Related Experiment Video
Updated: Sep 3, 2026

In Vivo Imaging of Reactive Oxygen Species in a Murine Wound Model
Published on: November 17, 2018
Early mRNA expression of pro-inflammatory cytokines and ADAMTS-5 in an acute ischemia/reperfusion-induced pressure
Mustafa Sağlam1, Burcu Yanık2, Eralp Erdoğan3
1Clinic of Physical Medicine and Rehabilitation, Bolu İzzet Baysal Physical Treatment and Rehabilitation Training and Research Hospital, Bolu, Türkiye.
Objectives:
This study aimed to determine the messenger ribonucleic acid (mRNA) expression levels of interleukin (IL)-1α, IL-1β, IL-6, IL-17, and A Disintegrin and Metalloproteinase with Thrombospondin Motifs (ADAMTS)-5 in an acute ischemia/reperfusion (I/R)-induced pressure ulcer (PU) model, in order to characterize the early inflammatory cytokine profile and explore the potential role of ADAMTS-5 in extracellular matrix (ECM) remodeling.
Patients And Methods:
Ten BALB/c mice were randomly allocated to control and PU groups. Acute PUs were generated on the dorsal skin using a repeated I/R protocol achieved with ceramic magnetic plaques. Skin biopsies obtained from ulcerated and control areas were examined histologically using hematoxylin-eosin staining. mRNA expression levels of IL-1α, IL-1β, IL-6, IL-17, and ADAMTS-5 were analyzed by quantitative real-time PCR and compared statistically between groups.
Results:
Compared with controls, mRNA expression levels of IL-1α, IL-6, IL-17, and ADAMTS-5 were significantly increased in the PU group (p<0.05). In contrast, IL-1β expression showed an increase that did not reach statistical significance.
Conclusion:
These findings indicate that proinflammatory cytokines and ADAMTS-5 are activated early during PU formation following I/R injury. The observed upregulation of ADAMTS-5, a molecule that has been rarely examined in PU models, suggests a possible role for early ECM degradation in ulcer development. Further experimental and clinical studies are warranted to clarify the relevance of these pathways for PU progression and targeted local therapies.

