Unveiling the Unexplored Multifactorial Potential of 5-Aminosalicylic Acid in Diabetic Wound Therapy.
Bharat Kumar Reddy SanapalliAshwini S DeshpandeVidyasrilekha YeleDilep Kumar SigalapalliPublished in: Diseases (Basel, Switzerland) (2024)
Diabetic wounds (DWs) are considered chronic complications observed in patients suffering from type 2 diabetes mellitus (DM). Usually, DWs originate from the interplay of inflammation, oxidation, impaired tissue re-epithelialization, vasculopathy, nephropathy, and neuropathy, all of which are related to insulin resistance and sensitivity. The conventional approaches available for the treatment of DWs are mainly confined to the relief of wound pressure, debridement of the wound, and management of infection. In this paper, we speculate that treatment of DWs with 5-aminosalicylic acid (5-ASA) and subsequent activation of peroxisome proliferator-activated receptor gamma (PPAR-γ) and transforming growth factor beta (TGF-β) via the AhR pathway might be highly beneficial for DW patients. This estimation is based on several lines of evidence showing that 5-ASA and PPAR-γ activation are involved in the restoration of insulin sensitivity, re-epithelialization, and microcirculation. Additionally, 5-ASA and TGF-β activate inflammation and the production of pro-inflammatory mediators. Suitable stabilized formulations of 5-ASA with high absorption rates are indispensable for scrutinizing its probable pharmacological benefits since 5-ASA is known to possess lower solubility profiles because of its reduced permeability through skin tissue. In vitro and in vivo studies with stabilized formulations and a control (placebo) are mandatory to determine whether 5-ASA indeed holds promise for the curative treatment of DWs.
Keyphrases
- transforming growth factor
- insulin resistance
- wound healing
- newly diagnosed
- type diabetes
- ejection fraction
- prognostic factors
- oxidative stress
- epithelial mesenchymal transition
- metabolic syndrome
- randomized controlled trial
- adipose tissue
- stem cells
- machine learning
- cardiovascular disease
- patient reported outcomes
- mesenchymal stem cells
- risk factors
- clinical trial
- hydrogen peroxide
- skeletal muscle
- chronic kidney disease
- risk assessment
- cardiovascular risk factors
- weight loss
- double blind
- open label
- binding protein
- patient reported
- placebo controlled