Evaluation of a potential bidirectional influence of metabolic syndrome and apical periodontitis: An animal‐based study

果糖 方差分析 代谢综合征 牙周炎 代谢物 臼齿 内科学 医学 内分泌学 生物 肥胖 牙科 生物化学
作者
Estéfano Borgo Sarmento,Luciana Moura Sassone,Karem Paula Pinto,Cláudio Malizia Alves Ferreira,Tatiana Kelly da Silva Fidalgo,Ricardo Tadeu Lopes,Adriana Terezinha Neves Novellino Alves,Liana Bastos Freitas‐Fernandes,Ana Paula Valente,Renata Heisler Neves,Emmanuel João Nogueira Leal Silva
出处
期刊:International Endodontic Journal [Wiley]
卷期号:58 (3): 467-483 被引量:1
标识
DOI:10.1111/iej.14189
摘要

Abstract Aim This study aimed to explore the possible bidirectional interrelations between fructose‐induced metabolic syndrome (MS) and apical periodontitis (AP). Methodology Twenty‐eight male Wistar rats were distributed into four groups ( n = 7, per group): Control (C), AP, Fructose Consumption (FRUT) and Fructose Consumption and AP (FRUT+AP). The rats in groups C and AP received filtered water, while those in groups FRUT and FRUT+AP received a 20% fructose solution mixed with water to induce MS. The groups AP and FRUT+AP had the pulp of their right mandibular first molar exposed to induce AP. Food consumption, murinometric measurements, blood glucose levels and glucose tolerance were monitored. Fifty‐six days after the start of the experiment, the animals were euthanized, and serum samples were collected for metabolomic analysis. Mandibles, livers and right kidneys were also collected. The area and volume of the periapical lesions were calculated using micro‐computed tomography. Histopathological evaluation was performed. Kruskal–Wallis followed by the Student–Newman–Keuls or Mann–Whitney tests and one‐way anova followed by Tukey's or Independent t ‐test were used for non‐parametric and parametric data, respectively ( p < .05). Multivariate analysis and variable importance in projection score were applied to assess metabolite profile differences among groups ( p < .05). Results FRUT and FRUT+AP groups showed significantly increased fluid intake, body mass, abdominal circumference, blood glucose levels, liver weight and visceral fat weight ( p < .05), indicating the development of MS. The analyses of the metabolite profile suggest increasing glucose, histidine, lactate, fatty acid and phenylalanine in the FRUT+AP group. There were no significant differences in volume and area of periapical lesions in micro‐CT analyses ( p = .1048 and p = .7494, respectively). Histopathological analysis of the hemimandibles demonstrated areas of inflammatory response, necrosis and microabscess in the periapical region. Hepatic histopathological observations indicated notable differences in cell appearance, with the FRUT and FRUT+AP groups showing signs of microsteatosis. Kidney analysis revealed Bowman's space dilation in the FRUT and AP groups, while the FRUT+AP group exhibited retracted Bowman's space, suggesting a possible alteration in renal filtration capacity. Conclusions MS had no impact on the progression of AP in rats. However, AP exacerbated the systemic state affected by MS, with changes in liver and kidney tissues and metabolite levels.
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