High-fat diet-induced obesity augments the deleterious effects of estrogen deficiency on bone: Evidence from ovariectomized mice
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
36217558
PubMed Central
PMC9741509
DOI
10.1111/acel.13726
Knihovny.cz E-zdroje
- Klíčová slova
- Aging, bone fragility, accelerated aging, bone marrow adiposity, menopause, obesity, osteoporosis, senescence,
- MeSH
- diabetes mellitus 2. typu * komplikace MeSH
- dieta s vysokým obsahem tuků * škodlivé účinky MeSH
- estrogeny MeSH
- kosti a kostní tkáň metabolismus MeSH
- lidé MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- obezita komplikace metabolismus MeSH
- ovarektomie škodlivé účinky MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- estrogeny MeSH
Several epidemiological studies have suggested that obesity complicated with insulin resistance and type 2 diabetes exerts deleterious effects on the skeleton. While obesity coexists with estrogen deficiency in postmenopausal women, their combined effects on the skeleton are poorly studied. Thus, we investigated the impact of high-fat diet (HFD) on bone and metabolism of ovariectomized (OVX) female mice (C57BL/6J). OVX or sham operated mice were fed either HFD (60%fat) or normal diet (10%fat) for 12 weeks. HFD-OVX group exhibited pronounced increase in body weight (~86% in HFD and ~122% in HFD-OVX, p < 0.0005) and impaired glucose tolerance. Bone microCT-scanning revealed a pronounced decrease in trabecular bone volume/total volume (BV/TV) (-15.6 ± 0.48% in HFD and -37.5 ± 0.235% in HFD-OVX, p < 0.005) and expansion of bone marrow adipose tissue (BMAT; +60.7 ± 9.9% in HFD vs. +79.5 ± 5.86% in HFD-OVX, p < 0.005). Mechanistically, HFD-OVX treatment led to upregulation of genes markers of senescence, bone resorption, adipogenesis, inflammation, downregulation of gene markers of bone formation and bone development. Similarly, HFD-OVX treatment resulted in significant changes in bone tissue levels of purine/pyrimidine and Glutamate metabolisms, known to play a regulatory role in bone metabolism. Obesity and estrogen deficiency exert combined deleterious effects on bone resulting in accelerated cellular senescence, expansion of BMAT and impaired bone formation leading to decreased bone mass. Our results suggest that obesity may increase bone fragility in postmenopausal women.
Biomechanics Section Department of Mechanical Engineering KU Leuven Heverlee Belgium
Molecular Physiology of Bone Institute of Physiology Czech Academy of Sciences Prague Czech Republic
Steno Diabetes Center Odense Odense University Hospital Odense Denmark
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Nutrition and Bone Marrow Adiposity in Relation to Bone Health