Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries

Research output: Other contributionResearch

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Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries. / Jensen, Lars J.

22 p. 2601 ed. MDPI - Open Access Publishing. 2024.

Research output: Other contributionResearch

Harvard

Jensen, LJ 2024, Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries. MDPI - Open Access Publishing. https://doi.org/10.3390/ijms25052601

APA

Jensen, L. J. (2024, Feb 23). Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries. (2601 ed.) MDPI - Open Access Publishing. https://doi.org/10.3390/ijms25052601

Vancouver

Jensen LJ. Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries. 2024. 22 p. https://doi.org/10.3390/ijms25052601

Author

Jensen, Lars J. / Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries. 2024. MDPI - Open Access Publishing. 22 p.

Bibtex

@misc{e69957dfd2714bf0b9c48e849499cff1,
title = "Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries",
abstract = "The normal ageing process affects resistance arteries, leading to various functional and structural changes. Systolic hypertension is a common occurrence in human ageing, and it is associated with large artery stiffening, heightened pulsatility, small artery remodeling, and damage to critical microvascular structures. Starting from young adulthood, a progressive elevation in the mean arterial pressure is evidenced by clinical and epidemiological data as well as findings from animal models. The myogenic response, a protective mechanism for the microcirculation, may face disruptions during ageing. The dysregulation of calcium entry channels (L-type, T-type, and TRP channels), dysfunction in intracellular calcium storage and extrusion mechanisms, altered expression of potassium channels, and a change in smooth muscle calcium sensitization may contribute to the age-related dysregulation of myogenic tone. Flow-mediated vasodilation, a hallmark of endothelial function, is compromised in ageing. This endothelial dysfunction is related to increased oxidative stress, lower nitric oxide bioavailability, and a low-grade inflammatory response, further exacerbating vascular dysfunction. Resistance artery remodeling in ageing emerges as a hypertrophic response of the vessel wall that is typically observed in conjunction with outward remodeling (in normotension), or as inward hypertrophic remodeling (in hypertension). The remodeling process involves oxidative stress, inflammation, reorganization of actin cytoskeletal components, and extracellular matrix fiber proteins. Reactive oxygen species (ROS) signaling and chronic low-grade inflammation play substantial roles in age-related vascular dysfunction. Due to its role in the regulation of vascular tone and structural proteins, the RhoA/Rho-kinase pathway is an important target in age-related vascular dysfunction and diseases. Understanding the intricate interplay of these factors is crucial for developing targeted interventions to mitigate the consequences of ageing on resistance arteries and enhance the overall vascular health.",
keywords = "ageing, resistance artery, myogenic tone, flow-mediated vasodilation, structural remodeling, hypertension, cardiovascular disease, neurodegenerative disease, proteomics",
author = "Jensen, {Lars J.}",
year = "2024",
month = feb,
day = "23",
doi = "10.3390/ijms25052601",
language = "English",
isbn = "1422-0067",
volume = "25",
publisher = "MDPI - Open Access Publishing",
edition = "2601",
type = "Other",

}

RIS

TY - GEN

T1 - Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries

AU - Jensen, Lars J.

PY - 2024/2/23

Y1 - 2024/2/23

N2 - The normal ageing process affects resistance arteries, leading to various functional and structural changes. Systolic hypertension is a common occurrence in human ageing, and it is associated with large artery stiffening, heightened pulsatility, small artery remodeling, and damage to critical microvascular structures. Starting from young adulthood, a progressive elevation in the mean arterial pressure is evidenced by clinical and epidemiological data as well as findings from animal models. The myogenic response, a protective mechanism for the microcirculation, may face disruptions during ageing. The dysregulation of calcium entry channels (L-type, T-type, and TRP channels), dysfunction in intracellular calcium storage and extrusion mechanisms, altered expression of potassium channels, and a change in smooth muscle calcium sensitization may contribute to the age-related dysregulation of myogenic tone. Flow-mediated vasodilation, a hallmark of endothelial function, is compromised in ageing. This endothelial dysfunction is related to increased oxidative stress, lower nitric oxide bioavailability, and a low-grade inflammatory response, further exacerbating vascular dysfunction. Resistance artery remodeling in ageing emerges as a hypertrophic response of the vessel wall that is typically observed in conjunction with outward remodeling (in normotension), or as inward hypertrophic remodeling (in hypertension). The remodeling process involves oxidative stress, inflammation, reorganization of actin cytoskeletal components, and extracellular matrix fiber proteins. Reactive oxygen species (ROS) signaling and chronic low-grade inflammation play substantial roles in age-related vascular dysfunction. Due to its role in the regulation of vascular tone and structural proteins, the RhoA/Rho-kinase pathway is an important target in age-related vascular dysfunction and diseases. Understanding the intricate interplay of these factors is crucial for developing targeted interventions to mitigate the consequences of ageing on resistance arteries and enhance the overall vascular health.

AB - The normal ageing process affects resistance arteries, leading to various functional and structural changes. Systolic hypertension is a common occurrence in human ageing, and it is associated with large artery stiffening, heightened pulsatility, small artery remodeling, and damage to critical microvascular structures. Starting from young adulthood, a progressive elevation in the mean arterial pressure is evidenced by clinical and epidemiological data as well as findings from animal models. The myogenic response, a protective mechanism for the microcirculation, may face disruptions during ageing. The dysregulation of calcium entry channels (L-type, T-type, and TRP channels), dysfunction in intracellular calcium storage and extrusion mechanisms, altered expression of potassium channels, and a change in smooth muscle calcium sensitization may contribute to the age-related dysregulation of myogenic tone. Flow-mediated vasodilation, a hallmark of endothelial function, is compromised in ageing. This endothelial dysfunction is related to increased oxidative stress, lower nitric oxide bioavailability, and a low-grade inflammatory response, further exacerbating vascular dysfunction. Resistance artery remodeling in ageing emerges as a hypertrophic response of the vessel wall that is typically observed in conjunction with outward remodeling (in normotension), or as inward hypertrophic remodeling (in hypertension). The remodeling process involves oxidative stress, inflammation, reorganization of actin cytoskeletal components, and extracellular matrix fiber proteins. Reactive oxygen species (ROS) signaling and chronic low-grade inflammation play substantial roles in age-related vascular dysfunction. Due to its role in the regulation of vascular tone and structural proteins, the RhoA/Rho-kinase pathway is an important target in age-related vascular dysfunction and diseases. Understanding the intricate interplay of these factors is crucial for developing targeted interventions to mitigate the consequences of ageing on resistance arteries and enhance the overall vascular health.

KW - ageing

KW - resistance artery

KW - myogenic tone

KW - flow-mediated vasodilation

KW - structural remodeling

KW - hypertension

KW - cardiovascular disease

KW - neurodegenerative disease

KW - proteomics

U2 - 10.3390/ijms25052601

DO - 10.3390/ijms25052601

M3 - Other contribution

SN - 1422-0067

VL - 25

PB - MDPI - Open Access Publishing

ER -

ID: 384479076