Antiosteoporosis effect of bryodulcosigenin on ovariectomy-induced osteoporosis in experimental rats

Kai Sun, Lin Qin
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Abstract

ABSTRACT Purpose: Osteoporosis is a bone disease which commonly occurred in postmenopausal women. Almost 10 percent of world population and approximately 30% of women (postmenopausal) suffer from this disease. Alternative medicine has great success in the treatment of osteoporosis disease. Bryodulcosigenin, a potent phytoconstituent, already displayed the anti-inflammatory and antioxidant effect. In this study, we made effort to analyze the antiosteoporosis effect of bryodulcosigenin against ovariectomy (OVX) induced osteoporosis in rats. Methods: Swiss albino Wistar rats were grouped into fIve groups and given an oral dose of bryodulcosigenin (10, 20 and 30 mg/kg) for eight weeks. Body weight, uterus, bone mineral density, cytokines, hormones parameters, transforming growth factor (TGF)-β, insulin-like growth factor (IGF), osteoprotegerin (OPG), receptor activator of nuclear factor kappa-Β ligand (RANKL), and its ratio were estimated. Results: Bryodulcosigenin significantly (p < 0.001) suppressed the body weight and enhanced the uterine weight and significantly (p < 0.001) increased the bone mineral density in whole femur, caput femoris, distal femur and proximal femur. Bryodulcosigenin significantly (P < 0.001) altered the level of biochemical parameters at dose dependent manner, significantly (P < 0.001) improved the level of estrogen and suppressed the level of follicle stimulating hormone and luteinizing hormone. Bryodulcosigenin significantly (P < 0.001) improved the level of OPG and suppressed the level of RANKL. Conclusions: Bryodulcosigenin reduced the cytokines level and suppressed the TGF-β and IGF. We concluded that bryodulcosigenin is an antiosteoporosis medication based on the findings.
白果苷对卵巢切除术诱发的实验大鼠骨质疏松症的抗骨质疏松症作用
ABSTRACT 目的:骨质疏松症是一种常见于绝经后妇女的骨病。全世界近 10% 的人口和约 30% 的妇女(绝经后)患有这种疾病。替代医学在治疗骨质疏松症方面取得了巨大成功。布洛陀甙元是一种强效植物成分,具有抗炎和抗氧化作用。在本研究中,我们试图分析白果苷元对卵巢切除术(OVX)诱导的大鼠骨质疏松症的抗骨质疏松症作用。研究方法将瑞士白化 Wistar 大鼠分为五组,分别口服 10、20 和 30 mg/kg 剂量的白果苷元,连续八周。对体重、子宫、骨矿物质密度、细胞因子、激素参数、转化生长因子(TGF)-β、胰岛素样生长因子(IGF)、骨保护素(OPG)、核因子卡帕Β配体受体活化因子(RANKL)及其比值进行估计。结果显示金银花苷元显著(P<0.001)抑制了体重,增加了子宫重量,并显著(P<0.001)增加了全股骨、股骨帽、股骨远端和股骨近端的骨矿物质密度。白果苷元以剂量依赖的方式显著(P < 0.001)改变了生化指标的水平,显著(P < 0.001)提高了雌激素水平,抑制了促卵泡激素和促黄体生成素的水平。白果苷元能明显(P < 0.001)改善 OPG 水平,抑制 RANKL 水平。结论白果苷元降低了细胞因子水平,抑制了 TGF-β 和 IGF。根据研究结果,我们认为白果苷元是一种抗骨质疏松症药物。
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