Effect of Deconditioning on Cortical and Cancellous Bone Growth in the Exercise Trained Young Rats

Exercise enhances bone growth and increases peak bone mass. The aim of this study was to determine whether or not 4 weeks of deconditioning after 8 weeks of exercise in growing rats would result in a decrease in bone gain or reverse the benefits of exercise. Fifty 4-week-old female Sprague-Dawley rats were randomized by a stratified weight method into 5 groups with 10 rats in each group: 8 weeks exercise (8EX), 8 weeks sedentary control (8S), 12 weeks exercise (12EX), 8 weeks exercise followed by 4 weeks sedentary (8EX4S), and 12 weeks sedentary control (12S). The exercise consisted of running on a treadmill with a 5° slope at 24 m/minute for 1 h/day and 5 days/week. After each period of exercise, cancellous and cortical bone histomorphometry were performed on double fluorescent labeled 5-μm-thick sections of the proximal tibia and 40-μm-thick sections of the tibial shaft, respectively. Eight and 12 weeks of exercise resulted in a significant increase in the body weight and gastrocnemius muscle weight by two-way analysis of variance (ANOVA). The femoral wet weight (mg; mean ± SD; 8EX, 781 ± 45.1 vs. 8S, 713 ± 40.5; p < 0.05; 12EX, 892 ± 41.6 vs. 12S, 807 ± 19.8; p < 0.05) was significantly higher in the exercise group than that in the respective control groups. The femoral wet weight and bone volume (BV) of the 8EX4S group (818 ± 46.2 mg and 531 ± 31.2 μl, respectively) were significantly lower than those of the 12EX group (p < 0.05) and did not differ significantly from those of the 12S groups. The cancellous BV was significantly higher in the 8EX and 12EX groups than that in the respective sedentary groups (p < 0.05). The cortical bone area of the tibial shaft was also significantly higher in the 12EX than that in the 12S group (p < 0.05). The increase in the cancellous BV or cortical bone area was caused by an increase in the mineral apposition rate (MAR), without a significant effect in the labeled perimeter. The bone formation rate (BFR; μm3/μm2 per day) in the cancellous bone (12EX, 27.9 ± 7.74 vs. 12S, 15.4 ± 4.56; p < 0.05) or periosteal surface (12EX, 127.6 ± 27.7 vs. 12S, 79.5 ± 18.6; p < 0.05) was significantly higher in the exercised groups than that in the respective control group (p < 0.05). Again, deconditioning resulted in a decrease in the cancellous BFR, BV, periosteal BFR, and cortical bone area to levels not significantly different from the 12S group. In conclusion, our findings showed that exercised growing rats, when deconditioned, lost the benefits gained through exercise and their bone parameters were reduced to levels not different from the sedentary control. Thus, continued exercise is required to maintain high bone mass.

[1]  J. Aloia,et al.  Expression of Concern Regarding “Effect of Deconditioning on Cortical and Cancellous Bone Growth in the Exercise Trained Young Rats” , 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[2]  J. Hopper,et al.  Self-reported ballet classes undertaken at age 10–12 years and hip bone mineral density in later life , 1998, Osteoporosis International.

[3]  C. L. Benhamou,et al.  Effect of physical training on bone mineral density in prepubertal girls: A comparative study between impact-loading and non-impact-loading sports , 2007, Osteoporosis International.

[4]  T. Ogihara,et al.  Alterations of bone mineral density of the femurs in hemiplegia , 1995, Calcified Tissue International.

[5]  A. Heinonen,et al.  Effects of unilateral strength training and detraining on bone mineral density and content in young women: A study of mechanical loading and deloading on human bones , 1994, Calcified Tissue International.

[6]  P. Kannus,et al.  Long-term unilateral loading and bone mineral density and content in female squash players , 1994, Calcified Tissue International.

[7]  L. Vico,et al.  Bone tissue response to four-month antiorthostatic bedrest: A bone histomorphometric study , 1992, Calcified Tissue International.

[8]  J. Aloia,et al.  Differential effect of treadmill exercise on three cancellous bone sites in the young growing rat. , 1999, Bone.

[9]  J. Iwamoto,et al.  Effects of Exercise on Bone Mineral Density in Mature Osteopenic Rats , 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[10]  G Pearce,et al.  Exercise Before Puberty May Confer Residual Benefits in Bone Density in Adulthood: Studies in Active Prepubertal and Retired Female Gymnasts , 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[11]  K. Oizumi,et al.  Accelerated bone remodeling in patients with poststroke hemiplegia. , 1998, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

[12]  H. Kawahara,et al.  Inhibition of Bone Resorption by Pamidronate Cannot Restore Normal Gain in Cortical Bone Mass and Strength in Tail‐Suspended Rapidly Growing Rats , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[13]  D. Hartmann,et al.  Effects of 1- and 6-month spaceflight on bone mass and biochemistry in two humans. , 1997, Bone.

[14]  J. Anderson,et al.  Peak bone mass development of females: can young adult women improve their peak bone mass? , 1996, Journal of the American College of Nutrition.

[15]  Y. Ma,et al.  Time responses of cancellous and cortical bones to sciatic neurectomy in growing female rats. , 1996, Bone.

[16]  C. Weaver,et al.  Previous physical activity relates to bone mineral measures in young women. , 1996, Medicine and science in sports and exercise.

[17]  S. Palle,et al.  Effects of physical training on bone adaptation in three zones of the rat tibia , 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[18]  Ari Heinonen,et al.  Effect of Starting Age of Physical Activity on Bone Mass in the Dominant Arm of Tennis and Squash Players , 1995, Annals of Internal Medicine.

[19]  P. Egger,et al.  Childhood growth, physical activity, and peak bone mass in women , 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[20]  H. Frost,et al.  Perspectives: A vital biomechanical model of the endochondral ossification mechanism , 1994, The Anatomical record.

[21]  H. Frost,et al.  Perspectives: Applications of a biomechanical model of the endochondral ossification mechanism , 1994, The Anatomical record.

[22]  S L Hui,et al.  Influences on skeletal mineralization in children and adolescents: evidence for varying effects of sexual maturation and physical activity. , 1994, The Journal of pediatrics.

[23]  H C Kemper,et al.  Weight‐bearing activity during youth is a more important factor for peak bone mass than calcium intake , 1994, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[24]  J. Aloia,et al.  Effect of treadmill exercise on tibial cortical bone in aged female rats: a histomorphometry and dual energy x-ray absorptiometry study. , 1994, Bone.

[25]  E. Alhava,et al.  Development of bone mass and bone density of the spine and femoral neck--a prospective study of 65 children and adolescents. , 1993, Bone and mineral.

[26]  N. Willows,et al.  Mechanical loading regime and its relationship to bone mineral density in children. , 1993, Medicine and science in sports and exercise.

[27]  J. Aloia,et al.  Influence of exercise on cancellous bone of the aged female rat , 1993 .

[28]  J. Anderson,et al.  Contributions of dietary calcium and physical activity to primary prevention of osteoporosis in females. , 1993, Journal of the American College of Nutrition.

[29]  J. Aloia,et al.  Effects of exercise and immobilization on bone formation and resorption in young rats. , 1993, The American journal of physiology.

[30]  W. Jee,et al.  Adaptation of cancellous bone to aging and immobilization in growing rats , 1992, The Anatomical record.

[31]  H. Frost,et al.  On the rat model of human osteopenias and osteoporoses. , 1992, Bone and mineral.

[32]  V. Matkovic Calcium and peak bone mass , 1992, Journal of internal medicine.

[33]  S L Hui,et al.  Role of physical activity in the development of skeletal mass in children , 1991, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[34]  V. Matkovic,et al.  Factors that influence peak bone mass formation: a study of calcium balance and the inheritance of bone mass in adolescent females. , 1990, The American journal of clinical nutrition.

[35]  A. Leblanc,et al.  Bone mineral loss and recovery after 17 weeks of bed rest , 1990, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[36]  J. Aloia,et al.  Deconditioning increases bone resorption and decreases bone formation in the rat. , 1990, Metabolism: clinical and experimental.

[37]  H. Frost Skeletal structural adaptations to mechanical usage (SATMU): 2. Redefining Wolff's Law: The remodeling problem , 1990, The Anatomical record.

[38]  D B Burr,et al.  Errors in bone remodeling: toward a unified theory of metabolic bone disease. , 1989, The American journal of anatomy.

[39]  A. Ehsani,et al.  Weight-bearing exercise training and lumbar bone mineral content in postmenopausal women. , 1988, Annals of internal medicine.

[40]  M. Drezner,et al.  Bone histomorphometry: Standardization of nomenclature, symbols, and units: Report of the asbmr histomorphometry nomenclature committee , 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[41]  H. Frost Bone “mass” and the “mechanostat”: A proposal , 1987, The Anatomical record.

[42]  H. Evans,et al.  Changes in total body calcium balance with exercise in the rat. , 1983, Journal of applied physiology: respiratory, environmental and exercise physiology.

[43]  J M Vogel,et al.  Effect of prolonged bed rest on bone mineral. , 1970, Metabolism: clinical and experimental.