Institute of Biomedical Research of Salamanca, University Hospital of Salamanca, University of Salamanca, CSIC, Salamanca, Spain.
Institute of Functional Biology and Genomics, University of Salamanca, CSIC, Salamanca, Spain.
Neurochem Res. 2021 Jan;46(1):51-63. doi: 10.1007/s11064-020-03016-z. Epub 2020 Mar 18.
A new era for neuroprotective strategies is emerging in ischemia/reperfusion. This has forced to review the studies existing to date based in neuroprotection against oxidative stress, which have undoubtedly contributed to clarify the brain endogenous mechanisms, as well as to identify possible therapeutic targets or biomarkers in stroke and other neurological diseases. The efficacy of exogenous administration of neuroprotective compounds has been shown in different studies so far. However, something must be missing to get these treatments successfully applied in the clinical environment. Here, the mechanisms involved in neuronal protection against physiological level of ROS and the main neuroprotective signaling pathways induced by excitotoxic and ischemic stimuli are reviewed. Also, the endogenous ischemic tolerance in terms of brain self-protection mechanisms against subsequent cerebral ischemia is revisited to highlight how the preconditioning has emerged as a powerful tool to understand these phenomena. A better understanding of endogenous defense against exacerbated ROS and metabolism in nervous cells will therefore aid to design pharmacological antioxidants targeted specifically against oxidative damage induced by ischemic injury, but also might be very valuable for translational medicine.
在缺血/再灌注中,神经保护策略正在迎来一个新时代。这迫使我们对迄今为止基于抗氧化应激的神经保护的研究进行回顾,这些研究无疑有助于阐明大脑内源性机制,并确定中风和其他神经疾病的潜在治疗靶点或生物标志物。迄今为止,已有不同研究表明外源性给予神经保护化合物的疗效。然而,要使这些治疗方法成功应用于临床环境,还必须解决一些问题。在这里,我们回顾了神经元在生理水平的 ROS 下的保护机制,以及兴奋性毒性和缺血性刺激诱导的主要神经保护信号通路。此外,还回顾了缺血性耐受的内在机制,即大脑自身对随后的脑缺血的保护机制,以强调预处理如何成为理解这些现象的有力工具。因此,更好地理解神经细胞中针对过度 ROS 和代谢的内源性防御,将有助于设计针对缺血性损伤引起的氧化损伤的靶向药理学抗氧化剂,这对于转化医学也非常有价值。