EFFECT OF DIETARY RESTRICTION ON BONE MINERAL CONTENT OF RHESUS MONKEYS
EFFECT OF DIETARY RESTRICTION ON BONE MINERAL CONTENT OF RHESUS MONKEYS
批准号:
6116415
负责人:
RICKI J COLMAN
金额:
$5.85万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-05-01 至 2000-04-30
中文摘要
点击翻译按钮获取中文摘要
英文摘要
OBJECTIVE To assess the effect of dietary restriction and aging
upon bone metabolism in rhesus monkeys. RESULTS Bone mass was lower
in dietary restricted animals, however this reflects smaller body size
and not pathological osteopenia. In addition, dietary restriction may
protect against the development of spinal osteoarthritis. DISCUSSION
The pathogenesis of age-related bone loss is unclear. As dietary
restriction (DR) retards many aspects of aging, it may also alter
skeletal changes. The purpose of this study was to examine the
effects of moderate DR (30% reduction in caloric intake from
individual baseline values) on bone. Bone mass (dual-energy X-ray
absorptiometry), turnover (osteocalcin, ICTP, and NTx) and lumbar
spine osteoarthritis (OA; radiographs) were examined longitudinally in
male (15 Control [C], 15 Restricted [R]; after 96 months of DR) rhesus
macaques 8-14 years of age at the onset of DR. Total body bone mass
was lower in R compared to C males and females. In the females, R
bone mass was also lower than C at the posterior-anterior spine and
radius (except for distal radius bone mineral content). Serum
turnover markers, and calcium and phosphorus concentration were not
different between C and R groups. In addition, testosterone and FSH
in the males were unchanged. There was less evidence of spi nal OA in
R males. We believe the lower bone mass reflects the smaller body
size, and not pathological osteopenia. In this model, DR does not
cause deleterious endocrine effects and may afford protection against
spinal OA. FUTURE DIRECTIONS We plan to continue using DXA,
radiographs and markers of bone metabolism to better characterize the
skeletal aging process in rhesus monkeys, making them better
understood models for osteoporosis research. KEY WORDS osteoporosis,
bone density, aging, bone metabolism, DXA FUNDING NIH PO1 AG11915
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