Kunimi Hiromitsu, Miwa Yukihiro, Katada Yusaku, Tsubota Kazuo, Kurihara Toshihide
Department of Ophthalmology, School of Medicine, Keio University, Tokyo, Japan.
Laboratory of Photobiology, School of Medicine, Keio University, Tokyo, Japan.
PeerJ. 2019 Oct 4;7:e7849. doi: 10.7717/peerj.7849. eCollection 2019.
The therapeutic approach for retinal ganglion cell (RGC) degeneration has not been fully established. Recently, it has been reported that hypoxia-inducible factor (HIF) may be involved with retinal neurodegeneration. In this study, we investigated neuroprotective effects of a HIF inhibitor against RGC degeneration induced in a murine model of retinal ischemia-reperfusion (I/R).
Eight-weeks-old male C57/BL6J mice were treated with intraperitoneal injection of a HIF inhibitor topotecan (1.25 mg/kg) for 14 days followed by a retinal I/R procedure. Seven days after the I/R injury, the therapeutic effect was evaluated histologically and electrophysiologically.
The increase of HIF-1α expression and the decrease of retinal thickness and RGC number in I/R were significantly suppressed by administration of topotecan. Impaired visual function in I/R was improved by topotecan evaluated with electroretinogram and visual evoked potentials.
Topotecan administration suppressed HIF-1a expression and improved RGC survival resulting in a functional protection against retinal I/R. These data indicated that the HIF inhibitor topotecan may have therapeutic potentials for RGC degeneration induced with retinal ischemia or high intraocular pressure.
视网膜神经节细胞(RGC)变性的治疗方法尚未完全确立。最近,有报道称缺氧诱导因子(HIF)可能与视网膜神经变性有关。在本研究中,我们研究了一种HIF抑制剂对视网膜缺血再灌注(I/R)小鼠模型中诱导的RGC变性的神经保护作用。
对8周龄雄性C57/BL6J小鼠腹腔注射HIF抑制剂拓扑替康(1.25mg/kg),持续14天,随后进行视网膜I/R手术。I/R损伤7天后,通过组织学和电生理学评估治疗效果。
拓扑替康给药可显著抑制I/R中HIF-1α表达的增加以及视网膜厚度和RGC数量的减少。通过视网膜电图和视觉诱发电位评估,拓扑替康改善了I/R中受损的视觉功能。
拓扑替康给药可抑制HIF-1α表达并改善RGC存活,从而对视网膜I/R产生功能保护。这些数据表明,HIF抑制剂拓扑替康可能对视网膜缺血或高眼压诱导的RGC变性具有治疗潜力。