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1
Geranylgeraniol reverses alendronate-induced MC3T3 cell cytotoxicity and alteration of osteoblast function via cell cytoskeletal maintenance.香叶基香叶醇通过维持细胞细胞骨架,逆转阿仑膦酸钠诱导的 MC3T3 细胞毒性和破骨细胞功能改变。
J Oral Pathol Med. 2021 Feb;50(2):191-199. doi: 10.1111/jop.13120. Epub 2021 Jan 8.
2
Geranylgeraniol (GGOH) as a Mevalonate Pathway Activator in the Rescue of Bone Cells Treated with Zoledronic Acid: An In Vitro Study.香叶基香叶醇(GGOH)作为甲羟戊酸途径激活剂对唑来膦酸处理的骨细胞的挽救作用:一项体外研究
Stem Cells Int. 2019 Jan 9;2019:4351327. doi: 10.1155/2019/4351327. eCollection 2019.
3
Osteoporosis: A Review of Treatment Options.骨质疏松症:治疗方案综述
P T. 2018 Feb;43(2):92-104.
4
Effects of zoledronic acid and geranylgeraniol on the cellular behaviour and gene expression of primary human alveolar osteoblasts.唑来膦酸和香叶基香叶醇对原代人牙槽骨成骨细胞细胞行为和基因表达的影响。
Clin Oral Investig. 2016 Nov;20(8):2023-2035. doi: 10.1007/s00784-015-1706-y. Epub 2016 Jan 22.
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Low Bone Turnover in Chronic Kidney Disease Is Associated with Decreased VEGF-A Expression and Osteoblast Differentiation.慢性肾脏病中的低骨转换与血管内皮生长因子-A表达降低和成骨细胞分化减少有关。
Am J Nephrol. 2015;41(6):464-73. doi: 10.1159/000438461. Epub 2015 Jul 25.
6
American Association of Oral and Maxillofacial Surgeons position paper on medication-related osteonecrosis of the jaw--2014 update.美国口腔颌面外科医师协会关于药物相关性颌骨坏死的立场文件——2014年更新版
J Oral Maxillofac Surg. 2014 Oct;72(10):1938-56. doi: 10.1016/j.joms.2014.04.031. Epub 2014 May 5.
7
Alendronate-induced atypical bone fracture: evidence that the drug inhibits osteogenesis.阿仑膦酸钠引起的非典型骨折:该药物抑制骨生成的证据。
J Clin Pharm Ther. 2014 Aug;39(4):349-53. doi: 10.1111/jcpt.12149. Epub 2014 Mar 24.
8
Geranylgeraniol - a new potential therapeutic approach to bisphosphonate associated osteonecrosis of the jaw.香叶醇——双膦酸盐相关性颌骨骨坏死的一种新的潜在治疗方法。
Oral Oncol. 2011 Mar;47(3):195-201. doi: 10.1016/j.oraloncology.2010.12.003. Epub 2011 Jan 17.
9
Determination of the differentiation capacities of murines' primary mononucleated cells and MC3T3-E1 cells.检测鼠源原代单核细胞和 MC3T3-E1 细胞的分化能力。
Cancer Cell Int. 2010 Oct 28;10:42. doi: 10.1186/1475-2867-10-42.
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Alendronate inhibits VEGF expression in growth plate chondrocytes by acting on the mevalonate pathway.阿仑膦酸盐通过作用于甲羟戊酸途径抑制生长板软骨细胞中的血管内皮生长因子(VEGF)表达。
Open Orthop J. 2009 Oct 1;3:83-8. doi: 10.2174/1874325000903010083.

在阿仑膦酸盐条件下,添加香叶基香叶醇的时间会增加成骨细胞活性。

Timing of geranylgeraniol addition increases osteoblast activities under alendronate condition.

作者信息

Mungpayabarn Harikarn, Patntirapong Somying

机构信息

Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.

Thammasat University Research Unit in Dental and Bone Substitute Biomaterials, Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.

出版信息

J Oral Biol Craniofac Res. 2021 Jul-Sep;11(3):396-401. doi: 10.1016/j.jobcr.2021.04.005. Epub 2021 May 5.

DOI:10.1016/j.jobcr.2021.04.005
PMID:34026481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8134755/
Abstract

BACKGROUND

Alendronate (ALN), a nitrogen-containing bisphosphonate, is prescribed to treat bone diseases. ALN acts as an inhibitor of enzymes in the mevalonate pathway, which results in reducing osteoblast viability and mineralization. Geranylgeraniol (GGOH) is a substrate in mevalonate pathway and mediates protein prenylation in the cells.

OBJECTIVE

To investigate the effects of GGOH on ALN-treated osteoblast activities in order to improve the application of GGOH.

METHODS

MC3T3 cells were treated with ALN. GGOH were added at different time points. Cell activities were examined using alizarin red S, MTT assay, alkaline phosphatase (ALP) activity, and quantitative polymerase chain reaction.

RESULTS

ALN decreased mineralization. In the presence of ALN, GGOH addition at the first week of culture increased mineralization compared with the addition at other time points. ALN treatment for 7 days caused a reduction in osteoblast and pre-osteoblast viability compared with untreated cells. GGOH supplement partially rescued cell viability and increased total protein in cells treated with ALN. Furthermore, GGOH significantly upregulated gene expressions of Col I, OPN, VEGF, and VEGFR2.

CONCLUSION

GGOH could be best applied at the early stage of osteogenesis since GGOH helped increasing cell viability and differentiation at the first 7 day of treatment.

摘要

背景

阿仑膦酸盐(ALN)是一种含氮双膦酸盐,用于治疗骨疾病。ALN作为甲羟戊酸途径中酶的抑制剂,导致成骨细胞活力和矿化减少。香叶基香叶醇(GGOH)是甲羟戊酸途径中的一种底物,介导细胞中的蛋白质异戊二烯化。

目的

研究GGOH对ALN处理的成骨细胞活性的影响,以改善GGOH的应用。

方法

用ALN处理MC3T3细胞。在不同时间点添加GGOH。使用茜素红S、MTT法、碱性磷酸酶(ALP)活性和定量聚合酶链反应检测细胞活性。

结果

ALN降低矿化。在存在ALN的情况下,与在其他时间点添加相比,在培养第一周添加GGOH可增加矿化。与未处理的细胞相比,ALN处理7天导致成骨细胞和前成骨细胞活力降低。GGOH补充剂部分挽救了细胞活力,并增加了用ALN处理的细胞中的总蛋白。此外,GGOH显著上调了Col I、OPN、VEGF和VEGFR2的基因表达。

结论

GGOH在成骨早期应用效果最佳,因为GGOH在治疗的前7天有助于增加细胞活力和分化。