Protective effect of Korean Red Ginseng against glucocorticoid-induced osteoporosis in vitro and in vivo
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作者:
Kim, Jinhee
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机构:
Gachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South KoreaGachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
Kim, Jinhee
[1
]
Lee, Hyejin
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Gachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South KoreaGachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
Lee, Hyejin
[1
]
Kang, Ki Sung
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机构:
Gachon Univ, Coll Korean Med, Gyeonggi Do 461701, Seongnam, South KoreaGachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
Kang, Ki Sung
[2
]
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Chun, Kwang-Hoon
[3
]
Hwang, Gwi Seo
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机构:
Gachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
Gachon Univ, Coll Korean Med, Gyeonggi Do 461701, Seongnam, South KoreaGachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
Hwang, Gwi Seo
[1
,2
]
机构:
[1] Gachon Univ, Coll Korean Med, Lab Cell Differentiat Res, Gyeonggi Do 461701, Seongnam, South Korea
[2] Gachon Univ, Coll Korean Med, Gyeonggi Do 461701, Seongnam, South Korea
[3] Gachon Univ, Coll Pharm, Gachon Inst Pharmaceut Sci, Inchon, South Korea
dexamethasone;
Korean Red Ginseng;
osteoblast;
osteoporosis;
Panax ginseng;
PANAX-GINSENG;
POTENTIAL MECHANISMS;
ENDOTHELIAL-CELLS;
INDUCED APOPTOSIS;
BONE;
OSTEOBLASTS;
INHIBITION;
PREVENTION;
OSTEOCYTES;
RATS;
D O I:
10.1016/j.jgr.2014.06.001
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Background: Glucocorticoids (GCs) are commonly used in many chemotherapeutic protocols and play an important role in the normal regulation of bone remodeling. However, the prolonged use of GCs results in osteoporosis, which is partially due to apoptosis of osteoblasts and osteocytes. In this study, effects of Korean Red Ginseng (KRG) on GC-treated murine osteoblastic MC3T3-E1 cells and a GC-induced osteoporosis mouse model were investigated. Methods: MC3T3-E1 cells were exposed to dexamethasone (Dex) with or without KRG and cell viability was measured by the 344, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. Real-time polymerase chain reaction was performed to evaluate the apoptotic gene expression; osteogenic gene expression and alkaline phosphatase (ALP) activity were also measured. Western blotting was performed to evaluate the mitogen-activated protein kinase (MAPK) proteins. A GC-induced osteoporosis animal model was used for in vivo study. Results and conclusion: The MU assay revealed that Korean Red Ginseng (KRG) prevents loss of cell viability caused by Dex-induced apoptosis in MC3T3E1 cells. Real-time polymerase chain reaction data showed that groups treated with both Dex and KRG exhibited lower mRNA levels of caspase-3 and -9, whereas the mRNA levels of Bcl2, IAPs, and XIAP increased. Moreover, groups treated with both Dex and KRG demonstrated increased mRNA levels of ALP. RUNX2, and bone morphogenic proteins as well as increased ALP activity in MC3T3-E1 cells, compared to cells treated with Dex only. In addition, KRG increased protein kinase B (AKT) phosphorylation and decreased c-Jun N-terminal kinase (JNK) phosphorylation. Moreover, microcomputed tomography analysis of the femurs showed that GC implantation caused trabecular bone loss. However, a significant reduction of bone loss was observed in the KRG-treated group. These results suggest that the molecular mechanism of KRG in the GC-induced apoptosis may lead to the development of therapeutic strategies to prevent and/or delay osteoporosis. Copyright (C) 2014. The Korean Society of Ginseng. Published by Elsevier. All rights reserved.
机构:
Department of Internal Medicine, Ctr. Osteoporosis Metab. Bone Dis., Univ. of Arkansas for Med. Sciences, Little Rock
Univ. of Arkansas for Med. Sciences, Little Rock, AR 72205-7199, 4301 West Markham StreetDepartment of Internal Medicine, Ctr. Osteoporosis Metab. Bone Dis., Univ. of Arkansas for Med. Sciences, Little Rock