# The Effects of the Natriuretic Peptide System on Alveolar Epithelium in Heart Failure

**Authors:** Yara Knany, Safa Kinaneh, Emad E. Khoury, Yaniv Zohar, Zaid Abassi, Zaher S. Azzam

PMC · DOI: 10.3390/ijms26073374 · 2025-04-04

## TL;DR

This study explores how natriuretic peptides affect alveolar fluid clearance in heart failure, which could help improve treatments for severe heart failure.

## Contribution

The study reveals novel molecular mechanisms by which natriuretic peptides influence alveolar sodium transport and fluid clearance in heart failure.

## Key findings

- ANP and BNP significantly reduce alveolar fluid clearance rates in isolated lungs.
- Natriuretic peptides downregulate active sodium transport components and increase αENaC ubiquitination via Nedd4-2.
- ANP partially restores alveolar fluid clearance in decompensated heart failure.

## Abstract

Alveolar active sodium transport is essential for clearing edema from airspaces, in a process known as alveolar fluid clearance (AFC). Although it has been reported that atrial natriuretic peptide (ANP) attenuates AFC, little is known about the underlying molecular effects of natriuretic peptides (NPs). Therefore, we examined the contribution of NPs to AFC and their effects as mediators of active sodium transport. By using the isolated liquid-filled lungs model, we investigated the effects of NPs on AFC. The expression of NPs, Na+, K+-ATPase, and Na+ channels was assessed in alveolar epithelial cells. Congestive heart failure (CHF) was induced by using the aortocaval fistula model. ANP and brain NP (BNP) significantly reduced AFC rate from 0.49 ± 0.02 mL/h in sham rats to 0.26 ± 0.013 and 0.19 ± 0.005 in ANP and BNP-treated groups, respectively. These effects were mediated by downregulating the active Na+ transport components in the alveolar epithelium while enhancing the ubiquitination and degradation of αENaC in the lungs, as reflected by increased levels of Nedd4-2. In addition, AFC was reduced in compensated CHF rats treated with ANP, while in decompensated CHF, ANP partially restored AFC. In conclusion, NPs regulate AFC in health and CHF. This research could help optimize pharmacological treatments for severe CHF.

## Linked entities

- **Proteins:** nrv1 (nervana 1), NEDD4L (NEDD4 like E3 ubiquitin protein ligase)
- **Diseases:** heart failure (MONDO:0005252), congestive heart failure (MONDO:0005009)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Nedd4l (NEDD4 like E3 ubiquitin protein ligase) [NCBI Gene 291553] {aka Nedd4-2}, Nppb (natriuretic peptide B) [NCBI Gene 25105] {aka BNP, Bnf}, Nppa (natriuretic peptide A) [NCBI Gene 24602] {aka ANF, ANP, CDD, Pnd, RATANF}, Scnn1a (sodium channel epithelial 1 subunit alpha) [NCBI Gene 25122] {aka ENaCA}, Klk8 (kallikrein related-peptidase 8) [NCBI Gene 308565] {aka Klnh, bsp1}
- **Diseases:** edema (MESH:D004487), CHF (MESH:D006333), aortocaval fistula (MESH:D005402)
- **Chemicals:** Na+ (MESH:D012964)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11989889/full.md

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Source: https://tomesphere.com/paper/PMC11989889