# Raman Investigation of Cardiac Tissues with Sodium-Induced High Stiffness

**Authors:** Igor Artyukov, Gregory Arutyunov, Dmitrii Dragunov, Nikolay Melnik, Elena Perevedentseva, Vadim M. Mitrokhin, Anna Sokolova

PMC · DOI: 10.3390/molecules31030530 · Molecules · 2026-02-03

## TL;DR

This study explores how high sodium levels in heart tissue increase stiffness and change molecular structures using Raman spectroscopy and physiological tests.

## Contribution

The novel contribution is linking sodium accumulation to specific molecular changes in collagen and glycosaminoglycans using Raman spectroscopy.

## Key findings

- High-salt diets increased myocardial stiffness and altered contractile parameters in rats.
- Raman spectroscopy revealed structural modifications in glycosaminoglycan and collagen due to sodium accumulation.
- Proline-rich collagen showed increased contribution, consistent with elevated tissue rigidity.

## Abstract

This study investigates the molecular and mechanical effects of sodium accumulation in myocardial tissue using a combination of physiological measurements and Raman spectroscopy. Male Wistar rats were maintained on normal- and high-salt diets to induce differential sodium loading in cardiac tissue. Hemodynamic and mechanical analyses revealed increased myocardial stiffness and altered contractile parameters in the high-salt group. Raman microspectroscopy of myocardial sections demonstrated distinct spectral changes, particularly in regions corresponding to glycosaminoglycan (GAG), collagen, and its component, proline. Enhanced Raman signals near 1640 cm−1 in the Amide I range, 1246 cm−1 in the Amide III range, and in the 1030–1070 cm−1 range indicated structural modifications of the GAG–collagen complex and an increased contribution of proline-rich collagen, consistent with elevated tissue rigidity. These findings support the concept that sodium deposition in the myocardium alters its molecular architecture and mechanical properties through GAG-mediated binding and collagen remodeling. This study provides new insights into the biophysical mechanisms linking sodium homeostasis to myocardial stiffness and diastolic dysfunction.

## Linked entities

- **Chemicals:** sodium (PubChem CID 5360545)

## Full-text entities

- **Diseases:** diastolic dysfunction (MESH:D018487)
- **Chemicals:** proline (MESH:D011392), Sodium (MESH:D012964), Amide I (-), GAG (MESH:D006025), salt (MESH:D012492)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12900002/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12900002/full.md

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Source: https://tomesphere.com/paper/PMC12900002