Women Scientist, DBT-BIO-Care, Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Division of Endocrinology, CSIR-Central Drug Research Institute, Council of Scientific and Industrial Research, Lucknow 226031, India.
Biomed Pharmacother. 2019 Oct;118:109207. doi: 10.1016/j.biopha.2019.109207. Epub 2019 Jul 12.
A combination of diosmin and hesperidin (9:1 ratio) is marketed as a dietary supplement/nutraceutical for cardiovascular health. We studied the skeletal effect of this combination (90% diosmin and 10% hesperidin, henceforth named as DH). We showed that a) in rats with femur osteotomy, DH stimulated callus bone regeneration, b) in growing rats, DH promoted peak bone mass achievement and c) in OVX rats rendered osteopenic, DH completely restored femur trabecular bones and strength along with the increases in surface referent bone formation and serum osteogenic marker. Furthermore, DH suppressed bone resorption in OVX rats as well as in OVX rats treated with teriparatide (human parathyroid hormone 1-34) but did not affect the osteoanabolic effect of teriparatide. These data suggested that DH could prolong the anabolic window of teriparatide. To understand the mechanism of DH action, we performed pharmacokinetic studies and observed that upon its oral administration the only circulating metabolites was diosmetin (the aglycone form of diosmin) while none of the two input flavanones were detectable. Accordingly, subsequent experiments with diosmetin revealed that it was a selective estrogen receptor-β agonist that stimulated osteoblast differentiation and suppressed sclerostin the anti-osteoblastogenic Wnt antagonist. Taken together, our study defined a positive skeletal effect of DH.
地奥司明和橙皮苷(9:1 比例)的组合作为一种膳食补充剂/营养保健品,用于心血管健康。我们研究了这种组合(90%地奥司明和 10%橙皮苷,以下简称 DH)对骨骼的影响。我们发现:a) 在股骨切开术后的大鼠中,DH 刺激骨痂骨再生;b) 在生长中的大鼠中,DH 促进峰值骨量的获得;c) 在去卵巢大鼠中,DH 完全恢复了骨小梁和强度,同时增加了表面参考骨形成和血清成骨标志物。此外,DH 抑制了去卵巢大鼠和去卵巢大鼠中甲状旁腺素(人甲状旁腺激素 1-34)治疗的骨吸收,但不影响甲状旁腺素的促合成代谢作用。这些数据表明,DH 可以延长甲状旁腺素的合成代谢窗口。为了了解 DH 作用的机制,我们进行了药代动力学研究,观察到口服给药后唯一循环的代谢物是地奥司明(地奥司明的糖苷形式),而两种输入的黄烷酮均不可检测。因此,对地奥司明的后续实验表明,它是一种选择性雌激素受体-β激动剂,刺激成骨细胞分化,并抑制成骨细胞抑制剂 sclerostin。综上所述,我们的研究定义了 DH 的积极的骨骼作用。