Unknown

Dataset Information

0

Effects of Selective Peroxisome Proliferator Activated Receptor Agonists on Corneal Epithelial Wound Healing.


ABSTRACT: The effects of each subtype-selective peroxisome proliferator activated receptor (PPAR) agonist (?, ?/?, ?) on corneal epithelial wound healing were investigated using a rat corneal alkali burn model. After the alkali burn, each PPAR agonist or vehicle ophthalmic solution was instilled topically onto the rat's cornea. Corneal epithelial healing processes were evaluated by fluorescein staining. Pathological analyses and real-time reverse transcription polymerase chain reactions were performed to evaluate Ki67 (proliferative maker) expression and inflammatory findings. The area of the corneal epithelial defect at 12 h and 24 h after the alkali burn was significantly smaller in each PPAR group than in the vehicle group. Ki67 mRNA expression was increased in the PPAR?/? group, whereas mRNA expressions of inflammatory cytokines were suppressed in all of the PPAR agonist groups. Nuclear factor kappa B (NF-?B) was the most suppressed in the PPAR? group. The accelerated corneal epithelial healing effects of each PPAR ligand were thought to be related to the promotion of proliferative capacity and inhibition of inflammation.

SUBMITTER: Tobita Y 

PROVIDER: S-EPMC7911852 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Effects of Selective Peroxisome Proliferator Activated Receptor Agonists on Corneal Epithelial Wound Healing.

Tobita Yutaro Y   Arima Takeshi T   Nakano Yuji Y   Uchiyama Masaaki M   Shimizu Akira A   Takahashi Hiroshi H  

Pharmaceuticals (Basel, Switzerland) 20210125 2


The effects of each subtype-selective peroxisome proliferator activated receptor (PPAR) agonist (α, β/δ, γ) on corneal epithelial wound healing were investigated using a rat corneal alkali burn model. After the alkali burn, each PPAR agonist or vehicle ophthalmic solution was instilled topically onto the rat's cornea. Corneal epithelial healing processes were evaluated by fluorescein staining. Pathological analyses and real-time reverse transcription polymerase chain reactions were performed to  ...[more]

Similar Datasets

| S-EPMC4248330 | biostudies-literature
| S-EPMC6703246 | biostudies-literature
| S-EPMC3632601 | biostudies-literature
2008-11-25 | GSE12147 | GEO
| S-EPMC4669743 | biostudies-literature
| S-EPMC3359336 | biostudies-literature
| S-EPMC8430769 | biostudies-literature
| S-EPMC4212005 | biostudies-literature
| S-EPMC4138931 | biostudies-literature
| S-EPMC4627737 | biostudies-literature