Pregled bibliografske jedinice broj: 1262826
Wound Healing in Dipeptidyl-peptidase IV (DPP IV/CD26) Deficient Diabetic Mice
Wound Healing in Dipeptidyl-peptidase IV (DPP IV/CD26) Deficient Diabetic Mice // Book of Abstracts-OSCON / Pavlović, Vedrana (ur.).
Osijek: University of Osijek, 2022. str. 44-44 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1262826 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Wound Healing in Dipeptidyl-peptidase IV (DPP
IV/CD26) Deficient Diabetic Mice
Autori
Batičić, Lara ; Detel, Dijana ; Bedoić, Edvard ; Varljen, Jadranka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts-OSCON
/ Pavlović, Vedrana - Osijek : University of Osijek, 2022, 44-44
Skup
4th International Translational Medicine Congress of Students and Young Physicians
Mjesto i datum
Osijek, Hrvatska, 31.03.2022. - 02.04.2023
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Diabetes Mellitus ; DPP IV/CD26 ; Hyperglycemia
Sažetak
Introduction: Dipeptidyl-peptidase IV/CD26 molecule (DPP IV/CD26) is widely known, except for its involvement in a multitude of physiological and pathological processes, for the role in regulation of glycaemia. Complications caused by diabetes such as infections, ulcerations and gangrene are the main causes for hospitalization. DPP IV/CD26 inhibitors are available as a treatment option for patients with diabetes type II. Inhibition of DPP IV/CD26 accelerates healing of chronic diabetic ulcerations by induction of a histological pattern consistent with enhanced angiogenesis. We hypothesized a significant role of DPP IV/CD in mechanisms of cutaneous wound healing in hyperglycemia. Our aim was to research the process of wound healing in conditions of CD26 deficiency in experimental hyperglycemia in order to acquire more insights on the role of DPP IV/CD26 in cutaneous reparation and regeneration. Materials and methods: A streptozotocin-model of diabetes was induced in wild-type mice and CD26 deficient type. Experimental wounds were performed on mice dorsal regions and animals were sacrificed on determined time schedule. Pathohistological, histomorphometrical, immunohistochemical and immunobiochemical analyses were performed on wound samples and control skin while serum samples were analysed for DPP IV/CD26 activity and concentration of target angiogenic factors. Results: Our hypothesis was confirmed by this study since we shown that DPP IV/CD26 plays an important role in the regulation of blood glucose concentration and its inactivation improves state associated with hyperglycemia. Moreover, the process of cutaneous wound healing is improved in conditions of DPP IV/CD26 deficiency with elevated local expression of proangiogenic factors. Conclusion: Inhibition of DPP IV/CD26 has beneficial effects on the wound healing process in hyperglycemia, which supports the significance of DPP IV/CD26 inhibition as a therapeutic option for the treatment of diabetes.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka