Oleanolic Acid Exerts Osteoprotective Effects and Modulates Vitamin D Metabolism

被引:32
作者
Cao, Sisi [1 ]
Dong, Xiao-Li [1 ,2 ]
Ho, Ming-Xian [1 ]
Yu, Wen-Xuan [1 ]
Wong, Ka-Chun [1 ]
Yao, Xin-Sheng [3 ]
Wong, Man-Sau [1 ,2 ,4 ]
机构
[1] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Shenzhen Res Inst, Shenzhen Key Lab Food Biol Safety Control, Shenzhen 518057, Peoples R China
[3] Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Coll Pharm, Guangzhou 510632, Guangdong, Peoples R China
[4] Hong Kong Polytech Univ, Shenzhen Res Inst, State Key Lab Chinese Med & Mol Pharmacol Incubat, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金;
关键词
oleanolic acid; ovariectomised; aging; osteoporosis; calcium; vitamin D; LIGUSTRI-LUCIDI EXTRACT; INTESTINAL CALCIUM-ABSORPTION; BONE-MINERAL DENSITY; PARATHYROID-HORMONE; 1,25-DIHYDROXYVITAMIN D-3; 25-HYDROXYVITAMIN D-3; ETHANOL EXTRACT; GENE-EXPRESSION; 1-ALPHA-HYDROXYLASE GENE; D SUPPLEMENTATION;
D O I
10.3390/nu10020247
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Oleanolic acid (OA) is a triterpenoid with reported bone anti-resorption activities. The present study aimed to characterize its bone protective effects in vivo and to study its effects on vitamin D metabolism, both in vivo and in vitro. OA significantly increased bone mineral density, improved micro-architectural properties, reduced urinary Ca excretion, increased 1,25(OH)(2)D-3 and renal CYP27B1 mRNA expression in mature C57BL/6 ovariectomised (OVX) mice. OA also improved bone properties, Ca balance, and exerted modulatory effects on renal CYP27B1 and CYP24A1 expressions in aged normal female Sprague-Dawley rats. In addition, OA significantly increased renal CYP27B1 mRNA and promoter activity, and suppressed CYP24A1 mRNA and protein expressions in human proximal tubule HKC-8 cells. OA exerted bone protective effects in mature OVX mice and aged female rats. This action on bone might be, at least in part, associated with its effects on Ca and vitamin D metabolism. The present findings suggest that OA is a potential drug candidate for the management of postmenopausal osteoporosis.
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页数:20
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