Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Division of Pharmaceutics, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Nutrition. 2018 Sep;53:64-76. doi: 10.1016/j.nut.2017.12.003. Epub 2018 Feb 13.
Kaempferol, a dietary flavonoid found in fruits and vegetables, has been reported to reverse osteopenic condition in ovariectomized rats. Because kaempferol is endowed with osteogenic activity, the aim of this study was to determine whether it has a beneficial effect on glucocorticoid (GC)-induced bone loss.
Adult female rats were divided into four groups as control (vehicle; distilled water), methylprednisolone (MP; 5 mg•kg•d, subcutaneously), MP + kaempferol (5 mg•kg•d, oral), and MP + human parathyroid 1-34 (30 µg/kg, 5 times/wk, subcutaneously) and treated for 4 wk. To study the antagonizing effect of kaempferol on GC-induced inhibition of fracture healing, drill-hole injury was performed on control and GC-treated rats. An oral dose of kaempferol was given for 14 d to observe the effect on callus formation at the site of injury. After treatment, bones were collected for further analysis.
GC was associated with a decreased bone mineral density and impaired bone microarchitecture parameters. Consumption of kaempferol induced bone-sparing effects in GC-induced osteopenic condition. Additionally, improved callus formation at site of drill injury in femur diaphysis was observed with kaempferol consumption in animals on GC. Consistent with the in vivo data, kaempferol elicited a higher expression of osteogenic markers in vitro and antagonized the apoptotic effect of dexamethasone on calvarial osteoblasts.
These results suggested that kaempferol reduced GC-induced bone loss and enhanced bone regeneration at fractured site, thus emphasizing the positive role of flavonoids on bone health.
山柰酚是一种存在于水果和蔬菜中的膳食类黄酮,已被报道可逆转去卵巢大鼠的骨质疏松症。由于山柰酚具有成骨活性,本研究旨在确定其是否对糖皮质激素(GC)诱导的骨丢失具有有益作用。
成年雌性大鼠分为 4 组:对照组(载体;蒸馏水)、甲基强的松龙(MP;5mg·kg·d,皮下注射)、MP+山柰酚(5mg·kg·d,口服)和 MP+人甲状旁腺素 1-34(30µg/kg,每周 5 次,皮下注射),并治疗 4 周。为研究山柰酚对 GC 抑制骨折愈合的拮抗作用,对对照组和 GC 处理组大鼠进行钻孔损伤。给予山柰酚口服剂量 14d,观察对损伤部位骨痂形成的影响。治疗后收集骨骼进行进一步分析。
GC 导致骨密度降低和骨微结构参数受损。山柰酚的消耗在 GC 诱导的骨质疏松症中产生了骨保护作用。此外,在 GC 处理的动物中,山柰酚的消耗观察到股骨骨干钻孔损伤部位的骨痂形成得到改善。与体内数据一致,山柰酚在体外诱导了更高的成骨标志物表达,并拮抗了地塞米松对颅骨成骨细胞的凋亡作用。
这些结果表明,山柰酚减少了 GC 诱导的骨丢失,并增强了骨折部位的骨再生,从而强调了类黄酮对骨骼健康的积极作用。