# Post hoc comparison of the intrarenal and circulating renin‐angiotensin(‐aldosterone) systems in cats with ischemia‐induced chronic kidney disease

**Authors:** Jane H. C. Huang, Bianca N. Lourenço, Chad W. Schmiedt, Jaime L. Tarigo, Amanda E. Coleman

PMC · DOI: 10.14814/phy2.70417 · 2025-06-25

## TL;DR

This study compares the renin-angiotensin system in healthy and kidney-diseased cats, finding no link between blood and kidney system activity.

## Contribution

The study reveals no correlation between circulating and intrarenal RA(A)S markers in cats with CKD.

## Key findings

- Circulating angiotensin peptide levels did not correlate with renal concentrations.
- Intrarenal angiotensin I and AGT levels were positively correlated.
- ACE transcript levels were negatively correlated with serum creatinine.

## Abstract

Activities of the circulating and intrarenal renin‐angiotensin(‐aldosterone) systems (RA[A]S) are incompletely understood in people and cats with chronic kidney disease (CKD). We measured circulating and intrarenal RA(A)S markers in healthy cats (n = 8) and cats with induced CKD (n = 6 subjected to unilateral renal ischemia [RI group] and n = 5 subjected to RI and delayed contralateral nephrectomy [RI‐DCN group]). Serum equilibrium concentrations of angiotensin peptides and aldosterone, plasma renin activity, and urinary aldosterone‐to‐creatinine ratio were evaluated before and after renal injury in CKD cats and at a single timepoint in healthy cats. Renal tissular concentrations of angiotensin peptides and mRNA levels of RA(A)S‐related genes were measured in all cats. There was no significant correlation between circulating angiotensin peptide concentrations and their respective renal concentrations. Intrarenal angiotensin I concentrations and AGT transcript levels were positively correlated, and ACE transcript levels were negatively correlated with serum creatinine concentration. Circulating RA(A)S markers were not different between healthy and CKD groups, except for serum angiotensin 1–5, which was lower in the RI group compared to the healthy group. Intrarenal angiotensin peptide concentrations did not differ among groups. Compared to healthy cats, mRNA levels of ACE, AT1R, and REN were lower, and AGT levels were higher in one or both CKD group(s).

Samples from cats with CKD or healthy were used to compare circulating and intrarenal RA(A)S markers. There was no correlation between circulating concentrations of angiotensin peptides and their respective renal tissular concentrations.

## Linked entities

- **Genes:** ACE (angiotensin I converting enzyme) [NCBI Gene 1636], AGTR1 (angiotensin II receptor type 1) [NCBI Gene 185], REN (renin) [NCBI Gene 5972], AGT (angiotensinogen) [NCBI Gene 183]
- **Diseases:** chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** REN [NCBI Gene 101081695], AGT [NCBI Gene 101093714]
- **Diseases:** CKD (MESH:D051436), ischemia (MESH:D007511), renal injury (MESH:D007674)
- **Chemicals:** aldosterone (MESH:D000450), DCN (-), RA (MESH:D011883), creatinine (MESH:D003404)
- **Species:** Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12190553/full.md

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Source: https://tomesphere.com/paper/PMC12190553