Quercitrin attenuates osteoporosis in ovariectomized rats by regulating mitogen-activated protein kinase (MAPK) signaling pathways

被引:54
作者
Xing, Li-zhi [1 ]
Ni, Huai-jun [2 ]
Wang, Yu-ling [3 ]
机构
[1] Linyi Peoples Hosp, Dept Endocrinolog, Linyi 276000, Shandong, Peoples R China
[2] Linyi Chest Hosp, Dept Surg, Linyi 276000, Shandong, Peoples R China
[3] Linyi Peoples Hosp, Dept Rheumatol & Immunol, 48 Jiefang Rd, Linyi 276003, Shandong, Peoples R China
关键词
Quercitrin; MAPK; Osteoporosis; MESENCHYMAL STEM-CELLS; ESTROGEN DEFICIENCY; MC3T3-E1; CELLS; BONE; OSTEOCLASTOGENESIS; DIFFERENTIATION; OSTEOBLASTS; MICE;
D O I
10.1016/j.biopha.2017.02.073
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
MAPK signaling pathways are crucial in regulating osteogenesis, a genetic disorder affecting the bones. Quercitrin, a type of flavonoid, is widely distributed in nature and involved in many pharmacological activities. But its osteoprotective functions and mechanism in osteoporosis are far from being understood clearly. In this paper, the MAPK upregulation was observed in the ovariectomy- induced bone loss. Quercitrin was found to downregulate MAPK signaling pathways and prevent the ovariectomy-induced deterioration of bone mineral density (BMD), trabecular microstructure, and bone mechanical characteristics. In this study, quercitrin was seen to prevent the progression of the postmenopausal osteoporosis among the rats, which may be mediated by the downregulated MAPK signaling pathways. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1136 / 1141
页数:6
相关论文
共 24 条
[1]   Quercitrin a bioflavonoid improves the antioxidant status in streptozotocin: induced diabetic rat tissues [J].
Babujanarthanam, Ranganathan ;
Kavitha, Purushothaman ;
Rao, U. S. Mahadeva ;
Pandian, Moses Rajasekara .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2011, 358 (1-2) :121-129
[2]   Prevention of trabecular bone loss induced by estrogen deficiency by a selective p38α inhibitor [J].
Caverzasio, Joseph ;
Higgins, Linda ;
Ammann, Patrick .
JOURNAL OF BONE AND MINERAL RESEARCH, 2008, 23 (09) :1389-1397
[3]   Protective effect of quercitrin against hydrogen peroxide-induced dysfunction in osteoblastic MC3T3-E1 cells [J].
Choi, Eun Mi .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2012, 64 (03) :211-216
[4]   Immunomodulatory pretreatment with Kalanchoe pinnata extract and its quercitrin flavonoid effectively protects mice against fatal anaphylactic shock [J].
Cruz, E. A. ;
Da-Silva, S. A. G. ;
Muzitano, M. F. ;
Silva, P. M. R. ;
Costa, S. S. ;
Rossi-Bergmann, B. .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2008, 8 (12) :1616-1621
[5]   Inhibition of AP-1 and MAPK signaling and activation of Nrf2/ARE pathway by quercitrin [J].
Ding, Min ;
Zhao, Jinshun ;
Bowman, Linda ;
Lu, Yongju ;
Shi, Xianglin .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 36 (01) :59-67
[6]  
Fakhry Maya, 2013, World J Stem Cells, V5, P136, DOI 10.4252/wjsc.v5.i4.136
[7]   The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice [J].
Greenblatt, Matthew B. ;
Shim, Jae-Hyuck ;
Zou, Weiguo ;
Sitara, Despina ;
Schweitzer, Michelle ;
Hu, Dorothy ;
Lotinun, Sutada ;
Sano, Yasuyo ;
Baron, Roland ;
Park, Jin Mo ;
Arthur, Simon ;
Xie, Min ;
Schneider, Michael D. ;
Zhai, Bo ;
Gygi, Steven ;
Davis, Roger ;
Glimcher, Laurie H. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (07) :2457-2473
[8]   Osteoporosis: impact on health and economics [J].
Harvey, Nicholas ;
Dennison, Elaine ;
Cooper, Cyrus .
NATURE REVIEWS RHEUMATOLOGY, 2010, 6 (02) :99-105
[9]   Protective Effect of Components Isolated from Lindera erythrocarpa against Oxidative Stress-induced Apoptosis of H9c2 Cardiomyocytes [J].
Kim, Jeong Ah ;
Jung, Yi-Sook ;
Kim, Mi-Young ;
Yang, Seo Young ;
Lee, Sohyun ;
Kim, Young Ho .
PHYTOTHERAPY RESEARCH, 2011, 25 (11) :1612-1617
[10]   Emodin Regulates Bone Remodeling by Inhibiting Osteoclastogenesis and Stimulating Osteoblast Formation [J].
Kim, Ju-Young ;
Cheon, Yoon-Hee ;
Kwak, Sung Chul ;
Baek, Jong Min ;
Yoon, Kwon-Ha ;
Lee, Myeung Su ;
Oh, Jaemin .
JOURNAL OF BONE AND MINERAL RESEARCH, 2014, 29 (07) :1541-1553