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Histopathological, immunohistochemical, and molecular studies for determination of wound age and vitality in rats

机译:组织病理学,免疫组织化学和分子研究,用于测定大鼠的伤口年龄和活力

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In forensic medicine, it is vital to verify with the best attainable accuracy once injuries occurred during vital or post-mortem conditions. An immunohistochemical study was carried out to examine the time-dependent expression of macrophage-specific gene CD68 (cluster of differentiation 68), alpha-smooth muscle actin (alpha-SMA), and vascular endothelial growth factor (VEGF) in different skin wound timings (0, 1, 3, 5, 7, and 14 days) in rats. Histopathological studies were performed to assess the wound age and vitality. Eighteen male albino Wister rats (weighing 170-200 g) were used for wound induction. Rats (n = 3) were euthanised at 0, 1, 3, 5, 7, and 14 days from the starting point of wound induction. Histopathological examination showed that the epidermal re-epithelialisation was completed 14 days after skin incision. The inflammatory phase was recorded during the first 3 days of healing and reached the maximum levels at 5 days, then declined after 7 days, and completely removed at 14 days. The beginning of the proliferative phase was dated to day 3 and the peak at days 5 and 7. The initiation of the granulation tissue formation and remodelling phase of the healing process was observed 5 days after wounding. By immunohistochemical staining, negative VEGF gene expressions at early stages (0-3 days) were observed, as well as neither CD68+ macrophages nor alpha-SMA+ myofibroblast cells were detected. By increasing the wound ages (5-7 days), granulation tissue and angiogenesis were observed, with the migration of macrophages and fibroblast, which expressed VEGF, CD68, and alpha-SMA positive reaction. Time-dependent expression of the above markers suggested that they would be useful indicators for the determination of wound age. Both VEGF and transforming growth factor-beta 1 (TGFb1) mRNA levels were determined in different skin wound ages. The transcription of TGFb1 and VEGF increased shortly after wounding, until post-wounding day 7. It then declined constantly, reaching minimal values on day 14.
机译:在法医学中,一旦在生命或验尸后的损伤发生时,验证最好的可达到的准确性至关重要。进行了免疫组织化学研究以检查不同皮肤伤口定时的巨噬细胞特异性基因CD68(分化簇68),α-平滑肌肌动蛋白(α-SMA)和血管内皮生长因子(VEGF)的时间依赖性表达(0,1,3,5,7和14天)在大鼠中。进行组织病理学研究以评估伤口年龄和活力。 18只雄性白化的大鼠(称为170-200g)用于伤口诱导。在伤口诱导的起点,在0,1,3,5,7和14天内安乐死大鼠(n = 3)。组织病理学检查表明,皮肤切口后14天完成了表皮重新上皮化。在愈合的前3天期间记录炎症期,并在5天内达到最高水平,然后在7天后下降,并在14天内完全除去。增殖相的开始日期为第3天和第5天和第7天的峰值。在伤口后5天观察愈合过程的造粒组织形成和重塑阶段的开始。通过免疫组织化学染色,观察到早期阶段(0-3天)处的负VEGF基因表达,并且均未检测CD68 +巨噬细胞和α-SMA +肌纤维细胞。通过增加伤口(5-7天)(5-7天),观察造粒组织和血管生成,巨噬细胞和成纤维细胞的迁移,其表达VEGF,CD68和α-SMA阳性反应。上述标记的时间依赖性表达表明它们将是测定伤口年龄的有用指标。 VEGF和转化生长因子-β1(TGFB1)mRNA水平均在不同的皮肤伤口中测定。 TGFB1和VEGF的转录在伤害后不久会增加,直至伤后第7天。然后持续下降,第14天达到最小值。

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