| Project/Area Number |
15591846
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Ophthalmology
|
|---|
| Research Institution | Teikyo University |
|---|
Principal Investigator |
SUZUKI Yasuyuki Teikyo University, School of Medicine, Professor, 医学部, 教授 (80196881)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
TOMIDOKORO Atsuo Tokyo University Graduate School of Medicine, Department of Ophthalmology, Lecture, 医学部附属病院, 講師 (80227628)
|
|---|
| Project Period (FY) |
2003 – 2004
|
| Project Status |
Completed (Fiscal Year 2004)
|
| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2004: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2003: ¥2,000,000 (Direct Cost: ¥2,000,000)
|
|---|
| Keywords | glaucoma / neurofilament / phosphorylation of heavy neurofilament subunit / retinal ganglion cell damage / rat glaucoma model / N-methyl-D-aspartate / グルタミン酸 / NF-200 / SMI31 / ELISA / 網膜神経節細胞 |
|---|
| Research Abstract |
Early detection of retinal ganglion damage in animal glaucoma models has been difficult. Neurofilaments are major neuronal intermediate filaments expressed in most neurons. Dephosphorylation of heavy neurofilament subunit is reported to be involved in retinal ganglion cell damage. Evaluating the status of neurofilament in retinal ganglion cell may be a good indicator of early retinal ganglion cell damage. In this study, we evaluated the relationship between the status of neurofilament in retinal ganglion cell and retinal ganglion cell damage using rat models. First, a rat glaucoma model was constructed by cauterizing suprascleral veins. The retinal section was examined immunohistologically. The dephosphorylation level of heavy neurofilament subunit seemed correlated slightly with the retinal ganglion cell damage but not apparent. Next, the expression level of neurofilament was immunohistologically examined in another rat glaucoma model in which N-methyl-D-aspartate (NMDA) was injected into the vitreous cavity. The expression level of neurofilament was reduced in the eyes with retinal ganglion cell damage caused by NMDA injection. In order to study the dephosphorylation of heavy neurofilament subunit and the retinal ganglion cell damage further, the ELISA (enzyme-linked immunosorbent assay) for quantification of phosphorylated and unphosphorylated heavy neurofilament subunit was developed and applied to the rat glaucoma model. The ELISA system could evaluate the retinal ganglion cell damage quantitatively.
|
