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Updated: Jul 2, 2026

Assessment of Vascular Tone Responsiveness using Isolated Mesenteric Arteries with a Focus on Modulation by Perivascular Adipose Tissues
Published on: June 3, 2019
Effects of central arterial aging on the structure and function of the peripheral vasculature: implications for
1Cardiovascular Engineering, Inc., 1 Edgewater Dr., Suite 201A, Norwood, MA 02062, USA. GaryFMitchell@mindspring.com
Insights
Increased aortic stiffness contributes to cardiovascular diseases and aging-related conditions by affecting blood flow and causing tissue damage. This review explores vascular aging mechanisms and their link to organ dysfunction.
Area of Science:
- Cardiovascular Science
- Gerontology
- Nephrology
Background:
- Increased aortic stiffness is linked to major cardiovascular events like heart disease, stroke, and kidney disease.
- Excessive pressure pulsatility, driven by large artery stiffness, is increasingly associated with aging-related disorders, particularly those with microvascular origins such as kidney disease and cognitive impairment.
- These microvascular issues involve remodeling and impaired blood flow regulation, leading to diffuse microscopic tissue damage.
Purpose of the Study:
- To review age-related changes in aortic and peripheral vascular function.
- To discuss the mechanisms connecting large artery properties to pressure pulsatility, microvascular dysfunction, and end-organ damage.
Main Methods:
- Literature review of studies on aortic stiffness, pulsatility, and aging-related diseases.
- Analysis of mechanisms linking vascular changes to tissue damage.
Main Results:
- Large artery stiffness and pulsatility contribute to microvascular remodeling and impaired local blood flow regulation.
- These vascular changes are associated with diffuse microscopic tissue damage in aging-related conditions.
- Age-related vascular dysfunction impacts multiple organ systems.
Conclusions:
- Age-related stiffening of large arteries and increased pressure pulsatility are key contributors to microvascular dysfunction and end-organ damage.
- Understanding these mechanisms is crucial for addressing aging-related diseases.
- Further research into vascular aging pathways may reveal new therapeutic targets.
Abstract:
Over the past decade, numerous studies have shown that increased aortic stiffness is associated with major cardiovascular disease end points, including heart disease, stroke, and kidney disease. Cardiac abnormalities and enhanced atherogenesis in the setting of increased pulsatile load on heart and arteries have been well described. However, recent studies have shown a further association between excessive pressure pulsatility and a number of afflictions of aging that share a predominant microvascular etiology, including many forms of kidney disease and cognitive impairment. In these disorders, microvascular remodeling and impaired regulation of local blood flow, which are related to large artery stiffness and pressure pulsatility, are associated with evidence of diffuse microscopic tissue damage. This brief review will summarize age-related changes in aortic and peripheral vascular function and will discuss potential mechanisms leading from changes in properties of large arteries to excessive pressure pulsatility, abnormal microvascular structure and function, and end-organ dysfunction and damage.
Related Concept Videos
Peripheral Artery Disease I: Introduction
The Effect of Aging on Tissues
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests
Hypertension II: Pathophysiology
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