Abstract
<p>Periodontal disease has been involved in a variety of systemic disorders and suspected as a potential risk factor for fetal growth restriction. Periodontal pathogenic bacteria may actively regulate embryonic development, implantation and placental trophoblast cell invasion. This study aimed to analyze the role of TNF-α, IL-10 and caspase-3 to maintain fetal growth in <em>Porphyromonas</em><em> gingivalis</em>-infected pregnant rats. Female rats were infected with live-<em>Porphyromonas gingivalis</em> at concentration of 2x10<sup>9</sup> cells/ml into subgingival sulcus area of the maxillary first molar before and during pregnancy. They were sacrificed on gestational day (GD)-14 and GD20. The weight and length of placentas and fetuses were evaluated. The expression of TNF-α, IL-10 and caspase-3 in macrophages and trophoblast cells were detected by immunohistochemistry. On GD14, TNF-α (R<sup>2</sup>=0.416;<em>P</em>=0.000) and IL-10 (R<sup>2</sup>=0.187;<em>P</em>=0.012) had an important role to increase expression of caspase-3 in the placenta, but only TNF-α (R<sup>2</sup>=0.393;<em>P</em>=0.000 ) was able to increase the expression of caspase-3 on GD20. TNF-α and caspase-3 also had an important role (<em>P</em>&lt;0.000) to decrease fetal weight, fetal length and placental weight on GD14 and GD20, but it was not the case with IL-10 (<em>P</em>&gt;0.000). The increasing expressions of TNF-α and IL-10 did not only enhance immune protection, but also maintained the trophoblast cells survival by regulating expression of caspase-3. <em>Porphyromonas</em><em> gingivalis</em> infection in maternal periodontal tissue can lead to decrease in placental weight, fetal weight and fetal length which mediated by increasing expression of TNF-α, IL-10 and caspase-3 in the placenta.</p>
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