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双(7)-他克林对谷氨酸诱导的视网膜神经节细胞损伤的神经保护作用。

Neuroprotective effects of bis(7)-tacrine against glutamate-induced retinal ganglion cells damage.

机构信息

Department of Ophthalmology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

BMC Neurosci. 2010 Mar 3;11:31. doi: 10.1186/1471-2202-11-31.

Abstract

BACKGROUND

Glutamate-mediated excitotoxicity, primarily through N-methyl-D-aspartate (NMDA) receptors, may be an important cause of retinal ganglion cells (RGCs) death in glaucoma and several other retinal diseases. Bis(7)-tacrine is a noncompetitive NMDA receptors antagonist that can prevent glutamate-induced hippocampal neurons damage. We tested the effects of bis(7)-tacrine against glutamate-induced rat RGCs damage in vitro and in vivo.

RESULTS

In cultured neonatal rats RGCs, the MTT assay showed that glutamate induced a concentration- and time-dependent toxicity. Bis(7)-tacrine and memantine prevented glutamate-induced cell death in a concentration-dependent manner with IC50 values of 0.028 microM and 0.834 microM, respectively. The anti-apoptosis effects of bis(7)-tacrine were confirmed by annexin V-FITC/PI staining. In vivo, TUNEL analysis and retrograde labeling analysis found that pretreatment with bis(7)-tacrine(0.2 mg/kg) induced a significant neuroprotective effect against glutamate-induced RGCs damage.

CONCLUSIONS

Our results showed that bis(7)-tacrine had neuroprotective effects against glutamate-induced RGCs damage in vitro and in vivo, possibly through the drug's anti-NMDA receptor effects. These findings make bis(7)-tacrine potentially useful for treating a variety of ischemic or traumatic retinopathies inclusive of glaucoma.

摘要

背景

谷氨酸介导的兴奋性毒性,主要通过 N-甲基-D-天冬氨酸(NMDA)受体,可能是青光眼和其他几种视网膜疾病中视网膜神经节细胞(RGC)死亡的一个重要原因。双(7)-他克林是一种非竞争性 NMDA 受体拮抗剂,可防止谷氨酸诱导的海马神经元损伤。我们测试了双(7)-他克林对体外和体内谷氨酸诱导的大鼠 RGC 损伤的作用。

结果

在培养的新生大鼠 RGC 中,MTT 测定表明谷氨酸诱导的细胞毒性呈浓度和时间依赖性。双(7)-他克林和 memantine 以浓度依赖性方式防止谷氨酸诱导的细胞死亡,IC50 值分别为 0.028 microM 和 0.834 microM。双(7)-他克林的抗凋亡作用通过 Annexin V-FITC/PI 染色得到证实。在体内,TUNEL 分析和逆行标记分析发现,双(7)-他克林(0.2mg/kg)预处理对谷氨酸诱导的 RGC 损伤具有显著的神经保护作用。

结论

我们的结果表明,双(7)-他克林对体外和体内谷氨酸诱导的 RGC 损伤具有神经保护作用,这可能是通过药物的抗 NMDA 受体作用。这些发现使双(7)-他克林有可能用于治疗包括青光眼在内的多种缺血性或创伤性视网膜病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e27/2838896/3ec4ef6cd58f/1471-2202-11-31-1.jpg

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