Fabian Roderic H, Derry Paul J, Rea Harriett Charmaine, Dalmeida William V, Nilewski Lizanne G, Sikkema William K A, Mandava Pitchaiah, Tsai Ah-Lim, Mendoza Kimberly, Berka Vladimir, Tour James M, Kent Thomas A
Department of Neurology, Baylor College of Medicine, Michael E. DeBakey VA Medical Center, Houston, TX, United States.
Department of Neurology and Center for Translational Research on Inflammatory Diseases, Baylor College of Medicine, Michael E. DeBakey VA Medical Center, Houston, TX, United States.
Front Neurol. 2018 Apr 9;9:199. doi: 10.3389/fneur.2018.00199. eCollection 2018.
While oxidative stress can be measured during transient cerebral ischemia, antioxidant therapies for ischemic stroke have been clinically unsuccessful. Many antioxidants are limited in their range and/or capacity for quenching radicals and can generate toxic intermediates overwhelming depleted endogenous protection. We developed a new antioxidant class, 40 nm × 2 nm carbon nanoparticles, hydrophilic carbon clusters, conjugated to poly(ethylene glycol) termed PEG-HCCs. These particles are high-capacity superoxide dismutase mimics, are effective against hydroxyl radical, and restore the balance between nitric oxide and superoxide in the vasculature. Here, we report the effects of PEG-HCCs administered during reperfusion after transient middle cerebral artery occlusion (tMCAO) by suture in the rat under hyperglycemic conditions. Hyperglycemia occurs in one-third of stroke patients and worsens clinical outcome. In animal models, this worsening occurs largely by accelerating elaboration of reactive oxygen species (ROS) during reperfusion.
PEG-HCCs were studied for their protective ability against hydrogen peroxide in b.End3 brain endothelial cell line and E17 primary cortical neuron cultures. , hyperglycemia was induced by streptozotocin injection 2 days before tMCAO. 58 Male Sprague-Dawley rats were analyzed. They were injected IV with PBS or PEG-HCCs (4 mg/kg 2×) at the time of recanalization after either 90- or 120-min occlusion. Rats were survived for up to 3 days, and infarct volume characteristics and neurological functional outcome (modified Bederson Score) were assessed.
PEG-HCCs were protective against hydrogen peroxide in both culture models. improvement was found after PEG-HCCs with 90-min ischemia with reduction in infarct size (42%), hemisphere swelling (46%), hemorrhage score (53%), and improvement in Bederson score (70%) ( = 0.068-0.001). Early high mortality in the 2-h in the PBS control group precluded detailed analysis, but a trend was found in improvement in all factors, e.g., reduction in infarct volume (48%; = 0.034) and a 56% improvement in Bederson score ( = 0.055) with PEG-HCCs.
This nano-antioxidant showed some improvement in several outcome measures in a severe model of tMCAO when administered at a clinically relevant time point. Long-term studies and additional models are required to assess potential for clinical use, especially for patients hyperglycemic at the time of their stroke, as these patients have the worst outcomes.
虽然在短暂性脑缺血期间可以测量氧化应激,但缺血性中风的抗氧化疗法在临床上并未取得成功。许多抗氧化剂在淬灭自由基的范围和/或能力方面存在局限性,并且会产生有毒中间体,从而压倒耗尽的内源性保护机制。我们开发了一种新的抗氧化剂类别,即40纳米×2纳米的碳纳米颗粒,亲水性碳簇,与聚乙二醇共轭,称为聚乙二醇 - 亲水性碳簇(PEG - HCCs)。这些颗粒是高容量的超氧化物歧化酶模拟物,对羟基自由基有效,并能恢复血管系统中一氧化氮和超氧化物之间的平衡。在此,我们报告了在高血糖条件下,通过缝合在大鼠中短暂性大脑中动脉闭塞(tMCAO)后再灌注期间给予PEG - HCCs的效果。三分之一的中风患者会出现高血糖,这会使临床结果恶化。在动物模型中,这种恶化主要是通过在再灌注期间加速活性氧(ROS)的产生而发生的。
研究了PEG - HCCs在b.End3脑内皮细胞系和E17原代皮质神经元培养物中对过氧化氢的保护能力。在tMCAO前2天通过注射链脲佐菌素诱导高血糖。分析了58只雄性Sprague - Dawley大鼠。在闭塞90分钟或120分钟后的再通时,通过静脉注射给予它们PBS或PEG - HCCs(4毫克/千克,2次)。大鼠存活长达3天,并评估梗死体积特征和神经功能结局(改良的贝德森评分)。
在两种培养模型中,PEG - HCCs都对过氧化氢具有保护作用。在90分钟缺血后给予PEG - HCCs后发现有改善,梗死体积减小(42%)、半球肿胀减轻(46%)、出血评分降低(53%)以及贝德森评分改善(70%)(P = 0.068 - 0.001)。PBS对照组在2小时内早期死亡率高,妨碍了详细分析,但发现使用PEG - HCCs时所有因素都有改善趋势,例如梗死体积减小(48%;P = 0.034)和贝德森评分改善56%(P = 0.055)。
这种纳米抗氧化剂在临床相关时间点给药时,在严重的tMCAO模型中的几个结局指标上显示出一定改善。需要进行长期研究和更多模型来评估其临床应用潜力,特别是对于中风时高血糖的患者,因为这些患者的预后最差。