Glymphatic System and Mitochondrial Dysfunction as Two Crucial Players in Pathophysiology of Neurodegenerative Disorders

Int J Mol Sci. 2023 Jun 20;24(12):10366. doi: 10.3390/ijms241210366.

Abstract

Neurodegenerative diseases are a complex problem affecting millions of people around the world. The pathogenesis is not fully understood, but it is known that both insufficiency of the glymphatic system and mitochondrial disorders affect the development of pathology. It appears that these are not just two independent factors that coexist in the processes of neurodegeneration, but that they often interact and drive each other. Bioenergetics disturbances are potentially associated with the accumulation of protein aggregates and impaired glymphatic clearance. Furthermore, sleep disorders characteristic of neurodegeneration may impair the work of both the glymphatic system and the activity of mitochondria. Melatonin may be one of the elements linking sleep disorders with the function of these systems. Moreover, noteworthy in this context is the process of neuroinflammation inextricably linked to mitochondria and its impact not only on neurons, but also on glia cells involved in glymphatic clearance. This review only presents possible direct and indirect connections between the glymphatic system and mitochondria in the process of neurodegeneration. Clarifying the connection between these two areas in relation to neurodegeneration could lead to the development of new multidirectional therapies, which, due to the complexity of pathogenesis, seems to be worth considering.

Keywords: Alzheimer’s disease; Parkinson’s disease; glymphatic system; mitochondrial dysfunction; neurodegeneration; neuroinflammation; sleep disorders.

Publication types

  • Review

MeSH terms

  • Glymphatic System* / metabolism
  • Humans
  • Mitochondria / metabolism
  • Mitochondrial Diseases* / metabolism
  • Neurodegenerative Diseases* / metabolism
  • Sleep Wake Disorders* / metabolism

Grants and funding

This research received no external funding.