Pronto-Laborinho Ana Catarina, Pinto Susana, de Carvalho Mamede
Institute of Physiology, Faculty of Medicine, University of Lisbon, Avenida Professor Egas Moniz, 1649-028 Lisbon, Portugal ; Instituto de Medicina Molecular (IMM), Translational Clinical Physiology Unit, Avenida Professor Egas Moniz, 1649-028 Lisbon, Portugal.
Institute of Physiology, Faculty of Medicine, University of Lisbon, Avenida Professor Egas Moniz, 1649-028 Lisbon, Portugal ; Instituto de Medicina Molecular (IMM), Translational Clinical Physiology Unit, Avenida Professor Egas Moniz, 1649-028 Lisbon, Portugal ; Department of Neurosciences, Hospital Santa Maria, Centro Hospitalar Lisboa Norte, Avenida Professor Egas Moniz, 1649-028 Lisbon, Portugal.
Biomed Res Int. 2014;2014:947513. doi: 10.1155/2014/947513. Epub 2014 Apr 29.
Amyotrophic lateral sclerosis (ALS) is a fatal devastating neurodegenerative disorder, involving progressive degeneration of motor neurons in spinal cord, brainstem, and motor cortex. Riluzole is the only drug approved in ALS but it only confers a modest improvement in survival. In spite of a high number of clinical trials no other drug has proved effectiveness. Recent studies support that vascular endothelial growth factor (VEGF), originally described as a key angiogenic factor, also plays a key role in the nervous system, including neurogenesis, neuronal survival, neuronal migration, and axon guidance. VEGF has been used in exploratory clinical studies with promising results in ALS and other neurological disorders. Although VEGF is a very promising compound, translating the basic science breakthroughs into clinical practice is the major challenge ahead. VEGF-B, presenting a single safety profile, protects motor neurons from degeneration in ALS animal models and, therefore, it will be particularly interesting to test its effects in ALS patients. In the present paper the authors make a brief description of the molecular properties of VEGF and its receptors and review its different features and therapeutic potential in the nervous system/neurodegenerative disease, particularly in ALS.
肌萎缩侧索硬化症(ALS)是一种致命的毁灭性神经退行性疾病,涉及脊髓、脑干和运动皮层中运动神经元的进行性退化。利鲁唑是唯一被批准用于治疗ALS的药物,但它只能使生存期适度延长。尽管进行了大量临床试验,但没有其他药物被证明有效。最近的研究表明,血管内皮生长因子(VEGF)最初被描述为一种关键的血管生成因子,在神经系统中也起着关键作用,包括神经发生、神经元存活、神经元迁移和轴突导向。VEGF已用于探索性临床研究,在ALS和其他神经系统疾病中取得了有希望的结果。尽管VEGF是一种非常有前景的化合物,但将基础科学突破转化为临床实践是面临的主要挑战。VEGF-B具有单一的安全性,在ALS动物模型中可保护运动神经元免于退化,因此,测试其对ALS患者的疗效将特别有意义。在本文中,作者简要描述了VEGF及其受体的分子特性,并综述了其在神经系统/神经退行性疾病,特别是在ALS中的不同特征和治疗潜力。