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山茱萸对核因子κB受体激活剂配体(RANKL)诱导的破骨细胞分化的影响。

Effect of Cornus Officinalis on Receptor Activator of Nuclear Factor-kappaB Ligand (RANKL)-induced Osteoclast Differentiation.

作者信息

Kim Jung Young, Kim Yun-Kyung, Choi Min Kyu, Oh Jaemin, Kwak Han Bok, Kim Jeong-Joong

机构信息

Department of Anatomy, School of Medicine, Wonkwang University, Iksan, Korea.

Department of Oriental Pharmacy, Wonkwang University, Iksan, Korea. ; Wonkwang Oriental Medicines Research Institute, Wonkwang University, Iksan, Korea.

出版信息

J Bone Metab. 2012 Nov;19(2):121-7. doi: 10.11005/jbm.2012.19.2.121. Epub 2012 Nov 16.

Abstract

OBJECTIVES

Osteoporosis is a disease of bones that is thought to result from an imbalance between bone resorption and bone formation. Although osteoporosis itself has no symptoms, osteoporosis caused by osteoclasts leads to an increased risk of fracture. Here we examined the effects of cornus officinalis on receptor activator of nuclear factor-kappaB ligand (RANKL)-mediated osteoclast differentiation.

METHODS

We evaluated the effects of cornus officinalis on RANKL-induced osteoclast differentiation from bone marrow-derived macrophages (BMMs) and performed a cytotoxicity assay, reverse transcriptase-polymerase chain reaction (RT-PCR), and Western blot analysis.

RESULTS

Cornus officinalis significantly inhibits RANKL-mediated osteoclast differentiation in a dose-dependent manner, but without cytotoxicity against BMMs. The mRNA expression of tartrate-resistant acid phosphatase (TRAP), osteoclast-associated receptor (OSCAR), c-Fos, and nuclear factor of activated T cells cytoplasmic 1 (NFATc1) in BMMs treated with RANKL was considerably inhibited by cornus officinalis treatment. Also, cornus officinalis inhibits the protein expression of c-Fos and NFATc1. Cornus officinalis greatly inhibits RANKL-induced phosphorylation of p38 and c-JUN N-terminal kinase (JNK). Also, cornus officinalis significantly suppresses RANKL-induced degradation of I-κB.

CONCLUSIONS

Taken together, our results suggest that cornus officinalis may be a useful the treatment of osteoporosis.

摘要

目的

骨质疏松症是一种骨骼疾病,被认为是由骨吸收和骨形成之间的失衡所致。尽管骨质疏松症本身没有症状,但由破骨细胞引起的骨质疏松会导致骨折风险增加。在此,我们研究了山茱萸对核因子κB受体激活剂配体(RANKL)介导的破骨细胞分化的影响。

方法

我们评估了山茱萸对RANKL诱导的骨髓来源巨噬细胞(BMMs)破骨细胞分化的影响,并进行了细胞毒性试验、逆转录聚合酶链反应(RT-PCR)和蛋白质印迹分析。

结果

山茱萸以剂量依赖性方式显著抑制RANKL介导的破骨细胞分化,但对BMMs无细胞毒性。用RANKL处理的BMMs中,抗酒石酸酸性磷酸酶(TRAP)、破骨细胞相关受体(OSCAR)、c-Fos和活化T细胞核因子细胞质1(NFATc1)的mRNA表达受到山茱萸处理的显著抑制。此外,山茱萸抑制c-Fos和NFATc1的蛋白表达。山茱萸极大地抑制RANKL诱导的p38和c-JUN氨基末端激酶(JNK)的磷酸化。此外,山茱萸显著抑制RANKL诱导的I-κB降解。

结论

综上所述,我们的结果表明山茱萸可能是治疗骨质疏松症的有效药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cc2/3780920/a062bf0cf267/jbm-19-121-g001.jpg

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