Raghuvanshi Ashutosh, Kumar Amit, Tyagi Abdul M, Kureel Jyoti, Awasthi Pallavi, Purohit Deepak, Mansoori Mohd Nizam, Shukla Priyanka, Srivastava Kamini, Gautam Abnish K, Saxena Ruchi, Dwivedi Anila, Singh Divya, Goel Atul
Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Mol Cell Endocrinol. 2017 Jun 15;448:41-54. doi: 10.1016/j.mce.2017.03.010. Epub 2017 Mar 10.
A series of new 6H-benzofuro[3, 2-c]chromenes (BFC, pterocarpans) with structure-activity relationships were investigated for their potential use in osteoporosis treatment. One of the BFCs 3-piperidylethoxypterocarpan 20 promotes osteoblast differentiation and mineralization at a dose as low as 1 pM via activation of ER/P38MAPK/BMP-2 pathway. When evaluated for in-vivo osteogenic activity in female Sprague-Dawley rats, BFC 20 increased bone mineral density and new bone formation, compared with control at 1.0 and 10.0 mg/kg/body weight by oral gavage for 30 days. The compound was devoid of any uterotrophic effect and led to the new bone formation in adult ovariectomized osteopenic rats. BFC 20 compound also inhibited bone resorption by reducing Ovx induced increase in urinary CTx, thus exhibiting both bone anabolic and anti-catabolic action. Finally, BFC 20 treatment to Ovx rats led to improved trabecular microarchitectural restoration and exhibited therapeutic potential as a dual acting anti-osteoporotic agent for the management of osteoporosis.
研究了一系列具有构效关系的新型6H-苯并呋喃[3,2-c]色烯(BFC,紫檀烷)在骨质疏松症治疗中的潜在用途。其中一种BFC,即3-哌啶基乙氧基紫檀烷20,通过激活ER/P38MAPK/BMP-2途径,在低至1 pM的剂量下促进成骨细胞分化和矿化。在雌性Sprague-Dawley大鼠中评估其体内成骨活性时,与通过口服灌胃给予1.0和10.0 mg/kg体重剂量的对照相比,BFC 20增加了骨矿物质密度和新骨形成,持续30天。该化合物没有任何子宫营养作用,并在成年去卵巢骨质疏松大鼠中导致新骨形成。BFC 20化合物还通过减少去卵巢诱导的尿CTx增加来抑制骨吸收,从而表现出骨合成代谢和抗分解代谢作用。最后,对去卵巢大鼠进行BFC 20治疗导致小梁微结构恢复改善,并显示出作为双效抗骨质疏松剂治疗骨质疏松症的治疗潜力。