Wound healing in diabetes. An intervention study in db/db mice
Year: 2017
Type: dissertation
Abstract: The prevalence of diabetes is increasing globally. Certain microvascular and macrovascular complications such as cardiovascular disease, retinopathy, nephropathy, neuropathy, and impaired wound healing are associated with the disease. Prolonged exposure to hyperglycaemia plays an important role in their development. Glucose reacts with macromolecules including proteins, lipoproteins, and nucleic acids over time to form irreversible advanced glycation end products (AGEs) that could modify both extracellular matrix and plasma proteins and also alter cellular functions. \nIn skin of animals and humans with diabetes, increased cross-linking of collagen by glycation and subsequent accumulation of AGEs occur. This is associated with more stiffness and increased insolubility, and could potentially contribute to inhibition of cellular infiltration in the wound, blockage of angiogenesis and attenuation of wound contraction and closure. Furthermore, wound studies in diabetes have demonstrated an aberrant course of inflammation. Macrophages are crucial in inflammation and wound healing, and studies have revealed impaired functioning of these cells in diabetes. \nIn order to study wound healing, we used leptin receptor deficient db/db mice, the most widely used animal model for type 2 diabetes. The aims of our studies were to: 1) examine the effects of a macrophage stimulant, water-soluble aminated beta-1,3-D-glucan (AG) with or without additional glucose-lowering treatment with insulin, 2) study potential dose-response effects of AG, 3) investigate if there was an association between wound healing and metabolic variables, and 4) explore potential effects of aminoguanidine, an inhibitor of AGE formation. \nIn mice that were topically applied with AG, wound closure improved significantly compared to placebo treated controls. The addition of subcutaneous insulin treatment did not further accelerate wound healing. Subcutaneous insulin treatment alone did not promote wound healing. It lowered plasma glucose significantly, but did not normalise it. Experiments on different frequencies of topical AG administration onto the wound revealed dose-dependent effects on wound healing. Wounds applied with multiple AG doses (five or more) closed comparably to growth factor treatment (combined treatment with platelet-derived growth factor and insulin-like growth factor 1) during the early phase (days 0-17) of wound repair. In a separate study, wound closure did not show a significant association with plasma glucose, whereas change in body weight predicted wound healing in our model. Aminoguanidine, either administered topically or systemically, did not improve wound healing. However, the AGE-inhibitor was associated with favourable metabolic changes over time, that is, percentage weight loss and glycated hemoglobin A1c tended to decrease dose-dependently.
Author: Margrete Berdal
Language: English
Topic: Wound Healing and Treatments
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W2735389097