Caloric restriction reduces trabecular bone loss during aging and improves bone marrow adipocyte endocrine function in male mice

被引:0
作者
Rinne, Charlotte [1 ]
Soultoukis, George A. [1 ,2 ]
Oveisi, Masoome [1 ,2 ]
Leer, Marina [1 ,2 ]
Schmidt-Bleek, Oskar [3 ]
Burkhardt, Lisa-Marie [3 ,4 ,5 ,6 ]
Bucher, Christian H. [3 ]
Moussa, Eman Abou [7 ]
Makhlouf, Melanie [7 ]
Duda, Georg N. [3 ,8 ]
Saraiva, Luis R. [7 ,9 ]
Schmidt-Bleek, Katharina [3 ,8 ]
Schulz, Tim J. [1 ,2 ,10 ]
机构
[1] German Inst Human Nutr Potsdam Rehbrucke, Dept Adipocyte Dev & Nutr, Nuthetal, Germany
[2] German Ctr Diabet Res DZD, Munich, Germany
[3] Charite Univ Med Berlin, Julius Wolff Inst Biomech & Musculoskeletal Regene, Berlin Inst Hlth, Berlin, Germany
[4] Charite Univ Med Berlin, Berlin Ctr Adv Therapies BeCAT, Berlin, Germany
[5] Free Univ Berlin, Berlin, Germany
[6] Humboldt Univ, Berlin, Germany
[7] Sidra Med, Translat Med Div, Doha, Qatar
[8] Charite Univ Med Berlin, Berlin Inst Hlth Ctr Regenerat Therapies BCRT, Berlin Inst Hlth, Berlin, Germany
[9] Hamad Bin Khalifa Univ, Coll Hlth & Life Sci, Doha, Qatar
[10] Univ Potsdam, Inst Nutr Sci, Nuthetal, Germany
来源
FRONTIERS IN ENDOCRINOLOGY | 2024年 / 15卷
关键词
caloric restriction; aging; bone; bone marrow adipose tissue; osteogenesis; ADIPOSE-TISSUE; MINERAL DENSITY; METABOLISM; AGE; ADIPONECTIN; OVERWEIGHT; LIFELONG; DIET; MASS;
D O I
10.3389/fendo.2024.1394263
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Caloric restriction (CR) is a nutritional intervention that increases life expectancy while lowering the risk for cardio-metabolic disease. Its effects on bone health, however, remain controversial. For instance, CR has been linked to increased accumulation of bone marrow adipose tissue (BMAT) in long bones, a process thought to elicit detrimental effects on bone. Qualitative differences have been reported in BMAT in relation to its specific anatomical localization, subdividing it into physiological and potentially pathological BMAT. We here examine the local impact of CR on bone composition, microstructure and its endocrine profile in the context of aging.Methods Young and aged male C57Bl6J mice were subjected to CR for 8 weeks and were compared to age-matched littermates with free food access. We assessed bone microstructure and BMAT by micro-CT, bone fatty acid and transcriptomic profiles, and bone healing.Results CR increased tibial BMAT accumulation and adipogenic gene expression. CR also resulted in elevated fatty acid desaturation in the proximal and mid-shaft regions of the tibia, thus more closely resembling the biochemical lipid profile of the distally located, physiological BMAT. In aged mice, CR attenuated trabecular bone loss, suggesting that CR may revert some aspects of age-related bone dysfunction. Cortical bone, however, was decreased in young mice on CR and remained reduced in aged mice, irrespective of dietary intervention. No negative effects of CR on bone regeneration were evident in either young or aged mice.Discussion Our findings indicate that the timing of CR is critical and may exert detrimental effects on bone biology if administered during a phase of active skeletal growth. Conversely, CR exerts positive effects on trabecular bone structure in the context of aging, which occurs despite substantial accumulation of BMAT. These data suggest that the endocrine profile of BMAT, rather than its fatty acid composition, contributes to healthy bone maintenance in aged mice.
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页数:16
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