Arterial structure and function during and after long-duration spaceflight.

cardiovascular disease risk carotid intima-media thickness flow-mediated dilation inflammation oxidative stress

Journal

Journal of applied physiology (Bethesda, Md. : 1985)
ISSN: 1522-1601
Titre abrégé: J Appl Physiol (1985)
Pays: United States
ID NLM: 8502536

Informations de publication

Date de publication:
01 07 2020
Historique:
pubmed: 12 6 2020
medline: 24 6 2021
entrez: 12 6 2020
Statut: ppublish

Résumé

Spaceflight missions expose astronauts to increased risk of oxidative stress and inflammatory damage that might accelerate the development of asymptomatic cardiovascular disease. The purpose of this investigation was to determine whether long-duration spaceflight (>4 mo) results in structural and functional changes in the carotid and brachial arteries. Common carotid artery (CCA) intima-media thickness (cIMT), CCA distensibility and stiffness, and brachial artery endothelium-dependent and -independent vasodilation were measured in 13 astronauts (10 men, 3 women) ~180 and 60 days before launch, during the mission on ~15, 60, and 160 days of spaceflight, and within 1 wk after landing. Biomarkers of oxidative stress and inflammation were measured at corresponding times in fasting blood samples and urine samples from 24- or 48-h pools. Biomarkers of oxidative stress and inflammation increased during spaceflight, but most returned to preflight levels within 1 wk of landing. Mean cIMT, CCA stiffness, and distensibility were not significantly different from preflight at any time. As a group, neither mean endothelium-dependent nor -independent vasodilation changed from preflight to postflight, but changes within individuals in endothelial function related to some biomarkers of oxidative stress. Whereas biomarkers of oxidative stress and inflammation are elevated during spaceflight, CCA and brachial artery structure and function were not changed by spaceflight. It is unclear whether future exploration missions, with an extended duration in altered gravity fields and higher radiation exposure, may be problematic.

Identifiants

pubmed: 32525433
doi: 10.1152/japplphysiol.00550.2019
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

108-123

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Stuart M C Lee (SMC)

KBR, Houston, Texas.

L Christine Ribeiro (LC)

KBR, Houston, Texas.

David S Martin (DS)

KBR, Houston, Texas.

Sara R Zwart (SR)

University of Texas Medical Branch, Galveston, Texas.

Alan H Feiveson (AH)

NASA Johnson Space Center, Houston, Texas.

Steven S Laurie (SS)

KBR, Houston, Texas.

Brandon R Macias (BR)

KBR, Houston, Texas.

Brian E Crucian (BE)

NASA Johnson Space Center, Houston, Texas.

Stephanie Krieger (S)

KBR, Houston, Texas.

Daniela Weber (D)

Department of Molecular Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Nuthetal, Germany.

Tilman Grune (T)

Department of Molecular Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Nuthetal, Germany.
German Center for Cardiovascular Research (DZHK), Berlin, Germany.

Steven H Platts (SH)

NASA Johnson Space Center, Houston, Texas.

Scott M Smith (SM)

NASA Johnson Space Center, Houston, Texas.

Michael B Stenger (MB)

NASA Johnson Space Center, Houston, Texas.

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