# Improving depression-like behaviors caused by diabetes is likely to offer a new perspective for the treatment of non-healing chronic wounds

**Authors:** Zhiqin Dong, Jijin Wu, Hanchen Cao, Jinqiang Lu

PMC · DOI: 10.3389/fnbeh.2024.1348898 · Frontiers in Behavioral Neuroscience · 2024-02-19

## TL;DR

This study explores how diabetes-related depression might slow wound healing and suggests that treating depression could improve wound recovery in diabetic patients.

## Contribution

The study reveals a novel link between diabetes-induced depression and impaired wound healing, suggesting emotional health as a new therapeutic target.

## Key findings

- Diabetic mice show slower wound healing and depression-like behaviors.
- Inhibiting the lateral habenula reduces depressive symptoms and improves wound healing.
- Emotional health may be a key factor in treating non-healing chronic wounds.

## Abstract

Three phases are often involved in the intricate process of wound healing: inflammatory exudation, cell proliferation, and tissue remodeling. It is challenging for wounds to heal if conditions like ischemia, persistent pressure, infection, repetitive trauma, or systemic or localized illnesses arise during the healing process. Chronic wounds are persistent injuries that do not follow the normal healing process and fail to progress through the stages of healing within a reasonable timeframe, like diabetic ulcers, vascular ulcers, pressure sores, and infectious wounds. Various factors affect chronic wound healing. A large body of research has illuminated that psychological distress may often be related to wound healing in clinical settings. Our observations have indicated that the pace of wound healing in diabetic mice is generally slower than that of healthy mice, and mice induced by streptozotocin (STZ) and fed a high-fat diet generally exhibit depression-like behavior. Our experiment delves into whether there is an inherent correlation and provides new ideas for clinical treatment to promote wound healing.

In order to explore the relationship between diabetes, depression, and wound healing, we observed wound healing through HE staining, Masson's trichrome staining, and IHC staining for CD31 and detected the depressive condition through behavioral tests. Then, RT-PCR was used to detect the mRNA expression levels of α-SMA, Col1, CD31, and VEGF in wound tissue. Finally, the related brain areas were regulated through chemical genetic methods and the process of wound healing was observed.

It has been observed that the lateral habenula (LHb) areas are associated with depression-like behavior induced by diabetes. Inhibiting LHb neuronal activity mitigates these depressive symptoms and enhances wound healing. Refractory wounds can be improved by considering patients' emotional issues from a broad standpoint, which provides fresh concepts for potential clinical treatments in the future.

## Linked entities

- **Proteins:** ACTA1 (actin alpha 1, skeletal muscle), COL1 (CONSTANS-like 1), PECAM1 (platelet and endothelial cell adhesion molecule 1), VEGFA (vascular endothelial growth factor A)
- **Chemicals:** streptozotocin (PubChem CID 29327)
- **Diseases:** diabetes (MONDO:0005015), depression (MONDO:0002050), pressure sores (MONDO:0004646)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, Acta2 (actin alpha 2, smooth muscle, aorta) [NCBI Gene 11475] {aka 0610041G09Rik, Actvs, SMAalpha, SMalphaA, a-SMA, alphaSMA}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}
- **Diseases:** infection (MESH:D007239), infectious wounds (MESH:D003141), vascular ulcers (MESH:D014456), pressure sores (MESH:D003668), inflammatory (MESH:D007249), diabetes (MESH:D003920), psychological distress (MESH:D012128), trauma (MESH:D014947), diabetic ulcers (MESH:D017719), depression (MESH:D003866), ischemia (MESH:D007511)
- **Chemicals:** STZ (MESH:D013311)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10910048/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC10910048/full.md

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Source: https://tomesphere.com/paper/PMC10910048