Evidence map›Paper›PMID 33543238›Full record

ArticleEndocrinology2021

Importance of Adipose Tissue NAD+ Biology in Regulating Metabolic Flexibility.

Michael P Franczyk, Nathan Qi, Kelly L Stromsdorfer, Chengcheng Li, Shintaro Yamaguchi, Hiroshi Itoh, Mihoko Yoshino, Yo Sasaki, Rita T Brookheart, Brian N Finck and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 21 citations in OpenAlex.

  1. The Sirtuin Network: Linking NADDiabetes/metabolism research and reviews · 2026
    Review
  2. Article
  3. Review
  4. NADNature metabolism · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Adipocyte-specific inactivation of NAMPT, a key NADAmerican journal of physiology. Endocrinology and metabolism · 2024
    Article
  12. Article
  13. Adipocyte NMNAT1 expression is essential for nuclear NADBiochemical and biophysical research communications · 2023
    Article
  14. Review
  15. NAMPT-dependent NADProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Michael P FranczykCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Nathan QiDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Kelly L StromsdorferCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Chengcheng LiCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Shintaro YamaguchiCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Hiroshi ItohDivision of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Mihoko YoshinoCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Yo SasakiDepartment of Genetics, Washington University School of Medicine, St Louis, Missouri, USA.
Rita T BrookheartCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Brian N FinckCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Brian J DeBoschDepartment of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Samuel KleinCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Jun YoshinoCenter for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Washington University in St. Louis · USKeio University · JPUniversity of Michigan · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
Michigan Mouse Metabolic Phenotyping CenterU2CDK110768 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELIAS, CAROL FUZETI · 2016 to 2021
$6.2M
REGULATION OF SYSTEMIC GLUCOSE AND LIPID HOMEOSTASIS BY ADIPOCYTE NAD BIOSYNTHESISR01DK104995 · NIDDK · WASHINGTON UNIVERSITY · PI KLEIN, SAMUEL · 2016 to 2024
$3.5M
Treating secondary cardiomyopathies by mimicking the adaptive hepatic glucose fasting responseR01HL147968 · NHLBI · WASHINGTON UNIVERSITY · PI DEBOSCH, BRIAN JESSE · 2020 to 2024
$3.2M
NCATS NIH HHS UL1 TR002345NCCIH NIH HHS R21 AT010520NCI NIH HHS P30 CA091842NHLBI NIH HHS K01 HL145326NHLBI NIH HHS R01 HL147968NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK056341NIDDK NIH HHS P30 DK089503NIDDK NIH HHS P60 DK020572NIDDK NIH HHS P60 DK020579NIDDK NIH HHS R01 DK104995NIDDK NIH HHS R01 DK117657NIDDK NIH HHS R01 DK126622NIDDK NIH HHS R56 DK115764NIDDK NIH HHS U2C DK110768
6 · The paper itself

Abstract

Nicotinamide adenine dinucleotide (NAD+) is an essential coenzyme that regulates cellular energy metabolism in many cell types. The major purpose of the present study was to test the hypothesis that NAD+ in white adipose tissue (WAT) is a regulator of whole-body metabolic flexibility in response to changes in insulin sensitivity and with respect to substrate availability and use during feeding and fasting conditions. To this end, we first evaluated the relationship between WAT NAD+ concentration and metabolic flexibility in mice and humans. We found that WAT NAD+ concentration was increased in mice after calorie restriction and exercise, 2 enhancers of metabolic flexibility. Bariatric surgery-induced 20% weight loss increased plasma adiponectin concentration, skeletal muscle insulin sensitivity, and WAT NAD+ concentration in people with obesity. We next analyzed adipocyte-specific nicotinamide phosphoribosyltransferase (Nampt) knockout (ANKO) mice, which have markedly decreased NAD+ concentrations in WAT. ANKO mice oxidized more glucose during the light period and after fasting than control mice. In contrast, the normal postprandial stimulation of glucose oxidation and suppression of fat oxidation were impaired in ANKO mice. Data obtained from RNA-sequencing of WAT suggest that loss of NAMPT increases inflammation, and impairs insulin sensitivity, glucose oxidation, lipolysis, branched-chain amino acid catabolism, and mitochondrial function in WAT, which are features of metabolic inflexibility. These results demonstrate a novel function of WAT NAMPT-mediated NAD+ biosynthesis in regulating whole-body metabolic flexibility, and provide new insights into the role of adipose tissue NAD+ biology in metabolic health.

Indexed as

Adipose TissueAdultAnimalsCytokinesEnergy MetabolismFatty AcidsFemaleHumansLipolysisMaleMiceMice, Inbred C57BLMice, KnockoutMiddle AgedNADNicotinamide PhosphoribosyltransferaseCytokinesFatty AcidsNADNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, humannicotinamide phosphoribosyltransferase, mouseadiponectinadipose tissueinsulin sensitivitymetabolic flexibilityNAD+obesity

Identifiers

PMID33543238
PMCPMC7853299
OpenAlexW3120844915

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.