Evidence map›Paper›PMID 41481281›Full record

ArticleAmerican journal of physiology. Renal physiology2026

Protective effects of fermentable dietary fiber and propionate in Dahl salt-sensitive hypertension and renal damage.

Samuel D Walton, John Henry Dasinger, Emily C Burns-Ray, Lily N Hartenburg, Kaitlyn E Baldwin, Jeffrey Lin, Mary Cherian-Shaw, Ramakumar Tummala, Bina Joe, David L Mattson and 1 more

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Samuel D WaltonDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.ORCID 0000-0002-8460-2214
John Henry DasingerDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.ORCID 0000-0001-6667-0427
Emily C Burns-RayDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.ORCID 0000-0003-4653-609X
Lily N HartenburgDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.
Kaitlyn E BaldwinDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.
Jeffrey LinDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.
Mary Cherian-ShawDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.
Ramakumar TummalaDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio, United States.ORCID 0000-0002-3887-3566
Bina JoeDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio, United States.ORCID 0000-0002-2385-7061
David L MattsonDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.
Justine M Abais-BattadDepartment of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States.ORCID 0000-0001-5252-0903

Funding

The Impact of Obesity and Leptin on the Development of Immune System Dysfunction and Hypertension in Females with Systemic Lupus ErythematousU54HL169191 · NHLBI · AUGUSTA UNIVERSITY · PI Jennifer C Sullivan · 2023 to 2026
$7.4M
Deep South KUH Premier Research - Interdisciplinary Mentored Education (PRIME) Training CoreTL1DK139566 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVID M POLLOCK · 2023 to 2026
$3.6M
Deep South KUH Premier Research- Interdisciplinary Mentored Education (PRIME) Networking CoreU2CDK133422 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DEAN GEORGE ASSIMOS, Orlando M Gutierrez · 2023 to 2026
$2.8M
Gut Metabolites, T cells, and Salt-Sensitive HypertensionR01HL166458 · NHLBI · AUGUSTA UNIVERSITY · PI David L. Mattson, Aaron James Polichnowski · 2023 to 2026
$2.4M
Conjugated bile acids as nutritionally re-programmable antihypertensive metabolitesR01HL171401 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BINA JOE · 2024 to 2026
$2.3M
CD14 and Salt-Sensitive HypertensionR01HL161231 · NHLBI · AUGUSTA UNIVERSITY · PI MATTSON, DAVID L. · 2022 to 2025
$2.0M
Sex Differences in Gut Metabolite-Immune Interplay in Hypertension and Renal End-Organ DamageR56HL169434 · NHLBI · AUGUSTA UNIVERSITY · PI ABAIS-BATTAD, JUSTINE M · 2024 to 2024
$639k
American Heart Association (AHA) 25SFRNPCKMS1467444American Heart Association-American Stroke Association 25SFRNPCKMS1467444Georgia Research Alliance (GRA)HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL161231HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL166458HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL171401HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R56HL169434HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) U54HL169191NHLBI NIH HHS R01 HL161231NHLBI NIH HHS R01 HL166458NHLBI NIH HHS R01 HL171401NHLBI NIH HHS R56 HL169434NHLBI NIH HHS U54 HL169191NIDDK NIH HHS TL1 DK139566NIDDK NIH HHS U2C DK133422
6 · The paper itself

Abstract

The Dahl salt-sensitive (SS) rat is an established model of hypertensive kidney injury, where the gut microbiota has been shown to causally contribute to disease progression. Gut bacteria-derived metabolites serve as mechanistic links between the microbiota and disease, with dietary fiber providing a critical source of protective metabolites such as short-chain fatty acids (SCFAs). The current study hypothesized that the substitution of nonfermentable fiber cellulose with the fermentable fiber inulin would attenuate hypertension and renal damage in SS rats via increased circulating SCFAs. Male and female SS rats were placed on the 0.4% NaCl (low-salt, LS) inulin diet for 1 wk before the switch to a 4.0% NaCl (high-salt, HS) inulin diet for 4 wk. Controls were maintained on diets containing cellulose. Rats consuming inulin had a reduction in mean arterial pressure compared with cellulose, though the antihypertensive effect was more robust in females. The inulin diet significantly protected both sexes from albuminuria, medullary protein cast formation, and renal immune cell infiltration, and was associated with specific changes to the fecal microbiota. Assessed by mass spectrometry, inulin consumption resulted in increased circulating propionate and butyrate, and the administration of these SCFAs revealed a protective effect of propionate against salt-sensitive hypertension and kidney damage in males, which coincided with an expansion of renal T regulatory cells. In conclusion, substitution of cellulose for the fermentable fiber inulin lowered blood pressure and significantly attenuated salt-induced renal damage in both sexes, which may be attributed to greater production of the protective, anti-inflammatory SCFA propionate.

Indexed as

Dietary FiberGastrointestinal MicrobiomeHypertensionInulinKidneyKidney DiseasesPropionatesAnimalsArterial PressureDisease Models, AnimalFatty Acids, VolatileFemaleFermentationMaleRatsRats, Inbred DahlDietary FiberFatty Acids, VolatileInulinPropionatesSodium Chloride, Dietarydietary fiberkidney damagemicrobiotasalt-sensitive hypertensionSCFAs

Identifiers

PMID41481281
PMCPMC12908570

What OpenQuestion holds

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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.