在雪貂模型中,爆炸暴露后视网膜炎症的时间动力学。

IF 1.8 Q3 CLINICAL NEUROLOGY
Neurotrauma reports Pub Date : 2025-04-09 eCollection Date: 2025-01-01 DOI:10.1089/neur.2024.0127
Rex Jeya Rajkumar Samdavid Thanapaul, Chetan Pundkar, Gaurav Phuyal, Manoj Y Govindarajulu, Ashwathi Menon, Joseph B Long, Peethambaran Arun
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引用次数: 0

摘要

爆炸引起的外伤性眼损伤(bTOI)是近期作战行动中军事人员视力丧失的主要原因。然而,其潜在机制仍然知之甚少,阻碍了有效治疗的发展。本研究使用雪貂模型研究了爆炸暴露后视网膜中关键炎症标志物的时间表达模式。雪貂(n = 40)使用先进的爆炸模拟器遭受两次紧密耦合的爆炸(20 psi)。分别于细胞爆炸后4小时、24小时和28天收集视网膜组织。利用实时定量聚合酶链反应评估爆炸暴露后toll样受体(TLRs: 1-9)、细胞因子(IL: 1β、6和10)和环氧化酶(COX: 1和2)mRNA表达的差异,并与假对照组进行比较。我们的研究结果显示,在爆炸暴露后,视网膜中的多个tlr(1、2、4、5、7和8)快速且持续上调,表明存在强烈的炎症反应。与此同时,促炎性和抗炎性细胞因子(IL-1β、IL-6、IL-10和COX2)在细胞爆炸后4小时显著增加,提示它们参与了bTOI的急性发病机制。我们的研究结果强调了早期先天免疫反应和慢性炎症在bTOI中的关键作用,强调了及时治疗干预的重要性。针对这些炎症途径可能为减轻视网膜损伤和改善眼功能提供治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal Dynamics of Retinal Inflammation Following Blast Exposure in a Ferret Model.

Blast-induced traumatic ocular injury (bTOI) is a major cause of vision loss in military personnel involved in recent combat operations. However, its underlying mechanisms remain poorly understood, hindering the development of effective treatments. This study investigated the temporal expression patterns of key inflammatory markers in the retina after blast exposure using a ferret model. Ferrets (n = 40) were subjected to two tightly coupled blasts (20 psi) using an advanced blast simulator. Retinal tissues were collected at 4 h, 24 h, or 28 days post-blast. Differential mRNA expression of Toll-like receptors (TLRs: 1-9), cytokines (IL: 1β, 6, and 10), and cyclooxygenase enzymes (COX: 1 and 2) was assessed using quantitative real-time polymerase chain reaction after blast exposure and compared with sham controls. Our results revealed a rapid and sustained upregulation of multiple TLRs (1, 2, 4, 5, 7, and 8) in the retina following blast exposure, indicating a robust inflammatory response. This was accompanied by a significant increase in pro- and anti-inflammatory cytokines (IL-1β, IL-6 IL-10, and COX2) at 4 h post-blast, suggesting their involvement in the acute pathogenesis of bTOI. Our findings emphasize the critical role of early innate immune responses and the potential for chronic inflammation in bTOI, highlighting the importance of timely therapeutic interventions. Targeting these inflammatory pathways may offer therapeutic avenues for mitigating retinal damage and improving ocular function.

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来源期刊
CiteScore
2.40
自引率
0.00%
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审稿时长
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