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小鼠动物模型中创伤性视神经病变急性处理中的全身低温治疗

Systemic Hypothermia in the Acute Management of Traumatic Optic Neuropathy in a Murine Animal Model.

作者信息

Tse Brian C, Wang Hua, Dvoriantchikova Galina, Pelaez Daniel, Tse David T

机构信息

Department of Ophthalmology, Dr. Nasser Al-Rashid Orbital Vision Research Center, Bascom Palmer Eye Institute, University of Miami, Miami, Florida, U.S.A.

出版信息

Ophthalmic Plast Reconstr Surg. 2025;41(3):293-298. doi: 10.1097/IOP.0000000000002821. Epub 2024 Dec 10.

DOI:10.1097/IOP.0000000000002821
PMID:39656522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12088910/
Abstract

PURPOSE

To examine the effects of systemic hypothermia on retinal ganglion cell survival and visual outcomes after optic nerve trauma in a sonication-inducted traumatic optic neuropathy murine animal model.

METHODS

Twenty mice underwent sonication-inducted traumatic optic neuropathy. Afterward, 10 mice were placed on a warming pad set to 36°C, and 10 mice were placed on a table. General anesthesia was maintained for 3 hours with subcutaneous injections of ketamine. The rectal temperature was measured every 15 minutes. Pattern electroretinograms were obtained at 2, 4, and 6 weeks. Mice were sacrificed at 6 weeks, and retinal ganglion cell counts were performed.

RESULTS

The hypothermia group had an average rectal temperature of 23.1°C; the control group was 33.3°C. At 6 weeks, the hypothermia group had larger a-wave amplitudes (18.19 µV) than the control group (12.75 µV) ( p < 0.05). At 6 weeks, retinal ganglion cell density over the entire retina was significantly higher in the hypothermia group versus the control ( p < 0.0001).

CONCLUSIONS

The hypothermia treatment group had significantly higher retinal ganglion cell density and pattern electroretinogram a-wave amplitudes 6 weeks after injury than the control group. Systemic hypothermia may have a neuroprotective effect when initiated immediately after sonication-inducted traumatic optic neuropathy.

摘要

目的

在超声诱导的外伤性视神经病变小鼠动物模型中,研究全身低温对视神经损伤后视网膜神经节细胞存活及视觉结果的影响。

方法

20只小鼠接受超声诱导的外伤性视神经病变。之后,10只小鼠置于温度设定为36°C的加热垫上,10只小鼠置于桌上。通过皮下注射氯胺酮维持全身麻醉3小时。每15分钟测量一次直肠温度。在第2、4和6周时进行图形视网膜电图检查。在第6周时处死小鼠并进行视网膜神经节细胞计数。

结果

低温组的平均直肠温度为23.1°C;对照组为33.3°C。在第6周时,低温组的a波振幅(18.19 μV)大于对照组(12.75 μV)(p < 0.05)。在第6周时,低温组整个视网膜的视网膜神经节细胞密度显著高于对照组(p < 0.0001)。

结论

损伤后6周,低温治疗组的视网膜神经节细胞密度和图形视网膜电图a波振幅显著高于对照组。在超声诱导的外伤性视神经病变后立即开始全身低温治疗可能具有神经保护作用。

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本文引用的文献

1
Cold protection allows local cryotherapy in a clinical-relevant model of traumatic optic neuropathy.冷保护允许创伤性视神经病变的临床相关模型中的局部冷冻疗法。
Elife. 2022 Mar 30;11:e75070. doi: 10.7554/eLife.75070.
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Mitochondrial targeted therapy with elamipretide (MTP-131) as an adjunct to tumor necrosis factor inhibition for traumatic optic neuropathy in the acute setting.线粒体靶向治疗联合肿瘤坏死因子抑制剂治疗创伤性视神经病变的急性期。
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肿瘤坏死因子抑制在创伤性视神经病变的急性治疗中的应用。
Invest Ophthalmol Vis Sci. 2018 Jun 1;59(7):2905-2912. doi: 10.1167/iovs.18-24431.
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Traumatic optic neuropathy treatment trial (TONTT): open label, phase 3, multicenter, semi-experimental trial.创伤性视神经病变治疗试验(TONTT):开放标签、3期、多中心、半实验性试验。
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A Novel Mouse Model of Traumatic Optic Neuropathy Using External Ultrasound Energy to Achieve Focal, Indirect Optic Nerve Injury.一种使用外部超声能量实现局灶性间接视神经损伤的创伤性视神经病变新型小鼠模型。
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Hypothermia Prevents Retinal Damage Generated by Optic Nerve Trauma in the Rat.低温可预防大鼠视神经损伤所致的视网膜损伤。
Sci Rep. 2017 Jul 31;7(1):6966. doi: 10.1038/s41598-017-07294-6.
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The Outcome of Endoscopic Transethmosphenoid Optic Canal Decompression for Indirect Traumatic Optic Neuropathy with No-Light-Perception.经鼻内镜视神经管减压术治疗无光感间接性外伤性视神经病变的疗效
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