User menu

Effects of tail suspension on serum testosterone and molecular targets regulating muscle mass

Bibliographic reference De Naeyer, Hélène ; Lamon, Séverine ; Russell, Aaron P ; Everaert, Inge ; De Spaey, Annelies ; et. al. Effects of tail suspension on serum testosterone and molecular targets regulating muscle mass. In: Muscle & Nerve, Vol. 52, no.2, p. 278-288 (2015)
Permanent URL http://hdl.handle.net/2078.1/175833
  1. Morey-Holton Emily R., Globus Ruth K., Hindlimb unloading rodent model: technical aspects, 10.1152/japplphysiol.00969.2001
  2. CLARK BRIAN C., In Vivo Alterations in Skeletal Muscle Form and Function after Disuse Atrophy : , 10.1249/mss.0b013e3181a645a6
  3. Kamiya Hiroyuki, Sasaki Shoichi, Ikeuchi Takahito, Umemoto Yukihiro, Tatsura Hiroyuki, Hayashi Yutaro, Kaneko Shigeo, Kohri Kenjiro, Effect of Simulated Microgravity on Testosterone and Sperm Motility in Mice, 10.1002/j.1939-4640.2003.tb03140.x
  4. Wimalawansa Sunishka M., Wimalawansa Sunil J., Simulated weightlessness-induced attenuation of testosterone production may be responsible for bone loss, 10.1007/bf02738624
  5. Royland Joyce E., Weber L.J., Fitzpatrick M., Testes size and testosterone levels in a model for weightlessness, 10.1016/0024-3205(94)90005-1
  6. Tash Joseph S., Johnson Donald C., Enders George C., Long-term (6-wk) hindlimb suspension inhibits spermatogenesis in adult male rats, 10.1152/japplphysiol.00931.2001
  7. Hadley, J Appl Physiol, 72, 748 (1992)
  8. DEMURA R., SUZUKI T., NAKAMURA S., KOMATU H., ODAGIRI E., DEMURA H., Effect of Immobilization Stress on Testosterone and Inhibin in Male Rats, 10.1002/j.1939-4640.1989.tb00089.x
  9. Bhasin, J Clin Endocrinol Metab, 82, 407 (1997)
  10. Wimalawansa, J Appl Physiol, 86, 1841 (1999)
  11. Tsika, J Appl Physiol, 63, 2128 (1987)
  12. Joumaa W. H., Bouhlel A., Bigard X., Leoty C., Nandrolone decanoate pre-treatment attenuates unweighting-induced functional changes in rat soleus muscle, 10.1046/j.1365-201x.2002.01035.x
  13. Hoffman Eric P, Nader Gustavo A, Balancing muscle hypertrophy and atrophy, 10.1038/nm0604-584
  14. Bodine Sue C., Stitt Trevor N., Gonzalez Michael, Kline William O., Stover Gretchen L., Bauerlein Roy, Zlotchenko Elizabeth, Scrimgeour Angus, Lawrence John C., Glass David J., Yancopoulos George D., 10.1038/ncb1101-1014
  15. Yin Hui-Nan, Chai Jia-Ke, Yu Yong-Ming, Shen Chuan-An, Wu Yan-Qiu, Yao Yong-Ming, Liu Hui, Liang Li-Ming, Tompkins Ronald G., Sheng Zhi-Yong, Regulation of Signaling Pathways Downstream of IGF-I/Insulin by Androgen in Skeletal Muscle of Glucocorticoid-Treated Rats : , 10.1097/ta.0b013e31817e7420
  16. Haren M. T., Siddiqui A. M., Armbrecht H. J., Kevorkian R. T., Kim M. J., Haas M. J., Mazza A., Kumar Vijaya B., Green M., Banks W. A., Morley J. E., Testosterone modulates gene expression pathways regulating nutrient accumulation, glucose metabolism and protein turnover in mouse skeletal muscle : Testosterone and muscle gene expression, 10.1111/j.1365-2605.2010.01061.x
  17. White James P., Gao Song, Puppa Melissa J., Sato Shuichi, Welle Stephen L., Carson James A., Testosterone regulation of Akt/mTORC1/FoxO3a signaling in skeletal muscle, 10.1016/j.mce.2012.10.019
  18. Sandri Marco, Sandri Claudia, Gilbert Alex, Skurk Carsten, Calabria Elisa, Picard Anne, Walsh Kenneth, Schiaffino Stefano, Lecker Stewart H, Goldberg Alfred L, Foxo Transcription Factors Induce the Atrophy-Related Ubiquitin Ligase Atrogin-1 and Cause Skeletal Muscle Atrophy, 10.1016/s0092-8674(04)00400-3
  19. Stitt Trevor N., Drujan Doreen, Clarke Brian A., Panaro Frank, Timofeyva Yekatarina, Kline William O., Gonzalez Michael, Yancopoulos George D., Glass David J., The IGF-1/PI3K/Akt Pathway Prevents Expression of Muscle Atrophy-Induced Ubiquitin Ligases by Inhibiting FOXO Transcription Factors, 10.1016/s1097-2765(04)00211-4
  20. Bodine S. C., Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy, 10.1126/science.1065874
  21. Gomes M. D., Lecker S. H., Jagoe R. T., Navon A., Goldberg A. L., Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy, 10.1073/pnas.251541198
  22. Ibebunjo C., Eash J. K., Li C., Ma Q., Glass D. J., Voluntary running, skeletal muscle gene expression, and signaling inversely regulated by orchidectomy and testosterone replacement, 10.1152/ajpendo.00402.2010
  23. Pires-Oliveira M., Maragno A. L. G. C., Parreiras-e-Silva L. T., Chiavegatti T., Gomes M. D., Godinho R. O., Testosterone represses ubiquitin ligases atrogin-1 and Murf-1 expression in an androgen-sensitive rat skeletal muscle in vivo, 10.1152/japplphysiol.00490.2009
  24. Trendelenburg A. U., Meyer A., Rohner D., Boyle J., Hatakeyama S., Glass D. J., Myostatin reduces Akt/TORC1/p70S6K signaling, inhibiting myoblast differentiation and myotube size, 10.1152/ajpcell.00105.2009
  25. Carlson, Am J Physiol, 277, R601 (1999)
  26. Wehling, FASEB J, 14, 103 (2000)
  27. Jones, FASEB J, 18, 1025 (2004)
  28. Chen Yi-Wen, Gregory Chris M., Scarborough Mark T., Shi Rongye, Walter Glenn A., Vandenborne Krista, Transcriptional pathways associated with skeletal muscle disuse atrophy in humans, 10.1152/physiolgenomics.00115.2006
  29. Diel P., Friedel A., Geyer H., Kamber M., Laudenbach-Leschowsky U., Schänzer W., Schleipen B., Thevis M., Vollmer G., Zierau O., The prohormone 19-norandrostenedione displays selective androgen receptor modulator (SARM) like properties after subcutaneous administration, 10.1016/j.toxlet.2008.01.014
  30. Mendler Luca, Baka Zsuzsanna, Kovács-Simon Andrea, Dux László, Androgens negatively regulate myostatin expression in an androgen-dependent skeletal muscle, 10.1016/j.bbrc.2007.07.023
  31. Brugarolas J., Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex, 10.1101/gad.1256804
  32. Kelleher A. R., Kimball S. R., Dennis M. D., Schilder R. J., Jefferson L. S., The mTORC1 signaling repressors REDD1/2 are rapidly induced and activation of p70S6K1 by leucine is defective in skeletal muscle of an immobilized rat hindlimb, 10.1152/ajpendo.00409.2012
  33. Wu Yong, Zhao Weidong, Zhao Jingbo, Zhang Yuanfei, Qin Weiping, Pan Jiangping, Bauman William A., Blitzer Robert D., Cardozo Christopher, REDD1 Is a Major Target of Testosterone Action in Preventing Dexamethasone-Induced Muscle Loss, 10.1210/en.2009-0530
  34. Jänne, Endocrinology, 140, 4166 (1999)
  35. Taieb J., Testosterone Measured by 10 Immunoassays and by Isotope-Dilution Gas Chromatography-Mass Spectrometry in Sera from 116 Men, Women, and Children, 10.1373/49.8.1381
  36. McNamara K.M., Harwood D.T., Simanainen U., Walters K.A., Jimenez M., Handelsman D.J., Measurement of sex steroids in murine blood and reproductive tissues by liquid chromatography–tandem mass spectrometry, 10.1016/j.jsbmb.2010.02.001
  37. Glass David, Roubenoff Ronenn, Recent advances in the biology and therapy of muscle wasting : Glass & Roubenoff, 10.1111/j.1749-6632.2010.05809.x
  38. Okamoto Takeshi, Torii Suguru, Machida Shuichi, Differential gene expression of muscle-specific ubiquitin ligase MAFbx/Atrogin-1 and MuRF1 in response to immobilization-induced atrophy of slow-twitch and fast-twitch muscles, 10.1007/s12576-011-0175-6
  39. Axell A.-M., Continuous testosterone administration prevents skeletal muscle atrophy and enhances resistance to fatigue in orchidectomized male mice, 10.1152/ajpendo.00058.2006
  40. Vanderschueren, Endocrinology, 141, 1642 (2000)
  41. Fiers Tom, Casetta Bruno, Bernaert Brigitte, Vandersypt Eric, Debock Martine, Kaufman Jean-Marc, Development of a highly sensitive method for the quantification of estrone and estradiol in serum by liquid chromatography tandem mass spectrometry without derivatization, 10.1016/j.jchromb.2012.02.034
  42. Vandesompele Jo, De Preter Katleen, Pattyn Filip, Poppe Bruce, Van Roy Nadine, De Paepe Anne, Speleman Frank, 10.1186/gb-2002-3-7-research0034
  43. Wallace Marita A., Hock M. Benjamin, Hazen Bethany C., Kralli Anastasia, Snow Rod J., Russell Aaron P., Striated muscle activator of Rho signalling (STARS) is a PGC-1α/oestrogen-related receptor-α target gene and is upregulated in human skeletal muscle after endurance exercise : STARS is upregulated by endurance exercise, 10.1113/jphysiol.2011.205468
  44. Wheeler G, Cumming D, Burnham R, Maclean I, Sloley B D, Bhambhani Y, Steadward R D, Testosterone, cortisol and catecholamine responses to exercise stress and autonomic dysreflexia in elite quadriplegic athletes, 10.1038/sc.1994.51
  45. Lennartsson Anna-Karin, Kushnir Mark M., Bergquist Jonas, Billig Håkan, Jonsdottir Ingibjörg H., Sex steroid levels temporarily increase in response to acute psychosocial stress in healthy men and women, 10.1016/j.ijpsycho.2012.03.001
  46. SAPOLSKY ROBERT M., Stress-Induced Suppression of Testicular Function in the Wild Baboon: Role of Glucocorticoids*, 10.1210/endo-116-6-2273
  47. Gardetto, J Appl Physiol, 66, 2739 (1989)
  48. Miokovic T., Armbrecht G., Felsenberg D., Belavy D. L., Heterogeneous atrophy occurs within individual lower limb muscles during 60 days of bed rest, 10.1152/japplphysiol.00611.2012
  49. Svensson J., Moverare-Skrtic S., Windahl S., Swanson C., Sjogren K., Stimulation of both estrogen and androgen receptors maintains skeletal muscle mass in gonadectomized male mice but mainly via different pathways, 10.1677/jme-09-0165
  50. Inoue Kazuo, Yamasaki Sho, Fushiki Tohru, Okada Yoshimune, Sugimoto Etsuro, Androgen receptor antagonist suppresses exercise-induced hypertrophy of skeletal muscle, 10.1007/bf00867933
  51. Ahtiainen Juha P., Hulmi Juha J., Kraemer William J., Lehti Maarit, Nyman Kai, Selänne Harri, Alen Markku, Pakarinen Arto, Komulainen Jyrki, Kovanen Vuokko, Mero Antti A., Häkkinen Keijo, Heavy resistance exercise training and skeletal muscle androgen receptor expression in younger and older men, 10.1016/j.steroids.2010.10.012
  52. Awede Bonaventure, Thissen Jean-Paul, Gailly Phillipe, Lebacq Jean, Regulation of IGF-I, IGFBP-4 and IGFBP-5 gene expression by loading in mouse skeletal muscle, 10.1016/s0014-5793(99)01469-6
  53. Hanson Andrea M., Harrison Brooke C., Young Mary H., Stodieck Louis S., Ferguson Virginia L., Longitudinal characterization of functional, morphologic, and biochemical adaptations in mouse skeletal muscle with hindlimb suspension : Characterization of Hindlimb Suspension, 10.1002/mus.23753
  54. Sugiura T., Changes in PKB/Akt and calcineurin signaling during recovery in atrophied soleus muscle induced by unloading, 10.1152/ajpregu.00688.2004
  55. Childs T. E., Spangenburg E. E., Vyas D. R., Booth F. W., Temporal alterations in protein signaling cascades during recovery from muscle atrophy, 10.1152/ajpcell.00478.2002
  56. LAWLER JOHN M., KWAK HYO-BUM, KIM JONG-HEE, LEE YANG, HORD JEFFREY M., MARTINEZ DANIEL A., Biphasic Stress Response in the Soleus during Reloading after Hind Limb Unloading : , 10.1249/mss.0b013e31823ab37a
  57. Dupont E., Cieniewski-Bernard C., Bastide B., Stevens L., Electrostimulation during hindlimb unloading modulates PI3K-AKT downstream targets without preventing soleus atrophy and restores slow phenotype through ERK, 10.1152/ajpregu.00793.2009
  58. Gustafsson T., Osterlund T., Flanagan J. N., von Walden F., Trappe T. A., Linnehan R. M., Tesch P. A., Effects of 3 days unloading on molecular regulators of muscle size in humans, 10.1152/japplphysiol.00110.2009
  59. Reich K. A., Chen Y.-W., Thompson P. D., Hoffman E. P., Clarkson P. M., Forty-eight hours of unloading and 24 h of reloading lead to changes in global gene expression patterns related to ubiquitination and oxidative stress in humans, 10.1152/japplphysiol.00444.2010
  60. Krawiec B. J., Hindlimb casting decreases muscle mass in part by proteasome-dependent proteolysis but independent of protein synthesis, 10.1152/ajpendo.00126.2005
  61. Dong Feng, Hua Yinan, Zhao Peng, Ren Jun, Du Min, Sreejayan Nair, Chromium supplement inhibits skeletal muscle atrophy in hindlimb-suspended mice, 10.1016/j.jnutbio.2008.09.006
  62. Maki Taiki, Yamamoto Daisuke, Nakanishi Shiho, Iida Keiji, Iguchi Genzo, Takahashi Yutaka, Kaji Hidesuke, Chihara Kazuo, Okimura Yasuhiko, Branched-chain amino acids reduce hindlimb suspension-induced muscle atrophy and protein levels of atrogin-1 and MuRF1 in rats, 10.1016/j.nutres.2012.07.005
  63. Labeit Siegfried, Kohl Christine H., Witt Christian C., Labeit Dittmar, Jung Jeong, Granzier Henk, Modulation of Muscle Atrophy, Fatigue and MLC Phosphorylation by MuRF1 as Indicated by Hindlimb Suspension Studies on MuRF1-KO Mice, 10.1155/2010/693741
  64. Drummond Micah J., Glynn Erin L., Lujan Heidi L., Dicarlo Stephen E., Rasmussen Blake B., Gene and protein expression associated with protein synthesis and breakdown in paraplegic skeletal muscle, 10.1002/mus.20976
  65. Salanova M., Schiffl G., Püttmann B., Schoser B. G., Blottner D., Molecular biomarkers monitoring human skeletal muscle fibres and microvasculature following long-term bed rest with and without countermeasures, 10.1111/j.1469-7580.2008.00854.x
  66. Chen Guoan, Gharib Tarek G., Huang Chiang-Ching, Taylor Jeremy M. G., Misek David E., Kardia Sharon L. R., Giordano Thomas J., Iannettoni Mark D., Orringer Mark B., Hanash Samir M., Beer David G., Discordant Protein and mRNA Expression in Lung Adenocarcinomas, 10.1074/mcp.m200008-mcp200
  67. Lichtinghagen Ralf, Musholt Petra B, Lein Michael, Römer Andreas, Rudolph Birgit, Kristiansen Glen, Hauptmann Steffen, Schnorr Dietmar, Loening Stefan A, Jung Klaus, Different mRNA and Protein Expression of Matrix Metalloproteinases 2 and 9 and Tissue Inhibitor of Metalloproteinases 1 in Benign and Malignant Prostate Tissue, 10.1016/s0302-2838(02)00324-x
  68. Lee S.-J., McPherron A. C., Regulation of myostatin activity and muscle growth, 10.1073/pnas.151270098
  69. Chen S. N., Czernuszewicz G., Tan Y., Lombardi R., Jin J., Willerson J. T., Marian A. J., Human Molecular Genetic and Functional Studies Identify TRIM63, Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy, 10.1161/circresaha.112.270207