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Erschienen in: Calcified Tissue International 2/2018

19.02.2018 | Original Research

The Time Point-Specific Effect of Beta-Adrenergic Blockade in Attenuating High Fat Diet-Induced Obesity and Bone Loss

verfasst von: Kyunghwa Baek, Jiho Kang, Jinu Lee, Min Kim, Jeong-Hwa Baek

Erschienen in: Calcified Tissue International | Ausgabe 2/2018

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Abstract

We aimed to clarify the key factor determining the effect of beta blocker attenuating high fat diet- induced obesity and bone loss. Six-week-old C57BL/6 male mice were assigned to groups reflecting different relative onset of obesity and beta blocker administration, different diet (control vs. high fat), and treatment (vehicle vs. beta blocker: propranolol). Mice in Group 1 were fed a control diet (CON) or high fat diet (HIGH) with vehicle or propranolol for 12 weeks. Mice in Group 2 were fed a CON or HIGH without pharmaceutical treatment for the first 12 weeks, followed by another 12 weeks of treatment with vehicle or propranolol. Mice in Group 3 were fed a CON without pharmaceutical treatment for the first 12 weeks, followed by stratification into diet-based subgroups and another 12 weeks of treatment with vehicle or propranolol. Propranolol attenuated the HIGH-induced increase in body weight/fat mass in Group 1 mice and in Group 3 mice, but not in Group 2 mice. Propranolol mitigated HIGH-induced reduction in femoral trabecular bone mineral density and bone architecture deterioration in Group 1 mice but not in Group 2 mice. HIGH feeding in Group 3 did not compromise skeletal integrity. Taken together, propranolol attenuates HIGH-induced body weight increases while weight gain is in progress but not once obesity has already been established. HIGH feeding during the growth period results in compromised bone mass/architecture; which can be attenuated by propranolol administration during the growth period, but not by propranolol administration after obesity has already been established.
Literatur
2.
Zurück zum Zitat Takeda S, Elefteriou F, Levasseur R, Liu X, Zhao L, Parker KL, Armstrong D, Ducy P, Karsenty G (2002) Leptin regulates bone formation via the sympathetic nervous system. Cell 111:305–317CrossRefPubMed Takeda S, Elefteriou F, Levasseur R, Liu X, Zhao L, Parker KL, Armstrong D, Ducy P, Karsenty G (2002) Leptin regulates bone formation via the sympathetic nervous system. Cell 111:305–317CrossRefPubMed
3.
Zurück zum Zitat Elefteriou F, Ahn JD, Takeda S, Starbuck M, Yang X, Liu X, Kondo H, Richards WG, Bannon TW, Noda M, Clement K, Vaisse C, Karsenty G (2005) Leptin regulation of bone resorption by the sympathetic nervous system and CART. Nature 434:514–520CrossRefPubMed Elefteriou F, Ahn JD, Takeda S, Starbuck M, Yang X, Liu X, Kondo H, Richards WG, Bannon TW, Noda M, Clement K, Vaisse C, Karsenty G (2005) Leptin regulation of bone resorption by the sympathetic nervous system and CART. Nature 434:514–520CrossRefPubMed
4.
Zurück zum Zitat Baek K, Bloomfield SA (2009) Beta-adrenergic blockade and leptin replacement effectively mitigate disuse bone loss. J Bone Miner Res 24:792–799CrossRefPubMed Baek K, Bloomfield SA (2009) Beta-adrenergic blockade and leptin replacement effectively mitigate disuse bone loss. J Bone Miner Res 24:792–799CrossRefPubMed
5.
Zurück zum Zitat Bonnet N, Beaupied H, Vico L, Dolleans E, Laroche N, Courteix D, Benhamou CL (2007) Combined effects of exercise and propranolol on bone tissue in ovariectomized rats. J Bone Miner Res 22:578–588CrossRefPubMed Bonnet N, Beaupied H, Vico L, Dolleans E, Laroche N, Courteix D, Benhamou CL (2007) Combined effects of exercise and propranolol on bone tissue in ovariectomized rats. J Bone Miner Res 22:578–588CrossRefPubMed
6.
Zurück zum Zitat Tatsumi S, Ito M, Asaba Y, Tsutsumi K, Ikeda K (2008) Life-long caloric restriction reveals biphasic and dimorphic effects on bone metabolism in rodents. Endocrinology 149:634–641CrossRefPubMed Tatsumi S, Ito M, Asaba Y, Tsutsumi K, Ikeda K (2008) Life-long caloric restriction reveals biphasic and dimorphic effects on bone metabolism in rodents. Endocrinology 149:634–641CrossRefPubMed
7.
Zurück zum Zitat da Silva AA, do Carmo J, Dubinion J, Hall JE (2009) The role of the sympathetic nervous system in obesity-related hypertension. Curr Hypertens Rep 11:206–211CrossRefPubMedPubMedCentral da Silva AA, do Carmo J, Dubinion J, Hall JE (2009) The role of the sympathetic nervous system in obesity-related hypertension. Curr Hypertens Rep 11:206–211CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Baek K, Hwang HR, Park HJ, Kwon A, Qadir AS, Baek JH (2014) Propranolol, a beta-adrenergic antagonist, attenuates the decrease in trabecular bone mass in high calorie diet fed growing mice. BMB Rep 47:506–511CrossRefPubMedPubMedCentral Baek K, Hwang HR, Park HJ, Kwon A, Qadir AS, Baek JH (2014) Propranolol, a beta-adrenergic antagonist, attenuates the decrease in trabecular bone mass in high calorie diet fed growing mice. BMB Rep 47:506–511CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Perez-Castrillon JL, De Luis DA, Duenas-Laita A (2009) Are beta-blockers useful in the prevention of osteoporotic fractures? Eur Rev Med Pharmacol Sci 13:157–162PubMed Perez-Castrillon JL, De Luis DA, Duenas-Laita A (2009) Are beta-blockers useful in the prevention of osteoporotic fractures? Eur Rev Med Pharmacol Sci 13:157–162PubMed
10.
Zurück zum Zitat Bonnet N, Gadois C, McCloskey E, Lemineur G, Lespessailles E, Courteix D, Benhamou CL (2007) Protective effect of beta blockers in postmenopausal women: influence on fractures, bone density, micro and macroarchitecture. Bone 40:1209–1216CrossRefPubMed Bonnet N, Gadois C, McCloskey E, Lemineur G, Lespessailles E, Courteix D, Benhamou CL (2007) Protective effect of beta blockers in postmenopausal women: influence on fractures, bone density, micro and macroarchitecture. Bone 40:1209–1216CrossRefPubMed
11.
Zurück zum Zitat de Vries F, Souverein PC, Cooper C, Leufkens HG, van Staa TP (2007) Use of beta-blockers and the risk of hip/femur fracture in the United Kingdom and The Netherlands. Calcif Tissue Int 80:69–75CrossRefPubMedPubMedCentral de Vries F, Souverein PC, Cooper C, Leufkens HG, van Staa TP (2007) Use of beta-blockers and the risk of hip/femur fracture in the United Kingdom and The Netherlands. Calcif Tissue Int 80:69–75CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Pasco JA, Henry MJ, Sanders KM, Kotowicz MA, Seeman E, Nicholson GC, Geelong Osteoporosis S (2004) Beta-adrenergic blockers reduce the risk of fracture partly by increasing bone mineral density: Geelong Osteoporosis Study. J Bone Miner Res 19:19–24CrossRefPubMed Pasco JA, Henry MJ, Sanders KM, Kotowicz MA, Seeman E, Nicholson GC, Geelong Osteoporosis S (2004) Beta-adrenergic blockers reduce the risk of fracture partly by increasing bone mineral density: Geelong Osteoporosis Study. J Bone Miner Res 19:19–24CrossRefPubMed
13.
Zurück zum Zitat Rejnmark L, Vestergaard P, Mosekilde L (2006) Treatment with beta-blockers, ACE inhibitors, and calcium-channel blockers is associated with a reduced fracture risk: a nationwide case-control study. J Hypertens 24:581–589CrossRefPubMed Rejnmark L, Vestergaard P, Mosekilde L (2006) Treatment with beta-blockers, ACE inhibitors, and calcium-channel blockers is associated with a reduced fracture risk: a nationwide case-control study. J Hypertens 24:581–589CrossRefPubMed
14.
Zurück zum Zitat Schlienger RG, Kraenzlin ME, Jick SS, Meier CR (2004) Use of beta-blockers and risk of fractures. Jama 292:1326–1332CrossRefPubMed Schlienger RG, Kraenzlin ME, Jick SS, Meier CR (2004) Use of beta-blockers and risk of fractures. Jama 292:1326–1332CrossRefPubMed
15.
Zurück zum Zitat Schoo M, Sturkenboom M, Van Leeuwen J, Stricker B, Pols H (2005) Use of beta-blockers is associated with BMD and fracture risk. Bone. Elsevier Science Inc., New York, pp S129–S130 Schoo M, Sturkenboom M, Van Leeuwen J, Stricker B, Pols H (2005) Use of beta-blockers is associated with BMD and fracture risk. Bone. Elsevier Science Inc., New York, pp S129–S130
16.
Zurück zum Zitat Levasseur R, Dargent-Molina P, Sabatier JP, Marcelli C, Breart G (2005) Beta-blocker use, bone mineral density, and fracture risk in older women: results from the Epidemiologie de l’Osteoporose prospective study. J Am Geriatr Soc 53:550–552CrossRefPubMed Levasseur R, Dargent-Molina P, Sabatier JP, Marcelli C, Breart G (2005) Beta-blocker use, bone mineral density, and fracture risk in older women: results from the Epidemiologie de l’Osteoporose prospective study. J Am Geriatr Soc 53:550–552CrossRefPubMed
17.
Zurück zum Zitat Meisinger C, Heier M, Lang O, Doring A (2007) Beta-blocker use and risk of fractures in men and women from the general population: the MONICA/KORA Augsburg cohort study. Osteoporos Int 18:1189–1195CrossRefPubMed Meisinger C, Heier M, Lang O, Doring A (2007) Beta-blocker use and risk of fractures in men and women from the general population: the MONICA/KORA Augsburg cohort study. Osteoporos Int 18:1189–1195CrossRefPubMed
18.
Zurück zum Zitat Reid IR, Gamble GD, Grey AB, Black DM, Ensrud KE, Browner WS, Bauer DC (2005) Beta-blocker use, BMD, and fractures in the study of osteoporotic fractures. J Bone Miner Res 20:613–618CrossRefPubMed Reid IR, Gamble GD, Grey AB, Black DM, Ensrud KE, Browner WS, Bauer DC (2005) Beta-blocker use, BMD, and fractures in the study of osteoporotic fractures. J Bone Miner Res 20:613–618CrossRefPubMed
19.
Zurück zum Zitat Rejnmark L, Vestergaard P, Kassem M, Christoffersen BR, Kolthoff N, Brixen K, Mosekilde L (2004) Fracture risk in perimenopausal women treated with beta-blockers. Calcif Tissue Int 75:365–372CrossRefPubMed Rejnmark L, Vestergaard P, Kassem M, Christoffersen BR, Kolthoff N, Brixen K, Mosekilde L (2004) Fracture risk in perimenopausal women treated with beta-blockers. Calcif Tissue Int 75:365–372CrossRefPubMed
20.
Zurück zum Zitat Boxall BW, Clark AL (2012) Beta-blockers and weight change in patients with chronic heart failure. J Card Fail 18:233–237CrossRefPubMed Boxall BW, Clark AL (2012) Beta-blockers and weight change in patients with chronic heart failure. J Card Fail 18:233–237CrossRefPubMed
21.
Zurück zum Zitat Rossner S, Taylor CL, Byington RP, Furberg CD (1990) Long term propranolol treatment and changes in body weight after myocardial infarction. Bmj 300:902–903CrossRefPubMedPubMedCentral Rossner S, Taylor CL, Byington RP, Furberg CD (1990) Long term propranolol treatment and changes in body weight after myocardial infarction. Bmj 300:902–903CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Pischon T, Sharma AM (2001) Use of beta-blockers in obesity hypertension: potential role of weight gain. Obes Rev 2:275–280CrossRefPubMed Pischon T, Sharma AM (2001) Use of beta-blockers in obesity hypertension: potential role of weight gain. Obes Rev 2:275–280CrossRefPubMed
23.
Zurück zum Zitat Dempster B (2013) National rationing of MRI in Australia has impact on use of CT. Bmj 346:f3929CrossRefPubMed Dempster B (2013) National rationing of MRI in Australia has impact on use of CT. Bmj 346:f3929CrossRefPubMed
24.
Zurück zum Zitat Parfitt AM (1987) Trabecular bone architecture in the pathogenesis and prevention of fracture. Am J Med 82:68–72CrossRefPubMed Parfitt AM (1987) Trabecular bone architecture in the pathogenesis and prevention of fracture. Am J Med 82:68–72CrossRefPubMed
25.
Zurück zum Zitat Baek K, Bloomfield SA (2012) Blocking beta-adrenergic signaling attenuates reductions in circulating leptin, cancellous bone mass, and marrow adiposity seen with dietary energy restriction. J Appl Physiol 113:1792–1801CrossRefPubMed Baek K, Bloomfield SA (2012) Blocking beta-adrenergic signaling attenuates reductions in circulating leptin, cancellous bone mass, and marrow adiposity seen with dietary energy restriction. J Appl Physiol 113:1792–1801CrossRefPubMed
26.
Zurück zum Zitat Veldhuis-Vlug AG, Tanck MW, Limonard EJ, Endert E, Heijboer AC, Lips P, Fliers E, Bisschop PH (2015) The effects of beta-2 adrenergic agonist and antagonist on human bone metabolism: a randomized controlled trial. Bone 71:196–200CrossRefPubMed Veldhuis-Vlug AG, Tanck MW, Limonard EJ, Endert E, Heijboer AC, Lips P, Fliers E, Bisschop PH (2015) The effects of beta-2 adrenergic agonist and antagonist on human bone metabolism: a randomized controlled trial. Bone 71:196–200CrossRefPubMed
27.
28.
Zurück zum Zitat Wellen KE, Hotamisligil GS (2003) Obesity-induced inflammatory changes in adipose tissue. J Clin Investig 112:1785–1788CrossRefPubMed Wellen KE, Hotamisligil GS (2003) Obesity-induced inflammatory changes in adipose tissue. J Clin Investig 112:1785–1788CrossRefPubMed
29.
Zurück zum Zitat Evans AL, Paggiosi MA, Eastell R, Walsh JS (2015) Bone density, microstructure and strength in obese and normal weight men and women in younger and older adulthood. J Bone Miner Res 30:920–928CrossRefPubMed Evans AL, Paggiosi MA, Eastell R, Walsh JS (2015) Bone density, microstructure and strength in obese and normal weight men and women in younger and older adulthood. J Bone Miner Res 30:920–928CrossRefPubMed
30.
Zurück zum Zitat Ionova-Martin SS, Wade JM, Tang S, Shahnazari M, Ager JW 3rd, Lane NE, Yao W, Alliston T, Vaisse C, Ritchie RO (2011) Changes in cortical bone response to high-fat diet from adolescence to adulthood in mice. Osteoporos Int 22:2283–2293CrossRefPubMed Ionova-Martin SS, Wade JM, Tang S, Shahnazari M, Ager JW 3rd, Lane NE, Yao W, Alliston T, Vaisse C, Ritchie RO (2011) Changes in cortical bone response to high-fat diet from adolescence to adulthood in mice. Osteoporos Int 22:2283–2293CrossRefPubMed
Metadaten
Titel
The Time Point-Specific Effect of Beta-Adrenergic Blockade in Attenuating High Fat Diet-Induced Obesity and Bone Loss
verfasst von
Kyunghwa Baek
Jiho Kang
Jinu Lee
Min Kim
Jeong-Hwa Baek
Publikationsdatum
19.02.2018
Verlag
Springer US
Erschienen in
Calcified Tissue International / Ausgabe 2/2018
Print ISSN: 0171-967X
Elektronische ISSN: 1432-0827
DOI
https://doi.org/10.1007/s00223-018-0407-3

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