Pathological mechanisms of amyotrophic lateral Sclerosis

Neural Regen Res. 2024 May;19(5):1036-1044. doi: 10.4103/1673-5374.382985.

Abstract

Amyotrophic lateral sclerosis refers to a neurodegenerative disease involving the motor system, the cause of which remains unexplained despite several years of research. Thus, the journey to understanding or treating amyotrophic lateral sclerosis is still a long one. According to current research, amyotrophic lateral sclerosis is likely not due to a single factor but rather to a combination of mechanisms mediated by complex interactions between molecular and genetic pathways. The progression of the disease involves multiple cellular processes and the interaction between different complex mechanisms makes it difficult to identify the causative factors of amyotrophic lateral sclerosis. Here, we review the most common amyotrophic lateral sclerosis-associated pathogenic genes and the pathways involved in amyotrophic lateral sclerosis, as well as summarize currently proposed potential mechanisms responsible for amyotrophic lateral sclerosis disease and their evidence for involvement in amyotrophic lateral sclerosis. In addition, we discuss current emerging strategies for the treatment of amyotrophic lateral sclerosis. Studying the emergence of these new therapies may help to further our understanding of the pathogenic mechanisms of the disease.

Keywords: amyotrophic lateral sclerosis; cellular pathways; disease mechanisms; motor neuron; neurodegenerative disease.

Grants and funding

Funding: This work was in part supported by the National Natural Science Foundation of China, Nos. 30560042, 81160161, 81360198, and 82160255; Education Department of Jiangxi Province, Nos. GJJ13198 and GJJ170021; Jiangxi Provincial Department of Science and Technology, No. 20192BAB205043; and Health and Family Planning Commission of Jiangxi Province, Nos. 20181019 and 202210002 (all to RX).