Physiological ReportsPhysiologyPeer-reviewed journal article
Glenn circulation causes early and progressive shunting in a surgical model of pulmonary arteriovenous malformations
Tina C. WaniD, Henry Rousseau, Carol Mattern, Madeline Tabor, Matthew Robert HodgesiD, Ramani RamchandraniD, Andrew D. SpearmaniD
Abstract
BackgroundPulmonary arteriovenous malformations (PAVMs) universally develop in patients with single ventricle congenital heart disease (CHD). Single ventricle PAVMs have been recognized for over 50 years, yet they are poorly understood, and we lack any medical therapies. To improve our understanding of single ventricle PAVM initiation and progression, we developed a surgical rat model of Glenn circulation and characterized PAVM physiology over multiple time points. MethodsUsing adult rats, we performed a left thoracotomy and end-to-end anastomosis of the left superior vena cava to the left pulmonary artery (unilateral Glenn), or sham surgical control. To assess for PAVM physiology in the left lung, we quantified intrapulmonary shunting using two independent methods (bubble echocardiography and fluorescent microsphere injection) at 2 weeks, 2 months, and 6 months. Additionally, we performed arterial blood gas measurements to assess oxygenation and plethysmography to assess ventilation. ResultsWe identified pathologic intrapulmonary shunting by bubble echocardiography as early as 2 weeks post-Glenn surgery, and shunting continued chronically at 2- and 6-months post-Glenn. Shunting also progressed over time, demonstrated by increased shunting of 10{micro}m microspheres at 6 months. Shunting was accompanied by mildly decreased arterial oxygenation, but there were no differences in ventilation as quantified by plethysmography. ConclusionsOur surgical animal model of unilateral Glenn circulation re-creates the clinical condition of single ventricle PAVMs with early and progressive intrapulmonary shunting. This model is poised to characterize single ventricle PAVM pathophysiology and lead to mechanistic and therapeutic discovery. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=78 SRC="FIGDIR/small/588015v1_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@b1c722org.highwire.dtl.DTLVardef@1889af9org.highwire.dtl.DTLVardef@1767519org.highwire.dtl.DTLVardef@1c230_HPS_FORMAT_FIGEXP M_FIG C_FIG
- Citations
- 4
- FWCI
- 1.10
- Field percentile
- top 22%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Decreased endothelial cell retinoic acid signaling accelerates progression of single ventricle pulmonary arteriovenous malformations
Henry Rousseau, Tina C. Wan, … Andrew D. Spearman·bioRxiv·Dec 21, 2025
- Pulmonary Vascular Endothelial Dysfunction is Induced by Non-Pulsatile Pulmonary Blood Flow in an Ovine Classic Glenn Model
Jonathan Hyde, Michael A. Smith, … Jeffrey R. Fineman·Comprehensive physiologyPeer-reviewed·Nov 10, 2025
- Pulsatile flow dynamics determine pulmonary arterial architecture
Stephen B. Spurgin, Lauren Thai, … Ondine B. Cleaver·bioRxiv·Jun 30, 2025
- Switching the left and the right hearts: A novel bi-ventricle mechanical support strategy with spared native single-ventricle
E. Sisli, K. Pekkan, … M. Ozbaran·Annals of Biomedical EngineeringPeer-reviewed·Aug 27, 2023
- Postnatal Pulmonary Artery Development from Transcript to Tissue
Erica L. Schwarz, Abhay B. Ramachandra, … Jay D. Humphrey·Journal of The Royal Society InterfacePeer-reviewed·Jun 17, 2026
- Microvascular preservation and cardiomyocyte hyperplasia underlie adaptive right ventricular development in congenital heart disease-associated pulmonary arterial hypertension
Michael A. Smith, Eleana Stephanie Guardado, … Jeffrey R. Fineman·American Journal of Physiology-Heart and Circulatory PhysiologyPeer-reviewed·Sep 9, 2025