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首页|期刊导航|浙江中医药大学学报|葛根素调控P2X7/NLRP3通路影响过敏性鼻炎小鼠肥大细胞活性

葛根素调控P2X7/NLRP3通路影响过敏性鼻炎小鼠肥大细胞活性

王娇娇 程静凯 王娟 朱珊

浙江中医药大学学报2025,Vol.49Issue(9):1105-1114,10.
浙江中医药大学学报2025,Vol.49Issue(9):1105-1114,10.DOI:10.16466/j.issn1005-5509.2025.09.003

葛根素调控P2X7/NLRP3通路影响过敏性鼻炎小鼠肥大细胞活性

Effect of Puerarin Regulating the P2X7/NLRP3 Pathway on the Activity of Mast Cells in Mice with Allergic Rhinitis

王娇娇 1程静凯 2王娟 1朱珊3

作者信息

  • 1. 河南中医药大学第五临床医学院(郑州人民医院) 郑州 450000
  • 2. 河南省中医院(河南中医药大学第二附属医院)
  • 3. 河南中医药大学第二临床医学院
  • 折叠

摘要

Abstract

[Objective]To investigate the effects of puerarin regulation of purinergic receptor P2X ligand-gated ion channel 7(P2X7)/nucleotide-binding oligomeric domain receptor protein 3(NLRP3)pathway on mast cell activity in mice with allergic rhinitis(AR).[Methods]BALB/c mice were randomly divided into normal group,AR group,puerarin low-dose group,puerarin high-dose group,dexamethasone group,puerarin high-dose+P2X7 activator adenosine triphosphate(ATP)group,with 12 mice in each group.Except for normal group and the AR mouse models in the other groups received intraperitoneal ovalbumin-alum sensitization followed by intranasal ovalbumin challenge to induce AR.After successful modeling,the puerarin low-and high-dose groups were intragastrically administered with puerarin at 12.5 mg·kg-1 and 50 mg·kg-1 respectively;the dexamethasone group was intragastrically administered with dexamethasone at 1 mg·kg-1;the puerarin high-dose+ATP group was intragastrically administered with puerarin at 50 mg·kg-1,and simultaneously injected with ATP(7.5×10-3 mmol per mouse)via the tail vein;the normal group and the AR group were given equal amounts of 0.9%sodium chloride solution via both intragastric administration and tail vein injection.The treatment was performed once a day for 14 consecutive days.AR score,serum immunoglobulin E(IgE),leukotriene,histamine,tumor necrosis factor-α(TNF-α),interleukin-18(IL-18)and IL-1β levels were detected.Hematoxylin-eosin(HE)staining was used to detect nasal mucosa pathological Change.The number of mast cells,the number of degranulated mast cells and the degranulated rate were detected by toluidine blue staining.The mean optical density of Tryptase expression in nasal mucosa was detected by immunohistochemical staining.The expressions of P2X7,NLRP3,cleaved-Caspase-1 proteins in nasal mucosa were measured by Western blot.[Results]Compared with normal group,the nasal mucosal epithelium in AR group was significantly thickened,accompanied with a large number of inflammatory cell infiltration and significant mucosal interstitial edema.The levels of AR score,serum IgE,leukotriene,histamine and TNF-α,IL-18,IL-1β were raised(P<0.05).What's more,the number of mast cells and the number of degranulated mast cells were increased,with a corresponding rise in the degranulation rate(P<0.05).The mean optical density of Tryptase expression,as well as the expressions of P2X7,NLRP3 and cleaved-Caspase-1 in nasal mucosa were all amplified(P<0.05).Compared with AR group,the pathological injury of nasal mucosa in puerarin low-dose group,puerarin high-dose group and dexamethasone group was reduced.The levels of AR score,serum IgE,leukotriene,histamine,TNF-α,IL-18 and IL-1β were decreased.Additionally,the number of mast cells and the number of degranulated mast cells were reduced,with a corresponding decrease in the degranulation rate.The mean optical density of Tryptase expression,as well as the expressions of P2X7,NLRP3 and cleaved-Caspase-1 in nasal mucosa were also diminished(P<0.05).Compared with the puerarin high-dose group,the puerarin high-dose+ATP group showed more severe pathological damage to nasal mucosal tissues.The AR score,serum levels of IgE,leukotrienes,histamine,TNF-α,IL-18 and IL-1β were increased.Meanwhile,the number of mast cells and degranulated mast cells,the degranulation rate were significantly added,and the mean optical density of Tryptase expression,and the expressions of P2X7,NLRP3 and cleaved-Caspase-1 in nasal mucosa tissues were all amplified(P<0.05).[Conclusion]Puerarin may reduce the activity of mast cells in AR model mice by inhibiting the P2X7/NLRP3 pathway.

关键词

过敏性鼻炎/葛根素/P2X7/NLRP3通路/肥大细胞/脱颗粒/小鼠/鼻黏膜/炎症

Key words

allergic rhinitis/puerarin/P2X7/NLRP3 pathway/mast cells/degranulation/mice/nasal mucosa/inflammation

分类

医药卫生

引用本文复制引用

王娇娇,程静凯,王娟,朱珊..葛根素调控P2X7/NLRP3通路影响过敏性鼻炎小鼠肥大细胞活性[J].浙江中医药大学学报,2025,49(9):1105-1114,10.

基金项目

河南省自然科学基金面上项目(232300421188) He'nan Natural Science Foundation General Research Project(232300421188) (232300421188)

浙江中医药大学学报

1005-5509

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