de Almeida Fernanda Martins, Marques Suelen Adriani, Dos Santos Anne Caroline Rodrigues, Prins Caio Andrade, Dos Santos Cardoso Fellipe Soares, Dos Santos Heringer Luiza, Mendonça Henrique Rocha, Martinez Ana Maria Blanco
Laboratório de Neurodegeneração e Reparo, Programa de Pós-Graduação em Medicina: Anatomia Patológica, Departamento de Patologia, Faculdade de Medicina, Hospital Universitário Clementino Fraga Filho, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro; Instituto de Ciências Biomédicas, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Laboratório de Neurodegeneração e Reparo, Programa de Pós-Graduação em Medicina: Anatomia Patológica, Departamento de Patologia, Faculdade de Medicina, Hospital Universitário Clementino Fraga Filho, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro; Instituto de Biologia, Departamento de Neurobiologia, Laboratório de Regeneração Neural e Função, UFF, Rio de Janeiro, Brazil.
Neural Regen Res. 2023 Jan;18(1):23-30. doi: 10.4103/1673-5374.344830.
Injuries to the spinal cord result in permanent disabilities that limit daily life activities. The main reasons for these poor outcomes are the limited regenerative capacity of central neurons and the inhibitory milieu that is established upon traumatic injuries. Despite decades of research, there is still no efficient treatment for spinal cord injury. Many strategies are tested in preclinical studies that focus on ameliorating the functional outcomes after spinal cord injury. Among these, molecular compounds are currently being used for neurological recovery, with promising results. These molecules target the axon collapsed growth cone, the inhibitory microenvironment, the survival of neurons and glial cells, and the re-establishment of lost connections. In this review we focused on molecules that are being used, either in preclinical or clinical studies, to treat spinal cord injuries, such as drugs, growth and neurotrophic factors, enzymes, and purines. The mechanisms of action of these molecules are discussed, considering traumatic spinal cord injury in rodents and humans.
脊髓损伤会导致永久性残疾,限制日常生活活动。这些不良后果的主要原因是中枢神经元的再生能力有限以及创伤性损伤后形成的抑制性环境。尽管经过数十年的研究,脊髓损伤仍然没有有效的治疗方法。许多策略在临床前研究中进行了测试,这些研究侧重于改善脊髓损伤后的功能结果。其中,分子化合物目前正用于神经恢复,取得了令人鼓舞的结果。这些分子靶向轴突塌陷的生长锥、抑制性微环境、神经元和胶质细胞的存活以及重新建立失去的连接。在这篇综述中,我们重点关注了在临床前或临床研究中用于治疗脊髓损伤的分子,如药物、生长和神经营养因子、酶和嘌呤。考虑到啮齿动物和人类的创伤性脊髓损伤,讨论了这些分子的作用机制。