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组织蛋白酶 K 抑制剂对牙本质侵蚀的影响:一项体外研究。

Effects of Cathepsin K Inhibitors on Dentin Erosion: An in vitro Study.

机构信息

Fujian Key Laboratory of Oral Diseases and Fujian Provincial Engineering Research Center of Oral Biomaterial and Stomatological Key Laboratory of Fujian College and University, School and Hospital of Stomatology, Fujian Medical University, Fuzhou, China.

Department of Preventive Dentistry, Periodontology and Cariology, University Medical Center Göttingen, Göttingen, Germany.

出版信息

Caries Res. 2023;57(2):159-166. doi: 10.1159/000529621. Epub 2023 Feb 17.

Abstract

Cathepsin K (catK) modulates the degradation of dentin collagen. This study aimed to evaluate the effects of catK inhibitors on dentin erosion. Dentin beams were eroded (4 times/d for 5 days) and immersed in deionized water (negative control), 0.1 M NaCl, 0.3 M NaCl, 0.5 M NaCl, or 1 μm odanacatib (each n = 16) for 30 min after each erosive challenge. Erosive dentin loss (EDL) and demineralized organic matrix (DOM) thickness were evaluated profilometrically. Additionally, dentin beams were demineralized, immersed in the respective solutions for 30 min each (n = 5), and then incubated in artificial saliva for 5 days. Dentin collage degradation was evaluated by quantifying the levels of the C-terminal peptide of type I collagen (CTX), C-terminal cross-linked telopeptide of type I collagen (ICTP), and hydroxyproline (HYP) in the incubation media. Significantly lower EDL and dentin collagen degradation (CTX, ICTP, and HYP) and thicker DOM layers were observed in the samples treated with 0.3 m NaCl and 1 μm odanacatib than in those treated with deionized water (all p < 0.05). The samples treated with 1 μm odanacatib showed significantly lower levels of CTX and HYP than those treated with 0.3 M NaCl (all p < 0.05). The present findings support the potential use of catK inhibitors in controlling dentin erosion.

摘要

组织蛋白酶 K(catK)可调节牙本质胶原的降解。本研究旨在评估 catK 抑制剂对牙本质侵蚀的影响。牙本质梁进行侵蚀(每天 4 次,持续 5 天),然后在去离子水(阴性对照)、0.1MNaCl、0.3MNaCl、0.5MNaCl 或 1 μmodanacatib(每次 n = 16)中浸泡 30 分钟,每次侵蚀后都进行浸泡。采用轮廓法评估侵蚀性牙本质损失(EDL)和脱矿有机基质(DOM)厚度。此外,将牙本质梁脱矿,然后分别在各溶液中浸泡 30 分钟(n = 5),然后在人工唾液中孵育 5 天。通过定量测定 I 型胶原 C 端肽(CTX)、I 型胶原 C 端交联端肽(ICTP)和羟脯氨酸(HYP)在孵育介质中的水平来评估牙本质胶原降解。与去离子水处理的样本相比,用 0.3MNaCl 和 1 μmodanacatib 处理的样本的 EDL 和牙本质胶原降解(CTX、ICTP 和 HYP)更低,DOM 层更厚(所有 p < 0.05)。用 1 μmodanacatib 处理的样本的 CTX 和 HYP 水平明显低于用 0.3MNaCl 处理的样本(所有 p < 0.05)。本研究结果支持使用 catK 抑制剂控制牙本质侵蚀的潜力。

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