Evidence map›Paper›PMID 43026630›Full record

ArticleBiology of sex differences2026

Persistent metabolic remodeling after dietary salt reduction reveals sex differences in the adaptation to chronic high-salt intake.

Sevilay Şahoğlu Göktaş, Peter Spégel, Martin Magnusson, Anja Meissner, João M N Duarte

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Article in Biology of sex differences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Sevilay Şahoğlu GöktaşWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0001-8701-1172
Peter SpégelDepartment of Chemistry, Centre for Analysis and Synthesis, Lund University, Lund, 223 62, Sweden.ORCID https://orcid.org/0000-0002-6092-2387
Martin MagnussonWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0003-1710-5936
Anja Meissner *Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0002-0793-7213
João M N Duarte *Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden. joao.duarte@med.lu.se.ORCID https://orcid.org/0000-0001-5984-1574

Funding

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6 · The paper itself

Abstract

backgroundExcessive salt intake is a risk factor for cardiovascular disease, yet its systemic metabolic consequences and its relationship to differential cardiovascular adaptations in males and females remain poorly understood. Here, we performed plasma metabolite profiling in male and female mice subjected to long-term high-salt diet (HSD) exposure during aging.

methodsMice were fed HSD (8.6% NaCl) or low-salt normal diet (ND; 0.6% NaCl) from 9 to 23 months of age, with a subset of mice undergoing diet reversal to ND after 7 months of HSD. Plasma metabolites were analyzed using gas chromatography/mass spectrometry and related to previously reported measurements of arterial blood pressure and cardiac function.

resultsFemale mice developed salt-sensitive hypertension driven by vascular dysfunction, whereas male mice exhibited cardiac and vascular remodeling independent of blood pressure. Among 48 measured metabolites, HSD induced substantial alterations in levels of glucose, glycerol, glycerol phosphates, and fatty acids. Males showed a near-complete normalization of metabolite profiles following 7 months of salt reduction, whereas females retained a metabolomic signature different from ND despite normalization of blood pressure. In particular, metabolites related to energy metabolism, lipid handling, and osmotic balance were influenced by both diet and sex, with linoleate showing a significant sex-diet interaction. Correlation analyses demonstrated associations between metabolite profiles and cardiovascular parameters with different patterns in males and females.

conclusionOur findings demonstrate that chronic high-salt consumption induces persistent plasma metabolite alterations displaying different patterns in male and female mice that are not fully reversed by a salt-lowering dietary intervention. The dissociation between physiological recovery and metabolic normalization, particularly in females, suggests that metabolic alterations may represent an additional layer of cardiovascular risk beyond blood pressure control in mice.

Indexed as

Adaptation, PhysiologicalDiet, Sodium-RestrictedSex CharacteristicsSodium Chloride, DietaryAnimalsBlood PressureFemaleHypertensionMaleMetabolomeMiceMice, Inbred C57BLSodium Chloride, DietaryCardiac remodelingDietary saltHypertensionMetabolism

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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.