Boosting NAD preferentially blunts Th17 inflammation via arginine biosynthesis and redox control in healthy and psoriasis subjects.


Journal

Cell reports. Medicine
ISSN: 2666-3791
Titre abrégé: Cell Rep Med
Pays: United States
ID NLM: 101766894

Informations de publication

Date de publication:
19 09 2023
Historique:
received: 01 12 2022
revised: 23 05 2023
accepted: 18 07 2023
medline: 22 9 2023
pubmed: 17 8 2023
entrez: 16 8 2023
Statut: ppublish

Résumé

To evaluate whether nicotinamide adenine dinucleotide-positive (NAD

Identifiants

pubmed: 37586364
pii: S2666-3791(23)00310-5
doi: 10.1016/j.xcrm.2023.101157
pmc: PMC10518596
pii:
doi:

Substances chimiques

NAD 0U46U6E8UK
Sequestosome-1 Protein 0
Antioxidants 0
NF-E2-Related Factor 2 0

Banques de données

ClinicalTrials.gov
['NCT01934660', 'NCT02812238', 'NCT01143454', 'NCT00001846']

Types de publication

Journal Article Research Support, N.I.H., Intramural Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101157

Subventions

Organisme : Medical Research Council
ID : MR/P011705/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P011705/2
Pays : United Kingdom
Organisme : NIH HHS
ID : S10 OD021562
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA HL005102
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of interests The NR and matching placebo were supplied by Chromadex Inc. (Los Angeles, CA, USA) under a Cooperative and Development Research Agreement (CRADA).

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Auteurs

Kim Han (K)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Komudi Singh (K)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Allison M Meadows (AM)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA; Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK.

Rahul Sharma (R)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Shahin Hassanzadeh (S)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Jing Wu (J)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Haley Goss-Holmes (H)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.

Rebecca D Huffstutler (RD)

Cardiovascular Branch, NHLBI, NIH, Bethesda, MD, USA.

Heather L Teague (HL)

Laboratory of Cardiometabolic Disease and Inflammation, NHLBI, NIH, Bethesda, MD, USA.

Nehal N Mehta (NN)

Laboratory of Cardiometabolic Disease and Inflammation, NHLBI, NIH, Bethesda, MD, USA.

Julian L Griffin (JL)

Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK; The Rowett Institute, School of Medicine, Medical Sciences and Nutrition, Foresterhill Campus, Aberdeen, UK.

Rong Tian (R)

Mitochondria and Metabolism Center, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA.

Javier Traba (J)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA; Instituto Universitario de Biología Molecular-UAM (IUBM-UAM), Departamento de Biología Molecular, Universidad Autónoma de Madrid, Madrid, Spain; Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain.

Michael N Sack (MN)

Laboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA; Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK. Electronic address: sackm@nih.gov.

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Classifications MeSH