| Literature DB >> 31306971 |
Sharmistha Bhattacharyya1, Subhashis Pal2, Riyazuddin Mohamed3, Priya Singh2, Sourav Chattopadhyay4, Shyamsundar Pal China2, Konica Porwal2, Sabyasachi Sanyal4, Jiaur R Gayen3, Naibedya Chattopadhyay5.
Abstract
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.Entities:
Keywords: Bone regeneration; Estrogen receptors; Nutraceutical; Osteoporosis; Parathyroid hormone; Sclerostin
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Year: 2019 PMID: 31306971 DOI: 10.1016/j.biopha.2019.109207
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529