The role of uncoupling protein 2 in experimental periodontitis-associated renal injury in rats.

Qiong Li, Haonan Ma, Yaqi Shang, Xirui Xin, Xinchan Liu, Zhou Wu, Weixian Yu
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Abstract

Objectives: This study aims to explore changes in uncoupling protein 2 (UCP2) in experimental periodontitis-associated renal injury induced by ligation and investigate the effect of UCP2 on renal injury induced by periodontitis.

Methods: Twelve Wistar male rats were randomly divided into two groups: control and periodontitis groups. A periodontal model was built by ligating the maxillary first molars area with 0.2 mm orthodontic ligature wire. After 8 weeks, the intraoral condition of the rats was observed and periodontal clinical indices such as gingival bleeding index (BI), periodontal probing depth (PD), and tooth mobility (TM) were detected. The maxillary bone was scanned by Micro CT to observe the alveolar bone resorption. The tissue mineral density (TMD), bone mineral density (BMD), bone volume fraction (BV/TV), trabecular thickness (Tb.Th), trabecular bone separation (Tb.Sp) were recorded, and the distance from the enamel bone boundary to the alveolar crest (CEJ-ABC) of the maxillary first molar was measured. The oxidative stress indexes such as malondialdehyde, glutathione (GSH), and superoxide dismutase (SOD) were detected using frozen rat kidney tissue. The gene expression of UCP2, nuclear factor erythroid 2-related factor 2 (Nrf2), and peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α) was observed by quantitative real-time polymerase chain reaction (qRT-PCR) test. The gingival tissue of the rats was used for immunohistochemical staining to observe the expression of the UCP2 protein. The fixed rat kidney tissue was used for hematoxylin-eosin (HE), periodic acid-schiff (PAS), MitoSOX Red, JC-1, and immunohistochemical staining to observe the renal histopathology, the level of reactive oxygen species (ROS), the level of mitochondrial membrane potential, and the expression of UCP2, Nrf2, and PGC-1α protein. Rat serum was collected to detect renal function indices, namely, blood urea nitrogen (BUN), creatinine (Cre), and albumin (Alb).

Results: Compared with the control group, the periodontitis group showed red, swollen, and soft gingival tissue, with gingival probing bleeding, periodontal PD increased, tooth loosening, alveolar bone resorption, decreased TMD, BMD, BV/TV, and Tb.Th indices, and increased Tb.Sp index, CEJ-ABC, and gingival UCP2 protein expression. Compared with the control group, the levels of MDA and ROS in the kidney tissue of periodontitis rats and the gene and protein expression of UCP2 increased, and the levels of MMP, GSH, and SOD and the gene and protein expression of Nrf2 and PGC-1α decreased. Renal functional indices, namely, BUN, Cre, and Alb, were not significantly different between the two groups.

Conclusions: UCP2 may play a role in renal injury induced by periodontitis through oxidative stress.

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解偶联蛋白 2 在大鼠实验性牙周炎相关肾损伤中的作用
研究目的本研究旨在探讨解偶联蛋白2(UCP2)在实验性牙周炎相关肾损伤结扎中的变化,并研究UCP2对牙周炎引起的肾损伤的影响:方法:将12只雄性Wistar大鼠随机分为两组:对照组和牙周炎组。方法:将 12 只 Wistar 雄性大鼠随机分为两组:对照组和牙周炎组。8 周后,观察大鼠的口腔内状况,检测牙龈出血指数(BI)、牙周探诊深度(PD)和牙齿活动度(TM)等牙周临床指标。用显微 CT 扫描上颌骨,观察牙槽骨吸收情况。记录组织矿物质密度(TMD)、骨矿物质密度(BMD)、骨体积分数(BV/TV)、骨小梁厚度(Tb.Th)、骨小梁分离度(Tb.Sp),并测量上颌第一磨牙釉骨边界到牙槽嵴顶的距离(CEJ-ABC)。使用冷冻大鼠肾组织检测丙二醛、谷胱甘肽(GSH)和超氧化物歧化酶(SOD)等氧化应激指标。通过实时聚合酶链式反应(qRT-PCR)定量检测,观察了 UCP2、核因子红细胞 2 相关因子 2(Nrf2)和过氧化物酶体增殖激活受体 gamma 辅激活剂-1α(PGC-1α)的基因表达。对大鼠牙龈组织进行免疫组化染色,观察 UCP2 蛋白的表达。固定的大鼠肾组织用于苏木精-伊红(HE)、周期性酸-希夫(PAS)、MitoSOX Red、JC-1和免疫组化染色,以观察肾组织病理学、活性氧(ROS)水平、线粒体膜电位水平以及UCP2、Nrf2和PGC-1α蛋白的表达。采集大鼠血清检测肾功能指标,即血尿素氮(BUN)、肌酐(Cre)和白蛋白(Alb):与对照组相比,牙周炎组牙龈组织红肿、柔软,探龈出血,牙周PD增加,牙齿松动,牙槽骨吸收,TMD、BMD、BV/TV、Tb.Th指数下降,Tb.Sp指数、CEJ-ABC、牙龈UCP2蛋白表达增加。与对照组相比,牙周炎大鼠肾组织中 MDA 和 ROS 的水平以及 UCP2 的基因和蛋白表达增加,MMP、GSH 和 SOD 的水平以及 Nrf2 和 PGC-1α 的基因和蛋白表达降低。两组患者的肾功能指标(即 BUN、Cre 和 Alb)无明显差异:结论:UCP2可能通过氧化应激在牙周炎引起的肾损伤中发挥作用。
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