In diabetic mice with incisional wounds, cibinetide significantly improved the increased wound malondialdehyde seen with vehicle.
In plain wordsIn diabetic mice, cibinetide improved the raised oxidative damage marker in wounds, compared with vehicle.
- Peptide
- Cibinetide (ARA-290)
- Outcome
- DecreaseWound malondialdehyde (MAL)
- Study
mousen: not reported in source
Incisional wound model in genetic diabetic (db+/db+) mice- Comparator
- Vehicle
- Outcome group
- Wound healing · Skin and wound
- Studied dose
- 30 µg/kg · subcutaneous · up to 14 daysAs given in this study (mouse).
Source sentences
Throughout the wound healing process diabetic animals treated with vehicle exhibited increased wound MAL with reduced VEGF, pAkt, peNOS and nitrite/nitrate, all associated with poor re-epitheliziation, angiogenesis, and wound breaking strength. Cibenitide administration significantly improved these abnormalities.
2 context sentences(design, population, supporting numbers)
A specific IRR agonist cibinetide was administered in an incisional wound healing model performed mice with genetic diabetes (db+/db+) and compared to the normal wild-type.
Animals were treated daily with cibinetide (30μg/kg/s.c.) or vehicle and euthanized 3, 7, and 14days after the injury to quantitate vascular endothelial growth factor (VEGF), malondialdehyde (MAL), phospho-Akt (pAkt), phospho e-NOS (p-eNOS), and nitrite/nitrate content within the wound.