Nakamura Makoto
Division of Ophthalmology, Department of Surgery, Kobe University Graduate School of Medicine, Chuo-ku, Kobe, Japan.
Nippon Ganka Gakkai Zasshi. 2012 Mar;116(3):298-344; discussion 345-6.
Glaucomatous optic neuropathy is a primary pathological condition responsible for visual dysfunction due to glaucoma. However, how intraocular pressure and other risk factors lead to glaucomatous optic neuropathy is not fully understood. Given that static or kinetic visual field tests for evaluating visual dysfunction in glaucomatous optic neuropathy are a subjective assessments based on a psychophysical principle, the development of a tool for objective assessment of the visual field is needed. In this study, we attempt to elucidate the pathophysiology of glaucomatous optic neuropathy and to refine a modality for the objective assessment of the visual dysfunction due to it. Aquaporin (AQP) water channels are located primarily in the plasma membrane. These proteins form either a homo- or hetero-tetramer and allow water to cross the plasma membrane bi-directionally. The transmembrane water movement through AQPs is critically involved in the maintenance of normal neuronal activity. Among the 13 isoforms indentified so far, AQP-4 is known to be expressed in the retrobulbar portion of the optic nerve. However, the optic nerve head, the primary pathological site of glaucomatous optic neuropathy, reportedly does not express AQP-4. We found that in control rats, astrocytes throughout the optic nerve express AQP-9. The chronic elevation of intraocular pressure due to cauterization of three episcleral veins substantially reduced both gene expression and immunoreactivity of AQP-9, whereas it did not change the AQP-4 gene or protein expression in the retrobulbar portion of the optic nerve. These findings are implicated in the chronic elevation of intraocular pressure in astrocytes. Similar findings were also observed in the eyes of a monkey with angle-laser-induced ocular hypertension and of a human with primary open-angle glaucoma. AQP-9 was also expressed in the cell bodies of retinal ganglion cells in control rats and its expression was significantly reduced in the eyes of rats with ocular hypertension. Recently, the astrocyte-to-neuron lactate shuttle hypothesis has been proposed. This hypothesis suggests that lactate generated by glucose during glycolysis in astrocytes is used by neurons as an energy substrate. Given that AQP-9 belongs to an aquaglyceroporin subfamily and allows solutes other than water (e.g., lactate) to cross the plasma membrane, chronic ocular hypertension may perturb this physiological passage of lactate. Thus, lactate as the energy substrate may be unable to be transported from astrocytes to retinal ganglion cells at the cell bodies and axons due to the reduction of AQP-9 expression by astrocytes at the optic nerve head and retinal ganglion cells. The multifocal visual evoked potential (mfVEP) is an objective visual field test, which enables the recording of cortical potential corresponding to 60 local retinal areas simultaneously. Evidence is accumulating that the signal-to-noise ratio (SNR) has been enhanced by recording mfVEPs from multiple channels at the same time. However, previous studies evaluated the mfVEPs mostly in Caucasians. It has not yet been proven whether this strategy is applicable to Japanese people who have a skull frame that may be different from that of Caucasians. We calculated the relative position of the calcarine landmark for electrode placement during the mfVEP recording, from brain MRI images of 200 individuals, which were found to be 1 cm lower than those reported in Caucasians with a statistical significance. Then, we recorded mfVEPs from 110 normal controls using three channels and conducted receiver-operating characteristic (ROC) curve analysis of the overlap of SNR distribution at signal and noise windows. We found that a combination of one horizontal channel straddling the inion with either one of the two perpendicular vertical channels yielded the largest area under the ROC curve (AUC). Next, we showed that the SNR-AUC exhibited a similar diagnostic performance to, and a significant correlation with, a total deviation of the Humphrey visual field in 56 eyes with mild to moderate glaucomatous damage, which exhibited a mean deviation of -15 dB or less, and in 62 control eyes. In contrast, a topographical agreement in defining abnormal locations based on probability plots between the Humphrey visual field and mfVEP testing was moderate. The SNR-AUC may be used as a global index, analogous to the mean deviation of the Humphrey visual field, to quantify diffuse functional loss due to glaucomatous optic neuropathy, in contrast to the previously proposed cluster analysis of the mfVEP probability plots, which is a strategy more suitable to diagnosing local sensitivity loss.
青光眼性视神经病变是一种导致青光眼所致视觉功能障碍的原发性病理状况。然而,眼内压及其他风险因素如何导致青光眼性视神经病变尚未完全明确。鉴于用于评估青光眼性视神经病变视觉功能障碍的静态或动态视野检查是基于心理物理学原理的主观评估,因此需要开发一种用于客观评估视野的工具。在本研究中,我们试图阐明青光眼性视神经病变的病理生理学,并完善一种用于客观评估其所致视觉功能障碍的方法。水通道蛋白(AQP)水通道主要位于质膜。这些蛋白质形成同四聚体或异四聚体,使水能够双向穿过质膜。通过水通道蛋白的跨膜水转运对于维持正常神经元活动至关重要。在迄今已鉴定出的13种异构体中,已知水通道蛋白4(AQP-4)在视神经球后部分表达。然而,据报道,青光眼性视神经病变的主要病理部位视神经乳头不表达AQP-4。我们发现,在对照大鼠中,整个视神经的星形胶质细胞表达AQP-9。通过烧灼三条巩膜静脉导致的眼内压慢性升高显著降低了AQP-9的基因表达和免疫反应性,而对视神经球后部分的AQP-4基因或蛋白表达没有影响。这些发现与星形胶质细胞中眼内压的慢性升高有关。在激光诱导房角型青光眼的猴子和原发性开角型青光眼患者的眼中也观察到了类似的结果。在对照大鼠的视网膜神经节细胞胞体中也表达AQP-9,在高眼压大鼠的眼中其表达显著降低。最近,提出了星形胶质细胞-神经元乳酸穿梭假说。该假说表明,星形胶质细胞在糖酵解过程中由葡萄糖产生的乳酸被神经元用作能量底物。鉴于AQP-9属于水甘油通道蛋白亚家族,允许水以外的溶质(如乳酸)穿过质膜,慢性高眼压可能会扰乱这种乳酸的生理转运途径。因此,由于视神经乳头和视网膜神经节细胞处星形胶质细胞AQP-9表达降低,作为能量底物的乳酸可能无法从星形胶质细胞转运至视网膜神经节细胞的胞体和轴突。多焦视觉诱发电位(mfVEP)是一种客观视野检查,能够同时记录对应于60个局部视网膜区域的皮质电位。越来越多的证据表明,通过同时从多个通道记录mfVEP可提高信噪比(SNR)。然而,以往研究大多在白种人中评估mfVEP。尚未证实这种策略是否适用于颅骨结构可能与白种人不同的日本人。我们从200名个体的脑部MRI图像计算了mfVEP记录期间用于电极放置的距状地标相对位置,发现其比白种人报道的低1cm,具有统计学意义。然后,我们使用三个通道从110名正常对照者记录mfVEP,并对信号和噪声窗口处SNR分布的重叠进行受试者操作特征(ROC)曲线分析。我们发现,一条横跨枕外隆凸的水平通道与两条垂直通道之一的组合在ROC曲线下面积(AUC)最大。接下来,我们表明,在56只轻度至中度青光眼性损害(平均偏差为-15dB或更低)的眼睛和62只对照眼中,SNR-AUC与Humphrey视野的总偏差表现出相似的诊断性能且具有显著相关性。相比之下,基于Humphrey视野和mfVEP测试的概率图定义异常位置的地形一致性为中等。SNR-AUC可作为一个全局指标,类似于Humphrey视野的平均偏差,用于量化青光眼性视神经病变所致的弥漫性功能丧失,这与先前提出的mfVEP概率图聚类分析相反,后者是一种更适合诊断局部敏感性丧失的策略。