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丹酚酸B和丹参素通过上调一氧化氮途径诱导大鼠骨髓间充质干细胞的成骨分化。

Salvianolic acid B and danshensu induce osteogenic differentiation of rat bone marrow stromal stem cells by upregulating the nitric oxide pathway.

作者信息

Zhang Xinle, Zou Liyi, Li Jin, Xu Bilian, Wu Tie, Fan Huanqiong, Xu Weiming, Yao Weimin, Yang Yajun, Liu Yuyu, Cui Liao

机构信息

Department of Pharmacology, Guangdong Medical University, Zhanjiang, Guangdong 524023, P.R. China.

Department of Respiratory Medicine, The Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524023, P.R. China.

出版信息

Exp Ther Med. 2017 Oct;14(4):2779-2788. doi: 10.3892/etm.2017.4914. Epub 2017 Aug 9.

Abstract

The aim of the present study was to investigate the effect of salvianolic acid B (Sal B) and danshensu (DSU) on the osteogenic differentiation of bone marrow mesenchymal stem cells (MSCs) and the mechanisms of the effects. The osteogenic differentiation of MSCs in culture was assessed by measuring alkaline phosphatase (ALP) activity, osteocalcin (OCN) production, nitric oxide (NO) production and the mRNA expression levels of osteoprotegerin (OPG) and its ligand by MSCs. MSCs were successfully induced to differentiate into osteoblasts and adipocytes. Sal B and DSU increased the ALP activity and the production of OCN in the absence of an ossification inducer. The increase in ALP activity was more pronounced when induction was combined with the osteogenic inducer, Sal B, which enhanced the expression of OPG; however, Sal B reduced the expression of receptor activator of nuclear factor-κB ligand (RANKL) by MSCs. Sal B reversed the inhibitory effect of N-nitro L-arginine methylester on the MSCs and increased ALP activity, OCN content and the OPG/RANKL ratio. Based on these results, it was concluded that Sal B increases the osteogenic differentiation of MSCs, most likely by regulating the nitric oxide pathway.

摘要

本研究旨在探讨丹酚酸B(Sal B)和丹参素(DSU)对骨髓间充质干细胞(MSCs)成骨分化的影响及其作用机制。通过检测培养的MSCs中碱性磷酸酶(ALP)活性、骨钙素(OCN)生成、一氧化氮(NO)生成以及MSCs中骨保护素(OPG)及其配体的mRNA表达水平,评估MSCs的成骨分化情况。MSCs成功诱导分化为成骨细胞和脂肪细胞。在无骨化诱导剂的情况下,Sal B和DSU增加了ALP活性和OCN的生成。当诱导与成骨诱导剂Sal B联合使用时,ALP活性的增加更为明显,Sal B增强了OPG的表达;然而,Sal B降低了MSCs中核因子κB受体活化因子配体(RANKL)的表达。Sal B逆转了N-硝基-L-精氨酸甲酯对MSCs的抑制作用,增加了ALP活性、OCN含量和OPG/RANKL比值。基于这些结果,得出结论:Sal B可能通过调节一氧化氮途径增加MSCs的成骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/444d/5615234/e0bee5383300/etm-14-04-2779-g00.jpg

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