Evidence map›Paper›PMID 30816906›Full record

ArticleGenetics and molecular biology

NFAT5 is differentially expressed in Sprague-Dawley rat tissues in response to high salt and high fructose diets.

Braden A Herman, Kaylee M Ferguson, Jared V B Fernandez, Samantha Kauffman, Jason T Spicher, Rachel J King, Julia A Halterman

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In one paragraph

Article in Genetics and molecular biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. TonEBP as a key regulator of hypothalamic leptin signaling and resistance.Cellular and molecular life sciences : CMLS · 2026
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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

7 authors at 1 institution in 1 country.

Braden A HermanDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.
Kaylee M FergusonDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.
Jared V B FernandezMaster's in Biomedicine Program, Eastern Mennonite University, Harrisonburg, VA, USA.
Samantha KauffmanDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.
Jason T SpicherDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.
Rachel J KingDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.
Julia A HaltermanDepartment of Biology, Eastern Mennonite University, Harrisonburg, VA, USA.ORCID http://orcid.org/0000-0002-7323-249X
Eastern Mennonite University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current diets contain an increasing amount of salt and high fructose corn syrup, but it remains unclear as to how dietary salt and fructose affect organ function at the molecular level. This study aimed to test the hypothesis that consumption of high salt and fructose diets would increase tissue-specific expression of two critical osmotically-regulated genes, nuclear factor of activated T-cells 5 (NFAT5) and aldose reductase (AR). Fifty Sprague-Dawley rats were placed on a control, 4% NaCl, 8% NaCl, or 64% fructose diet for eight weeks. Fourteen different tissue samples were harvested and snap-frozen, followed by RNA purification, cDNA synthesis, and NFAT5 and AR gene expression quantification by real-time PCR.Our findings demonstrate that NFAT5 and AR expression are up-regulated in the kidney medulla, liver, brain, and adipose tissue following consumption of a high salt diet. NFAT5 expression is also up-regulated in the kidney cortex following consumption of a 64% fructose diet. These findings highlight the kidney medulla, liver, brain, and adipose tissue as being "salt-responsive" tissues and reveal that a high fructose diet can lead to enhanced NFAT5 expression in the kidney cortex. Further characterization of signaling mechanisms involved could help elucidate how these diets affect organ function long term.

Identifiers

PMID30816906
PMCPMC6726159
OpenAlexW2918212372

What OpenQuestion holds

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LicenceCC BY
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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.