Cannabinoid 2 receptor is a novel anti-inflammatory target in experimental proliferative vitreoretinopathy

被引:28
作者
Szczesniak, Anna-Maria [1 ]
Porter, Richard F. [1 ]
Toguri, James T. [1 ]
Borowska-Fielding, Joanna [1 ]
Gebremeskel, Simon [3 ,4 ]
Siwakoti, Anuja [2 ,3 ,4 ]
Johnston, Brent [3 ,4 ]
Lehmann, Christian [1 ,2 ,3 ,4 ,5 ,6 ]
Kelly, Melanie E. M. [1 ,2 ,7 ,8 ]
机构
[1] Dalhousie Univ, Dept Pharmacol, 5850 Coll St, Halifax, NS B3H 4R2, Canada
[2] Dalhousie Univ, Dept Anesthesia, Halifax, NS, Canada
[3] Dalhousie Univ, Dept Microbiol, Halifax, NS, Canada
[4] Dalhousie Univ, Dept Immunol, Halifax, NS, Canada
[5] Dalhousie Univ, Dept Physiol, Halifax, NS, Canada
[6] Dalhousie Univ, Dept Biophys, Halifax, NS, Canada
[7] Dalhousie Univ, Dept Ophthalmol, Halifax, NS, Canada
[8] Dalhousie Univ, Dept Vis Sci, Halifax, NS, Canada
基金
加拿大健康研究院;
关键词
Proliferative vitreoretinopathy; Endocannabinoid system; Cannabinoid; 2; receptor; Inflammation; Anti-inflammatory agents; CB2; RECEPTOR; RETINAL-DETACHMENT; ENDOCANNABINOID SYSTEM; MICROGLIAL CELLS; POTENTIAL ROLE; EXPRESSION; ACTIVATION; PROTECTS; INFLAMMATION; MODULATION;
D O I
10.1016/j.neuropharm.2016.08.030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Proliferative vitreoretinopathy (PVR) can develop after ocular trauma or inflammation and is a common complication of surgery to correct retinal detachment. Currently, there are no pharmacological treatments for PVR. Cannabinoids acting at cannabinoid 2 receptor (CB2R) can decrease inflammation and fibrosis. The objective of this study was to examine the anti-inflammatory actions of CB2R as a candidate novel therapeutic target in experimental PVR. PVR was induced by intravitreal injection of dispase in wild-type (WT) and CB2R genetic knockout (CB2R(-/-)) mice. Ocular pathology was studied at 24 h or one week after dispase injection. CB2R modulation was examined in WT mice, using the CB2R agonist, HU308, and the CB2R antagonist, AM630. Histopathological scoring and quantification of microglia was used to evaluate tissue pathology. Quantitative PCR and multiplex assays were used to assess changes in proinflammatory cytokines. Intravital microscopy (IVM) was used to visualize and quantify leukocyte endothelial adhesion to the iridial microcirculation. Activation of CB2R with HU308 in WT mice with PVR decreased mean histopathological scores, the number of microglia, and leukocyte adhesion compared to vehicle-treated animals. Conversely, an increase in histopathological scores and activated microglia was observed in PVR animals after treatment with AM630. CB2R(-/-) mice with PVR exhibited exacerbated ocular histopathology, increased microglia numbers, and elevated protein levels of cytokines as compared to WT mice. In conclusion, our results indicate that intervention at early stage PVR with CB2R agonists reduces ocular inflammation and disease severity. CB2R may represent a therapeutic target to prevent PVR progression and vision loss. This article is part of the Special Issue entitled `Lipid Sensing G Protein-Coupled Receptors in the CNS'. Crown Copyright (C) 2016 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:627 / 638
页数:12
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