School of Biochemistry and Immunology, Trinity College, Dublin 2, Ireland.
Department of Surgery, Royal College of Surgeons in Ireland (RCSI), York House, York Street, Dublin, Ireland.
J Neural Transm (Vienna). 2020 Feb;127(2):213-230. doi: 10.1007/s00702-019-02133-6. Epub 2020 Jan 1.
6-Hydroxydopamine (6-OHDA), which is a neurotoxin that selectively destroys catecholaminergic nerves in sympathetically innervated tissues, has been used to provide a model of Parkinson's disease in experimental animals. It is rapidly autoxidised to yield potentially toxic products and reactive oxygen species. Its ability to release Fe(II) from protein storage sites also results in the formation of hROS. This account will consider how this family of toxic products may contribute to the observed effects of 6-OHDA.
6-羟多巴胺(6-OHDA)是一种神经毒素,可选择性破坏交感神经支配组织中的儿茶酚胺能神经,已被用于为实验动物提供帕金森病模型。它会迅速自氧化生成潜在毒性产物和活性氧。它从蛋白质储存部位释放 Fe(II)的能力也导致了 hROS 的形成。本报告将考虑这一家族的毒性产物如何导致观察到的 6-OHDA 效应。