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使用京尼平进行巩膜交联会损害树鼩的视网膜结构和功能。

Scleral crosslinking using genipin can compromise retinal structure and function in tree shrews.

机构信息

Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, AL, USA.

Department of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Exp Eye Res. 2022 Jun;219:109039. doi: 10.1016/j.exer.2022.109039. Epub 2022 Mar 24.

Abstract

Scleral crosslinking using genipin has been identified as a promising treatment approach for myopia control. The efficacy of genipin to alter biomechanical properties of the sclera has been shown in several animal models of myopia but its safety profile remains unclear. In this safety study, we aim to investigate the effect of scleral crosslinking using retrobulbar injections of genipin on retinal structure and function at genipin doses that were shown to be effective in slowing myopia progression in juvenile tree shrews. To this end, three or five retrobulbar injections of genipin at 0 mM (sham), 10 mM, or 20 mM were performed in one eye every other day. Form deprivation myopia was induced in the injected eye. We evaluated retinal function using full-field electroretinography and retinal structure using in vivo optical coherence tomography imaging and ex vivo histology. The optical coherence tomography results revealed significant thinning of the peripapillary retinal nerve fiber layer in all genipin treated groups including the lowest dose group, which showed no significant treatment effect in slowing myopia progression. In contrast, inducing form deprivation myopia alone and in combination with sham injections caused no obvious thinning of the retinal nerve fiber layer. Electroretinography results showed a significant desensitizing shift of the b-wave semi-saturation constant in the sham group and the second highest genipin dose group, and a significant reduction in b-wave maxima in the two highest genipin dose groups. The ex vivo histology revealed noticeable degeneration of photoreceptors and retinal pigment epithelium in one of two investigated eyes of the highest genipin dose group. While scleral crosslinking using genipin may still be a feasible treatment option for myopia control, our results suggest that repeated retrobulbar injections of genipin at 10 mM or higher are not safe in tree shrews. An adequate and sustained delivery strategy of genipin at lower concentrations will be needed to achieve a safe and effective scleral crosslinking treatment for myopia control in tree shrews. Caution should be taken if the proposed treatment approach is translated to humans.

摘要

使用京尼平进行巩膜交联已被确定为一种有前途的近视控制治疗方法。在几种近视动物模型中已显示京尼平改变巩膜生物力学特性的效果,但安全性尚不清楚。在这项安全性研究中,我们旨在研究巩膜交联使用 retrobulbar 注射京尼平对视网膜结构和功能的影响在京尼平剂量,这被证明是有效的减缓近视进展在幼年树鼩。为此,每隔一天在一只眼的每只眼进行三次或五次 retrobulbar 注射京尼平 0 毫米(假),10 毫米或 20 毫米。在注射的眼中诱导剥夺性近视。我们使用全视野视网膜电图评估视网膜功能,并使用活体光学相干断层扫描成像和离体组织学评估视网膜结构。光学相干断层扫描结果显示,所有京尼平处理组包括最低剂量组的视盘周围视网膜神经纤维层均有明显变薄,而最低剂量组在减缓近视进展方面没有明显的治疗效果。相比之下,单独诱导剥夺性近视和结合假注射不会导致视网膜神经纤维层明显变薄。视网膜电图结果显示,假组和第二高京尼平剂量组的 b 波半饱和常数有明显的脱敏移位,两个最高京尼平剂量组的 b 波最大值均有明显降低。离体组织学显示,在两个研究眼的最高京尼平剂量组中的一个眼中,可见光感受器和视网膜色素上皮退化。虽然使用京尼平进行巩膜交联可能仍然是一种可行的近视控制治疗选择,但我们的结果表明,在树鼩中重复 retrobulbar 注射 10 毫米或更高浓度的京尼平并不安全。需要一种适当和持续的京尼平传递策略,以实现安全有效的树鼩巩膜交联治疗近视。如果将提议的治疗方法转化为人类,应谨慎行事。

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