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Akiko Kasai(2010). The Increase of D-Amino Acids in Alzheimerfs Disease?Related Proteins Isolated from the Brains of SAMP8 Mice. J. of SJWS 11: 57-64

The Increase of D-Amino Acids in Alzheimerfs Disease?Related
ProteinsIsolated from the Brains of SAMP8 Mice

Akiko Kasai

1 Faculty of Pharmacy, Research Institute of Pharmaceutical Science, Musashino
University, 1-1-20Shinmachi, Nishitokyo-shi, Tokyo, 202-8585, Japan,
2 Department of Psychiatry, Tokyo WomenfsMedical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan

Abstract: Recently, the presence and function of D-amino acids in mammals, including humans, have been reported. In particular, a relationship between an increase in the D-amino acid content of specific proteins and aging and senescence-related diseases has been proposed. However, this hypothesis remains unproven. Here, we focused on Alzheimerfs disease, a well known senescence-related disease, and used high performance liquid chromatography (HPLC) to analyze the degree of change in the D-amino acid content in the Alzheimerfs disease?related proteins PP1C, GLRX1 and NF-L. Cerebrums of SAM (senescence-accelerated mice), an animal model of Alzheimerfs disease, were used. Increases in D-serine and D-aspartic acid contents with aging in PP1C were found. PP1C is a catalytic subunit of PP1 (serine/threonine phosphatase 1). Tau, one of the most important molecules involved in Alzheimerfs disease, is a target of PP1C. Hyperphosphorylation of Tau is thought to be a trigger of Alzheimerfs disease. Moreover, the involvement of PP1C in cognitive function and memory, independently of dephosphorylation of Tau, has been suggested. The results of this study suggest that substitution of L-amino acids with D-amino acids alters the physical properties of PP1C, and this, in turn, causes its malfunction, which may lead to the onset of Alzheimerfs disease.

Key words: Alzheimerfs disease, D-amino acid, SAMP8, proteinphosphatase 1, aging


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