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根管内药物与根尖乳头干细胞的相互作用:通过甲基噻唑基四氮唑、台盼蓝和乳酸脱氢酶进行定量细胞毒性评估。

Interaction of intracanal medicaments with apical papilla stem cells: quantitative cytotoxicity assessment by methyl thiazolyl tetrazolium, trypan blue and lactate dehydrogenase.

作者信息

Saberi Eshaghali, Farhad-Mollashahi Narges, Saberi Mersad

机构信息

Department of Endodontics, Oral and Dental Diseases Research Center, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran.

Department of Endodontics, Oral and Dental Diseases Research Center, Faculty of Dentistry, Zahedan University of Medical Sciences, Zahedan, Iran -

出版信息

Minerva Stomatol. 2019 Feb;68(1):36-41. doi: 10.23736/S0026-4970.18.04172-9. Epub 2019 Jan 7.

Abstract

BACKGROUND

Chemical residues often have cytotoxic effects on the stem cells. This study aimed to assess the cytotoxic effects of intracanal medicaments on stem cells of the apical papilla (SCAPs) using methyl thiazolyl tetrazolium (MTT), trypan blue exclusion (TBE) and lactate dehydrogenase release (LDHR) assays.

METHODS

SCAPs were cultured and exposed to 0.125, 0.25, 1, 5 and 10 mg/mL concentrations of modified triple antibiotic paste (mTAP)/distilled water (DW), mTAP/chlorhexidine (CHX), calcium hydroxide(Ca(OH)2)/CHX and Ca(OH)2/DW. Cell viability was quantitatively analyzed using the MTT, LDHR and TBE assays. Data were analyzed using one-way ANOVA and Tukey's test.

RESULTS

All three assessment methods yielded the same results. Ca(OH)2/ DW resulted in the highest and mTAP/CHX resulted in the lowest cell viability. In contrast to Ca(OH)2, mTAP decreased cell viability in a dose-dependent manner. Also, addition of CHX to mTAP and Ca(OH)2 increased their cytotoxicity.

CONCLUSIONS

In contrast to the proliferative effects of Ca(OH)2, even low concentrations of mTAP have cytotoxic effects on SCAPs.

摘要

背景

化学残留物通常对干细胞具有细胞毒性作用。本研究旨在使用甲基噻唑基四氮唑蓝(MTT)、台盼蓝排斥试验(TBE)和乳酸脱氢酶释放试验(LDHR)评估根管内药物对根尖乳头干细胞(SCAPs)的细胞毒性作用。

方法

培养SCAPs,并将其暴露于浓度为0.125、0.25、1、5和10mg/mL的改良三联抗生素糊剂(mTAP)/蒸馏水(DW)、mTAP/氯己定(CHX)、氢氧化钙(Ca(OH)2)/CHX和Ca(OH)2/DW中。使用MTT、LDHR和TBE试验对细胞活力进行定量分析。数据采用单因素方差分析和Tukey检验进行分析。

结果

三种评估方法得出相同结果。Ca(OH)2/DW导致细胞活力最高,mTAP/CHX导致细胞活力最低。与Ca(OH)2不同,mTAP以剂量依赖方式降低细胞活力。此外,向mTAP和Ca(OH)2中添加CHX会增加它们的细胞毒性。

结论

与Ca(OH)2的增殖作用相反,即使是低浓度的mTAP对SCAPs也具有细胞毒性作用。

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