Medical Hypotheses
Volume 65, Issue 3 , Pages 498-500, 2005

Etiology of sporadic Alzheimer’s disease: Somatostatin, neprilysin, and amyloid β peptide

  • E. Hama
  • ,
  • T.C. Saido

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +81 48 467 9715; fax: +81 48 467 9716

Laboratory for Proteolytic Neuroscience, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan

Received 15 February 2005; accepted 19 February 2005. published online 26 May 2005.

Summary 

We recently demonstrated that amyloid β peptide (Aβ) is catabolized primarily by a neutral endopeptidase, neprilysin, in the brain and that a neuropeptide, somatostatin (SST), regulates brain Aβ level via modulation of neprilysin activity. Because SST expression in the brain declines upon aging in various mammals including rodents, apes and humans, we hypothesize that the aging-dependent reduction of SST triggers accumulation of Aβ in the brain by suppressing neprilysin action. This hypothesis accounts for the fact that aging is the predominant risk factor for Sporadic Alzheimer’s disease.

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PII: S0306-9877(05)00177-5

doi:10.1016/j.mehy.2005.02.045

Medical Hypotheses
Volume 65, Issue 3 , Pages 498-500, 2005