Neural Regeneration Research ›› 2022, Vol. 17 ›› Issue (9): 1881-1884.doi: 10.4103/1673-5374.335138

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Intranasal neprilysin rapidly eliminates amyloid-beta plaques, but causes plaque compensations: the explanation why the amyloid-beta cascade may fail?

Christian Humpel*   

  1. Laboratory of Psychiatry and Experimental Alzheimer’s Research, Medical University of Innsbruck, Innsbruck, Austria
  • Online:2022-09-15 Published:2022-03-03
  • Contact: Christian Humpel, PhD, christian.humpel@i-med.ac.at.

Abstract: Neurodegenerative brain disorders are a major burden in our society, such as Alzheimer´s disease. In order to repair or prevent such diseases, drugs are designed which enter the brain, but the blood-brain barrier limits their entry and the search for alternative pathways is important. Recently, we reported that intranasal delivery of the amyloid-beta degrading enzyme neprilysin eliminated amyloid-beta plaques in transgenic Alzheimer´s disease mice. This review describes the anatomical structure of the intranasal pathway, explains the intranasal delivery of pure neprilysin, cell-loaded neprilysin (platelets) and collagen-embedded neprilysin to destruct amyloid-beta plaques in Alzheimer´s disease in transgenic APP_SweDI mice and hypothesizes why this may cause compensation and why the amyloid-beta cascade hypothesis may fail.

Key words: amyloid-beta, amyloid-beta degrading enzyme, clear plaque, collagen biomaterial, intranasal, neprilysin, nose-to-brain