D28-16 Transcriptomic Remodeling of Kidneys in Preclinical Models of Pulmonary Hypertension and Right Heart Failure
Abstract
Abstract Rationale Pulmonary hypertension (PH) is a progressive pulmonary vascular disease characterized by elevated pulmonary artery pressures leading to right ventricular failure (RVF) and death. Growing evidence suggests that PH is associated with extrapulmonary manifestations. The Renin-Angiotensin-Aldesterone System (RAAS) plays a central role in PH, due to the fundamental connection between the heart, lungs, liver, and kidneys. Currently, there is a paucity of data on changes in the kidneys secondary to PH and RVF. We hypothesized that severe PH and RVF in pre-clinical models is associated with remodeling in the kidneys. Methods PH and RVF were induced in male Sprague Dawley rats with either monocrotaline (MCT) (60 mg/kg; subcutaneous; 4-week protocol; n = 6) or Sugen with hypoxia (SuHx) (20 mg/kg; 3-week hypoxia 10%O2, 2-week normoxia; n = 6). Saline treated rats served as control (n = 6). Serial echocardiography and terminal cardiac catheterization were performed. RV hypertrophy index, RV systolic pressure, and RV function were recorded. Kidneys were processed for histology and bulk RNA sequencing and bioinformatics analysis was conducted. Results MCT and SuHx rats developed severe PH and RVF as demonstrated by significantly increased RV systolic pressure and RV hypertrophy index, and significantly reduced RV function (p < 0.05 for all parameters). Subsequent transcriptomic analysis on the kidneys revealed transcriptomic remodeling in the diseased rats. There were a total of 13 unique pathways in the MCT rats, 16 in the SuHx rats, and 10 common pathways significant between both models. Common upregulated pathways included apoptosis and several inflammatory pathways including, IL-6/JAK/STAT3 signaling and interferon gamma response. Additionally, a total of 463 genes specific to MCT, 675 genes specific to SuHx, and 97 genes common between both rat models were significant compared to control rats (padj
Fields of Study & Subjects
Pulmonary Hypertension Research and Treatments
Eicosanoids and Hypertension Pharmacology
Cardiovascular Disease and Adiposity
Publication details
- Journal / source
- American Journal of Respiratory and Critical Care Medicine
- Publisher
- Oxford University Press (OUP)
- Volume
- 212
- Issue
- Supplement_2
- Publication date
- 1 June 2026
- Language
- EN