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Updated: Apr 28, 2026

Invasive Hemodynamic Characterization of the Portal-hypertensive Syndrome in Cirrhotic Rats
Published on: August 1, 2018
Vascular pathobiology in chronic liver disease and cirrhosis - current status and future directions
Yasuko Iwakiri1, Vijay Shah2, Don C Rockey3
1The Section of Digestive Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
Insights
Chronic liver disease alters liver vasculature, leading to portal hypertension. Understanding hepatic vascular cell signaling is key to developing new treatments for this condition.
Area of Science:
- Vascular Biology
- Hepatology
- Gastroenterology
Background:
- Chronic liver disease causes significant intra- and extrahepatic vascular changes.
- Portal hypertension is closely linked to alterations in liver vasculature and vascular biology.
- Hepatic vascular cells, including sinusoidal endothelial cells and hepatic stellate cells, play critical roles in liver fibrosis and portal hypertension pathogenesis.
Purpose of the Study:
- To review the current understanding of the basic biology of portal hypertension.
- To focus on the physiology, pathophysiology, and cell signaling within the liver and mesenteric vasculature.
- To highlight translational implications and future research directions.
Main Methods:
- This is a review article, synthesizing existing research.
- Focuses on cellular and molecular mechanisms of portal hypertension.
- Examines signaling pathways involving growth factors and vasoactive peptides.
Main Results:
- Increased intra-hepatic resistance is an early feature of liver injury, driven by hepatic vascular cell changes.
- Complex signaling pathways involving cytokines and vasoactive peptides contribute to portal hypertension.
- Vascular changes in the liver propagate to the extrahepatic circulation, worsening portal hypertension through collateral formation and vasodilation.
Conclusions:
- Hepatic vascular cells and their signaling pathways are central to the development of portal hypertension in chronic liver disease.
- Understanding these mechanisms is crucial for developing targeted therapies.
- Further research into cellular signaling and vascular dynamics holds promise for translational applications.
Abstract:
Chronic liver disease is associated with remarkable alterations in the intra- and extrahepatic vasculature. Because of these changes, the fields of liver vasculature and portal hypertension have recently become closely integrated within the broader vascular biology discipline. As developments in vascular biology have evolved, a deeper understanding of vascular processes has led to a better understanding of the mechanisms of the dynamic vascular changes associated with portal hypertension and chronic liver disease. In this context, hepatic vascular cells, such as sinusoidal endothelial cells and pericyte-like hepatic stellate cells, are closely associated with one another, where they have paracrine and autocrine effects on each other and themselves. These cells play important roles in the pathogenesis of liver fibrosis/cirrhosis and portal hypertension. Further, a variety of signaling pathways have recently come to light. These include growth factor pathways involving cytokines such as transforming growth factor β, platelet derived growth factor, and others as well as a variety of vasoactive peptides and other molecules. An early and consistent feature of liver injury is the development of an increase in intra-hepatic resistance; this is associated with changes in hepatic vascular cells and their signaling pathway that cause portal hypertension. A critical concept is that this process aggregates signals to the extrahepatic circulation, causing derangement in this system's cells and signaling pathways, which ultimately leads to the collateral vessel formation and arterial vasodilation in the splanchnic and systemic circulation, which by virtue of the hydraulic derivation of Ohm's law (pressure = resistance × flow), worsens portal hypertension. This review provides a detailed review of the current status and future direction of the basic biology of portal hypertension with a focus on the physiology, pathophysiology, and signaling of cells within the liver, as well as those in the mesenteric vascular circulation. Translational implications of recent research and the future directions that it points to are also highlighted.
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