Osteogenic activity of constituents from Butea monosperma

被引:75
作者
Maurya, Rakesh [1 ]
Yadav, Dinesh K. [1 ]
Singh, Geetu [1 ]
Bhargavan, Biju [2 ]
Murthy, P. S. Narayana [2 ]
Sahai, Mahendra [3 ]
Singh, Man Mohan [2 ]
机构
[1] Cent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, India
[2] Cent Drug Res Inst, Div Endocrinol, Lucknow 226001, Uttar Pradesh, India
[3] Banaras Hindu Univ, Inst Med Sci, Dept Med Chem, Varanasi 221005, Uttar Pradesh, India
关键词
Flame of Forest; Butea monosperma; Isoflavonoids; Osteogenic; Osteoblast proliferation; Differentiation; Mineralization; NUCLEAR-MAGNETIC-RESONANCE; LIPID CONSTITUENTS; BARK; TRANSFORMATION; ISOFLAVONOIDS; PTEROCARPAN; TRITERPENES; FLAVONOIDS; COUMESTAN; FRONDOSA;
D O I
10.1016/j.bmcl.2008.12.064
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Phytochemical investigation from the stem bark of Butea monosperma, led to the isolation and identification of three new compounds named buteaspermin A ( 1), buteaspermin B ( 2) and buteaspermanol ( 3), along with 19 known compounds. The structure of compounds 1-22 were established on the basis of their spectroscopic data. The isolated compounds 2-17 were evaluated using neonatal (1-3 day old) rat calvaria derived primary osteoblast cultures. Five of these compounds 7, 10-13 showed promising osteogenic activity, attributed to increased osteoblast proliferation, differentiation and mineralization as evidenced by marked increase in expression of alkaline phosphatase, an early phase differentiation marker, and alizarin Red S staining of osteoblasts cultured for 48 h and von Kossa silver staining of nodules formed 15 days after culture with these compounds. Quanti. cation of mineralization by optical density measurement of Alizarin Red S extracted from stained osteoblasts cultured for 7 days in presence of these compounds showed significant ( P < 0.05, vs corresponding vehicle control group) increase in mineralization. On the basis of biological results, structure-activity relationships are discussed. (c) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:610 / 613
页数:4
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