Evidence map›Paper›PMID 24882067›Full record

ArticleCell metabolism2014

Resveratrol prevents high fat/sucrose diet-induced central arterial wall inflammation and stiffening in nonhuman primates.

Julie A Mattison, Mingyi Wang, Michel Bernier, Jing Zhang, Sung-Soo Park, Stuart Maudsley, Steven S An, Lakshmi Santhanam, Bronwen Martin, Shakeela Faulkner and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
13.4field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 202 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Effects of resveratrol supplementation on cardiac remodeling in hypertensive patients: a randomized controlled clinical trial.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
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  4. Resveratrol Improves Vascular Function and Mitochondrial Number but Not Glucose Metabolism in Older Adults.The journals of gerontology. Series A, Biological sciences and medical sciences · 2017
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65 more citing papers are in PubMed but not listed here.

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

21 authors at 8 institutions in 1 country.

Julie A MattisonTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Mingyi WangLaboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Michel BernierTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Jing ZhangLaboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Sung-Soo ParkLaboratory of Neurosciences, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Stuart MaudsleyLaboratory of Neurosciences, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Steven S AnProgram in Respiratory Biology and Lung Disease, Johns Hopkins Bloomberg School of Public Health, Room E7616, 615 North Wolfe Street, Baltimore, MD 21205, USA.
Lakshmi SanthanamDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University, School of Medicine, Ross 1150, 720 Rutland Avenue, Baltimore, MD 21205, USA.
Bronwen MartinLaboratory of Clinical Investigation, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Shakeela FaulknerTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Christopher MorrellLaboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA; Mathematics and Statistics Department, Loyola University Maryland, Baltimore, MD 21210, USA.
Joseph A BaurDepartment of Physiology and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Room 12-114, 3400 Civic Center Boulevard, Philadelphia, PA 19104, USA.
Leonid PeshkinSystems Biology, Harvard Medical School, WA 536, Boston, MA 02115, USA.
Danuta SosnowskaReynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma, BRC 1303, 975 Northeast 10th Street, Oklahoma City, OK 73104, USA.
Anna CsiszarReynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma, BRC 1303, 975 Northeast 10th Street, Oklahoma City, OK 73104, USA.
Richard L HerbertNational Institute of Allergy and Infectious Disease, NIH Animal Center, Building 102, 16701 Elmer School Road, Dickerson, MD 20842, USA.
Edward M TilmontTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Zoltan UngvariReynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma, BRC 1303, 975 Northeast 10th Street, Oklahoma City, OK 73104, USA.
Kevin J PearsonDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, C.T. Wethington Building, Room 591, 900 South Limestone, Lexington, KY 40536, USA.
Edward G LakattaLaboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Rafael de CaboTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, NIH, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA. Electronic address: decabora@mail.nih.gov.
National Institute on Aging · USUniversity of Oklahoma Health Sciences Center · USJohns Hopkins University · USHarvard University · USLoyola University Maryland · USNational Institute of Allergy and Infectious Diseases · USUniversity of Kentucky · USUniversity of Pennsylvania · US

Funding

Comparative Medicine Infectious Diseases- BethesdaZIGAI001047 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ELKINS, WILLIAM · 2009 to 2025
$535.6M
Aging Intervention ProgramZIAAG000363 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$9.0M
Effects of Aging on Experimental Atherosclerosis in Nonhuman PrimatesZIAAG000238 · NIA · NATIONAL INSTITUTE ON AGING · PI LAKATTA, EDWARD · 2009 to 2025
$4.5M
Nrf2 as a critical determinant of smooth muscle functionR01HL107361 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI AN, STEVEN S · 2011 to 2015
$2.0M
Role of SIRT1 in vasoprotectionR01AT006526 · NCCIH · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI UNGVARI, ZOLTAN ISTVAN · 2010 to 2014
$1.8M
Resveratrol treatment in monkeysZIAAG000369 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTISON, JULIE · 2009 to 2017
$858k
Intramural NIH HHS ZIA AG000363NCCIH NIH HHS R01 AT006526NHLBI NIH HHS HL107361.NHLBI NIH HHS R01 HL107361
6 · The paper itself

Abstract

Central arterial wall stiffening, driven by a chronic inflammatory milieu, accompanies arterial diseases, the leading cause of cardiovascular (CV) morbidity and mortality in Western society. An increase in central arterial wall stiffening, measured as an increase in aortic pulse wave velocity (PWV), is a major risk factor for clinical CV disease events. However, no specific therapies to reduce PWV are presently available. In rhesus monkeys, a 2 year diet high in fat and sucrose (HFS) increases not only body weight and cholesterol, but also induces prominent central arterial wall stiffening and increases PWV and inflammation. The observed loss of endothelial cell integrity, lipid and macrophage infiltration, and calcification of the arterial wall were driven by genomic and proteomic signatures of oxidative stress and inflammation. Resveratrol prevented the HFS-induced arterial wall inflammation and the accompanying increase in PWV. Dietary resveratrol may hold promise as a therapy to ameliorate increases in PWV.

Indexed as

Diet, High-FatAldehydesAnimalsAortaCaspase 3Cell AdhesionCells, CulturedEndothelial CellsHumansInflammationMonocytesPrimatesPulse Wave AnalysisResveratrolStilbenesSucrose4-hydroxy-2-nonenalAldehydesCaspase 3ResveratrolStilbenesSucrose

Identifiers

PMID24882067
PMCPMC4254394
OpenAlexW2054670968

What OpenQuestion holds

Textmetadata
LicenceTDM
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.