Protection of retinal cells from ischemia by a novel gap junction inhibitor

被引:21
作者
Das, Satyabrata [1 ]
Lin, Dingbo [1 ]
Jena, Snehalata [1 ]
Shi, Aibin [2 ]
Battina, Srinivas [2 ]
Hua, Duy H. [2 ]
Allbaugh, Rachel [3 ]
Takemoto, Dolores J. [1 ]
机构
[1] Kansas State Univ, Dept Biochem, Manhattan, KS 66506 USA
[2] Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
[3] Kansas State Univ, Vet Med Teaching Hosp, Manhattan, KS 66506 USA
关键词
ischemia; cobalt chloride (CoCl2); gap junctions; retinal degeneration; hypoxia; caspase-3; HIF1-alpha; PQ1;
D O I
10.1016/j.bbrc.2008.06.069
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu M. 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. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:504 / 508
页数:5
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