Cellular Stress Response and Signal Transduction Research Laboratory, Faculty of Medicine, Department of Medical Pharmacology, Gazi University, Beşevler, 06500, Ankara, Turkey.
Institute of Experimental Pharmacology and Toxicology, CEM, Slovak Academy of Sciences, Dubravska cesta 9, 84104, Bratislava, Slovakia.
Neurotox Res. 2021 Apr;39(2):210-226. doi: 10.1007/s12640-020-00305-x. Epub 2020 Nov 4.
Cellular redox dysregulation produced by aldose reductase (AR) in the presence of high blood sugar is a mechanism involved in neurodegeneration commonly observed in diabetes mellitus (DM) and Parkinson's disease (PD); therefore, AR is a key target for treatment of both diseases. The substituted triazinoindole derivatives 2-(3-thioxo-2H-[1,2,4]triazino[5,6-b]indol-5(3H)-yl) acetic acid (cemtirestat or CMTI) and 2-(3-oxo-2H-[1,2,4]triazino[5,6-b]indol-5(3H)-yl) acetic acid (COTI) are well-known AR inhibitors (ARIs). The neuroprotective properties of CMTI, COTI, the clinically used epalrestat (EPA), and the pyridoindole antioxidants stobadine and SMe1EC2 were all tested in the neurotoxic models produced by hyperglycemic glucotoxicity (HG, 75 mM D-glucose, 72 h), 6-hydroxydopamine (6-OHDA), and HG+6-OHDA models in PC12 cells. Cell viability decreased in all toxic models, increased by 1-5 μM EPA, and decreased by COTI at ≥ 2.5 μM. In the HG model alone, where compounds were present in the medium for 24 h after a continuous 24-h exposure to HG, cell viability was improved by 100 nM-5 μM EPA, 1-10 μM ARIs, and the antioxidants studied, but decreased by EPA at ≥ 10 μM. In the 6-OHDA model alone, where cells were treated with compounds for 24 h and further exposed to 100 μM 6-OHDA (8 h), only the antioxidants protected cell viability. In the HG+6-OHDA model, where cells were treated with all compounds (1 nM to 50 μM) for 48 h and exposed to 75 mM glucose for 24 h followed by incubation with 6-OHDA for 8 h, cell viability was protected by 100 nM-10 μM ARIs and 100-500 nM EPA, but not by antioxidants. All ARIs inhibited the HG+6-OHDA-induced increase in iNOS, IL-1β, TNF-α, 3-NT, and total oxidant status at 1-50 μM, while increased SOD, CAT, GPx, and total antioxidant status at 1-10 μM. EPA and CMTI also reduced the HG+6-OHDA-induced increase in the cellular levels of nuclear factor kB (NF-KB). The neuroprotective potential of the novel ARIs and the pyridoindole antioxidants studied constitutes a promising tool for the development of therapeutic strategies against DM-induced and PD-related neurodegeneration.
醛糖还原酶(AR)在高血糖环境下产生的细胞氧化还原失调是糖尿病(DM)和帕金森病(PD)中常见的神经退行性变机制;因此,AR 是治疗这两种疾病的关键靶点。取代的三嗪并吲哚衍生物 2-(3-硫代-2H-[1,2,4]三嗪并[5,6-b]吲哚-5(3H)-基)乙酸(cemtirestat 或 CMTI)和 2-(3-氧代-2H-[1,2,4]三嗪并[5,6-b]吲哚-5(3H)-基)乙酸(COTI)是众所周知的 AR 抑制剂(ARIs)。CMTI、COTI、临床使用的依帕司他(EPA)以及吡啶并吲哚抗氧化剂 Stobadine 和 SMe1EC2 的神经保护特性在高血糖毒性(HG,75 mM D-葡萄糖,72 h)、6-羟多巴胺(6-OHDA)和 HG+6-OHDA 模型中在 PC12 细胞中进行了测试。所有毒性模型中的细胞活力均下降,1-5 μM EPA 可增加细胞活力,而 COTI 则在≥2.5 μM 时降低细胞活力。在仅存在 HG 的模型中,在连续暴露于 HG 24 小时后,化合物在培养基中存在 24 小时,100 nM-5 μM EPA、1-10 μM ARIs 和研究的抗氧化剂可提高细胞活力,但 EPA 在≥10 μM 时降低细胞活力。在仅存在 6-OHDA 的模型中,细胞用化合物处理 24 小时,然后进一步用 100 μM 6-OHDA(8 小时)处理,只有抗氧化剂可保护细胞活力。在 HG+6-OHDA 模型中,细胞用所有化合物(1 nM 至 50 μM)处理 48 小时,并用 75 mM 葡萄糖孵育 24 小时,然后用 6-OHDA 孵育 8 小时,100 nM-10 μM ARIs 和 100-500 nM EPA 可保护细胞活力,但抗氧化剂则不行。所有 ARIs 在 1-50 μM 时抑制 HG+6-OHDA 诱导的 iNOS、IL-1β、TNF-α、3-NT 和总氧化剂状态的增加,而在 1-10 μM 时增加 SOD、CAT、GPx 和总抗氧化状态。EPA 和 CMTI 还降低了 HG+6-OHDA 诱导的核因子 kB(NF-KB)细胞内水平的增加。研究中新型 ARIs 和吡啶并吲哚抗氧化剂的神经保护潜力为开发针对 DM 诱导的和 PD 相关的神经退行性变的治疗策略提供了有希望的工具。