Abstract

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.

Highlights

  • Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disorder characterized by rapidly progressive degeneration of motor neurons in the spinal cord, brainstem, and motor cortex [1,2,3,4], leading to severe weakness and atrophy of voluntary muscles

  • An immunohistochemical study reported that VEGF receptors (VEGFR)-2 immunostaining in neuropil was decreased in the spinal cord of ALS patients when compared to controls [210, 249]

  • The results showed a differentiation of transplanted cells human umbilical cord blood (HUCB) in vascular endothelial cells (ECs) and an increased survival of motor neuron in these mice [271]

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Summary

Introduction

Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disorder characterized by rapidly progressive degeneration of motor neurons in the spinal cord, brainstem, and motor cortex [1,2,3,4], leading to severe weakness and atrophy of voluntary muscles. VEGF is a proangiogenic factor that confers neuroprotection by promoting neuron survival in vivo and in vitro [37,38,39], in particular increasing life expectancy of the ALS mice model [40,41,42,43]. It exerts protective effects on other cells, such as lung epithelia, bone marrow, and bone cells. We highlight the role of VEGF in ALS and its association with a potential therapeutic use

Biology of VEGF
VEGF Receptors Nontyrosine Kinases
VEGF in the Nervous System
Animal Models
VEGF in Human ALS
Therapeutical Potential of VEGF in ALS
Role of VEGF
Use of VEGF in ALS Patients
Concluding Remarks
Findings
Conflict of Interests
Full Text
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