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依巴斯汀对Balb/c小鼠特应性皮炎模型的作用研究
引用本文:华思瑞,徐可佳,王琳. 依巴斯汀对Balb/c小鼠特应性皮炎模型的作用研究[J]. 中国麻风皮肤病杂志, 2022, 38(6): 355-358. DOI: 10.12144/zgmfskin202206355
作者姓名:华思瑞  徐可佳  王琳
作者单位:四川大学华西医院皮肤科,四川成都,610041
摘    要:目的:评价抗组胺药依巴斯汀对2,4-二硝基氟苯(DNFB)诱导的特应性皮炎(AD)小鼠模型的疗效及可能机制.方法:将18只6~8周龄Balb/c雌性小鼠随机分为治疗组、阴性对照组、空白对照组,每组6只.DNFB外涂小鼠背部皮肤制备AD小鼠模型,造模2周后治疗组和阴性对照组每天分别予0.2 mL(浓度为0.41 mg/m...

关 键 词:特应性皮炎  依巴斯汀  抗组胺药

Effect of ebastine on Balb/c mouse model of atopic dermatitis
HUA Sirui,XU Kejia,WANG Lin. Effect of ebastine on Balb/c mouse model of atopic dermatitis[J]. China Journal of Leprosy and Skin Diseases, 2022, 38(6): 355-358. DOI: 10.12144/zgmfskin202206355
Authors:HUA Sirui  XU Kejia  WANG Lin
Affiliation:West China Hospital, Sichuan University, Chengdu 610041, China
Abstract:Objective: To access the effect and possible mechanism of antihistamine ebastine on atopic dermatitis (AD) mouse model induced by 2,4-dinitrofluorobenzene (DNFB). Methods: Eighteen Balb/c female mice aged 6-8 weeks were randomly divided into treatment group, negative control group and blank group. The AD mouse model was prepared by coating DNFB on the back skin of mice, and the mice in the blank group were not treated. After 2 weeks of modeling, the treatment group was given ebastine of concentration of 0.41 mg/mL, 0.2mL, by gavage, once a day, and the negative control group was given the same amount of normal saline. After 2 weeks of administration, the changes of body weight, skin lesion and scratching behavior of mice were assessed, the thickness of skin lesions and the number of eosinophils were observed by HE staining, and the level of serum interleukin-4 (IL-4) was detected by ELISA. Results: Typical AD lesions such as erythema, edema, exudation, crust and skin thickening appeared in the back skin of the model mice. The weight of mice in the treatment group and the blank group increased after the experiment (P<0.05), but there was no significant change in the negative control group (P>0.05). Compared with the negative control group, there was no significant difference in the score of skin lesion in the treatment group before treatment (P>0.05). After treatment, the score of skin lesion in the treatment group decreased significantly (P<0.05). In addition, the scratching times, epidermal thickness, eosinophil number and serum IL-4 in the treatment group were lower than those in the negative control group (P<0.05). Conclusion: Ebastine has certain therapeutic effect on AD mouse model, which may through inhibiting Th2 immune response in vivo.
Keywords:atopic dermatitis  ebastine  antihistamine  
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