Neuropeptides, Inflammation, Biofilms, and diabetic Foot Ulcers

التفاصيل البيبلوغرافية
العنوان: Neuropeptides, Inflammation, Biofilms, and diabetic Foot Ulcers
المؤلفون: Yiwen Yang, Shaoling Yang, Rui Han, Liye Hu
المصدر: Experimental and Clinical Endocrinology & Diabetes. 130:439-446
بيانات النشر: Georg Thieme Verlag KG, 2021.
سنة النشر: 2021
مصطلحات موضوعية: 0301 basic medicine, Calcitonin Gene-Related Peptide, Endocrinology, Diabetes and Metabolism, Macrophage polarization, Inflammation, Proinflammatory cytokine, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Diabetes mellitus, Diabetes Mellitus, Internal Medicine, medicine, Humans, Wound Healing, business.industry, General Medicine, medicine.disease, Diabetic foot, Diabetic Foot, 030104 developmental biology, Diabetic foot ulcer, Biofilms, Immunology, Chronic inflammatory response, medicine.symptom, business, Wound healing
الوصف: A diabetic foot ulcer (DFU) is a serious complication in patients with diabetes mellitus (DM). A DFU is the most common cause of non-traumatic limb amputation, and patients with DFUs have increased mortality rates within 5 years after amputation. DFUs also increase the risk of cardiovascular and cerebrovascular diseases; therefore, with the increasing incidence and prevalence of diabetic foot wounds, DFUs are gradually becoming a major public health problem. The pathophysiology of DFUs is complicated and remains unclear. In recent years, many studies have demonstrated that the pathophysiology of DFUs is especially associated with neuropeptides, inflammation, and biofilms. Neuropeptides, especially substance P (SP) and calcitonin gene-related peptide (CGRP), play an important role in wound healing. SP and CGRP accelerate the healing of cutaneous wounds by promoting neovascularization, inhibiting the release of certain proinflammatory chemokines, regulating macrophage polarization, and so on. However, the expression of SP and CGRP was downregulated in DM and DFUs. DFUs are characterized by a sustained inflammatory phase. Immune cells such as neutrophils and macrophages are involved in the sustained inflammatory phase in DFUs by extracellular traps (NETs) and dysregulated macrophage polarization, which delays wound healing. Furthermore, DFUs are at increased risk of biofilm formation. Biofilms disturb wound healing by inducing a chronic inflammatory response, inhibiting macrophage phagocytosis and keratinocyte proliferation migration, and transferring antimicrobial resistance genes. To understand the relationships among neuropeptides, inflammation, biofilms, and DFUs, this review highlights the recent scientific advances that provide possible pathophysiological insights into the delayed healing of DFUs.
تدمد: 1439-3646
0947-7349
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5a67c55041215de43f766b4b06f9daTest
https://doi.org/10.1055/a-1493-0458Test
رقم الانضمام: edsair.doi.dedup.....4c5a67c55041215de43f766b4b06f9da
قاعدة البيانات: OpenAIRE