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. 2020 Oct;34(10):932-936.
doi: 10.13201/j.issn.2096-7993.2020.10.015.

[The experimental study on the biological rhythm expression of substance P in allergic airway inflammation mice]

[Article in Chinese]
Affiliations

[The experimental study on the biological rhythm expression of substance P in allergic airway inflammation mice]

[Article in Chinese]
Ting Zhang et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Oct.

Abstract

Objective:To establish the murine models of allergic airway inflammation, and to investigate the biological rhythm expression of substance P in it. Method:Eighty-four BALB/c mice were divided into 14 groups, which were airway inflammation groups(0: 00 group, 04: 00 group, 08: 00 group, 12: 00 group, 16: 00 group, 20: 00 group, 24: 00 group) and normal control groups(0: 00 group, 04: 00 group, 08: 00 group, 12: 00 group, 16: 00 group, 20: 00 group, 24: 00 group). The allergic airway inflammation models of mice were established by intraperitoneal injection of ovalbumin(OVA), nasal challenge and aerosol inhalation with OVA. The plasma substance P levels were measured by ELISA. The expression of substance P in nasal mucosa, left lung tissue and left bronchial tissue during different time periods was obversed with RT-PCR and immunohistochemical technique. Result:In allergic airway inflammation groups, the plasma substance P levels were higher than in normal control groups(P<0.05), and 0: 00 group(321.99±28.93) pg/mL, 04: 00 group(310.76±25.31) pg/mL and 24: 00 group(335.62±28.29) pg/mL were higher than other experimental groups(P<0.05). The expression of substance P mRNA in nasal mucosa, left lung tissue and left bronchial tissue was higher than control groups(P<0.01). By observing immunohistochemical sections, the expression of substance P in allergic airway inflammation groups was higer than control groups. Conclusion:The expression of substance P is high in allergic airway inflammation mice and the peaks are during 04: 00-08: 00 in the early morning, which may provide new basis for treating allergic airway inflammation.

目的:建立变应性气道炎症小鼠模型,探讨P物质在变应性气道炎症小鼠中的生物节律性表达。 方法:将84只BABL/c小鼠随机分为14个组,分别为实验组7组(0:00组,04:00组,08:00组,12:00组,16:00组,20:00组,24:00组)和对照组7组(0:00组,04:00组,08:00组,12:00组,16:00组,20:00组,24:00组),每组6只。采用卵清蛋白腹腔注射+鼻腔局部激发+雾化吸入的方法制备小鼠变应性气道炎症模型。对实验动物血液进行ELISA法测量上清液P物质含量,采用RT-PCR技术检测不同时间段内P物质在鼻腔组织、肺组织及支气管组织中基因表达的分布及含量。取小鼠鼻腔组织、左肺组织及左主支气管组织行免疫组织化学染色,观察组织切片中P物质阳性细胞的表达及分布。 结果:实验组各时间段内血浆中P物质含量明显高于对照组(P<0.05),其中,实验组中0:00组(321.99±28.93) pg/mL、04:00组(310.76±25.31) pg/mL及24:00组(335.62±28.29) pg/mL的P物质含量明显高于实验组其他时间段(P<0.05)。实验组小鼠鼻腔组织、左肺组织及左主支气管组织中P物质mRNA表达明显高于对应的对照组(P<0.01)。实验组小鼠鼻腔组织、左肺及左主支气管免疫组织化学切片中P物质表达显著高于对照组。 结论:P物质在变应性气道炎症小鼠模型中呈现高表达,且在凌晨及上午04:00~08:00表达出现峰值,这可能为治疗变应性气道炎症的给药时间提供新的依据。.

Keywords: allergic airway inflammation; biological rhythm; substance P.

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Conflict of interest statement

The authors of this article and the planning committee members and staff have no relevant financial relationships with commercial interests to disclose.

Figures

图 1
图 1
造模周期图
图 2
图 2
血液与组织中P物质表达趋势
图 3
图 3
病理形态学观察

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