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Protection of retinal cells from ischemia by a novel gap junction inhibitor
Authors:Das Satyabrata  Lin Dingbo  Jena Snehalata  Shi Aibin  Battina Srinivas  Hua Duy H  Allbaugh Rachel  Takemoto Dolores J
Institution:aDepartment of Biochemistry, Kansas State University, 141 Chalmers Hall, Manhattan, KS 66506, USA;bDepartment of Chemistry, Kansas State University, Manhattan, KS 66506, USA;cVet Med Teaching Hospital, Kansas State University, Manhattan, KS 66506, USA
Abstract:Retinal cells which become ischemic will pass apoptotic signal to adjacent cells, resulting in the spread of damage. This occurs through open gap junctions. A class of novel drugs, based on primaquine (PQ), was tested for binding to connexin 43 using simulated docking studies. A novel drug has been synthesized and tested for inhibition of gap junction activity using R28 neuro-retinal cells in culture. Four drugs were initially compared to mefloquine, a known gap junction inhibitor. The drug with optimal inhibitory activity, PQ1, was tested for inhibition and was found to inhibit dye transfer by 70% at 10 μM. Retinal ischemia was produced in R28 cells using cobalt chloride as a chemical agent. This resulted in activation of caspase-3 which was prevented by PQ1, the gap junction inhibitor. Results demonstrate that novel gap junction inhibitors may provide a means to prevent retinal damage during ischemia.
Keywords:Ischemia  Cobalt Chloride (CoCl2)  Gap junctions  Retinal degeneration  Hypoxia  Caspase-3  HIF1α    PQ1
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