Lambuk Lidawani, Jafri Azliana Jusnida Ahmad, Iezhitsa Igor, Agarwal Renu, Bakar Nor Salmah, Agarwal Puneet, Abdullah Aimy, Ismail Nafeeza Mohd
Center for Neuroscience Research (NeuRon), Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh Campus, Sungai Buloh 47000, Selangor Darul Ehsan, Malaysia.
Research Institute of Pharmacology, Volgograd State Medical University, Volgograd 400131, Russian Federation.
Int J Ophthalmol. 2019 May 18;12(5):746-753. doi: 10.18240/ijo.2019.05.08. eCollection 2019.
To investigate dose-dependent effects of N-methyl-D-aspartate (NMDA) on retinal and optic nerve morphology in rats.
Sprague Dawley rats, 180-250 g in weight were divided into four groups. Groups 1, 2, 3 and 4 were intravitreally administered with vehicle and NMDA at the doses 80, 160 and 320 nmol respectively. Seven days after injection, rats were euthanized, and their eyes were taken for optic nerve toluidine blue and retinal hematoxylin and eosin stainings. The TUNEL assay was done for detecting apoptotic cells.
All groups treated with NMDA showed significantly reduced ganglion cell layer (GCL) thickness within inner retina, as compared to control group. Group NMDA 160 nmol showed a significantly greater GCL thickness than the group NMDA 320 nmol. Administration of NMDA also resulted in a dose-dependent decrease in the number of nuclei both per 100 µm GCL length and per 100 µm of GCL. Intravitreal NMDA injection caused dose-dependent damage to the optic nerve. The degeneration of nerve fibres with increased clearing of cytoplasm was observed more prominently as the NMDA dose increased. In accordance with the results of retinal morphometry analysis and optic nerve grading, TUNEL staining demonstrated NMDA-induced excitotoxic retinal injury in a dose-dependent manner.
Our results demonstrate dose-dependent effects of NMDA on retinal and optic nerve morphology in rats that may be attributed to differences in the severity of excitotoxicity and oxidative stress. Our results also suggest that care should be taken while making dose selections experimentally so that the choice might best uphold study objectives.
研究N-甲基-D-天冬氨酸(NMDA)对大鼠视网膜和视神经形态的剂量依赖性影响。
将体重180 - 250克的Sprague Dawley大鼠分为四组。第1、2、3和4组分别经玻璃体腔内注射溶剂和剂量为80、160和320纳摩尔的NMDA。注射后7天,对大鼠实施安乐死,并取出其眼睛用于视神经甲苯胺蓝染色以及视网膜苏木精-伊红染色。采用TUNEL检测法检测凋亡细胞。
与对照组相比,所有接受NMDA治疗的组视网膜内层神经节细胞层(GCL)厚度均显著降低。NMDA 160纳摩尔组的GCL厚度显著大于NMDA 320纳摩尔组。NMDA给药还导致每100微米GCL长度和每100微米GCL内的细胞核数量呈剂量依赖性减少。玻璃体腔内注射NMDA对视神经造成剂量依赖性损伤。随着NMDA剂量增加,观察到神经纤维变性,细胞质清除增加更为明显。根据视网膜形态计量学分析和视神经分级结果,TUNEL染色显示NMDA诱导的兴奋性毒性视网膜损伤呈剂量依赖性。
我们的结果表明,NMDA对大鼠视网膜和视神经形态具有剂量依赖性影响,这可能归因于兴奋性毒性和氧化应激严重程度的差异。我们的结果还表明,在实验中进行剂量选择时应谨慎,以便该选择可能最符合研究目标。