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2
Intravitreal homocysteine-thiolactone injection leads to the degeneration of multiple retinal cells, including photoreceptors.玻璃体内注射同型半胱氨酸硫内酯会导致包括光感受器在内的多种视网膜细胞退化。
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Homocysteine-mediated modulation of mitochondrial dynamics in retinal ganglion cells.同型半胱氨酸介导的视网膜神经节细胞中线粒体动力学的调节。
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Anterior ischemic optic neuropathy in a patient with Crohn's disease and aberrant MTHFR and GPIIIa gene variants.伴有异常 MTHFR 和 GPIIIa 基因突变的克罗恩病患者的前部缺血性视神经病变。
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Levels of plasma homocysteine in pseudoexfoliation glaucoma.血浆同型半胱氨酸水平在假性剥脱性青光眼。
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8
Complete deficiency of methylenetetrahydrofolate reductase in mice is associated with impaired retinal function and variable mortality, hematological profiles, and reproductive outcomes.在小鼠中,亚甲基四氢叶酸还原酶完全缺乏与视网膜功能受损以及可变的死亡率、血液学特征和生殖结果有关。
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9
Levels of circulating homocysteine, vitamin B6, vitamin B12, and folate in different types of open-angle glaucoma.不同类型开角型青光眼患者血液中同型半胱氨酸、维生素 B6、维生素 B12 和叶酸水平。
Clin Interv Aging. 2010 Apr 26;5:133-9. doi: 10.2147/cia.s9918.
10
Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2.表达 CLCN2 早期终止突变的小鼠中的光感受器变性、无精子症、脑白质病和异常 RPE 细胞功能。
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胱硫醚-β-合酶突变小鼠,高同型半胱氨酸血症模型,视觉功能随年龄变化。

Age-related changes in visual function in cystathionine-beta-synthase mutant mice, a model of hyperhomocysteinemia.

机构信息

Department of Ophthalmic Research, Cole Eye Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.

出版信息

Exp Eye Res. 2012 Mar;96(1):124-31. doi: 10.1016/j.exer.2011.12.011. Epub 2011 Dec 16.

DOI:10.1016/j.exer.2011.12.011
PMID:22197750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3368555/
Abstract

Homocysteine is an amino acid required for the metabolism of methionine. Excess homocysteine is implicated in cardiovascular and neurological disease and new data suggest a role in various retinopathies. Mice lacking cystathionine-beta-synthase (cbs(-/-)) have an excess of retinal homocysteine and develop anatomical abnormalities in multiple retinal layers, including photoreceptors and ganglion cells; heterozygous (cbs(+/-)) mice demonstrate ganglion cell loss and mitochondrial abnormalities in the optic nerve. The purpose of the present study was to determine whether elevated homocysteine, due to absent or diminished cbs, alters visual function. We examined cbs(-/-) (3 weeks) and cbs(+/-) mice (5, 10, 15, 30 weeks) and results were compared to those obtained from wild type (WT) littermates. Conventional dark- and light-adapted ERGs were recorded, along with dc-ERG to assess retinal pigment epithelial (RPE) function. The visual evoked potential (VEP) was used to assess transmission to the visual cortex. The amplitudes of the major ERG components were reduced in cbs(-/-) mice at age 3 weeks and VEPs were delayed markedly. These findings are consistent with the early retinal disruption observed anatomically in these mice. In comparison, at 3 weeks of age, responses of cbs(+/-) mice did not differ significantly from those of WT mice. Functional abnormalities were not observed in cbs(+/-) mice until 15 weeks of age, at which time amplitude reductions were noted for the ERG a- and b-wave and the light peak component, but not for other components generated by the RPE. VEP implicit times were delayed in cbs(+/-) mice at 15 and 30 weeks, while VEP amplitudes were unaffected. The later onset of functional defects in cbs(+/-) mice is consistent with a slow loss of ganglion cells reported previously in the heterozygous mutant. Light peak abnormalities indicate that RPE function is also compromised in older cbs(+/-) mice. The data suggest that severe elevations of homocysteine are associated with marked alterations of retinal function while modest homocysteine elevation is reflected in milder and delayed alterations of retinal function. The work lays the foundation to explore the role of homocysteine in retinal diseases such as glaucoma and optic neuropathy.

摘要

同型半胱氨酸是甲硫氨酸代谢所需的一种氨基酸。过量的同型半胱氨酸与心血管和神经疾病有关,新数据表明其在各种视网膜病变中也有作用。缺乏胱硫醚-β-合酶(cbs(-/-))的小鼠视网膜同型半胱氨酸含量过高,并在多个视网膜层中出现解剖异常,包括光感受器和节细胞;杂合子(cbs(+/-))小鼠表现出视神经节细胞丢失和线粒体异常。本研究的目的是确定由于 cbs 的缺失或减少而导致的同型半胱氨酸升高是否会改变视觉功能。我们检查了 cbs(-/-)(3 周)和 cbs(+/-)(5、10、15、30 周)小鼠,并将结果与野生型(WT)同窝仔鼠进行比较。记录了常规暗适应和明适应 ERG,以及 dc-ERG 以评估视网膜色素上皮(RPE)功能。视觉诱发电位(VEP)用于评估向视觉皮层的传递。cbs(-/-)小鼠在 3 周龄时,主要 ERG 成分的振幅降低,VEP 明显延迟。这些发现与这些小鼠在解剖学上观察到的早期视网膜破坏一致。相比之下,在 3 周龄时,cbs(+/-)小鼠的反应与 WT 小鼠没有显著差异。直到 15 周龄,cbs(+/-)小鼠才出现功能异常,此时 ERG a-和 b-波和光峰成分的振幅降低,但 RPE 产生的其他成分不受影响。cbs(+/-)小鼠在 15 和 30 周龄时的 VEP 潜伏期延迟,而 VEP 振幅不受影响。cbs(+/-)小鼠功能缺陷的发病较晚与先前报道的杂合突变体中节细胞缓慢丢失一致。光峰异常表明,在老年 cbs(+/-)小鼠中,RPE 功能也受到损害。数据表明,同型半胱氨酸的严重升高与视网膜功能的显著改变有关,而轻度升高的同型半胱氨酸则反映在视网膜功能的轻度和延迟改变中。这项工作为探索同型半胱氨酸在青光眼和视神经病变等视网膜疾病中的作用奠定了基础。