# Protective Effect of Deer Heart Peptide on Cardiac Injury in Mice

**Authors:** Qun Zhang, Hongjin Li, Dongshu Jia, Wei Chen, Xinao Jia, Qi Lin, Jiyi Zhang, Yujiao Tang

PMC · DOI: 10.1155/2024/6661371 · International Journal of Inflammation · 2024-05-14

## TL;DR

This study shows that deer heart peptides can protect mice from alcohol-induced heart damage by reducing inflammation and boosting antioxidants.

## Contribution

The novel contribution is the empirical evidence of deer heart peptides' anti-inflammatory and antioxidant effects in a mouse model of cardiac injury.

## Key findings

- Deer heart peptides reduced inflammatory markers TNF-α, IL-6, and IL-1β in cardiac tissues.
- Peptides increased antioxidant enzymes CAT and SOD in serum and improved myocardial enzyme profiles.
- Histological analysis showed significant improvement in myocardial disorders in treated mice.

## Abstract

Peptides are widely used as natural bio-small molecules because of their various pharmacological activities such as enhancing immunity, promoting wound healing, and improving inflammation. Alcoholic heart injury has become one of the major health problems worldwide, and alcohol consumption is now the main cause of alcoholic cardiomyopathy. In this study, deer heart peptides were extracted from deer hearts by enzymatic digestion and the antioxidant activity of deer heart peptides extracted at different times was evaluated by three in vitro antioxidant methods, and the active peptide with the best enzymatic effect has been selected for in vivo animal experiments. The anti-inflammatory and antioxidant properties of deer heart enzymatic extracts were evaluated in in vivo experiments in mice. In this study, mice were orally gavaged with white wine (12 mL/kg body weight) to induce a mouse model of cardiac injury, while mice were orally administered a single dose of 100 mg/kg/bw and 200 mg/kg/bw of deer heart enzyme digest and were examined for body weight, dietary intake, water intake, and coat gloss, as well as for general behaviors, adverse effects, and mortality. Histology, serum, anti-inflammatory factors, and oxidative stress parameters were subsequently assessed. In all modeled mice, no four-way or any significant behavioral changes were observed in all groups, but in the modeled group, mice showed weight loss, decreased diet and water intake, and decreased cardiac index. For in vivo tests, the extract inhibited the anti-inflammatory activity with a significant decrease in inflammatory factors of TNF-α, IL-6, and IL-1β in cardiac tissues, a significant increase in serum levels of both CAT and SOD, an increase in MDA content, and a remarkable increase in the level of the marker CK in the cardiac myocardial enzyme profile. Significant improvement in myocardial disorders by deer heart peptide could be observed from heart tissue sections. The present study emphasizes the anti-inflammatory and antioxidant activity of deer heart peptide, an enzymatic digest of deer heart, which provides empirical as well as supportive role for the anti-inflammatory properties of traditional medicine.

## Linked entities

- **Chemicals:** IL-6 (PubChem CID 165368475), MDA (PubChem CID 1614), CK (PubChem CID 10477)
- **Diseases:** alcoholic cardiomyopathy (MONDO:0006643)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}
- **Diseases:** alcoholic cardiomyopathy (MESH:D002310), weight loss (MESH:D015431), Alcoholic heart injury (MESH:D006335), Cardiac Injury (MESH:D006331), myocardial disorders (MESH:D009202), inflammation (MESH:D007249)
- **Chemicals:** alcohol (MESH:D000438), white wine (-), MDA (MESH:D015104)
- **Species:** Cervidae (deer, family) [taxon 9850], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11208793/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC11208793/full.md

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Source: https://tomesphere.com/paper/PMC11208793