# Dietary modifications affect renal recovery during the healing phase following ischemic acute ischemic kidney injury

**Authors:** Junseok Jeon, Kyungho Lee, Hojin Jeon, Kyeong Eun Yang, Cheol-Jung Lee, Jung Eun Lee, Ghee Young Kwon, Wooseong Huh, Hye Ryoun Jang

PMC · DOI: 10.3389/fcell.2025.1494660 · Frontiers in Cell and Developmental Biology · 2025-05-22

## TL;DR

This study shows that extreme diets during kidney injury recovery can worsen healing, highlighting the need for balanced nutrition.

## Contribution

The study reveals how specific dietary modifications impact renal healing after ischemic injury in mice and human cell models.

## Key findings

- Low-salt/fat/protein diets worsened kidney fibrosis and inflammation after bilateral injury.
- High-salt diets increased tubular damage and TGF-β expression in mice.
- High lipid diets promoted cell proliferation in hypoxic kidney cells.

## Abstract

The effects of dietary modifications, such as varying amounts of salt, fat, and protein intake on the healing phase of acute kidney injury (AKI) remain to be elucidated. We investigated the effects of low- or high-salt/fat/protein diets on the intrarenal immunologic micromilieu and healing after renal ischemia-reperfusion injury (IRI) using murine ischemic AKI and human kidney-2 (HK-2) cell hypoxia models.

Three cohorts of male C57BL/6 mice (9-weeks old) were fed the designated diet from the third day following renal IRI until sacrifice (6 or 12 weeks after bilateral or unilateral IRI, respectively) in groups as follows: cohort 1, control, high- and low-salt/fat/protein; cohort 2, control, high- and low-salt; cohort 3, control, high- and low-fat/protein. Hypoxic HK-2 cells were treated with sodium chloride, amino acids, or fatty acids.

Low-salt/fat/protein diet aggravated interstitial fibrosis, enhanced TGF-β expression, and induced more proinflammatory changes after bilateral IRI. High-salt diet aggravated renal tubular damage and enhanced the expression of intrarenal TGF-β after bilateral IRI, whereas low-salt diet enhanced the expression of intrarenal TGF-β after unilateral IRI. Low-salt diet induced more proinflammatory changes after bilateral IRI. Blood urea nitrogen levels were lower in the low fat/protein group than that in the control group following IRI. However, low-fat/protein diet aggravated interstitial fibrosis and enhanced intrarenal TGF-β expression after unilateral IRI. High sodium- or protein-containing media suppressed the proliferation of hypoxic HK-2 cells, whereas high lipid-containing media enhanced the proliferation of hypoxic HK-2 cells.

Excessive low or high salt, low fat, and low protein diet may adversely affect the healing process following renal IRI, supporting the importance of adequate and balanced nutrition during the recovery phase of ischemic AKI.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1)
- **Chemicals:** sodium chloride (PubChem CID 5234), fatty acids (PubChem CID 264)
- **Diseases:** acute kidney injury (MONDO:0002492)
- **Species:** Mus musculus (taxon 10090), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}
- **Diseases:** ischemic (MESH:D002545), renal (MESH:D006030), renal IRI (MESH:D007511), AKI (MESH:D058186), IRI (MESH:D015427), fibrosis (MESH:D005355), hypoxia (MESH:D000860), Hypoxic (MESH:D002534), ischemic kidney injury (MESH:D007674)
- **Chemicals:** sodium (MESH:D012964), sodium chloride (MESH:D012965), salt (MESH:D012492), fat (MESH:D005223), fatty acids (MESH:D005227), amino acids (MESH:D000596), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HK-2 — Homo sapiens (Human), Transformed cell line (CVCL_0302)

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12137256/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12137256/full.md

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Source: https://tomesphere.com/paper/PMC12137256