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Cited 8 time in webofscience Cited 8 time in scopus
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The ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in miceopen access

Authors
Tse, Dennis Y.Kim, Seong JaeChung, InyoungHe, FengWensel, Theodore G.Wu, Samuel M.
Issue Date
18-Sep-2017
Publisher
IJO PRESS
Keywords
simvastatin; retina; electroretinography; high-performance liquid chromatography; electron microscopy; intravitreal injection
Citation
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, v.10, no.9, pp 1361 - 1369
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY
Volume
10
Number
9
Start Page
1361
End Page
1369
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/13476
DOI
10.18240/ijo.2017.09.05
ISSN
2222-3959
2227-4898
Abstract
AIM: To investigate the retinal toxicity and pharmacokinetics of simvastatin intravitreally injected into mice. METHODS: Forty-eight 6-8-week-old C57BL/6J mice were used in this study. Simvastatin was intravitreally injected into the right eye of each mouse; the left eye was injected with vehicle and was used as a control. Bilateral dark-adapted electroretinography (ERG) was performed 1 and 7d following injection. Histology was examined using a combination of light, fluorescence and electron microscopy. High-performance liquid chromatography (HPLC) was used to determine the decay in the retinal simvastatin concentration. RESULTS: ERG revealed no significant changes in the simvastatin-injected eyes compared to control. Histologic studies showed normal retinal morphology in eyes injected with simvastatin up to a final vitreal concentration of 200 mu mol/L. No significant changes in the number of photoreceptors, bipolar cells or ganglion cells were found. The retinal simvastatin concentration decayed exponentially, with a half-life of 1.92-2.41 h. CONCLUSION: Intravitreal injection of up to 200 mu mol/L simvastatin produced no signs of adverse effects in the mouse retina. Simvastatin reaches the retina shortly after intravitreal injection and has a short half-life.
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