MODULATING ROLE OF DIETARY-FAT, ENERGY RESTRICTION, AND THE EFFECT OFAGE ON THE EXPRESSION OF PROLIFERATING CELL NUCLEAR ANTIGEN AND PROTEIN-KINASE-C ACTIVITY IN PROSTATE-GLANDS OF RATS
Kq. Yao et al., MODULATING ROLE OF DIETARY-FAT, ENERGY RESTRICTION, AND THE EFFECT OFAGE ON THE EXPRESSION OF PROLIFERATING CELL NUCLEAR ANTIGEN AND PROTEIN-KINASE-C ACTIVITY IN PROSTATE-GLANDS OF RATS, Journal of nutritional biochemistry, 9(4), 1998, pp. 236-241
The present study investigated the role of dietary fat and energy rest
riction (ER) on the proliferative status and the protein kinase c (PKC
) activity in the prostate glands in young (3-week-old, n = 40) and ad
ult rats (10-week-old, n = 40). F344 male rats, young and adult, were
allocated to four dietary groups (n = 10/group): high fat (23% wt/wt)
or low fat (5% w/w) ad libitum (HFAL or LFAL) and high- or low-fat ene
rgy restriction (HFER or LFER). Energy-restricted rats were fed 80% of
the energy intake of the ad libitum fed rats. After 12 weeks of feedi
ng, the proliferating cell nuclear antigen (PCNA) labeling index in pr
ostate glands was higher in young rats than in adult rats. Both the HF
AL and LFAL groups had higher PCNA labeling index than both the HFER a
nd LFER groups in each age group. In addition, the HFAL group had high
er PCNA labeling index than the LFAL group. Dietary fat and ER markedl
y affected the PKC activity which decreased in the order HFAL > HFER =
LFAL > LFER for both young and adult animals. The effect of high-fat
diet and ER were more evident in the younger animals than in the adult
animals. Among the young animals, the absolute total PKC activity was
higher (P less than or equal to 0.05) in the high-fat groups than in
the low-fat groups and a higher proportion of the total PKC was associ
ated with the membrane fraction. In both young and adult rats, ER decr
eased the total PKC activity and the ratio of PKC activity in the cyto
sol to the membrane fractions compared with the ad lib counterparts. W
e conclude that age, a high-fat diet, and energy restriction modulate
PCNA expression and the PKC activity of prostatic tissue. (C) Elsevier
Science Inc. 1998.