Evidence mapPaperPMID 39005372Full record

ArticlebioRxiv : the preprint server for biology2024

Sulfur Amino Acid Restriction Enhances Exercise Capacity in Mice by Boosting Fat Oxidation in Muscle.

Charlotte G Mann, Michael R MacArthur, Jing Zhang, Songlin Gong, Jenna E AbuSalim, Craig J Hunter, Wenyun Lu, Thomas Agius, Alban Longchamp, Florent Allagnat and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Charlotte G MannDepartment of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.ORCID 0000-0003-2005-7752
Michael R MacArthurDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0003-3593-6995
Jing ZhangDepartment of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.
Songlin GongDepartment of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.
Jenna E AbuSalimLewis-Sigler Institute of Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Craig J HunterDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Wenyun LuDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0003-1787-2617
Thomas AgiusDepartment of Vascular Surgery, Lausanne University Hospital (CHUV), Lausanne 1005, Switzerland.ORCID 0000-0001-6917-0831
Alban LongchampDepartment of Vascular Surgery, Lausanne University Hospital (CHUV), Lausanne 1005, Switzerland.ORCID 0000-0002-1743-4935
Florent AllagnatDepartment of Vascular Surgery, Lausanne University Hospital (CHUV), Lausanne 1005, Switzerland.ORCID 0000-0001-6528-679X
Joshua RabinowitzDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-1247-4727
James R MitchellDepartment of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.ORCID 0000-0003-1565-603X
Katrien De BockDepartment of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.ORCID 0000-0001-8232-4663
Sarah J MitchellLudwig Institute for Cancer Research, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-4027-3754

Funding

Revealing cancer metabolism via mass spectrometry and isotope tracersR50CA211437 · PRINCETON UNIVERSITY · 2025 to 2025
$125k
NCI NIH HHS R50 CA211437NIA NIH HHS P01 AG055369
6 · The paper itself

Abstract

Dietary restriction of the sulfur-containing amino acids methionine and cysteine (SAAR) improves body composition, enhances insulin sensitivity, and extends lifespan; benefits seen also with endurance exercise. Yet, the impact of SAAR on skeletal muscle remains largely unexplored. Here we demonstrate that one week of SAAR in sedentary, young, male mice increases endurance exercise capacity. Indirect calorimetry showed that SAAR increased lipid oxidation at rest and delayed the onset of carbohydrate utilization during exercise. Transcriptomic analysis revealed increased expression of genes involved in fatty acid catabolism especially in glycolytic muscle following SAAR. These findings were functionally supported by increased fatty acid circulatory turnover flux and muscle β-oxidation. Reducing lipid uptake from circulation through endothelial cell (EC)-specific CD36 deletion attenuated the running phenotype. Mechanistically, VEGF-signaling inhibition prevented exercise increases following SAAR, without affecting angiogenesis, implicating noncanonical VEGF signaling and EC CD36-dependent fatty acid transport in regulating exercise capacity by influencing muscle substrate availability.

Identifiers

PMID39005372
PMCPMC11244859

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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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 Socratic graph.