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

被引:4
作者
Baek, Kyunghwa [1 ,2 ]
Kang, Jiho [3 ,4 ]
Lee, Jinu [3 ,4 ]
Kim, Min [1 ,2 ]
Baek, Jeong-Hwa [3 ,4 ,5 ,6 ]
机构
[1] Gangneung Wonju Natl Univ, Dept Pharmacol, Coll Dent, Kangnung 210702, Gangwondo, South Korea
[2] Gangneung Wonju Natl Univ, Res Inst Oral Sci, Kangnung 210702, Gangwondo, South Korea
[3] Seoul Natl Univ, Sch Dent, Dept Mol Genet, Seoul 08826, South Korea
[4] Seoul Natl Univ, Dent Res Inst, Seoul 08826, South Korea
[5] Seoul Natl Univ, Sch Dent, Dept Mol Genet, Seoul 110749, South Korea
[6] Seoul Natl Univ, Dent Res Inst, Seoul 110749, South Korea
基金
新加坡国家研究基金会;
关键词
Propranolol; Beta-adrenergic receptor blockade; Obesity; Bone loss; High fat diet; SYMPATHETIC-NERVOUS-SYSTEM; FRACTURE RISK; OSTEOPOROTIC FRACTURES; MINERAL DENSITY; BLOCKERS; WOMEN; LEPTIN; PROPRANOLOL; WEIGHT; RESTRICTION;
D O I
10.1007/s00223-018-0407-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:217 / 226
页数:10
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