute and chronic pulmonary hypertensive
syndromes is a significant determinant of short-and long-term outcomes. Although …

Murine models of heart failure with preserved ejection fraction: a “fishing expedition”

M Valero-Muñoz, W Backman, F Sam - Basic to Translational Science, 2017 - jacc.org
Heart failure with preserved ejection fraction (HFpEF) is characterized by signs and
symptoms of heart failure in the presence of a normal left ventricular ejection fraction …

Endothelial HIF-2α contributes to severe pulmonary hypertension due to endothelial-to-mesenchymal transition

H Tang, A Babicheva, KM McDermott… - … of Physiology-Lung …, 2018 - journals.physiology.org
Pulmonary vascular remodeling characterized by concentric wall thickening and intraluminal
obliteration is a major contributor to the elevated pulmonary vascular resistance in patients …

Intravascularly infused extracellular matrix as a biomaterial for targeting and treating inflamed tissues

MT Spang, R Middleton, M Diaz, J Hunter… - Nature biomedical …, 2023 - nature.com
Decellularized extracellular matrix in the form of patches and locally injected hydrogels has
long been used as therapies in animal models of disease. Here we report the safety and …

Bone morphogenetic proteins in vascular homeostasis and disease

MJ Goumans, A Zwijsen… - Cold Spring Harbor …, 2018 - cshperspectives.cshlp.org
It is well established that control of vascular morphogenesis and homeostasis is regulated
by vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), Delta-like 4 …

Exploring the monocrotaline animal model for the study of pulmonary arterial hypertension: A network approach

R Nogueira-Ferreira, R Vitorino, R Ferreira… - Pulmonary …, 2015 - Elsevier
Pulmonary arterial hypertension (PAH) is responsible for the premature death mainly
because of progressive and severe heart failure. This disease is characterized by increased …

Group 3 pulmonary hypertension: from bench to bedside

N Singh, P Dorfmüller, OA Shlobin… - Circulation …, 2022 - Am Heart Assoc
Pulmonary hypertension (PH) because of chronic lung disease is categorized as Group 3
PH in the most recent classification system. Prevalence of these diseases is increasing over …

Animal models of pulmonary hypertension: Getting to the heart of the problem

JP Dignam, TE Scott, BK Kemp‐Harper… - British Journal of …, 2022 - Wiley Online Library
Despite recent therapeutic advances, pulmonary hypertension (PH) remains a fatal disease
due to the development of right ventricular (RV) failure. At present, no treatments targeted at …

Interplay of low-density lipoprotein receptors, LRPs, and lipoproteins in pulmonary hypertension

L Calvier, J Herz, G Hansmann - Basic to Translational Science, 2022 - jacc.org
The low-density lipoprotein receptor (LDLR) gene family includes LDLR, very LDLR, and
LDL receptor–related proteins (LRPs) such as LRP1, LRP1b (aka LRP-DIT), LRP2 (aka …

TGFβ and BMPRII signalling pathways in the pathogenesis of pulmonary arterial hypertension

B Tielemans, M Delcroix, C Belge, R Quarck - Drug Discovery Today, 2019 - Elsevier
Highlights•Dysregulation of the BMP–TGFβ axis is a major concern in pulmonary arterial
hypertension.•Reduced BMPRII expression causes an imbalance of BMP–TGFβ …