Glycocalyx-Sodium Interaction in Vascular Endothelium.

CVD endothelial-glycocalyx glypicans hyaluronan hypertension proteoglycans sodium chloride-salt syndecans

Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
25 Jun 2023
Historique:
received: 20 05 2023
revised: 19 06 2023
accepted: 22 06 2023
medline: 17 7 2023
pubmed: 14 7 2023
entrez: 14 7 2023
Statut: epublish

Résumé

The glycocalyx generally covers almost all cellular surfaces, where it participates in mediating cell-surface interactions with the extracellular matrix as well as with intracellular signaling molecules. The endothelial glycocalyx that covers the luminal surface mediates the interactions of endothelial cells with materials flowing in the circulating blood, including blood cells. Cardiovascular diseases (CVD) remain a major cause of morbidity and mortality around the world. The cardiovascular risk factors start by causing endothelial cell dysfunction associated with destruction or irregular maintenance of the glycocalyx, which may culminate into a full-blown cardiovascular disease. The endothelial glycocalyx plays a crucial role in shielding the cell from excessive exposure and absorption of excessive salt, which can potentially cause damage to the endothelial cells and underlying tissues of the blood vessels. So, in this mini review/commentary, we delineate and provide a concise summary of the various components of the glycocalyx, their interaction with salt, and subsequent involvement in the cardiovascular disease process. We also highlight the major components of the glycocalyx that could be used as disease biomarkers or as drug targets in the management of cardiovascular diseases.

Identifiants

pubmed: 37447199
pii: nu15132873
doi: 10.3390/nu15132873
pmc: PMC10343370
pii:
doi:

Substances chimiques

Sodium 9NEZ333N27
Sodium Chloride 451W47IQ8X

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Lawrence Fred Sembajwe (LF)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Abdul M Ssekandi (AM)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Agnes Namaganda (A)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Haruna Muwonge (H)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Josephine N Kasolo (JN)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Robert Kalyesubula (R)

Department of Medical Physiology, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Annettee Nakimuli (A)

Department of Obstetrics and Gynecology, School of Medicine, Makerere University College of Health Sciences, Kampala P.O. Box 7072, Uganda.

Mwesigwa Naome (M)

Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

Kaushik P Patel (KP)

Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, NE 68198, USA.

Sepiso K Masenga (SK)

Department of Physiological Sciences, School of Medicine and Health Sciences, Mulungushi University, Kabwe P.O. Box 80415, Zambia.

Annet Kirabo (A)

Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

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