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The protective effects of triptolide on age-related bone loss in old male rats
Deqing Luo1, Hongyue Ren2, Huantang Zhang3
1Orthopaedic Center of People's Liberation Army, The Affiliated Southeast Hospital of Xiamen University, Zhangzhou, 363000, Fujian, China.
Background:
Previous studies have showed that triptolide have a critical role in inhibiting osteoclast formation, bone resorption and attenuating regional osteoporosis. However, the protective role of triptolide on age-related bone loss has not been investigated. In the study, we assessed the effect of triptolide supplementation on bone microstructure and bone remolding in old male rat lumbars.
Methods:
Fifty-two 22-month-old male Sprague-Dawley rats were randomly assigned to either triptolide treatment group or control group. Triptolide (15 μg/kg/d) or normal saline was administered to the rats of assigned group for 8 weeks. Lumbar bone mineral density (BMD) and bone microstructure were analyzed by micro-CT. Fluorochrome labeling of the bones was performed to measure the mineral apposition rate (MAR) and bone formation rate (BFR). Osteoclast number was also measured by TRAP staining. Plasma level of osteocalcin and tartrate-resistant acid phosphatase 5b (Tracp 5b) was also analyzed.
Results:
Micro-CT results revealed that triptolide-treated rats had significant higher BMD, bone volume over total volume (BV/TV), trabecular thickness (Tb.Th), bone trabecular number (Tb.N), and lower trabecular separation (Tb.Sp) compared to the control group. Although fluorochrome labeling result showed no significant difference in MAR and BFR between the groups, triptolide decreased osteoclast number in vivo. In addition, a significant higher level of plasma Tracp 5b was observed in the triptolide-treated rats. Furthermore, triptolide also reduced the expression of receptor for activation of NF-κB ligand (RANKL) and increased osteoprotegerin (OPG) expression in the lumbars.
Conclusion:
These results suggested that triptolide had a protective effect on age-related bone loss at least in part by reducing osteoclast number in elder rats. Therefore, triptolide might be a feasible therapeutic approach for senile osteoporosis.
Insights
Triptolide supplementation improved bone microarchitecture and reduced osteoclast number in aged rats, suggesting it may combat age-related bone loss and senile osteoporosis.
Area of Science:
- Bone biology and aging research.
- Pharmacological interventions for osteoporosis.
Background:
- Triptolide is known to inhibit osteoclast formation and bone resorption.
- The effect of triptolide on age-related bone loss was previously uninvestigated.
Purpose of the Study:
- To assess the impact of triptolide on bone microstructure and remodeling in aged male rats.
- To determine triptolide's potential as a therapeutic agent for age-related bone loss.
Main Methods:
- Aged male rats received daily triptolide (15 μg/kg/d) or saline for 8 weeks.
- Evaluated lumbar bone mineral density (BMD), micro-CT, fluorochrome labeling (MAR, BFR), osteoclast number (TRAP staining), and plasma markers (osteocalcin, Tracp 5b).
Main Results:
- Triptolide significantly increased lumbar BMD, bone volume, trabecular thickness, and trabecular number, while decreasing trabecular separation.
- Triptolide reduced osteoclast number, RANKL expression, and increased OPG expression, despite no significant changes in MAR or BFR.
Conclusions:
- Triptolide demonstrates a protective effect against age-related bone loss in elderly rats, primarily by reducing osteoclast activity.
- Triptolide shows promise as a potential therapeutic strategy for senile osteoporosis.
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