Evidence map›Paper›PMID 36086823›Full record

ArticleThe Journal of physiology2023

Regulation of metabolic health by dietary histidine in mice.

Victoria Flores, Alexandra B Spicer, Michelle M Sonsalla, Nicole E Richardson, Deyang Yu, Grace E Sheridan, Michaela E Trautman, Reji Babygirija, Eunhae P Cheng, Jennifer M Rojas and 11 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Quantifying the Impact of Co-Housing on Murine Aging Studies.bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Bioscience of microbiota, food and health · 2024
    Article
  13. Article
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 1 country.

Victoria FloresWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Alexandra B SpicerDepartment of Population Health Sciences, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
Michelle M SonsallaWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Nicole E RichardsonWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Deyang YuWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Grace E SheridanWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Michaela E TrautmanWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Reji BabygirijaWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Eunhae P ChengWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Jennifer M RojasDepartment of Physiology and Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania, Philadelphia, PA, USA.
Shany E YangWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Matthew H WakaiWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Ryan HubbellWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Ildiko KaszaMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0001-5736-1956
Jay L TomasiewiczWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Cara L GreenWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Claudia DantoinWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Caroline M AlexanderMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-7830-8043
Joseph A BaurDepartment of Physiology and Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania, Philadelphia, PA, USA.
Kristen C MaleckiDepartment of Population Health Sciences, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
Dudley W LammingWilliam S. Middleton Memorial Veterans Hospital, Madison, WI, USA.ORCID 0000-0002-0079-4467
University of Wisconsin–Madison · USUniversity of Wisconsin System · USUniversity of Pennsylvania · USWilliam S. Middleton Memorial Veterans Hospital · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Patrick Seale · 1986 to 2026
$48.3M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
TRAINING IN NUTRITIONT32DK007665 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GUY E GROBLEWSKI, Chi- Liang Eric Yen · 1993 to 2026
$9.2M
The regulation of health and longevity by branched-chain amino acidsR01AG056771 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Dudley William Lamming · 2018 to 2026
$3.1M
The regulation of health and longevity by branched-chain amino acidsRF1AG056771 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM · 2023 to 2023
$2.1M
Comparative analysis of geroprotective interventions in established and novel mouse models of Alzheimer's diseaseR01AG062328 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM, MERRINS, MATTHEW J. · 2018 to 2022
$2.0M
Dietary regulation of the hepatic epigenomeR01DK125859 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI DENU, JOHN M, LAMMING, DUDLEY WILLIAM · 2021 to 2023
$1.8M
The regulation of health and longevity by branched-chain amino acidsR56AG056771 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM · 2017 to 2017
$573k
Translation analysis of a novel intervention for diet-induced obesityR21AG061635 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI COLMAN, RICKI J, LAMMING, DUDLEY WILLIAM · 2019 to 2020
$426k
Promoting metabolic health through the reduction of dietary branched chain amino acidsI01BX004031 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI LAMMING, DUDLEY WILLIAM · 2018 to 2022
–
BLRD VA I01 BX004031BLRD VA IS1 BX005524NCI NIH HHS P30 CA014520NIA NIH HHS R01 AG056771NIA NIH HHS R01 AG062328NIA NIH HHS R21 AG061635NIA NIH HHS R56 AG056771NIA NIH HHS RF1 AG056771NIA NIH HHS T32 AG000213NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK125859NIDDK NIH HHS T32 DK007665
6 · The paper itself

Abstract

Low-protein (LP) diets are associated with a decreased risk of diabetes in humans, and promote leanness and glycaemic control in both rodents and humans. While the effects of an LP diet on glycaemic control are mediated by reduced levels of the branched-chain amino acids, we have observed that reducing dietary levels of the other six essential amino acids leads to changes in body composition. Here, we find that dietary histidine plays a key role in the response to an LP diet in male C57BL/6J mice. Specifically reducing dietary levels of histidine by 67% reduces the weight gain of young, lean male mice, reducing both adipose and lean mass without altering glucose metabolism, and rapidly reverses diet-induced obesity and hepatic steatosis in diet-induced obese male mice, increasing insulin sensitivity. This normalization of metabolic health was associated not with caloric restriction or increased activity, but with increased energy expenditure. Surprisingly, the effects of histidine restriction do not require the energy balance hormone Fgf21. Histidine restriction that was started in midlife promoted leanness and glucose tolerance in aged males but not females, but did not affect frailty or lifespan in either sex. Finally, we demonstrate that variation in dietary histidine levels helps to explain body mass index differences in humans. Overall, our findings demonstrate that dietary histidine is a key regulator of weight and body composition in male mice and in humans, and suggest that reducing dietary histidine may be a translatable option for the treatment of obesity. KEY POINTS: Protein restriction (PR) promotes metabolic health in rodents and humans and extends rodent lifespan. Restriction of specific individual essential amino acids can recapitulate the benefits of PR. Reduced histidine promotes leanness and increased energy expenditure in male mice. Reduced histidine does not extend the lifespan of mice when begun in midlife. Dietary levels of histidine are positively associated with body mass index in humans.

Indexed as

HistidineThinnessAgedAnimalsDietEnergy MetabolismHumansMaleMiceMice, Inbred C57BLObesityProteinsHistidineProteinsamino acidsBMIbody compositionFGF21histidineprotein restriction

Identifiers

PMID36086823
PMCPMC9995620
OpenAlexW4295491496

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Registered trials

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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.