NIH-funded research R01 grant

How molecular changes in the liver cause portal hypertension

Official title: A Molecular Approach to the Pathogenesis of Portal Hypertension

Funded at Medical University of South Carolina · NIH-11290437 · Data updated 2026-11-12

This project looks at how changes in proteins that control nitric oxide in liver blood vessel cells lead to portal hypertension in people with liver injury.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionMedical University of South Carolina
NIH-funded
Lab location1 site (Charleston, United States)
Project startFebruary 15, 2024
Project endJanuary 31, 2028
Funding year2026
Award (this year)$458,793
NIH project number5R01DK113159-07
Project IDNIH-11290437 on NIH RePORTER

Who could benefit from this research

Could help

Patients with liver injury or cirrhosis who have or are at risk for portal hypertension would be the most relevant group.

Less likely to help

People without liver disease or whose portal hypertension is due to non-liver causes (for example, portal vein thrombosis) would be unlikely to benefit directly from this work.

What this research studies

Researchers are studying why the tiny blood vessels in the liver make less nitric oxide after injury, which raises resistance to blood flow and leads to portal hypertension. They will examine biochemical changes in sinusoidal endothelial cells, focusing on how eNOS phosphorylation is altered by a protein complex that includes GIT1, β-PIX, and β-arrestins. Using molecular and cellular lab techniques and building on prior preliminary data, the team will test whether these defects explain the endothelial dysfunction seen after liver injury. The work is laboratory-focused and may include human-derived samples, with the goal of identifying targets that could be translated into treatments.

Why it matters

Potential benefit: If successful, this work could point to new drug targets to restore nitric oxide signaling and reduce portal pressure in patients with liver injury.

How similar studies have gone: Previous research has shown loss of eNOS-derived nitric oxide contributes to portal hypertension, but targeting the GIT1/β-PIX regulatory complex is a novel approach not yet tested clinically.

Where this research is happening

  • Medical University of South Carolina
    Charleston, United States
    Active

Researchers

  • Principal investigator: Rockey, Don C. — Medical University of South Carolina
  • Study coordinator: Rockey, Don C.

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.