NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models.
8-Hydroxy-2'-Deoxyguanosine
/ genetics
Animals
Corneal Injuries
/ chemically induced
Disease Models, Animal
Dry Eye Syndromes
/ chemically induced
Epithelial Cells
/ drug effects
Epithelium, Corneal
/ drug effects
Gene Expression Regulation
/ drug effects
Glutamate-Cysteine Ligase
/ genetics
Humans
Keratitis
/ chemically induced
NAD(P)H Dehydrogenase (Quinone)
/ genetics
NF-E2-Related Factor 2
/ genetics
Oxidative Stress
/ drug effects
RNA, Messenger
/ drug effects
Rats
Reactive Oxygen Species
/ metabolism
Scopolamine
/ toxicity
Triterpenes
/ pharmacology
Wound Healing
/ drug effects
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
28
09
2019
accepted:
05
02
2020
entrez:
23
4
2020
pubmed:
23
4
2020
medline:
2
7
2020
Statut:
epublish
Résumé
Oxidative stress may cause ocular surface damage during the development of dry eye. Mammalian cells have defense systems against oxidative stress. A central regulator of the stress response is nuclear factor-erythroid 2-related factor 2 (NFE2L2). NFE2L2 is activated by the novel triterpenoid RS9 (a biotransformation compound of RTA 402). The purpose of this study was to assess the efficacy of RS9 against dry eye using in vitro and in vivo models. Bioactivity was estimated by the induction of mRNAs for two NFE2L2-targeted genes: NQO1 (prevents radical species) and GCLC (glutathione synthesis), using a corneal epithelial cell line (HCE-T). Protection against oxidation and cell damage was tested in vitro by culturing cells under hyperosmotic stress or by the addition of menadione, a generator of reactive oxygen species (ROS). Dry eye in vivo was induced by the injection of scopolamine into rats. Then, 930 nM of RS9 was applied to both eyes for 2 weeks. Oxidative stress was measured by the accumulation of 8-hydroxy-2'-deoxyguanosine (8-OHdG). Corneal wound healing was measured by scoring for superficial punctate keratitis (SPK). Corneal epithelial cell densities were evaluated histologically. RS9 and RTA 402 induced the expression of NQO1 and GCLC mRNAs in HCE-T cells. And both compounds suppressed hyperosmotic-ROS generation and menadione induced cellular damage. However RS9 had a stronger protective effect than RTA 402. Ocular instillation of RS9 also significantly upregulated the expression of Nqo1 mRNA in the corneal epithelium. Accumulation of 8-OHdG, increase of SPK scores and decrement of basal cell density were observed in corneal epithelium from scopolamine-injected rats. These changes were significantly ameliorated by the topical administration of RS9. RS9 induced Nfe2l2 activation and Nfe2l2-targeted genes, reduced oxidation, and ameliorated symptoms of dry eye using in vitro and in vivo models. Thus, RS9 might be a potent candidate agent against dry eye disease.
Identifiants
pubmed: 32320433
doi: 10.1371/journal.pone.0229421
pii: PONE-D-19-27264
pmc: PMC7176120
doi:
Substances chimiques
NF-E2-Related Factor 2
0
RNA, Messenger
0
RS9 triterpenoid
0
Reactive Oxygen Species
0
Triterpenes
0
8-Hydroxy-2'-Deoxyguanosine
88847-89-6
Scopolamine
DL48G20X8X
NAD(P)H Dehydrogenase (Quinone)
EC 1.6.5.2
NQO1 protein, rat
EC 1.6.5.2
Glutamate-Cysteine Ligase
EC 6.3.2.2
GCLC protein, rat
EC 6.3.2.2.
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0229421Déclaration de conflit d'intérêts
I have read the journal’s policy and the authors of this manuscript have the following competing interests: Yuka Matsuda, Mamiko Machida, Takeshi Nakajima and Mitsuyoshi Azuma are employees of Senju Pharmaceutical Co., Ltd. Yasuhiro Nakagami is a employee of Daiichi Sankyo Pharmaceutical Co., Ltd. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.
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