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布洛芬和双氯芬酸预处理对人牙髓干细胞活力和凋亡过程的影响。

Effects of Ibuprofen and Diclofenac Pre-Treatment on Viability and Apoptosis Processes in Human Dental Pulp Stem Cells.

机构信息

5th Department of Internal Medicine, Faculty of Medicine, Comenius University Bratislava, Špitálska 24, 81372 Bratislava, Slovakia.

Department of Pharmacology and Toxicology, University of Veterinary Medicine and Pharmacy, 04181 Košice, Slovakia.

出版信息

Medicina (Kaunas). 2024 May 9;60(5):787. doi: 10.3390/medicina60050787.

Abstract

: Stem cell-based regeneration strategies have shown therapeutic efficacy in various fields of regenerative medicine. These include bone healing after bone augmentation, often complicated by pain, which is managed by using nonsteroidal anti-inflammatory drugs (NSAIDs). However, information is limited about how NSAIDs affect the therapeutic potential of stem cells. : We investigated the effects of ibuprofen and diclofenac on the characteristics, morphology, and immunophenotype of human mesenchymal stromal cells isolated from the dental pulp () and cultured in vitro, as well as their effects on the expression of angiogenic growth factors ( and ) and selected genes in apoptosis signalling pathways (, , , , and 2). : Ibuprofen and diclofenac significantly reduced the viability of DPSCs, while the expression of mesenchymal stem cell surface markers was unaffected. Both ibuprofen and diclofenac treatment significantly upregulated the expression of , while the expression of remained unchanged. Ibuprofen significantly altered the expression of several apoptosis-related genes, including the upregulation of and , with decreased expression. BAK, CASP3, CASP9, and BCL2 expressions were significantly increased in the diclofenac-treated DPSCs, while no difference was demonstrated in BAX expression. : Our results suggest that concomitant use of the NSAIDs ibuprofen or diclofenac with stem cell therapy may negatively impact cell viability and alter the expression of apoptosis-related genes, affecting the efficacy of stem cell therapy.

摘要

基于干细胞的再生策略在再生医学的各个领域显示出了治疗效果。这些策略包括骨增量后骨愈合,通常伴有疼痛,可通过使用非甾体抗炎药(NSAIDs)来缓解。然而,关于 NSAIDs 如何影响干细胞的治疗潜力的信息有限。

我们研究了布洛芬和双氯芬酸对体外分离培养的牙髓间充质基质细胞()的特性、形态和免疫表型的影响,以及它们对血管生成生长因子(和)和凋亡信号通路中选定基因(、、、和 2)表达的影响。

布洛芬和双氯芬酸显著降低了 DPSCs 的活力,而间充质干细胞表面标志物的表达不受影响。布洛芬和双氯芬酸处理均显著上调了的表达,而的表达保持不变。布洛芬显著改变了几个与凋亡相关的基因的表达,包括上调和,同时下调的表达。BAK、CASP3、CASP9 和 BCL2 在双氯芬酸处理的 DPSCs 中的表达显著增加,而 BAX 的表达则没有差异。

我们的研究结果表明,NSAIDs 布洛芬或双氯芬酸与干细胞治疗同时使用可能会对细胞活力产生负面影响,并改变与凋亡相关基因的表达,从而影响干细胞治疗的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4da9/11123081/b8dae1a927d0/medicina-60-00787-g001.jpg

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