Alcohol alters whole body composition, inhibits bone formation, and increases bone marrow adiposity in rats

被引:85
作者
Maddalozzo, G. F. [1 ]
Turner, R. T. [1 ]
Edwards, C. H. T. [2 ]
Howe, K. S. [1 ]
Widrick, J. J. [1 ]
Rosen, C. J. [3 ,4 ]
Iwaniec, U. T. [1 ]
机构
[1] Oregon State Univ, Dept Nutr & Exercise Sci, Corvallis, OR 97331 USA
[2] Oregon State Univ, Dept Chem Engn, Corvallis, OR 97331 USA
[3] Maine Med Ctr, Res Inst, Scarborough, ME USA
[4] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
Adipocyte; Bone formation; Osteoporosis; Sarcopenia; Skeletal muscle; ACTIVELY GROWING RATS; SKELETAL-MUSCLE; PROTEIN-SYNTHESIS; HUMAN OSTEOBLASTS; MINERAL DENSITY; TRABECULAR BONE; ETHANOL ABUSE; ELDERLY-WOMEN; IN-VIVO; CONSUMPTION;
D O I
10.1007/s00198-009-0836-y
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Chronic alcohol abuse is a risk factor for osteoporosis and sarcopenia, but the long-term effects of alcohol on the immature musculoskeletal system are less clear. The present investigation in growing rats was designed to determine the effects of alcohol consumption on body composition, muscle mass, and bone mass, architecture, and turnover. Few studies have focused on the long-term effects of drinking on bone and muscle during skeletal maturation. Alcohol was included in the diet of 4-week-old male Sprague-Dawley rats (35% caloric intake) for 3 months. The controls were fed an isocaloric alcohol-free liquid diet ad libitum. A second study was performed in which the controls were pair-fed to the alcohol-fed animals. Compared to ad libitum-fed age-matched controls, alcohol-fed rats weighed less and had lower lean mass, fat mass, and percent body fat. In addition, they had lower slow- and fast-twitch muscle mass, lower total body bone mineral content and bone mineral density, and lower cancellous bone volume in the lumbar vertebra and proximal tibia. The effects of alcohol consumption on body composition were reduced when compared to the pair-fed control diet, indicating that caloric restriction was a comorbidity factor. In contrast, the effects of alcohol to decrease bone formation and serum leptin and IGF-I levels and to increase bone marrow adiposity appeared independent of caloric restriction. The skeletal abnormalities in growing alcohol-fed rats were due to a combination of effects specific to alcohol consumption and alcohol-induced caloric restriction.
引用
收藏
页码:1529 / 1538
页数:10
相关论文
共 48 条
[1]
Addolorato G, 2000, AM J GASTROENTEROL, V95, P2323
[2]
PPARγ insufficiency enhances osteogenesis through osteoblast formation from bone marrow progenitors [J].
Akune, T ;
Ohba, S ;
Kamekura, S ;
Yamaguchi, M ;
Chung, UI ;
Kubota, N ;
Terauchi, Y ;
Harada, Y ;
Azuma, Y ;
Nakamura, K ;
Kadowaki, T ;
Kawaguchi, H .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (06) :846-855
[3]
[Anonymous], AM BON HLTH STAT OST
[4]
Baron R., 1983, Bone histomorphometry: Techniques and interpretation, P13
[5]
Leptin reduces ovariectomy-induced bone loss in rats [J].
Burguera, B ;
Hofbauer, LC ;
Thomas, T ;
Gori, F ;
Evans, GL ;
Khosla, S ;
Riggs, BL ;
Turner, RT .
ENDOCRINOLOGY, 2001, 142 (08) :3546-3553
[6]
Caetano-Lopes J, 2007, ACTA REUMATOL PORT, V32, P103
[7]
Alcohol-induced bone loss and deficient bone repair [J].
Chakkalakal, DA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (12) :2077-2090
[8]
Chronic ethanol consumption results in deficient bone repair in rats [J].
Chakkalakal, DA ;
Novak, JR ;
Fritz, ED ;
Mollner, TJ ;
McVicker, DL ;
Lybarger, DL ;
McGuire, MH ;
Donohue, TM .
ALCOHOL AND ALCOHOLISM, 2002, 37 (01) :13-20
[9]
Leptin directly regulates bone cell function in vitro and reduces bone fragility in vivo [J].
Cornish, J ;
Callon, KE ;
Bava, U ;
Lin, C ;
Naot, D ;
Hill, BL ;
Grey, AB ;
Broom, N ;
Myers, DE ;
Nicholson, GC ;
Reid, IR .
JOURNAL OF ENDOCRINOLOGY, 2002, 175 (02) :405-415
[10]
Congenic mice provide in vivo evidence for a genetic locus that modulates serum insulin-like growth factor-I and bone acquisition [J].
Delahunty, K. M. ;
Shultz, K. L. ;
Gronowicz, G. A. ;
Koczon-Jaremko, B. ;
Adamo, M. L. ;
Horton, L. G. ;
Lorenzo, J. ;
Donahue, L. R. ;
Ackert-Bicknell, C. ;
Kream, B. E. ;
Beamer, W. G. ;
Rosen, C. J. .
ENDOCRINOLOGY, 2006, 147 (08) :3915-3923