Differences in trabecular bone of leptin-deficient ob/ob mice in response to biomechanical loading

被引:0
|
作者
Heep, Hansjoerg [1 ]
Wedemeyer, Christian [1 ]
Wegner, Alexander [1 ]
Hofmeister, Sebastian [1 ]
von Knoch, Marius [1 ]
机构
[1] Univ Duisburg Essen, Dept Orthopaed, D-45239 Essen, Germany
来源
关键词
bone mineral density; leptin; biomechanical loading; micro-CT; mice;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective: It is known that bone mineral density (BMD) and the strength of bone is predicted by body mass. Fat mass is a significant predictor of bone mineral density which correlates with body weight. This suggests that body fat regulates bone metabolism first by means of hormonal factors and second that the effects of muscle and loading are signaling factors in mechanotransduction. Leptin, a peptide hormone produced predominantly by white fat cells, is one of these hormonal factors. The aim of this study was to investigate and measure by micro-CT the different effects of weight-bearing on trabecular bone formation in mice without the stimulation of leptin. Results: Animals with an ad-libitum-diet (Group A) were found to increase body weight significantly at the age of six weeks in comparison with lean mice (Group B). From this point on, the difference increased constantly. At the age of twenty weeks the obese mice were almost twice as heavy as the lean mice. Significant statistical differences are shown between the two groups for body weight and bone mineral density. Examination of trabecular bone (BV/TV, trabecular number (Tb.N.), trabecular thickness (Tb.Th.)) revealed that the only statistically significant difference between the two groups was the Tb. N. for the proximal femur. High weight- bearing insignificantly improved all trabecular bone parameters in the obese mice. Compared with the control- diet Group B, the BV/TV and Tb.N. were slightly higher in the controlled- diet Group A, but not the Tb.Th.. However, correlation was found between Tb.N. and BMD on the one hand and body weight on the other hand. Conclusion: biomechanical loading led to decreased bone mineral density by a decrease in the number of trabeculae. Trabecular thickness was not increased by biomechanical loading in growing mice. Decreased body weight in leptin-deficient mice protects against bone loss. This finding is consistent with the principle of light-weight construction of bone. Differences in cortical and trabecular bone will be examined in later studies. It is not possible to conclude that these results also apply to human beings.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 50 条
  • [1] Osteoarthitis of Leptin-Deficient ob/ob Mice in Response to Biomechanical Loading in Micro-CT
    Heep, Hansjoerg
    Hilken, Gero
    Hofmeister, Sebastian
    Wedemeyer, Christian
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2009, 5 (03): : 265 - 275
  • [2] Leptin into the ventrolateral medulla facilitates chemorespiratory response in leptin-deficient (ob/ob) mice
    Bassi, M.
    Furuya, W. I.
    Menani, J. V.
    Colombari, D. S. A.
    do Carmo, J. M.
    da Silva, A. A.
    Hall, J. E.
    Moreira, T. S.
    Wenker, I. C.
    Mulkey, D. K.
    Colombari, E.
    [J]. ACTA PHYSIOLOGICA, 2014, 211 (01) : 240 - 248
  • [3] Osteoarthritis of young leptin-deficient ob/ob mice in response of body weight
    Heep, H.
    Xu, J.
    Hofmeister, S.
    Henschke, F.
    Wedemeyer, Ch
    [J]. OSTEOLOGIE, 2009, 18 (01) : 45 - 50
  • [4] Impaired steroidogenesis in the testis of leptin-deficient mice (ob/ob-/-)
    Martins, Fabiane Ferreira
    Aguila, Marcia Barbosa
    Mandarim-de-Lacerda, Carlos Alberto
    [J]. ACTA HISTOCHEMICA, 2017, 119 (05) : 508 - 515
  • [5] Pulmonary Mycobacterium tuberculosis infection in leptin-deficient ob/ob mice
    Wieland, CW
    Florquin, S
    Chan, ED
    Leemans, JC
    Weijer, S
    Verbon, A
    Fantuzzi, G
    van der Poll, T
    [J]. INTERNATIONAL IMMUNOLOGY, 2005, 17 (11) : 1399 - 1408
  • [6] Leptin treatment induces loss of bone marrow adipocytes and increases bone formation in leptin-deficient ob/ob mice
    Hamrick, MW
    Della-Fera, MA
    Choi, YH
    Pennington, C
    Baile, CA
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (06) : 994 - 1001
  • [7] Effect of leptin treatment on mitochondrial function in obese leptin-deficient ob/ob mice
    Holmstrom, Maria H.
    Tom, Robby Zachariah
    Bjornholm, Marie
    Garcia-Roves, Pablo M.
    Zierath, Juleen R.
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2013, 62 (09): : 1258 - 1267
  • [8] Leptin-deficient ob/ob mice are resistant to thioacetamide-induced fibrogenic response in the liver
    Hondo, H
    Ikejima, K
    Fukuda, T
    Nishiyama, D
    Shimizu, H
    Kitamura, T
    Takei, Y
    Sato, N
    [J]. HEPATOLOGY, 2000, 32 (04) : 188A - 188A
  • [9] Nitrosative stress and peripheral diabetic neuropathy in leptin-deficient (ob/ob) mice
    Vareniuk, Igor
    Pavlov, Ivan A.
    Drel, Viktor R.
    Lyzogubov, Valeriy V.
    Ilnytska, Olga
    Bell, Seth R.
    Tibrewala, Jyoti
    Groves, John T.
    Obrosova, Irina G.
    [J]. EXPERIMENTAL NEUROLOGY, 2007, 205 (02) : 425 - 436
  • [10] Central leptin gene therapy corrects skeletal abnormalities in leptin-deficient ob/ob mice
    Iwaniec, Urszula T.
    Boghossian, Stephane
    Lapke, Paul D.
    Turner, Russell T.
    [J]. PEPTIDES, 2007, 28 (05) : 1012 - 1019