CALCIUM AND VITAMIN-D ENRICHED DIETS INCREASE AND PRESERVE VERTEBRAL MINERAL-CONTENT IN AGING LABORATORY RATS

被引:63
作者
SCHAPIRA, D
LINN, S
SARID, M
MOKADI, S
KABALA, A
SILBERMANN, M
机构
[1] TECHNION ISRAEL INST TECHNOL, BRUCE RAPPAPORT FAC MED, IL-31096 HAIFA, ISRAEL
[2] RAMBAM MED CTR, B SHINE DEPT RHEUMATOL, HAIFA, ISRAEL
[3] RAMBAM MED CTR, H SCHUSSHEIM RHEUMATOL RES LAB, HAIFA, ISRAEL
[4] RAMBAM MED CTR, EPIDEMIOL UNIT, HAIFA, ISRAEL
[5] TECHNION ISRAEL INST TECHNOL, FAC FOOD ENGN & BIOTECHNOL, HAIFA, ISRAEL
关键词
RAT; VERTEBRAE; OSTEOPENIA; AGING; CALCIUM; VITAMIN-D;
D O I
10.1016/8756-3282(95)00088-U
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To assess the long-term effect of vitamin D of calcium supplementation on the skeletal metabolism of aging laboratory rodents, 1.5-month-old female Wistar rats were fed with diets containing twice the concentration of vitamin D (group 2) and of calcium (group 3) as in the usual rat chow, Follow-up to 24 months of age did not show significant differences between the enriched-diet groups and the controls (group 1) in terms of the vertebral body weight and protein content. Significantly higher bone mineral contents were found in groups 2 and 3 than were found in controls, as revealed by an increased bone mineral density (BMD: +62%, group 2; +48%, group 3) and vertebral calcium content (+73%, group 2; +84%, group 3). The vertebral alkaline phosphatase enzymatic activity was significantly lower in the enriched diet groups than in controls (-47%, group 2; -45%, group 3). The ratio alkaline phosphatase/acid phosphatase activity was markedly reduced in groups 2 and 3 (-57% and -59%, respectively), which might indicate a diminished rate of bone turnover. The trabecular bone volume (BV/TV) decreased in all groups during senescence, being significantly elevated in group 3 as compared to controls. Vitamin D and calcium dietary supplementations increase the axial mineral bone content in laboratory rats and might reduce the bone turnover. Their influence on the trabecular bone volume has yet to be examined.
引用
收藏
页码:575 / 582
页数:8
相关论文
共 75 条
[1]  
AMBRECHT HJ, 1986, BIOCHIM BIOPHYS ACTA, V882, P281
[2]  
BERNHART FW, 1972, J NUTR, V102, P1123
[3]  
BOIVIN G, 1987, BONE MINER, V3, P125
[4]   ULTRASTRUCTURAL DEVELOPMENT OF HYPEROSTEOIDOSIS IN 1,25(OH)2D3-TREATED RATS FED HIGH-LEVELS OF DIETARY CALCIUM [J].
BOYCE, RW ;
WEISBRODE, SE ;
KINDIG, O .
BONE, 1985, 6 (03) :165-172
[5]   EFFECT OF HORMONES AND GROWTH-FACTORS ON ALKALINE-PHOSPHATASE ACTIVITY AND COLLAGEN-SYNTHESIS IN CULTURED RAT CALVARIAE [J].
CANALIS, E .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1983, 32 (01) :14-20
[6]   DECREASE IN SERUM IMMUNOREACTIVE PARATHYROID-HORMONE IN RATS AND IN PARATHYROID-HORMONE SECRETION INVITRO BY 1,25-DIHYDROXYCHOLECALCIFEROL [J].
CHERTOW, BS ;
BAYLINK, DJ ;
WERGEDAL, JE ;
SU, MHH ;
NORMAN, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1975, 56 (03) :668-678
[7]  
CUMMING RG, 1990, CALCIFIED TISSUE INT, V47, P194
[8]  
ERDEN RG, 1992, CALCIFIED TISSUE INT, V50, P228
[9]   CALCITRIOL CORRECTS BONE LOSS INDUCED BY OOPHORECTOMY IN RATS [J].
FAUGERE, MC ;
OKAMOTO, S ;
DELUCA, HF ;
MALLUCHE, HH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 250 (01) :E35-E38
[10]   BIOCHEMICAL MARKERS OF BONE TURNOVER [J].
FRAHER, LJ .
CLINICAL BIOCHEMISTRY, 1993, 26 (06) :431-432