| Project/Area Number |
25462730
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Ophthalmology
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| Research Institution | Wakayama Medical University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
saika shizuya 和歌山県立医科大学, 医学部, 教授 (40254544)
okada yuka 和歌山県立医科大学, 医学部, 講師 (50264891)
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| Project Period (FY) |
2013-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2013: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
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| Keywords | 角膜 / 眼科学 / ドライアイ / 糖尿病 |
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| Outline of Final Research Achievements |
We create a dry eye model mice, compared with the wild-type mouse corneal tear secretion,epithelial disorder. Also inflammatory cytokines from excised lacrimal gland, a study of such immunostaining comparative study renal failure mouse be used, was scheduled to investigate the tear fluid dynamics in mice, did not lead to the announcement. Also divided the dialysis patients in diabetes patients and non-diabetic patients as a clinical study, did not lead to the announcement was scheduled to perform a comparative study.
Other was to study the dynamics of corneal neovascularization in TRPV1-deficient mice. The mouse the central cornea to heat coagulation, corneal neovascularization that stretched from the limbus was to suppress the extension compared by wild-type mice with TRPV1-deficient mice. The study was awarded a Docor of Medicine posted on Journal of Ophthalmology.
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