The response of bone to unloading

被引:189
作者
Bikle, DD [1 ]
Halloran, BP [1 ]
机构
[1] Univ Calif San Francisco, Vet Affairs Med Ctr, Endocrine Unit 111N, San Francisco, CA 94121 USA
关键词
bone; spaceflight; bed rest; IGF-I; mechanical load;
D O I
10.1007/s007740050090
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Skeletal unloading leads to decreased bone formation and decreased bone mass. Bone resorption is uncoupled from bone formation, contributing to the bone loss. During spaceflight bone is lost principally from the bones most loaded in the 1-g environment, and some redistribution of bone from the lower extremities to the head appears to take place. Although changes in calcitropic hormones have been demonstrated during skeletal unloading (PTH and 1,25(OH)2D decrease), it remains unclear whether such changes account for or are in response to the changes in bone formation and resorption. Bed rest studies with human volunteers and hindlimb elevation studies with rats have provided useful data to help explain the changes in bone formation during spaceflight. These models of skeletal unloading reproduce a number of the conditions associated with microgravity, and the findings from such studies confirm many of the observations made during spaceflight. Determining the mechanism(s) by which loading of bone is sensed and translated into a signal(s) controlling bone formation remains the holy grail in this field. Such investigations couple biophysics to biochemistry to cell and molecular biology. Although studies with cell cultures have revealed biochemical responses to mechanical loads comparable to that seen in intact bone, it seems likely that matrix-cell interactions underlie much of the mechanocoupling. The role for systemic hormones such as PTH, GH, and 1,25(OH)2D compared to locally produced factors such as IGF-I, PTHrP, BMPs, and TGF-β in modulating the cellular response to load remains unclear. As the mechanism(s) by which bone responds to mechanical load with increased bone formation are further elucidated, applications of this knowledge to other etiologies of osteoporosis are likely to develop. Skeletal unloading provides a perturbation in bone mineral homeostasis that can be used to understand the mechanisms by which bone mineral homeostasis is maintained, with the expectation that such understanding will lead to effective treatment for disuse osteoporosis.
引用
收藏
页码:233 / 244
页数:12
相关论文
共 132 条
[111]  
TURNER RT, 1995, AVIAT SPACE ENVIR MD, V66, P770
[112]   EFFECTS OF SPACEFLIGHT ON RAT HUMERUS GEOMETRY, BIOMECHANICS, AND BIOCHEMISTRY [J].
VAILAS, AC ;
ZERNICKE, RF ;
GRINDELAND, RE ;
KAPLANSKY, A ;
DURNOVA, GN ;
LI, KC ;
MARTINEZ, DA .
FASEB JOURNAL, 1990, 4 (01) :47-54
[113]  
VANLOON JJWA, 1995, J BONE MINER RES, V10, P550
[114]  
VICO L, 1987, BONE MINER, V2, P383
[115]   TRABECULAR BONE REMODELING AFTER 7 DAYS OF WEIGHTLESSNESS EXPOSURE (BIOCOSMOS-1667) [J].
VICO, L ;
CHAPPARD, D ;
PALLE, S ;
BAKULIN, AV ;
NOVIKOV, VE ;
ALEXANDRE, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02) :R243-R247
[116]   MICROGRAVITY AND BONE ADAPTATION AT THE TISSUE-LEVEL [J].
VICO, L ;
ALEXANDRE, C .
JOURNAL OF BONE AND MINERAL RESEARCH, 1992, 7 :S445-S447
[117]   HISTOMORPHOMETRIC ANALYSES OF CANCELLOUS BONE FROM COSMOS-2044 RATS [J].
VICO, L ;
BOURRIN, S ;
GENTY, C ;
PALLE, S ;
ALEXANDRE, C .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 75 (05) :2203-2208
[118]  
VICO L, 1991, AVIAT SPACE ENVIR MD, V62, P26
[119]  
VOGEL JM, 1977, NASA SP, V377, P183
[120]   PARATHYROID-HORMONE RESTORES BONE MASS AND ENHANCES OSTEOBLAST INSULIN-LIKE GROWTH-FACTOR-I GENE-EXPRESSION IN OVARIECTOMIZED RATS [J].
WATSON, P ;
LAZOWSKI, D ;
HAN, V ;
FRAHER, L ;
STEER, B ;
HODSMAN, A .
BONE, 1995, 16 (03) :357-365