In order to examine the effect of
Streptococcus lactis (ATCC 19435) cell preparation on the retarding of senile changes in Wistar and SHR rats, a comparatively large dose, namely 1.2×10
11cells or 120 mg in dry weight, was fed per capitafor life. Striking differences in appearance of Wistar rats at 27 months of age after weaning were observed between the control group which was fedcommercial pelletized feed and the study group which was fed the same plus 1% of
S. lactis preparation; remarkable kephosis and alopecia developed in the former, none in the latter. Other age-related changes significantly suppressed by such extended supplementation of the culture were fibrosis and calcification of cartilage matrix; aortic endothelial damage, segmental thickening, calcification and chondroid cells in intima; hypertension in aging SHR; disarray of hepatic cords and portal fibrosis; atrophy of epidermis and appendages, and increase in amorphous dermal matrix in Wistar; waxy degeneration and atrophy of psoas muscles. These morphological and histological changes in tissues on aging could be reflected in such biochemical changes as an increase in lipoperoxides in the serum, liver, and brain; increase in hydroxyproline content in aorta, mesenteric artery, and liver; reduction in cyclic AMP and GMP in the serum. The
S. lactis preparation also afforded mice protection against the X-ray irradiation (300 rad) as shownin primary antibody response and leukopenia. The present preparation of
S. lactis exhibited superoxide dismutase activity and presence of glutathione, and also was found digestible
in vivo and immediately phagocitized by Paneth's cells. Themechanism for the observed anti-aging effect of
S. lactis was discussed.
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