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A new ophthalmic pharmaceutical formulation, topical sulglycotide, enhances the ocular mucin secretion in desiccation stress-mediated dry eye diseaseoa mark
  • Lee, Hyesook ;
  • Jeon, Sangwon ;
  • Kim, Chae Eun ;
  • Park, Young Joon ;
  • Yang, Jaewook
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Publication Year
2019-03-01
Publisher
Association for Research in Vision and Ophthalmology Inc.
Citation
Investigative Ophthalmology and Visual Science, Vol.60, pp.1076-1087
Keyword
Conjunctival goblet cellDry eye diseaseInflammationMucinSulglycotide (SOS)
Mesh Keyword
Administration, OphthalmicAnimalsAnti-Ulcer AgentsDesiccationDisease Models, AnimalDrug CompoundingDry Eye SyndromesEnzyme-Linked Immunosorbent AssayFluorescent Antibody Technique, IndirectGoblet CellsImmunohistochemistryMiceMice, Inbred NODMucinsMuscarinic AntagonistsOphthalmic SolutionsOxidative StressReal-Time Polymerase Chain ReactionScopolamineSialoglycoproteinsTears
All Science Classification Codes (ASJC)
OphthalmologySensory SystemsCellular and Molecular Neuroscience
Abstract
PURPOSE. The aim of this study was the investigation of the effect of sulglycotide (SOS), a polysulfated glycopeptide derived from porcine duodenal mucin, for the treatment of dry eye disease. METHODS. NOD.B10.H2b mice were exposed to an air draft for 10 days, and, simultaneously, scopolamine hydrobromide was injected subcutaneously. The mice were randomly divided into nine groups as follows: four kinds of SOS formulations and three kinds of commercial medicine. After 10 days of treatment, we estimated the effect of treatment on tear production, epithelium stabilization, mucin secretion, and inflammation. RESULTS. The desiccation stress significantly decreased tear production and corneal epithelium stabilization, as well as markedly decreased the numbers of goblet cells and mucin-stained cells in conjunctiva. However, the topical 4% SOS eye drops markedly increased tear production and corneal stabilization, which recovered to baseline levels. In addition, topical 4% SOS significantly induced an increase in the numbers of goblet cells and the expression of membrane-associated mucins including MUC1, MUC4, and MUC16, as well as the gel-forming mucin, MUC5AC. Furthermore, SOS formulations provided anti-inflammatory improvement in a dose-dependent manner. CONCLUSIONS. In summary, we suggest that a new ophthalmic pharmaceutical formulation, topical sulglycotide, enhances the ocular mucin secretion in dry eye disease and can be used as a new ophthalmic pharmaceutical material to treat dry eye disease.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30657
DOI
https://doi.org/10.1167/iovs.18-24935
Fulltext

Type
Article
Funding
Supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (Grant HI15C1142). Disclosure: H. Lee, None; S. Jeon, None; C.E. Kim, None; Y.-J. Park, None; J. Yang, None
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