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李娟丽, 席克虎, 侯赟等. 18β-甘草次酸对变应性鼻炎大鼠鼻黏膜中CCL11、AQP1和EOS表达的影响[J]. 四川大学学报(医学版), 2015, 46(3): 389-393.
引用本文: 李娟丽, 席克虎, 侯赟等. 18β-甘草次酸对变应性鼻炎大鼠鼻黏膜中CCL11、AQP1和EOS表达的影响[J]. 四川大学学报(医学版), 2015, 46(3): 389-393.
LI Juan-li, XI Ke-hu, HOU Yun. et al. Effects of 18β-glycyrrhetinic Acid on the Expression of CCL11, AQP1 and EOS in Nasal Mucosa of AllergicRhinitis Rats[J]. Journal of Sichuan University (Medical Sciences), 2015, 46(3): 389-393.
Citation: LI Juan-li, XI Ke-hu, HOU Yun. et al. Effects of 18β-glycyrrhetinic Acid on the Expression of CCL11, AQP1 and EOS in Nasal Mucosa of AllergicRhinitis Rats[J]. Journal of Sichuan University (Medical Sciences), 2015, 46(3): 389-393.

18β-甘草次酸对变应性鼻炎大鼠鼻黏膜中CCL11、AQP1和EOS表达的影响

Effects of 18β-glycyrrhetinic Acid on the Expression of CCL11, AQP1 and EOS in Nasal Mucosa of AllergicRhinitis Rats

  • 摘要: 目的 观察18β-甘草次酸(glycyrrhetinic acid,GA)对变应性鼻炎(allergic rhinitis,AR)大鼠鼻黏膜中嗜酸粒细胞趋化因子11(CCL11)、水通道蛋白1(AQP1)和嗜酸粒细胞(EOS)表达的影响。方法 将Wistar大鼠随机分为生理盐水对照(NC)组、AR模型(AR)组、氯雷他定(LOA)组、18β-GA组。1~14 d腹腔注射卵清蛋白(OVA)和Al(OH)3基础致敏,14~21 d用OVA鼻腔激发建立AR模型,NC组均以生理盐水替代。第21 d始LOA和18β-GA组分别给予氯雷他定和18β-GA每日1次灌胃,NC与AR组以生理盐水替代。干预1、2、3周后比较各组大鼠行为学评分,取大鼠鼻黏膜行实时荧光定量PCR(RT-QPCR)检测CCL11基因、免疫组化(SP法)检测AQP1表达程度,HE染色观察鼻黏膜组织结构和EOS浸润程度。结果 AR组大鼠1、2、3周时均出现典型AR症状,行为学叠加评分>5分,鼻黏膜中CCL11、AQP1表达和EOS浸润较NC组增强(P<0.05);各时间点,LOA组大鼠上述结果均低于AR组(P<0.05);18β-GA组大鼠1周时上述各结果与AR组比较下降(P<0.05),2周后各结果接近于LOA组、NC组(P>0.05)。结论 18β-GA干预可降低CCL11、AQP1的表达水平及EOS浸润程度,抑制AR进展。

     

    Abstract: Objective To investigate the effects of 18β-glycyrrhetinic acid (GA) on the expression of eotaxin 1 (CCL11), aquaporin protein 1 (AQP1) and eosinophil (EOS) in nasal mucosa of allergic rhinitis (AR) rats. Methods Seventy six Wistar rats were randomly divided into 4 groups,normal control (NC) group, AR model (AR) group, loratadine (LOA) group and 18β-GA group.All the mice in AR, LOA and 18β-GA groups were sensitized intraperitoneally with OVA and AL(OH)3 from day 1-14, then induced by intranasal administration with OVA from day 14-21, while the mice in NC group were sensitized with saline. The mice in both LOA and 18β-GA group were given LOA and 18β-GA once a day respectively from the 21 d, while the mice in AR and NC groups were administrated with saline.At the end of 1 week, 2 weeks and 3 weeks, the behavioral changes of mice were observed and recorded, the level of CCL11 mRNA was measured by RT-QPCR, and AQP1 expression was investiaged by SP staing.EOS in nasal mucosa was studied with the methods of HE staining. Results Compared with NC group , AR group showed typical AR symptoms. With the treatments,AR symptom scores and the expression levels of CCL11, AQP1 and EOS in nasal mucosa were improved significantly (P<0.05). When compared with AR group, the above statistics in LOA group were down-regulated evidently at different points in time (P<0.05).At the end of 1 week, the above detection results in 18β-GA group were lower than those in AR group (P<0.05).At the end of 2 weeks, those parameters approached to the levels of LOA and NC group significantly. Conclusion 18β-GA administration could down-regulate the expression levels of CCL11, AQP1 and EOS in nasal mucosa of allergic rhinitis rats and cast effects on inhibiting the progress of AR.

     

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