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The Process of Acclimation to Chronic Hypoxia Leads to Submandibular Gland and Periodontal Alterations: An Insight on the Role of Inflammatory Mediators

机译:慢性低氧适应过程导致下颌下腺和牙周变化:炎症介质作用的见解。

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The exposition to hypoxia is a stressful stimulus, and the organism develops acclimation mechanisms to ensure homeostasis, but if this fails, it leads to the development of pathological processes. Considering the large number of people under hypoxic conditions, it is of utmost importance to study the mechanisms implicated in hypoxic acclimation in oral tissues and the possible alteration of some important inflammatory markers that regulate salivary and periodontal function. It is the aim of the present study to analyze submandibular (SMG) and periodontal status of animals chronically exposed to continuous (CCH) or intermittent (CIH) hypoxia in order to elucidate the underlying molecular mechanisms that may lead to hypoxic acclimation. Adult Wistar rats were exposed to CCH or CIH simulating 4200 meters of altitude during 90 days. Salivary secretion was decreased in animals exposed to hypoxia, being lower in CIH, together with increased prostaglandin E2 (PGE2) content, TBARS concentration, and the presence of apoptotic nuclei and irregular secretion granules in SMG. AQP-5 mRNA levels decreased in both hypoxic groups. Only the CCH group showed higher HIF-1α staining, while CIH alone exhibited interradicular bone loss and increased concentration of the bone resorption marker CTX-I. In summary, animals exposed to CIH show a worse salivary secretion rate, which related with higher levels of PGE2, suggesting a negative role of this inflammatory mediator during hypoxia acclimation. We link the weak immunorreactivity of HIF-1α in CIH with improper hypoxia acclimation, which is necessary to sustaining SMG physiology under this environmental condition. The alveolar bone loss observed in CIH rats could be due mainly to a direct effect of PGE2, as suggested by its higher content in gingival tissue, but also to the indirect effect of hyposalivation. This study may eventually contribute to finding therapeutics to treat the decreased salivary flow, improving in that way oral health.
机译:暴露于缺氧环境是一种压力刺激,生物体会发展适应机制以确保体内稳态,但是如果失败,则会导致病理过程的发展。考虑到许多人处于低氧条件下,研究与口腔组织中低氧适应有关的机制以及调节唾液和牙周功能的某些重要炎症标记可能发生改变的机制至关重要。本研究的目的是分析长期暴露于连续性(CCH)或间歇性(CIH)低氧的动物的颌下(SMG)和牙周状态,以阐明可能导致低氧适应的潜在分子机制。成年Wistar大鼠在90天内暴露于模拟4200米高度的CCH或CIH中。暴露于低氧环境的动物唾液分泌减少,CIH降低,同时前列腺素E2(PGE2)含量,TBARS浓度增加,并且SMG中存在凋亡核和不规则​​分泌颗粒。在两个缺氧组中,AQP-5 mRNA水平均下降。仅CCH组显示出较高的HIF-1α染色,而单独的CIH则显示出小梁间骨丢失和骨吸收标记物CTX-1浓度增加。总之,暴露于CIH的动物唾液分泌率较差,这与PGE2的水平升高有关,表明该炎症介质在低氧适应过程中具有负作用。我们将CIH中HIF-1α的弱免疫反应性与不当的低氧适应联系起来,这对于在这种环境条件下维持SMG生理是必要的。在CIH大鼠中观察到的牙槽骨丢失可能主要归因于PGE2的直接作用,正如其在牙龈组织中的含量较高所暗示的那样,还可能是唾液分泌不足的间接作用。这项研究可能最终有助于寻找治疗唾液流量减少的疗法,从而改善口腔健康。

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