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Glucosamines Attenuate Bone Loss Due to Menopause by Regulating Osteoclast Function in Ovariectomized Mice
Hironobu Asai1, Sachie Nakatani, Takuya Kato
1Faculty of Pharmaceutical Sciences, Josai University.
Glucosamine (GlcN) and N-acetylglucosamine (GlcNAc) supplementation increased bone mineral density in ovariectomized mice. These compounds inhibit osteoclast activity, suggesting a nonestrogenic approach to suppressing bone loss.
Area of Science:
- Bone Metabolism
- Endocrinology
- Nutritional Science
Background:
- Ovariectomized (OVX) mice are a model for postmenopausal osteoporosis.
- Glucosamine (GlcN) and N-acetylglucosamine (GlcNAc) are components of glycosaminoglycans involved in bone structure.
- The effects of GlcN and GlcNAc on bone metabolism in OVX models require further elucidation.
Purpose of the Study:
- To investigate the impact of dietary glucosamine (GlcN) and N-acetylglucosamine (GlcNAc) on bone metabolism in ovariectomized (OVX) mice.
- To determine if GlcN and GlcNAc can mitigate bone loss through nonestrogenic mechanisms.
Main Methods:
- OVX mice were fed diets containing 0.2% GlcN or 0.2% GlcNAc for 12 weeks.
- Femoral bone mineral density (BMD) was measured.
- Histomorphometric analysis of tibial bone was performed.
- Osteoclast differentiation and activity were assessed using tartrate-resistant acid phosphatase (TRAP) staining and erosion depth measurements.
Main Results:
- GlcN and GlcNAc supplementation significantly increased femoral BMD in OVX mice compared to controls.
- Histomorphometry revealed reduced osteogenesis and bone resorption rates in GlcN-fed mice.
- Osteoclast erosion depth and TRAP-positive osteoclast numbers were significantly reduced in GlcN- and GlcNAc-fed OVX mice.
- Uterine weight loss and increased serum calcium were observed in supplemented groups.
Conclusions:
- Dietary intake of GlcN and GlcNAc effectively suppresses bone loss in OVX mice.
- The mechanism involves the inhibition of osteoclast differentiation and activity.
- GlcN and GlcNAc offer a potential nonestrogenic therapeutic strategy for managing bone loss.
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