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Oral proton pump inhibitors disrupt horizontal cell-cone feedback and enhance visual hallucinations in macular degeneration patients

机译:口服质子泵抑制剂破坏黄斑变性患者的水平细胞锥体反馈并增强视觉幻觉

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Purpose. Visual hallucinations (VHs) occur in macular degeneration patients with poor vision but normal cognitive function. The underlying mechanisms are poorly understood. We report the identification of pharmaceutical agents that enhance VH and use these agents to examine the contribution of retinal neurons to this syndrome. Methods. We detail clinical observations on VH in five macular degeneration patients treated with proton pump inhibitors having the core structure, 2-pyridyl-methylsulfinyl-benzimidazole. We tested possible retinal mechanisms using paired whole cell recordings to examine effects of these compounds on feedback interactions between horizontal cells and cones in amphibian retina. Results. Five patients with advanced wet macular degeneration described patterned VHs that were induced or enhanced by oral proton pump inhibitors. The abnormal images increased with light, disappeared in the dark, and originated in the retina, based on ophthalmodynamometry. Simultaneous paired whole cell recordings from amphibian cones and horizontal cells showed that 2-pyridyl-methylsulfinyl-benzimidazoles blocked the negative shift in voltage dependence and increase in amplitude of the calcium current (ICa) in cones that is induced by changes in horizontal cell membrane potential. These effects disrupt the negative feedback from horizontal cells to cones that is important for the formation of center-surround receptive fields in bipolar and ganglion cells, and thus for normal spatial and chromatic perception. Conclusions. Our study suggests that changes in the output of retinal neurons caused by disturbances in outer retinal feedback mechanisms can enhance patterned visual hallucinations.
机译:目的。视幻觉(VH)发生在视力较差但认知功能正常的黄斑变性患者中。潜在的机制了解甚少。我们报告鉴定增强VH的药物,并使用这些药物来检查视网膜神经元对该综合征的贡献。方法。我们详细介绍了5名接受具有核心结构的2-吡啶基-甲基亚磺酰基-苯并咪唑质子泵抑制剂治疗的黄斑变性患者VH的临床观察。我们使用成对的全细胞记录来测试可能的视网膜机制,以检查这些化合物对两栖视网膜中水平细胞和视锥细胞之间反馈相互作用的影响。结果。五名患有晚期湿性黄斑变性的患者描述了由口服质子泵抑制剂诱导或增强的模式性VH。根据眼压测功,异常图像随光增加,在黑暗中消失,并起源于视网膜。两栖动物视锥细胞和水平细胞的同时成对全细胞记录显示,2-吡啶基-甲基亚磺酰基-苯并咪唑类药物阻断了视锥细胞中电压依赖性的负向移动,并阻止了视锥细胞中钙离子电流(ICa)幅度的增加,后者是由水平细胞膜电位的变化引起的。这些影响破坏了从水平细胞到视锥细胞的负反馈,这对于在双极和神经节细胞中形成中心-周围的感受野,从而对于正常的空间和色觉至关重要。结论。我们的研究表明,由外部视网膜反馈机制的紊乱引起的视网膜神经元输出变化可以增强图案化的幻觉。

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