Cutaneous wounds occur when the skin is injured
mechanically, chemically, or by extreme temperatures. Wound healing is a very
complex process composed of several phases in which precise events occur, both
temporally and spatially. However, when these processes go awry,
biofilm-forming bacteria become installed in the healing tissue, and the
patient has comorbidities, so the wounds do not heal and become chronic. In
this review, we describe the importance of high levels of oxidative stress (OS)
and bacteria from the skin microbiome in the initiation and development of
chronic wounds. The skin microbiome is diverse in humans, and its composition
is dependent on the environment in the specific areas of the body. OS is
critical for wound healing as it stimulates the immune system to destroy
pathogens and secrete cytokines and growth factors that stimulate healing. When
OS levels become high in the wound, and the bacteria of the skin install
themselves in the wound, chronicity ensues. However, neither OS nor the
bacteria of the skin alone can initiate chronicity. However, when present together,
chronic wounds develop. Given the complexity of chronic wound initiation,
developing treatment for these wounds has been difficult. Based on current
published findings, a potential approach to treating chronic wounds after
debridement was recently proposed. It was proposed that it is important to
treat the physiological problems related to the comorbidities these patients
have prior to and during wound treatment. Patients should also be put on a diet
that is rich in products that stimulate an increase in the levels of adenosine
triphosphate (ATP) to ensure that the cells have sufficient energy to function,
and is rich in α-tocopherol (Vit E) to decrease lipid peroxidation and cell
membrane damage, and patients should also take antioxidants to reduce OS. Here,
we also discuss the challenges of treating chronic wounds and offer a potential
sequence of approaches to treating these wounds after debridement.
Author(s) Details
Manuela Martins-Green
Department of Molecular, Cell and Systems Biology, University of California
Riverside, Riverside, CA 92521, USA.
Jane Kim and Klara
Aziz
Department of Molecular, Cell and Systems Biology, University of California
Riverside, Riverside, CA 92521, USA.
Please see the link:- https://doi.org/10.9734/bpi/mbrao/v6/6757
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