Key result
Diet-induced NAFLD in mice causes progressive bone loss linked to altered TNF-α, IL-6, and IGF-1.
Why the study?
NAFLD exhibits a close association with osteoporosis, and this work aimed to assess the potential effects of NAFLD on the progression of osteopenia in animal models.
Does a high fat diet inducing NAFLD affect the progression of osteopenia and levels of TNF-α, IGF-1, and IGFBP-1 in C57BL/6 female mice?
Does a high fat diet inducing NAFLD affect the progression of osteopenia and levels of TNF-α, IGF-1, and IGFBP-1 in C57BL/6 female mice?
p-value: p=<0.05
In a mouse model, NAFLD induced by a high-fat diet is associated with progressive bone loss and significant alterations in TNF-α, IL-6, IGF-1, and IGFBP-1 levels.
May link NAFLD to osteoblast dysfunction via IGF signaling in mice; leaves open relevance to human osteopenia.
Backgrounds: Nonalcoholic fatty liver disease (NAFLD) exhibits a close association with osteoporosis. This work aims to assess the potential effects of NAFLD on the progression of osteopenia in animal models. Methods: Forty-eight C57BL/6 female mice were randomly divided to wild-type (WT) group and high fat diet (HFD) group. The corresponding detections were performed after sacrifice at 16, 24 and 32 weeks, respectively . Results: At 16 weeks, an remarkable increase of body weight and lipid aggregation in the hepatocytes of HFD group was observed compared to the WT group, while the bone structure parameters showed no significant difference. At 24 weeks, the levels of TNF-α and IL-6 in NAFLD mice were significantly increased, while the level of Osteoprotegerin (OPG) mRNA in bone tissue was decreased, and the level of receptor activator of nuclear factor Kappa-B ligand (RANKL) mRNA was increased. Meanwhile, the function of osteoclasts was increased, and the bone microstructure parameters showed significant changes. At 32 weeks, in the HFD mice, the mRNA levels of insulin-like growth factor-1 (IGF-1), Runt-related transcription factor 2 (Runx2), and Osterix (OSX) mRNA were reduced, while the insulin-like growth factor binding protein-1 (IGFBP-1) level was increased. Meanwhile, the osteoblast function was decreased, and the differences in bone structure parameters were more significant, showing obvious osteoporosis. Conclusions: The bone loss in HFD mice is pronounced as NAFLD progresses, and the changes of the TNF-α, IL-6, IGF-1, and IGFBP-1 levels may play critical roles at the different stages of NAFLD in HFD.
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Wang et al. (2023) studied Non-alcoholic fatty liver disease (NAFLD) and osteopenia (n=48). High-fat diet vs. Normal diet (Wild-type group) was evaluated on Bone microarchitecture and mineralization (Tb.N, BV/TV, Tb.Th, c.Th, Conn.D, vBMD, and tBMD) (p=<0.05). High-fat diet-induced NAFLD in mice resulted in progressive bone loss and microstructural deterioration, associated with early increases in TNF-α and IL-6 and later reductions in IGF-1.
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