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[Pathogenesis of varicose ulcers of the lower extremities]
Insights
In patients with lower limb varicosity, elevated cathepsin enzyme activity contributes to skin destruction and ulcer formation. Treatment with aescusan reduced this activity, suggesting a protective effect on cellular membranes.
Area of Science:
- Biochemistry
- Dermatology
- Pathophysiology
Context:
- Lower limb varicosity is associated with significant skin damage and ulceration.
- The precise biochemical pathways leading to skin destruction in these patients are not fully understood.
- Cathepsins, a group of enzymes, are implicated in tissue degradation.
Purpose:
- To investigate the role of cathepsin enzymes (A, B, C, and D) in the biochemical mechanisms of skin destruction and ulcer formation in patients with lower limb varicosity.
- To assess the impact of aescusan treatment on cathepsin activity in affected skin.
- To elucidate the potential protective mechanisms of aescusan on cellular structures.
Summary:
- Cathepsin A, B, C, and D activity was measured in the skin of 57 patients with lower limb varicosity.
- Significantly increased activity of cathepsin D (183.8%), cathepsin B (140.2%), and cathepsin B (239%) was observed in the lower leg.
- Authors concluded that cathepsins, particularly cathepsin D, play a key role in skin destruction, with aescusan treatment reducing their activity by 15.4-24.1% and protecting lysosomal membranes.
Impact:
- This study identifies specific cathepsin enzymes as key mediators of skin destruction in lower limb varicosity.
- The findings provide biochemical evidence for the therapeutic efficacy of aescusan in managing skin complications associated with venous insufficiency.
- Understanding the role of cathepsins may lead to novel therapeutic strategies for preventing and treating venous ulcers.
Abstract:
The article discusses the biochemical mechanisms of skin destruction and ulcer formation in patients with varicosity of the lower limbs. Cathepsins A, B, C, and D were determined in the skin in various parts of the limb in 57 patients: in the lower third of the leg the activity of cathepsin D was increased by 183.8%, that of cathepsin B by 140.2%, and the activity of cathepsin B by 239%. On basis of the data obtained the authors conclude that cathepsins take part in skin destruction. Increased activity of cathepsin D plays the initiative role in this process. Cathepsin activity reduced after 14-16 day treatment with aescusan; D by 24.1%, B by 17.7%, and A by 15.4%. The authors link the effect of the treatment with the protective effect of the preparation on the lysosomal membranes.
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