Experimental Periodontitis Results in Prediabetes and Metabolic Alterations in Brain, Liver and Heart: Global Untargeted Metabolomic Analyses.

Vladimir Ilievski, Jason M Kinchen, Ramya Prabhu, Fadi Rim, Lara Leoni, Terry G Unterman, Keiko Watanabe
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引用次数: 19

Abstract

Results from epidemiological studies suggest that there is an association between periodontitis and prediabetes, however, causality is not known. The results from our previous studies suggest that induction of periodontitis leads to hyperinsulinemia glucose intolerance and insulin resistance, all hallmarks of prediabetes. However, global effects of periodontitis on critical organs in terms of metabolic alterations are unknown. We determined the metabolic effects of periodontitis on brain, liver, heart and plasma resulting from Porphyromonas gingivalis induced periodontitis in mice. Periodontitis was induced by oral application of the periodontal pathogen, Porphyromonas gingivalis for 22 weeks. Global untargeted biochemical profiles in samples from these organs/plasma were determined by liquid and gas chromatography/mass spectrometry and compared between controls and animals with periodontitis. Oral application of Porphyromonas gingivalis induced chronic periodontitis and hallmarks of prediabetes. The results of sample analyses indicated a number of changes in metabolic readouts, including changes in metabolites related to glucose and arginine metabolism, inflammation and redox homeostasis. Changes in biochemicals suggested subtle systemic effects related to periodontal disease, with increases in markers of inflammation and oxidative stress most prominent in the liver. Signs of changes in redox homeostasis were also seen in the brain and heart. Elevated bile acids in liver were suggestive of increased biosynthesis, which may reflect changes in liver function. Interestingly, signs of decreasing glucose availability were seen in the brain. In all three organs and plasma, there was a significant increase in the microbiome-derived bioactive metabolite 4-ethylphenylsulfate sulfate in animals with periodontitis. The results of metabolic profiling suggest that periodontitis/bacterial products alter metabolomic signatures of brain, heart, liver, and plasma in the prediabetic state. These data provide scientific community valuable metabolic signatures that become the basis for understanding the impact of periodontitis on a systemic disease and potentially targets for therapeutic intervention.

Abstract Image

Abstract Image

实验性牙周炎导致糖尿病前期和大脑、肝脏和心脏的代谢改变:全球非靶向代谢组学分析。
流行病学研究结果表明牙周炎和前驱糖尿病之间存在关联,但因果关系尚不清楚。我们之前的研究结果表明,牙周炎的诱发会导致高胰岛素血症、葡萄糖耐受不良和胰岛素抵抗,这些都是前驱糖尿病的特征。然而,就代谢改变而言,牙周炎对关键器官的整体影响尚不清楚。研究了牙龈卟啉单胞菌引起的牙周炎对小鼠大脑、肝脏、心脏和血浆代谢的影响。口腔应用牙周病原菌牙龈卟啉单胞菌诱导牙周炎22周。通过液相和气相色谱/质谱法测定这些器官/血浆样品的总体非靶向生化特征,并在对照组和牙周炎动物之间进行比较。口腔应用牙龈卟啉单胞菌引起的慢性牙周炎和前驱糖尿病的标志。样本分析的结果表明,代谢读数发生了一些变化,包括与葡萄糖和精氨酸代谢、炎症和氧化还原稳态相关的代谢物的变化。生物化学物质的变化表明与牙周病相关的微妙的全身影响,炎症和氧化应激标志物的增加在肝脏中最为突出。大脑和心脏也出现了氧化还原稳态改变的迹象。肝脏胆汁酸升高提示生物合成增加,这可能反映了肝功能的变化。有趣的是,大脑中出现了葡萄糖可用性降低的迹象。在患有牙周炎的动物的所有三个器官和血浆中,微生物衍生的生物活性代谢物4-乙基苯基硫酸酯显著增加。代谢分析结果表明,牙周炎/细菌产物改变了糖尿病前期大脑、心脏、肝脏和血浆的代谢组学特征。这些数据为科学界提供了有价值的代谢特征,为理解牙周炎对全身性疾病的影响和治疗干预的潜在目标奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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