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Vol. 283, Issue 1, 328-335, 1997
Research Laboratories, Yoshitomi Pharmaceutical Industries, Ltd.,
Chikujo-gun, Fukuoka 871, Japan
Our study was performed to assess the hypothesis that prolyl
endopeptidase (PEP) would be functionally involved in the
senescence-accelerated amyloid formation and that long-term inhibition
of prolyl endopeptidase would suppress the progression of A
-like
deposition in the hippocampus of the senescence-accelerated mouse
(SAM). Granular structures of A
-LI were observed in the hippocampus
and around cerebral microvessels of the SAM after immunohistochemical
staining with specific anti-A
antibody. Repeated treatment of the
SAM with Y-29794 (1, 10, 20 mg/kg, p.o.), a specific inhibitor of
prolyl endopeptidase, significantly reduced the number and density of A
-positive granular structures in the hippocampus of the SAM, after
digital image analysis with NIH Image software. Furthermore, the
characteristic biphasic distribution of the digitized density of the
granules was significantly modulated after the treatment with Y-29794.
These results suggest that chronic treatment of the SAM with Y-29794, a
nonpeptide inhibitor of prolyl endopeptidase, prevents the progression
of A
-like deposition in the hippocampus of the SAM.
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