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β肾上腺素能阻断在减轻高脂饮食诱导的肥胖和骨丢失中的时间点特异性作用。

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

机构信息

Department of Pharmacology, College of Dentistry and Research Institute of Oral Science, Gangneung-Wonju National University, Gangwondo, 210-702, Republic of Korea.

Department of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Calcif Tissue Int. 2018 Aug;103(2):217-226. doi: 10.1007/s00223-018-0407-3. Epub 2018 Feb 19.

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.

摘要

我们旨在阐明决定β受体阻滞剂减弱高脂饮食诱导肥胖和骨丢失效果的关键因素。将 6 周龄 C57BL/6 雄性小鼠分为反映肥胖和β受体阻滞剂给药相对起始时间不同、不同饮食(对照 vs. 高脂)和治疗(载体 vs. 普萘洛尔)的组。第 1 组小鼠给予对照饮食(CON)或高脂饮食(HIGH),并用载体或普萘洛尔处理 12 周。第 2 组小鼠前 12 周给予 CON 或 HIGH 饮食,不进行药物治疗,然后再用载体或普萘洛尔处理 12 周。第 3 组小鼠前 12 周给予 CON 饮食,不进行药物治疗,然后根据饮食分组,再用载体或普萘洛尔处理 12 周。普萘洛尔减弱了第 1 组和第 3 组小鼠中 HIGH 诱导的体重/脂肪量增加,但在第 2 组小鼠中没有。普萘洛尔减轻了第 1 组小鼠中 HIGH 诱导的股骨小梁骨密度降低和骨结构恶化,但在第 2 组小鼠中没有。第 3 组小鼠高脂饮食并未损害骨骼完整性。总之,普萘洛尔减弱了正在进行的体重增加,但一旦肥胖已经确立,就不能减轻体重增加。生长期间的 HIGH 喂养导致骨量/骨结构受损;生长期间给予普萘洛尔可减轻,但肥胖已经确立后给予普萘洛尔则不行。

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