Suppr超能文献

二甲双胍通过抑制成骨细胞缺氧诱导的凋亡来改善根尖病变。

Metformin Ameliorates Periapical Lesions through Suppression of Hypoxia-induced Apoptosis of Osteoblasts.

机构信息

Department of Dentistry, School of Dentistry, College of Medicine, Taipei, Taiwan.

Graduate Institute of Clinical Dentistry, School of Dentistry, College of Medicine, Taipei, Taiwan.

出版信息

J Endod. 2018 Dec;44(12):1817-1825. doi: 10.1016/j.joen.2018.08.002. Epub 2018 Oct 4.

Abstract

INTRODUCTION

Intramuscular injection of metformin has been shown to inhibit the progression of periapical lesions in rats by decreasing the number of receptor activator of nuclear factor-κβ ligand- and tartrate-resistant acid phosphatase-positive cells. In this study, we investigated the effect of metformin on hypoxia-induced apoptosis of osteoblasts and the therapeutic activity of intracanal metformin in induced periapical lesions in rats.

METHODS

The influence of metformin on hypoxia-induced mitochondrial superoxide production in human osteoblasts was examined by using MitoSOX (Invitrogen, Carlsbad, CA) fluorescence dye signaling. The release of cytochrome c from mitochondria and the cleavage of procaspase-9 and poly(adenosine diphosphate-ribose) polymerase were evaluated by Western blot analysis. Apoptotic cell fraction was assessed by DNA content flow cytometry. In a rat model of induced periapical lesions, the effect of intracanal metformin on disease progression was appraised by 2-dimensional radiography and micro-computed tomographic imaging. Oxidative lesions and apoptotic activity of osteoblasts in vivo were estimated, respectively, by 8-hydroxy-2'-deoxyguanosine staining and terminal deoxynucleotidyl transferase dUTP nick end labeling.

RESULTS

Metformin inhibited hypoxia-enhanced mitochondrial superoxide production in osteoblasts. Metformin suppressed hypoxia-induced cytochrome c release from mitochondria and the cleavage of procaspase-9 and poly(adenosine diphosphate-ribose) polymerase. Metformin repressed hypoxia-augmented apoptotic cell fraction. In a rat model, intracanal metformin diminished the size of periapical lesions and the oxidative damage and apoptotic activity in osteoblasts.

CONCLUSIONS

Hypoxia increased oxidative stress in osteoblasts and enhanced cell death through activation of the mitochondrial pathway of apoptosis. Metformin attenuated the oxidative and cytotoxic action of hypoxia. The therapeutic effect of metformin on periapical lesions is partially caused by its antioxidative activity.

摘要

简介

肌内注射二甲双胍已被证明通过减少核因子-κβ配体受体激活剂和抗酒石酸酸性磷酸酶阳性细胞的数量来抑制大鼠根尖周病变的进展。在这项研究中,我们研究了二甲双胍对缺氧诱导的成骨细胞凋亡的影响以及二甲双胍在大鼠诱导性根尖周病变中的根管内治疗活性。

方法

通过使用 MitoSOX(Invitrogen,Carlsbad,CA)荧光染料信号来检测二甲双胍对人成骨细胞缺氧诱导的线粒体超氧化物产生的影响。通过 Western blot 分析评估细胞色素 c 从线粒体中的释放以及 procaspase-9 和多聚(腺苷二磷酸核糖)聚合酶的裂解。通过 DNA 含量流式细胞术评估凋亡细胞分数。在诱导性根尖周病变的大鼠模型中,通过二维射线照相和微计算机断层扫描成像评估根管内二甲双胍对疾病进展的影响。通过 8-羟基-2'-脱氧鸟苷染色和末端脱氧核苷酸转移酶 dUTP 缺口末端标记分别评估体内成骨细胞的氧化损伤和凋亡活性。

结果

二甲双胍抑制了成骨细胞中缺氧增强的线粒体超氧化物产生。二甲双胍抑制了缺氧诱导的细胞色素 c 从线粒体中的释放以及 procaspase-9 和多聚(腺苷二磷酸核糖)聚合酶的裂解。二甲双胍抑制了缺氧增强的凋亡细胞分数。在大鼠模型中,根管内二甲双胍减少了根尖周病变的大小以及成骨细胞中的氧化损伤和凋亡活性。

结论

缺氧增加了成骨细胞中的氧化应激,并通过激活线粒体凋亡途径增强了细胞死亡。二甲双胍减轻了缺氧的氧化和细胞毒性作用。二甲双胍对根尖周病变的治疗效果部分是由于其抗氧化活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验