Bone mineral density and content are differentially impacted by aerobic and resistance training in the colon-26 mouse model of cancer cachexia

Springer Science and Business Media LLC - Tập 37 - Trang 1-10 - 2017
Andy V. Khamoui1,2, Ming-Chia Yeh1, Do-Houn Kim1, Bong-Sup Park1, Marcus L. Elam1,3, Edward Jo1,4, Bahram H. Arjmandi1,5, Jeong-Su Kim1,5
1Department of Nutrition, Food and Exercise Sciences, Florida State University, Tallahassee, USA
2Department of Exercise Science and Health Promotion, Florida Atlantic University, Boca Raton, USA
3Department of Human Nutrition and Food Science, California State Polytechnic University, Pomona, Pomona, USA
4Department of Kinesiology and Health Promotion, California State Polytechnic University, Pomona, USA
5Center for Advancing Exercise and Nutrition Research on Aging, Florida State University, Tallahassee, USA

Tóm tắt

Cancer cachexia is a debilitating paraneoplastic syndrome featuring unintended weight loss and skeletal muscle atrophy. Evidence suggests that bone health may also be compromised, further limiting mobility and quality of life. Aerobic and resistance training was recently reported to differentially affect skeletal muscle adaptations in cancer cachectic mice. The purpose of this investigation was to assess the effects of aerobic and resistance training on bone mineral density (BMD) and bone mineral content (BMC) in mice with colon-26 (C26) tumor-induced cachexia. Twelve-month old Balb/c mice were aerobic-trained (wheel running 5 days/week) or resistance-trained (weighted ladder climbing 3days/week) for 8 weeks prior to C26 cell injection, followed by an additional three weeks of exercise. BMD and BMC were assessed pre- and post-training by dual-energy x-ray absorptiometry. Resistance-trained C26 mice lost total BMD by 7% (p = 0.06), which did not occur in aerobic-trained C26 mice. In terms of pelvic bone, both resistance- and aerobic-trained C26 mice had significantly lower BMD values (−12%, p = 0.01 and −6%, p = 0.04, respectively), albeit to a lesser degree in aerobic-trained C26 mice. Furthermore, resistance-trained C26 mice tended to lose total BMC (−12%), whereas aerobic-trained C26 mice maintained total BMC. In mice without C26 tumors, resistance training significantly increased total BMD (+13%, p = 0.001). Aerobic and resistance training may differentially affect bone status in C26 cancer cachexia, with high resistance loading possibly being detrimental to total and pelvis BMD, a region expected to bear significant loading stress and contribute substantially to overall mobility. Because resistance training improved BMD in tumor-free mice, the C26 tumor burden appeared to impair the beneficial effect of resistance training on bone mass.

Tài liệu tham khảo

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