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利多卡因抑制人牙髓干细胞的成骨分化。

Lidocaine inhibits osteogenic differentiation of human dental pulp stem cells .

机构信息

Department of Dental Anaesthesia and Pain Medicine, School of Dentistry, Pusan National University, Dental Research Institute, Yangsan, Republic of Korea.

Department of Anaesthesia and Pain Medicine, School of Medicine, Pusan National University, Yangsan, Republic of Korea.

出版信息

J Int Med Res. 2023 Feb;51(2):3000605231152100. doi: 10.1177/03000605231152100.

Abstract

OBJECTIVE

Lidocaine is an amide local anaesthetic commonly used for pain control, however, few studies have investigated the effect of lidocaine on the osteogenic differentiation of human dental pulp stem cells (HDPSCs). The present study aimed to determine the effect of lidocaine on HDPSC viability and osteogenic differentiation.

METHODS

HDPSCs were incubated with 0, 0.05, 0.2, 0.5, and 1 mM lidocaine for 24, 48 and 72 h, after which, MTT assays were performed. HDPSCs cultured with the above lidocaine concentrations and osteogenic differentiation medium for 7 and 14 days were stained for alkaline phosphatase (ALP). Protein and mRNA levels of relevant osteogenic factors (bone morphogenetic protein-2 [BMP-2] and runt-related transcription factor 2 [RUNX2]) were examined using western blotting and real-time reverse-transcription polymerase chain reaction, respectively.

RESULTS

Lidocaine did not affect the viability of HDPSCs, however, lidocaine reduced ALP activity in HDPSCs. Levels of ALP, BMP-2, and RUNX2 mRNA were reduced with lidocaine, and levels of BMP-2 and RUNX2 proteins were decreased, versus controls.

CONCLUSIONS

Lidocaine inhibits osteogenic differentiation markers in HDPSCs , even at low concentrations, without cytotoxicity. This study suggests that lidocaine may inhibit osteogenic differentiation in HDPSC-mediated regenerative medicine, including pulp regeneration and repair.

摘要

目的

利多卡因是一种酰胺类局部麻醉剂,常用于疼痛控制,但很少有研究探讨利多卡因对人牙髓干细胞(HDPSCs)成骨分化的影响。本研究旨在确定利多卡因对 HDPSC 活力和成骨分化的影响。

方法

将 HDPSCs 分别用 0、0.05、0.2、0.5 和 1mM 利多卡因孵育 24、48 和 72h,然后进行 MTT 检测。用上述浓度的利多卡因和成骨分化培养基培养 HDPSCs 7 和 14 天,用碱性磷酸酶(ALP)染色。用 Western blot 和实时逆转录聚合酶链反应分别检测相关成骨因子(骨形态发生蛋白-2[BMP-2]和 runt 相关转录因子 2[RUNX2])的蛋白和 mRNA 水平。

结果

利多卡因不影响 HDPSC 的活力,但降低了 HDPSC 的 ALP 活性。与对照组相比,用利多卡因处理后,HDPSC 中的 ALP、BMP-2 和 RUNX2mRNA 水平降低,BMP-2 和 RUNX2 蛋白水平降低。

结论

低浓度的利多卡因抑制 HDPSC 中的成骨分化标志物,而没有细胞毒性。本研究提示利多卡因可能会抑制 HDPSC 介导的再生医学中的成骨分化,包括牙髓再生和修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cde/9909061/30a13a915c6c/10.1177_03000605231152100-fig1.jpg

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