Skin Dryness Induced in the KK-Ay/TaJcl Type 2 Diabetes Mouse Model Deteriorates Following Dapagliflozin Administration

Biol Pharm Bull. 2022 Jul 1;45(7):934-939. doi: 10.1248/bpb.b22-00241. Epub 2022 May 17.

Abstract

Various diabetic drugs have been developed as the number of patients with type 2 diabetes has increased. Sodium-glucose cotransporter (SGLT)-2 inhibitors have been developed as novel therapeutic agents. However, SGLT-2 inhibitors cause skin dryness. The mechanism through which SGLT-2 inhibitors cause skin dryness is unknown. The purpose of this study was to investigate the mechanism through which dapagliflozin, a SGLT-2 inhibitor, induces skin dryness. Specific pathogen-free KK-Ay/TaJcl (type 2 diabetes model) mice were orally administered with SGLT-2 inhibitor (dapagliflozin) daily for 4 weeks at a dose of 1 mg/kg/d. Skin dryness induced in KK-Ay/TaJcl mice became severe after dapagliflozin administration. Dapagliflozin treatment decreased collagen type I and hyaluronic acid levels in mice; additionally, it affected the transforming growth factor (TGF)-β/hyaluronan synthase pathway, further reducing hyaluronic acid levels. The results indicate that the reduction in hyaluronic acid levels plays an important role in the occurrence of dry skin in diabetes.

Keywords: collagen type I; hyaluronic acid; sodium-glucose cotransporter-2; transforming growth factor-β; type 2 diabetes.

MeSH terms

  • Animals
  • Benzhydryl Compounds / pharmacology
  • Benzhydryl Compounds / therapeutic use
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 2* / metabolism
  • Disease Models, Animal
  • Glucosides
  • Hyaluronic Acid
  • Hypoglycemic Agents / therapeutic use
  • Mice
  • Sodium-Glucose Transporter 2 Inhibitors* / therapeutic use

Substances

  • Benzhydryl Compounds
  • Blood Glucose
  • Glucosides
  • Hypoglycemic Agents
  • Sodium-Glucose Transporter 2 Inhibitors
  • dapagliflozin
  • Hyaluronic Acid