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Updated: Dec 13, 2025

A Rat Carotid Artery Pressure-Controlled Segmental Balloon Injury with Periadventitial Therapeutic Application
Published on: July 9, 2020
A Rat Carotid Artery Pressure-Controlled Segmental Balloon Injury with Periadventitial Therapeutic Application
Nicholas E Buglak1, Edward S M Bahnson2
1Department of Surgery, Division of Vascular Surgery, University of North Carolina at Chapel Hill; Center for Nanotechnology in Drug Delivery, University of North Carolina at Chapel Hill; Curriculum in Toxicology & Environmental Medicine, University of North Carolina at Chapel Hill; McAllister Heart Institute, University of North Carolina at Chapel Hill.
Insights
Atherosclerosis causes arterial narrowing, leading to restenosis after revascularization. This study details a rat carotid artery balloon injury model to investigate restenosis and test therapies, using advanced 3D imaging.
Area of Science:
- Cardiovascular Research
- Vascular Biology
- Preclinical Models
Background:
- Cardiovascular disease and atherosclerosis are leading global health issues.
- Revascularization procedures like angioplasty restore blood flow but can cause arterial restenosis.
- Restenosis, or re-narrowing, limits the long-term success of these interventions.
Purpose of the Study:
- To present a modified, pressure-controlled rat carotid artery balloon injury model.
- To demonstrate the local periadventitial application of therapeutics to inhibit neointimal hyperplasia.
- To introduce light sheet fluorescence microscopy for 3D arterial injury visualization.
Main Methods:
- Surgical protocol for a modified rat carotid artery balloon injury model.
- Histological analysis of arterial healing and neointimal hyperplasia.
- Application of therapeutics via local periadventitial delivery.
- 3D imaging using light sheet fluorescence microscopy.
Main Results:
- The described model effectively induces arterial injury and restenosis in rats.
- Local periadventitial delivery of therapeutics shows potential for inhibiting neointimal hyperplasia.
- Light sheet fluorescence microscopy provides detailed 3D visualization of arterial injury.
Conclusions:
- The rat carotid artery balloon injury model is a valuable tool for studying restenosis mechanisms.
- This model facilitates testing of novel therapeutic strategies for preventing arterial re-narrowing.
- Advanced imaging techniques enhance the understanding of vascular injury and healing processes.
Abstract:
Cardiovascular disease remains the leading cause of death and disability worldwide, in part due to atherosclerosis. Atherosclerotic plaque narrows the luminal surface area in arteries thereby reducing adequate blood flow to organs and distal tissues. Clinically, revascularization procedures such as balloon angioplasty with or without stent placement aim to restore blood flow. Although these procedures reestablish blood flow by reducing plaque burden, they damage the vessel wall, which initiates the arterial healing response. The prolonged healing response causes arterial restenosis, or re-narrowing, ultimately limiting the long-term success of these revascularization procedures. Therefore, preclinical animal models are integral for analyzing the pathophysiological mechanisms driving restenosis, and provide the opportunity to test novel therapeutic strategies. Murine models are cheaper and easier to operate on than large animal models. Balloon or wire injury are the two commonly accepted injury modalities used in murine models. Balloon injury models in particular mimic the clinical angioplasty procedure and cause adequate damage to the artery for the development of restenosis. Herein we describe the surgical details for performing and histologically analyzing the modified, pressure-controlled rat carotid artery balloon injury model. Additionally, this protocol highlights how local periadventitial application of therapeutics can be used to inhibit neointimal hyperplasia. Lastly, we present light sheet fluorescence microscopy as a novel approach for imaging and visualizing the arterial injury in three-dimensions.

