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Article Publish Status: FREE
Abstract Title:

Protective Effects of 2,3,5,4'-Tetrahydroxystilbene-2--β-d-glucoside on Ovariectomy Induced Osteoporosis Mouse Model.

Abstract Source:

Int J Mol Sci. 2018 Aug 28 ;19(9). Epub 2018 Aug 28. PMID: 30154383

Abstract Author(s):

Su-Jin Kim, Yun-Ho Hwang, Seul-Ki Mun, Seong-Gyeol Hong, Kwang-Jin Kim, Kyung-Yun Kang, Young-Jin Son, Sung-Tae Yee

Article Affiliation:

Su-Jin Kim

Abstract:

2,3,5,4'-Tetrahydroxystilbene-2--β-d-glucoside (TSG), an active polyphenolic component of, exhibits many pharmacological activities including antioxidant, anti-inflammation, and anti-aging effects. A previous study demonstrated that TSG protected MC3T3-E1 cells from hydrogen peroxide (H₂O₂) induced cell damage and the inhibition of osteoblastic differentiation. However, no studies have investigated the prevention of ovariectomy-induced bone loss in mice. Therefore, we investigated the effects of TSG on bone loss in ovariectomized mice (OVX). Treatment with TSG (1 and 3 μg/g;i.p.) for six weeks positively affected body weight, uterine weight, organ weight, bone length, and weight change because of estrogen deficiency. The levels of the serum biochemical markers of calcium (Ca), inorganic phosphorus (IP), alkaline phosphatase (ALP), and total cholesterol (TCHO) decreasedin the TSG-treated mice when compared with the OVX mice. Additionally, the serum bone alkaline phosphatase (BALP) levels in the TSG-treated OVX mice were significantly increased compared with the OVX mice, while the tartrate-resistant acid phosphatase (TRAP) activity was significantly reduced. Furthermore, the OVX mice treated with TSG showed a significantly reduced bone loss compared to the untreated OVX mice upon micro-computed tomography (CT) analysis. Consequently, bone destruction in osteoporotic mice as a result of ovariectomy was inhibited by the administration of TSG. These findings indicate that TSG effectively prevents bone loss in OVX mice; therefore, it can be considered as a potential therapeutic for the treatment of postmenopausal osteoporosis.

Study Type : Animal Study

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