Peer-reviewed veterinary case report
What causes heart muscle changes and inflammation in dogs
By Gasparini, Stefania et al.·Published in Veterinary pathology·2020·Institute of Veterinary Pathology·View original on PubMed →
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Original publication title: Canine Dilated Cardiomyopathy: Diffuse Remodeling, Focal Lesions, and the Involvement of Macrophages and New Vessel Formation.
- Species:
- dog
Plain-English summary
A group of dogs with dilated cardiomyopathy (DCM), a serious heart condition, showed changes in their heart tissue that could explain why they were experiencing heart problems. Researchers found that the heart muscle had increased collagen and inflammatory cells, which can lead to heart dilation and reduced function. They also noted specific markers in the heart tissue that indicated inflammation and remodeling. Understanding these changes could help in developing better treatments for dogs with DCM.
People also search for: dog heart disease symptoms · dilated cardiomyopathy in dogs treatment · signs of heart problems in dogs
Abstract
Dilated cardiomyopathy (DCM) is among the most common cardiac diseases in dogs. Its pathogenesis is not fully understood, but myocardial remodeling and inflammation are suspected to be involved. The present study aimed to characterize the pathological processes in canine DCM, investigating morphological changes in association with the expression of relevant cytokines and remodeling markers. The myocardium of 17 dogs with DCM and 6 dogs without cardiac diseases was histologically evaluated, and selected cases were further examined by immunohistochemistry, morphometry, and reverse transcription quantitative PCR. In DCM, the myocardium exhibited subtle but statistically significant diffuse quantitative changes. These comprised increased interstitial collagen deposition and macrophage numbers, as well as an overall reduced proportion of contractile tissue. This was accompanied by a significant increase in myocardial transcription of intracellular adhesion molecule (ICAM) 1, inflammatory cytokines, and remodeling enzymes. Laser microdissection showed that cardiomyocytes transcribed most relevant markers including ICAM-1, tumor necrosis factor α, transforming growth factor β (TGF-β), matrix metalloproteinase 2 (MMP-2), tissue inhibitor of MMP (TIMP) 1 and TIMP-2. In addition, there were multifocal cell-rich lesions characterized by fibrosis, neovascularization, macrophage infiltration, and cardiomyocyte degeneration. In these, macrophages were often found to express ICAM-1, TGF-β, and vascular endothelial growth factor; the former two were also expressed by cardiomyocytes. These results characterize the diffuse myocardial remodeling processes that occur in DCM. The observed multifocal cell-rich lesions might result from reduced tissue perfusion. Macrophages and cardiomyocytes seem to actively contribute to the remodeling processes, which ultimately lead to cardiac dilation and dysfunction. The precise role of the involved cells and the factors initiating the remodeling process still needs to be identified.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/32125251/