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仙灵骨葆对去卵巢大鼠骨代谢的有益作用及毒性研究

Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats.

作者信息

Wu Hao, Zhong Qingxiang, Wang Jing, Wang Man, Fang Fang, Xia Zhi, Zhong Rongling, Huang Houcai, Ke Zhongcheng, Wei Yingjie, Feng Liang, Shi Ziqi, Sun E, Song Jie, Jia Xiaobin

机构信息

Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese MedicineNanjing, China.

Key Laboratory of New Drug Delivery System of Chinese Materia Medica, Jiangsu Province Academy of Chinese MedicineNanjing, China.

出版信息

Front Pharmacol. 2017 May 22;8:273. doi: 10.3389/fphar.2017.00273. eCollection 2017.

Abstract

Xian-ling-gu-bao (XLGB) is a well-known patented traditional Chinese prescription widely used to treat osteoporosis, osteoarthritis, aseptic bone necrosis, or climacteric syndrome. However, recent reports have suggested that XLGB may cause liver injury in humans. In the present study, we aimed to evaluate the efficacy of XLGB in the prevention of osteoporosis in the zebrafish and ovariectomized (OVX) rats, both of which have been used as osteoporosis models. The safety of XLGB after long-term administration to OVX rats was also assessed. OVX rats were administered by oral gavage 270 mg/kg (recommended daily dose), 1350 mg/kg, and 1800 mg/kg of XLGB for 26 weeks. Bone mineral density, relative bone surface to bone volume, relative bone volume to total volume, trabecular number, mean trabecular thickness, and mean trabecular spacing in OVX rats were examined at the end of the 26-week dosing period. Additionally, OPG and RANKL expression in the femur were determined by western blot and immunohistochemical staining. To evaluate the safety of XLGB, body weight, hematology, serum biochemistry markers related to toxicology, and organ histopathology were determined in each group of OVX rats. Conversely, the zebrafish was treated with prednisolone to induce osteoporosis in the embryo. Disodium etidronate was used as a treatment control. XLGB was shown to be effective in preventing osteoporosis in both the OVX rats and the prednisolone-treated zebrafish. Similarly, XLGB increased OPG protein and decreased RANKL protein in OVX rats. Interestingly, no obvious toxicity was observed in the heart, liver, kidney, small intestine, or stomach at dosages of up to 1800 mg/kg after treating the OVX rats for 26 weeks. XLGB was shown to be very effective in treating osteoporosis in OVX rats. No obvious toxicity or adverse effects developed in OVX rats at dosages up to 1800 mg/kg, which is equivalent to six times the daily-recommended dose. Therefore, XLGB should be considered a good option for the treatment of post-menopausal osteoporosis.

摘要

仙灵骨葆(XLGB)是一种著名的专利中药方剂,广泛用于治疗骨质疏松症、骨关节炎、无菌性骨坏死或更年期综合征。然而,最近的报告表明,XLGB可能会导致人类肝损伤。在本研究中,我们旨在评估XLGB在预防斑马鱼和去卵巢(OVX)大鼠骨质疏松症方面的疗效,这两种动物都已被用作骨质疏松症模型。我们还评估了长期给OVX大鼠服用XLGB后的安全性。给OVX大鼠口服灌胃270 mg/kg(推荐日剂量)、1350 mg/kg和1800 mg/kg的XLGB,持续26周。在给药26周结束时,检测OVX大鼠的骨密度、骨表面与骨体积的相对比值、骨体积与总体积的相对比值、小梁数量、平均小梁厚度和平均小梁间距。此外,通过蛋白质印迹法和免疫组织化学染色测定股骨中骨保护素(OPG)和核因子κB受体活化因子配体(RANKL)的表达。为了评估XLGB的安全性,测定每组OVX大鼠的体重、血液学指标、与毒理学相关的血清生化标志物以及器官组织病理学。相反,用泼尼松龙处理斑马鱼胚胎以诱导骨质疏松症。依替膦酸钠用作治疗对照。结果表明,XLGB在预防OVX大鼠和泼尼松龙处理的斑马鱼骨质疏松症方面均有效。同样,XLGB增加了OVX大鼠的OPG蛋白含量并降低了RANKL蛋白含量。有趣的是,在给OVX大鼠治疗26周后,剂量高达1800 mg/kg时,在心脏、肝脏、肾脏、小肠或胃中未观察到明显毒性。结果表明,XLGB在治疗OVX大鼠骨质疏松症方面非常有效。在剂量高达1800 mg/kg(相当于每日推荐剂量的六倍)时,OVX大鼠未出现明显毒性或不良反应。因此,XLGB应被视为治疗绝经后骨质疏松症的一个良好选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6162/5438972/354d0a44504b/fphar-08-00273-g001.jpg

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