艾灸及艾烟调控p38 MAPK/NF-κB信号通路改善 哮喘大鼠气道炎症的机制研究
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1.河南中医药大学;2.河南中医药大学第三附属医院

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国家自然科学基金面上项目(No. 82074562);河南省科技攻关计划项目(No. 242102310543);国家自然科学基金青年科学(No. 81704174)


The effect of moxibustion and moxa smoke on the airway inflammation in the asthmatic rats by regulating the p38 MAPK/NF-κB signaling pathway
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1.Henan University of Chinese Medicine;2.The Third Affiliated Hospital of Henan University of Chinese Medicine

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    摘要:

    【】 目的 基于p38 MAPK/NF-κB信号通路,探讨艾灸及艾烟改善哮喘大鼠气道炎症的作用机制。方法 SD雄性大鼠随机分为正常组、模型组、地塞米松组、艾灸组、无烟艾灸组、艾烟熏吸组、香烟熏吸组,采用卵清白蛋白(OVA)致敏和激发建立哮喘大鼠模型,造模完成后,地塞米松组腹腔注射地塞米松磷酸钠溶液,艾灸组艾灸大鼠“肺俞”(双)、“大椎”、“风门”(双)穴30 min,无烟艾灸组治疗方法及疗程同艾灸组,以上干预均每日1次,连续14 d,模型组、正常组大鼠不做任何干预。观察大鼠肺组织病理学变化;酶联免疫吸附试验法(ELISA)法检测各组大鼠肺泡灌洗液中IL-4、IL-5、IL-13、iNOS含量;比色法检测大鼠肺组织中CAT活力及H2O2、NO的含量;免疫组化法检测大鼠肺组织中p-p38 MAPK、p38 MAPK、p-IκBα、IκBα、p-NF-κB p65、NF-κB p65蛋白的表达水平;实时荧光定量PCR法检测大鼠肺组织中p38 MAPK、IκBα、NF-κB p65 mRNA的表达水平。结果:与模型组相比,地塞米松组、艾灸组、无烟艾灸组肺组织病理形态均有不同程度的缓解,肺泡灌洗液中IL-4、IL-5、IL-13和iNOS含量显著降低(P<0.01),肺组织中H2O2、NO含量显著降低,CAT含量显著升高(P<0.01),肺组织p-p38 MAPK、p38 MAPK、p-IκBα、NF-κB p65和p-NF-κB p65蛋白表达量均明显降低(P<0.01),IκBα蛋白表达量明显升高(P<0.01),肺组织中p38 MAPK、NF-κB p65 mRNA表达量均明显降低,IκBα mRNA明显升高。与地塞米松组比较,艾灸组与无烟艾灸组以上指标差异无统计学意义(P>0.05)。与无烟艾灸组比较,艾灸组以上指标差异有统计学意义(P<0.05),表明艾烟在艾灸中起着不可缺少的作用。结论:艾灸及艾烟可能通过抑制p38 MAPK/NF-κB信号通路激活改善OVA诱导的哮喘大鼠的炎症反应。

    Abstract:

    【】Objective: To explore the mechanism of moxibustion and moxa smoke on airway inflammation in asthmatic rats based on the p38 MAPK/NF-κB signaling pathway. Methods: Male Sprague-Dawley (SD) rats were randomly divided into normal group, model group, dexamethasone group, moxibustion group, smokeless moxibustion group, moxa smoke inhalation group, and cigarette smoke inhalation group. The asthmatic rat model was established by ovalbumin (OVA) sensitization and challenge. After successful modeling, rats in the dexamethasone group received intraperitoneal injection of dexamethasone sodium phosphate solution. Rats in the moxibustion group were treated with moxibustion at bilateral Feishu (BL13), Dazhui (GV14), and bilateral Fengmen (BL12) acupoints for 30 min. The treatment method and course of the smokeless moxibustion group were identical to those of the moxibustion group. All interventions were performed once daily for 14 consecutive days. Rats in the model group and normal group received no intervention.Pathological changes of rat lung tissues were observed. The levels of IL-4, IL-5, IL-13 and iNOS in bronchoalveolar lavage fluid (BALF) were detected by enzyme-linked immunosorbent assay (ELISA). The activity of catalase (CAT) and the contents of H2O2 and NO in lung tissues were measured by colorimetry. The expression levels of p-p38 MAPK, p38 MAPK, p-IκBα, IκBα, p-NF-κB p65 and NF-κB p65 proteins in lung tissues were determined by immunohistochemistry. The mRNA expression levels of p38 MAPK, IκBα and NF-κB p65 in lung tissues were detected by quantitative real-time fluorescence polymerase chain reaction (qRT-PCR). Results:Compared with the model group, the pathological morphology of lung tissues was alleviated to varying degrees in the dexamethasone group, moxibustion group and smokeless moxibustion group. The levels of IL-4, IL-5, IL-13 and iNOS in BALF were significantly decreased (P<0.01); the contents of H2O2 and NO in lung tissues were markedly reduced, while CAT activity was significantly increased (P<0.01). The protein expression levels of p-p38 MAPK, p38 MAPK, p-IκBα, IκBα, p-NF-κB p65 and NF-κB p65 in lung tissues were significantly down-regulated (P<0.01), whereas the protein expression of IκBα was significantly up-regulated (P<0.01). The mRNA expression levels of p38 MAPK and NF-κB p65 in lung tissues were significantly decreased, and the mRNA expression of IκBα was significantly increased.There were no statistically significant differences in the above indexes between the moxibustion group, smokeless moxibustion group and dexamethasone group (P>0.05). Statistically significant differences in the above indexes were found between the moxibustion group and the smokeless moxibustion group (P<0.05), suggesting that moxa smoke plays an indispensable role in moxibustion.

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  • 收稿日期:2026-03-06
  • 最后修改日期:2026-07-09
  • 录用日期:2026-08-24
  • 在线发布日期: 2026-08-24
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