通气障碍小鼠动物模型嗅黏膜的组织学变化
发布时间:2018-03-22 13:20
本文选题:通气障碍 切入点:嗅黏膜 出处:《中国医科大学》2010年硕士论文 论文类型:学位论文
【摘要】: 目的 构建通气障碍小鼠动物的模型,观察不同时间点嗅黏膜的组织学变化情况。 方法 刚出生的昆明小鼠50只,随机分为实验组(20只)、对照组(30只)。实验组小鼠出生后立即在显微镜下用9-0线缝合左侧前鼻孔,造成左侧前鼻孔闭锁。术后第2周、4周、6周、8周时处理小鼠。嗅黏膜HE染色后,观察小鼠嗅上皮的厚度、细胞数量的变化;并且行免疫组织化学染色,用显微镜观察小鼠嗅上皮中成熟的嗅感觉神经元(olfactory receptor neurons, ORNs)及嗅黏膜的组织学变化情况。 结果 刚出生的小鼠(作为阳性对照和阴性对照),两侧鼻腔嗅上皮厚度、成熟的嗅感觉神经元数量大致相同。缝合小鼠左侧前鼻孔术后第2周时,与对照组同侧相比,实验组嗅上皮略薄、OMP阳性细胞数略少。第4周时,嗅上皮较明显变薄、OMP阳性细胞数较明显变少。第6周时,嗅上皮显著变薄、OMP阳性细胞数显著减少且降至最低水平,说明此时缝合小鼠左侧前鼻孔造成的影响已经达到最大程度。第8周时,嗅上皮略薄、OMP阳性细胞数略少且基本恢复至2周时水平。 结论 每个时间点上,实验组和对照组小鼠左侧鼻腔嗅黏膜的组织学情况都有差异,两组间嗅上皮OMP阳性细胞数的差异有统计学意义,说明缝合小鼠左侧前鼻孔可导致同侧鼻腔嗅上皮厚度变薄、成熟的嗅感觉神经元数量减少。 第6周时,实验组左侧鼻腔嗅上皮厚度、OMP阳性细胞数均降至最低水平,说明此时,缝合小鼠前鼻孔对嗅黏膜及成熟嗅感觉神经元造成的影响已经达到最大程度。 第8周时,嗅上皮厚度和OMP阳性细胞数基本恢复至2周时水平,可能提示:在本实验方法下,小鼠嗅感觉神经元的再生周期约为6周。 本实验显微镜下缝合小鼠前鼻孔,它可以作为构建通气障碍小鼠动物模型的可靠方法。
[Abstract]:Purpose. To establish the animal model of ventilatory disturbance and observe the histological changes of olfactory mucosa at different time points. Method. Fifty newly born Kunming mice were randomly divided into experimental group (n = 20) and control group (n = 30). The left anterior nostril atresia was caused. The mice were treated at 4 weeks and 6 weeks and 8 weeks after operation. After HE staining of olfactory mucosa, the thickness of olfactory epithelium and the number of cells in the olfactory epithelium were observed. The histological changes of olfactory receptor neurons (ORNs) and olfactory mucosa in the olfactory epithelium of mice were observed by microscope. Results. The thickness of nasal olfactory epithelium and the number of mature olfactory sensory neurons were approximately the same in newly born mice (as positive and negative controls). At the second week after the left anterior nostril was sutured, the thickness of olfactory epithelium on both sides of the nasal cavity was similar to that in the control group. In the experimental group, the number of OMP positive cells in the OMP cells was slightly smaller. At the 4th week, the number of OMP positive cells in the olfactory epithelium became significantly thinner than that in the OMP positive cells. At the 6th week, the number of OMP positive cells in the olfactory epithelium decreased significantly and decreased to the lowest level. At 8 weeks, the number of OMP positive cells in the olfactory epithelium was slightly smaller and returned to the level of 2 weeks after the left anterior nostril was sutured. Conclusion. At each time point, there were significant differences in the number of OMP positive cells in the olfactory epithelium between the experimental group and the control group. The results showed that the thickness of olfactory epithelium in the ipsilateral nasal cavity was thinned and the number of mature olfactory sensory neurons was decreased after the left anterior nostril was sutured. At the 6th week, the number of OMP positive cells in the left nasal cavity of the experimental group was reduced to the lowest level, indicating that the effect of the anterior nostril suture on the olfactory mucosa and mature olfactory sensory neurons in the experimental group had reached the maximum extent. At the 8th week, the thickness of olfactory epithelium and the number of OMP positive cells returned to the level of 2 weeks, which suggested that the regeneration period of olfactory sensory neurons in mice was about 6 weeks. The anterior nostril of mice was sutured under microscope. It can be used as a reliable method to construct the animal model of ventilatory disorders in mice.
【学位授予单位】:中国医科大学
【学位级别】:硕士
【学位授予年份】:2010
【分类号】:R-332;R361
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