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1 Division of Food Science, and 2 Division of Health Promotion, National Institute of Health and Nutrition, Tokyo 162 - 8636, Japan; and 3 Nutritional Science Center, Bioscience Laboratories, Meiji Seika Kaisha, Saitama 350-0298, Japan
There is evidence
that estrogen plays an important role in skeletal tissue in males as
well as females. We have reported that phytoestrogens, such as
genistein, selectively act on bone and exhibit cooperative effects on
bone mass when combined with exercise in ovariectomized mice. In this
study, we examined whether both interventions exhibit cooperative
effects on bone loss in androgen-deficient mice similar to those in
estrogen-deficient mice. Male mice aged 7 wk were either sham operated
or orchidectomized (ORX) and divided into six groups: 1)
sham; 2) ORX; 3) ORX and treated with genistein (0.4 mg/day) subcutaneously; 4) ORX, exercised on a
treadmill daily for 30 min/day at 12 m/min; 5) ORX, given
genistein, and exercised (ORX+ExG); and 6) ORX and treated
with 17
-estradiol (E2). Four weeks after the
intervention, seminal vesicle weight strikingly decreased in ORX mice,
and it was not affected by administration of genistein or
E2. Bone mineral density of whole femur was significantly reduced by ORX, and bone loss was prevented by the combined
intervention. Histomorphometric analysis showed that bone volume and
trabecular thickness in the distal femoral cancellous bone were
significantly lower in the ORX group than in the Sham group, and they
were completely restored in the ORX+ExG group, as in the ORX with
E2 group. These results indicate that the combined
intervention of moderate exercise and a low dose of genistein
administration shows an additive effect in preventing bone loss in ORX
mice similar to that in ovariectomized mice.
androgen deficiency; phytoestrogens; genistein; exercise; osteoporosis
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