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咪达唑仑在牙本质再生方面的药物重定位潜力。

Potential for Drug Repositioning of Midazolam for Dentin Regeneration.

机构信息

Department of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University,2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, Japan.

National Institute of Advanced Industrial Science & Technology, Central 6, 1-1-1 Higashi, Tsukuba,Ibaraki 305-8566, Japan.

出版信息

Int J Mol Sci. 2019 Feb 4;20(3):670. doi: 10.3390/ijms20030670.

Abstract

Drug repositioning promises the advantages of reducing costs and expediting approvalschedules. An induction of the anesthetic and sedative drug; midazolam (MDZ), regulatesinhibitory neurotransmitters in the vertebrate nervous system. In this study we show the potentialfor drug repositioning of MDZ for dentin regeneration. A porcine dental pulp-derived cell line(PPU-7) that we established was cultured in MDZ-only, the combination of MDZ with bonemorphogenetic protein 2, and the combination of MDZ with transforming growth factor-beta 1. Thedifferentiation of PPU-7 into odontoblasts was investigated at the cell biological and genetic level.Mineralized nodules formed in PPU-7 were characterized at the protein and crystal engineeringlevels. The MDZ-only treatment enhanced the alkaline phosphatase activity and mRNA levels ofodontoblast differentiation marker genes, and precipitated nodule formation containing a dentinspecificprotein (dentin phosphoprotein). The nodules consisted of randomly orientedhydroxyapatite nanorods and nanoparticles. The morphology, orientation, and chemicalcomposition of the hydroxyapatite crystals were similar to those of hydroxyapatite that hadtransformed from amorphous calcium phosphate nanoparticles, as well as the hydroxyapatite inhuman molar dentin. Our investigation showed that a combination of MDZ and PPU-7 cellspossesses high potential of drug repositioning for dentin regeneration.

摘要

药物重定位有望降低成本并加快审批进度。麻醉和镇静药物咪达唑仑(MDZ)可调节脊椎动物神经系统中的抑制性神经递质。在这项研究中,我们展示了 MDZ 用于牙本质再生的药物重定位的潜力。我们建立的一种来源于猪牙髓的细胞系(PPU-7),在仅用 MDZ、MDZ 与骨形态发生蛋白 2 的组合以及 MDZ 与转化生长因子-β1 的组合中进行培养。在细胞生物学和遗传学水平上研究了 PPU-7 向成牙本质细胞的分化。在蛋白质和晶体工程水平上对 PPU-7 中形成的矿化结节进行了表征。仅用 MDZ 处理可增强碱性磷酸酶活性和牙本质分化标志物基因的 mRNA 水平,并沉淀形成含有牙本质特异性蛋白(牙本质磷蛋白)的结节。这些结节由随机取向的羟磷灰石纳米棒和纳米颗粒组成。羟基磷灰石晶体的形态、取向和化学成分与从无定形磷酸钙纳米颗粒转化而来的羟基磷灰石以及人磨牙牙本质中的羟基磷灰石相似。我们的研究表明,MDZ 和 PPU-7 细胞的组合具有很高的药物重定位潜力,可用于牙本质再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a2/6387224/34dfeab0bbd1/ijms-20-00670-g001.jpg

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