GLP-1 Promotes Cortical and Medullary Perfusion in the Human Kidney and Maintains Renal Oxygenation During NaCl Loading.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
07 02 2023
Historique:
pubmed: 4 2 2023
medline: 9 2 2023
entrez: 3 2 2023
Statut: ppublish

Résumé

Background GLP-1 (glucagon-like peptide-1) receptor agonists exert beneficial long-term effects on cardiovascular and renal outcomes. In humans, the natriuretic effect of GLP-1 depends on GLP-1 receptor interaction, is accompanied by suppression of angiotensin II, and is independent of changes in renal plasma flow. In rodents, angiotensin II constricts vasa recta and lowers medullary perfusion. The current randomized, controlled, crossover study was designed to test the hypothesis that GLP-1 increases renal medullary perfusion in healthy humans. Methods and Results Healthy male participants (n=10, aged 27±4 years) ingested a fixed sodium intake for 4 days and were examined twice during a 1-hour infusion of either GLP-1 (1.5 pmol/kg per minute) or placebo together with infusion of 0.9% NaCl (750 mL/h). Interleaved measurements of renal arterial blood flow, oxygenation (R

Identifiants

pubmed: 36734354
doi: 10.1161/JAHA.122.027712
pmc: PMC9973647
doi:

Substances chimiques

Angiotensin II 11128-99-7
Glucagon-Like Peptide 1 89750-14-1
Sodium Chloride 451W47IQ8X

Banques de données

ClinicalTrials.gov
['NCT04337268']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e027712

Subventions

Organisme : Medical Research Council
ID : MR/R02264X/1
Pays : United Kingdom

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Auteurs

Bryan Haddock (B)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Kasper B Kristensen (KB)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Mahvish Tayyab (M)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Henrik B W Larsson (HBW)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Ulrich Lindberg (U)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Mark Vestergaard (M)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Susan Francis (S)

Sir Peter Mansfield Magnetic Resonance Centre School of Physics and Astronomy University of Nottingham United Kingdom.

Boye L Jensen (BL)

Department of Cardiovascular and Renal Research, Institute of Molecular Medicine University of Southern Denmark Odense Denmark.

Ulrik B Andersen (UB)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Ali Asmar (A)

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.
Department of Clinical Physiology and Nuclear Medicine, Bispebjerg and Frederiksberg Hospital Copenhagen University Hospital Copenhagen Denmark.
Department of Clinical Medicine University of Copenhagen Copenhagen Denmark.

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