Article(id=1307264800841556307, tenantId=1146029695717560320, journalId=1302318977290174537, issueId=1307264617252680149, articleNumber=null, orderNo=null, doi=10.19664/j.cnki.1002-2392.260154, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1751472000000, receivedDateStr=2025-07-03, revisedDate=1773244800000, revisedDateStr=2026-03-12, acceptedDate=null, acceptedDateStr=null, onlineDate=1789605816325, onlineDateStr=2026-09-17, pubDate=1787155200000, pubDateStr=2026-08-20, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1789605816325, onlineIssueDateStr=2026-09-17, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1789605816325, creator=13701087609, updateTime=1789605816325, updator=13701087609, issue=Issue{id=1307264617252680149, tenantId=1146029695717560320, journalId=1302318977290174537, year='2026', volume='54', issue='8', pageStart='1', pageEnd='128', issueExtLink='null', onlineDate='null', pubDate='1787155200000', pubDateStr='2026-08-20', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1789605772555, creator='13701087609', updateTime=1789605772555, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=6, endPage=13, ext={EN=ArticleExt(id=1307264800996745556, articleId=1307264800841556307, tenantId=1146029695717560320, journalId=1302318977290174537, language=EN, title=Therapeutic Effect and Mechanism of Xiaoqinglong Decoction in Treating Allergic Rhinitis via Activating Autophagy and Inhibiting the IL-33/ST2 Pathway, columnId=null, journalTitle=Acta Chinese Medicine and Pharmacology, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective:

To investigate the potential mechanism of Xiaoqinglong Decoction (XQLD) in treating allergic rhinitis (AR) through autophagy and the IL -33/ST2 pathway.

Methods:

An ovalbumin (OVA)-sensitized mouse model of allergic rhinitis was established. Twenty-four mice were randomly assigned to four groups: control group, model group, dexamethasone (Dex) group, and XQLD group. All groups except the control received intraperitoneal injections of PBS containing 50 μg OVA and 2 mg aluminum hydroxide on days 1, 7, and 14 for sensitization. From days 21 to 27, mice were challenged intranasally with 400 μg OVA every 24 hours (4 total challenges). Interventions: The XQLD group received XQLD (10. 14 g/kg), the dexamethasone group received dexamethasone disodium phosphate (1 mg/kg), while the model and control groups received equivalent volumes of PBS. All treatments were administered once daily via gavage for 7 days. At 24 h after the final challenge, nasal symptoms (sneezing, scratching, rhinorrhea) were evaluated using a double-blind protocol. Serum was collected for the detection of OVA-specific IgE (OVA-sIgE) and Th1/Th2 cytokines (IL-2, IL-12, IL-5, IL-13) using ELISA. Nasal mucosa tissues underwent Hematoxylin and Eosin (H&E) staining, and immunohistochemical analysis was performed for IL-2, IL-12, IL-5, IL-13, IL-33, ST2, Beclin1, and P62.

Results:

compared to the control group, mice in the model group exhibited significantly elevated symptom scores (P < 0.01). The nasal mucosa showed pathological changes including epithelial desquamation, vasodilation, glandular hyperplasia, and extensive inflammatory cell infiltration. Serum OVA-sIgE, IL-5, and IL-13 levels were significantly increased (P < 0.01), while IL-2 and IL-12 levels were decreased (P < 0.01). In nasal mucosa tissue, the protein expression of IL-5, IL-13, IL-33, ST2, and P62 was elevated (P < 0.01), whereas the expression of IL-2, IL-12, and Beclin1 was decreased (P < 0.01). Compared to the model group, mice treated with XQLD and Dex groups showed significantly reduced symptom scores (P < 0.01) and improved nasal mucosal pathology. Serum OVA-sIgE, IL-5, and IL-13 levels decreased (P <0.01), while IL-2 and IL-12 levels increased (P <0.01). In nasal mucosa tissue, the protein expression of IL-2, IL-12, and Beclin1 increased (P <0.01), while the expression of IL-5, IL-13, IL-33, ST2, and P62 decreased (P < 0.01). No statistically significant differences were observed between the XQLD group and the Dex group regarding symptom scores, serum IL-2, IL-12, IL-5, OVA- sIgE levels, and nasal mucosa tissue IL-2, IL-12, IL-5, IL-13, Beclin1, and P62 protein expression (P >0.05).

Conclusion:

XQLD alleviates nasal symptoms and pathological damage in AR mice by synergistically regulating Th1/Th2 immune balance through autophagy activation and IL -33/ST2 pathway inhibition.

, authors=Yunsong LI1, Ronggang YANG1, *, Youqing LIANG2, authorsList=Yunsong LI, Ronggang YANG, Youqing LIANG, authorCompany=null, correspAuthors=Ronggang YANG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1307264801424564565, articleId=1307264800841556307, tenantId=1146029695717560320, journalId=1302318977290174537, language=CN, title=小青龙汤通过激活自噬与抑制IL-33/ ST2通路治疗变应性鼻炎的作用及机制研究, columnId=1303760926633652690, journalTitle=中医药学报, columnName=实验研究, runingTitle=null, highlight=null, articleAbstract=
目的:

探讨小青龙汤通过自噬与IL -33/ST2通路治疗变应性鼻炎的可能作用机制。

方法:

采用卵清蛋白(OVA)致敏建立变应性鼻炎小鼠模型。24只小鼠随机分为对照组、模型组、地塞米松组及小青龙汤组。除对照组外,其余各组第1、7、14天腹腔注射含50 μg OVA与2 mg氢氧化铝的PBS溶液致敏;第21 ~ 27天每24 h鼻腔滴注400 μg OVA激发(共4次)。小青龙汤组给予小青龙汤(10.14 g/kg),地塞米松组给予地塞米松磷酸二钠(1 mg/kg),模型组和对照组给予对应量PBS,采用灌胃给药1次/d,共7 d。末次激发24 h后,通过双盲法评估鼻部症状(喷嚏、鼻痒、鼻涕)。采集血清应用ELISA法检测OVA-sIgE及Th1/Th2细胞因子(IL-2、IL-12、IL-5、IL-13),取鼻黏膜组织行HE染色及IL-2、IL-12、IL-5、IL-13、IL-33、ST2、Beclin1、P62免疫组化分析。

结果:

与对照组比较,模型组小鼠症状评分显著升高(P <0.01),鼻黏膜呈现上皮剥脱、血管扩张和腺体增生并伴有大量炎症浸润,血清OVA-sIgE、IL-5、IL-13水平显著升高(P <0.01),IL-2、IL-12水平降低(P <0.01),鼻黏膜组织IL-5、IL-13、IL-33、ST2、P62蛋白表达升高(P <0.01),IL-2、IL-12、Beclin1表达降低(P <0.01)。与模型组比较,小青龙汤组及地塞米松组小鼠症状评分显著降低(P <0.01),鼻黏膜病理改善,血清OVA-sIgE、IL-5、IL-13降低(P <0.01)而IL-2、IL-12升高(P <0.01),鼻黏膜组织IL-2、IL-12、Beclin1蛋白表达均升高(P <0.01),而IL-5、IL-13、IL -33、ST2、P62蛋白表达均降低(P <0.01)。与地塞米松组比较,小青龙汤组小鼠症状评分,血清IL-2、IL-12、IL-5、OVA-sIgE含量,鼻黏膜组织IL-2、IL-12、IL-5、IL-13、Beclin1和P62蛋白表达差异均无统计学意义(P >0.05)。

结论:

小青龙汤可以通过激活细胞自噬与抑制IL -33/ST2通路协同调节Th1/Th2免疫平衡显著缓解变应性鼻炎小鼠鼻部症状及鼻黏膜病理损伤。

, authors=李云松1, 杨荣刚1, *, 梁友情2, authorsList=李云松, 杨荣刚, 梁友情, authorCompany=null, correspAuthors=杨荣刚, authorNote=

李云松(1990-),男,硕士,主治医师,主要从事中西医结合治疗耳鼻喉疾病的研究。

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* 杨荣刚(1977-),男,博士,副教授,副主任医师,主要从事中医药对耳鼻喉疾病的研究。
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李云松(1990-),男,硕士,主治医师,主要从事中西医结合治疗耳鼻喉疾病的研究。

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李云松(1990-),男,硕士,主治医师,主要从事中西医结合治疗耳鼻喉疾病的研究。

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小青龙汤通过激活自噬与抑制IL-33/ ST2通路治疗变应性鼻炎的作用及机制研究
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李云松 1 , 杨荣刚 1, * , 梁友情 2
中医药学报 | 实验研究 2026,54(8): 6-13
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中医药学报 |实验研究 2026 , 54 (8) : 6 -13
小青龙汤通过激活自噬与抑制IL-33/ ST2通路治疗变应性鼻炎的作用及机制研究
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李云松1, 杨荣刚1, *, 梁友情2
作者信息
  • 1.贵州中医药大学,贵州 贵阳 550025
  • 2.贵州中医药大学第二附属医院,贵州 贵阳 550001
通讯作者:
* 杨荣刚(1977-),男,博士,副教授,副主任医师,主要从事中医药对耳鼻喉疾病的研究。
作者简介:

李云松(1990-),男,硕士,主治医师,主要从事中西医结合治疗耳鼻喉疾病的研究。

Therapeutic Effect and Mechanism of Xiaoqinglong Decoction in Treating Allergic Rhinitis via Activating Autophagy and Inhibiting the IL-33/ST2 Pathway
Yunsong LI1, Ronggang YANG1, *, Youqing LIANG2
Affiliations
  • 1.Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
  • 2.The Second Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang 550001, China
出版时间: 2026-08-20 doi: 10.19664/j.cnki.1002-2392.260154
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目的:

探讨小青龙汤通过自噬与IL -33/ST2通路治疗变应性鼻炎的可能作用机制。

方法:

采用卵清蛋白(OVA)致敏建立变应性鼻炎小鼠模型。24只小鼠随机分为对照组、模型组、地塞米松组及小青龙汤组。除对照组外,其余各组第1、7、14天腹腔注射含50 μg OVA与2 mg氢氧化铝的PBS溶液致敏;第21 ~ 27天每24 h鼻腔滴注400 μg OVA激发(共4次)。小青龙汤组给予小青龙汤(10.14 g/kg),地塞米松组给予地塞米松磷酸二钠(1 mg/kg),模型组和对照组给予对应量PBS,采用灌胃给药1次/d,共7 d。末次激发24 h后,通过双盲法评估鼻部症状(喷嚏、鼻痒、鼻涕)。采集血清应用ELISA法检测OVA-sIgE及Th1/Th2细胞因子(IL-2、IL-12、IL-5、IL-13),取鼻黏膜组织行HE染色及IL-2、IL-12、IL-5、IL-13、IL-33、ST2、Beclin1、P62免疫组化分析。

结果:

与对照组比较,模型组小鼠症状评分显著升高(P <0.01),鼻黏膜呈现上皮剥脱、血管扩张和腺体增生并伴有大量炎症浸润,血清OVA-sIgE、IL-5、IL-13水平显著升高(P <0.01),IL-2、IL-12水平降低(P <0.01),鼻黏膜组织IL-5、IL-13、IL-33、ST2、P62蛋白表达升高(P <0.01),IL-2、IL-12、Beclin1表达降低(P <0.01)。与模型组比较,小青龙汤组及地塞米松组小鼠症状评分显著降低(P <0.01),鼻黏膜病理改善,血清OVA-sIgE、IL-5、IL-13降低(P <0.01)而IL-2、IL-12升高(P <0.01),鼻黏膜组织IL-2、IL-12、Beclin1蛋白表达均升高(P <0.01),而IL-5、IL-13、IL -33、ST2、P62蛋白表达均降低(P <0.01)。与地塞米松组比较,小青龙汤组小鼠症状评分,血清IL-2、IL-12、IL-5、OVA-sIgE含量,鼻黏膜组织IL-2、IL-12、IL-5、IL-13、Beclin1和P62蛋白表达差异均无统计学意义(P >0.05)。

结论:

小青龙汤可以通过激活细胞自噬与抑制IL -33/ST2通路协同调节Th1/Th2免疫平衡显著缓解变应性鼻炎小鼠鼻部症状及鼻黏膜病理损伤。

小青龙汤  /  变应性鼻炎  /  自噬  /  IL -33/ST2通路  /  Th1/Th2平衡
Objective:

To investigate the potential mechanism of Xiaoqinglong Decoction (XQLD) in treating allergic rhinitis (AR) through autophagy and the IL -33/ST2 pathway.

Methods:

An ovalbumin (OVA)-sensitized mouse model of allergic rhinitis was established. Twenty-four mice were randomly assigned to four groups: control group, model group, dexamethasone (Dex) group, and XQLD group. All groups except the control received intraperitoneal injections of PBS containing 50 μg OVA and 2 mg aluminum hydroxide on days 1, 7, and 14 for sensitization. From days 21 to 27, mice were challenged intranasally with 400 μg OVA every 24 hours (4 total challenges). Interventions: The XQLD group received XQLD (10. 14 g/kg), the dexamethasone group received dexamethasone disodium phosphate (1 mg/kg), while the model and control groups received equivalent volumes of PBS. All treatments were administered once daily via gavage for 7 days. At 24 h after the final challenge, nasal symptoms (sneezing, scratching, rhinorrhea) were evaluated using a double-blind protocol. Serum was collected for the detection of OVA-specific IgE (OVA-sIgE) and Th1/Th2 cytokines (IL-2, IL-12, IL-5, IL-13) using ELISA. Nasal mucosa tissues underwent Hematoxylin and Eosin (H&E) staining, and immunohistochemical analysis was performed for IL-2, IL-12, IL-5, IL-13, IL-33, ST2, Beclin1, and P62.

Results:

compared to the control group, mice in the model group exhibited significantly elevated symptom scores (P < 0.01). The nasal mucosa showed pathological changes including epithelial desquamation, vasodilation, glandular hyperplasia, and extensive inflammatory cell infiltration. Serum OVA-sIgE, IL-5, and IL-13 levels were significantly increased (P < 0.01), while IL-2 and IL-12 levels were decreased (P < 0.01). In nasal mucosa tissue, the protein expression of IL-5, IL-13, IL-33, ST2, and P62 was elevated (P < 0.01), whereas the expression of IL-2, IL-12, and Beclin1 was decreased (P < 0.01). Compared to the model group, mice treated with XQLD and Dex groups showed significantly reduced symptom scores (P < 0.01) and improved nasal mucosal pathology. Serum OVA-sIgE, IL-5, and IL-13 levels decreased (P <0.01), while IL-2 and IL-12 levels increased (P <0.01). In nasal mucosa tissue, the protein expression of IL-2, IL-12, and Beclin1 increased (P <0.01), while the expression of IL-5, IL-13, IL-33, ST2, and P62 decreased (P < 0.01). No statistically significant differences were observed between the XQLD group and the Dex group regarding symptom scores, serum IL-2, IL-12, IL-5, OVA- sIgE levels, and nasal mucosa tissue IL-2, IL-12, IL-5, IL-13, Beclin1, and P62 protein expression (P >0.05).

Conclusion:

XQLD alleviates nasal symptoms and pathological damage in AR mice by synergistically regulating Th1/Th2 immune balance through autophagy activation and IL -33/ST2 pathway inhibition.

Xiaoqinglong Decoction  /  Allergic rhinitis  /  Autophagy  /  IL -33/ST2 pathway  /  Th1/Th2 balance
李云松, 杨荣刚, 梁友情. 小青龙汤通过激活自噬与抑制IL-33/ ST2通路治疗变应性鼻炎的作用及机制研究. 中医药学报, 2026 , 54 (8) : 6 -13 . DOI: 10.19664/j.cnki.1002-2392.260154
Yunsong LI, Ronggang YANG, Youqing LIANG. Therapeutic Effect and Mechanism of Xiaoqinglong Decoction in Treating Allergic Rhinitis via Activating Autophagy and Inhibiting the IL-33/ST2 Pathway[J]. Acta Chinese Medicine and Pharmacology, 2026 , 54 (8) : 6 -13 . DOI: 10.19664/j.cnki.1002-2392.260154
  • 国家自然科学基金项目(82260955)
  • 贵州省中医药管理局科研项目(QZYY-2020-003)
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2026年第54卷第8期
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doi: 10.19664/j.cnki.1002-2392.260154
  • 接收时间:2025-07-03
  • 首发时间:2026-09-17
  • 出版时间:2026-08-20
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  • 收稿日期:2025-07-03
  • 修回日期:2026-03-12
基金
国家自然科学基金项目(82260955)
贵州省中医药管理局科研项目(QZYY-2020-003)
作者信息
    1.贵州中医药大学,贵州 贵阳 550025
    2.贵州中医药大学第二附属医院,贵州 贵阳 550001

通讯作者:

* 杨荣刚(1977-),男,博士,副教授,副主任医师,主要从事中医药对耳鼻喉疾病的研究。
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
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