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河南中医药大学第三附属医院
纸质出版日期:2020
移动端阅览
胡晓京, 邵素菊, 华金双, 等. 针灸“肺俞”“大椎”“风门”对哮喘大鼠肺组织中CC趋化因子配体1、CC趋化因子受体8表达的影响[J]. 针刺研究, 2020,45(5):363-367.
HU Xiao-jing, SHAO Su-ju, HUA Jin-shuang, et al. Effect of acupuncture and moxibustion at “Feishu”“Dazhui” and “Fengmen” on the expression of CC chemokine ligand 1 and CC chemokine receptor 8 in lung tissue of rats with asthma[J]. Acupuncture research, 2020, 45(5): 363-367.
胡晓京, 邵素菊, 华金双, 等. 针灸“肺俞”“大椎”“风门”对哮喘大鼠肺组织中CC趋化因子配体1、CC趋化因子受体8表达的影响[J]. 针刺研究, 2020,45(5):363-367. DOI: 10.13702/j.1000-0607.190394.
HU Xiao-jing, SHAO Su-ju, HUA Jin-shuang, et al. Effect of acupuncture and moxibustion at “Feishu”“Dazhui” and “Fengmen” on the expression of CC chemokine ligand 1 and CC chemokine receptor 8 in lung tissue of rats with asthma[J]. Acupuncture research, 2020, 45(5): 363-367. DOI: 10.13702/j.1000-0607.190394.
目的:观察针灸对哮喘大鼠肺组织中CC趋化因子配体1(CCL1)、CC趋化因子受体8(CCR8)表达的影响
探讨针灸"肺俞""大椎""风门"治疗哮喘的作用机制。方法:将SD大鼠随机分为空白组、模型组、针刺组和艾灸组
每组10只。采用卵白蛋白腹腔注射致敏法制备哮喘大鼠模型。针刺组和艾灸组分别针刺"肺俞""大椎""风门"穴20 min或回旋灸10 min进行治疗
每天1次
共治疗7 d。HE染色法观察各组大鼠肺组织形态学改变;荧光定量PCR法检测肺组织中信号转导和转录激活因子6(STAT6)mRNA的表达;免疫组织化学法检测肺组织中CCL1和CCR8蛋白表达。结果:空白组大鼠支气管管腔规则
支气管周围未见炎性细胞浸润
肺泡排列规律;模型组大鼠支气管周围有大量炎性细胞浸润和聚集
支气管管腔狭窄、管壁增厚
肺泡结构紊乱;针刺组和艾灸组支气管周围有少量炎性细胞
支气管管腔狭窄、管壁增厚程度均较模型组轻
肺泡排列较规则。模型组肺组织中CCL1、CCR8蛋白及STAT6 mRNA表达明显高于空白组(P<0.05);针刺组、艾灸组CCL1、CCR8蛋白及STAT6 mRNA表达较模型组明显减少(P<0.05)。结论:针灸能通过抑制肺组织中CCL1、CCR8蛋白及STAT6 mRNA的表达干预气道炎性反应
这可能是针灸治疗哮喘的作用机制之一。
Objective To investigate the protein expression of CC chemokine ligand 1(CCL1) and CC chemokine receptor 8(CCR8) in the lung tissue of rats and the mechanism of acupuncture and moxibustion at "Feishu"(BL13)
"Dazhui"(GV14) and "Fengmen"(BL12) in the treatment of asthma. Methods Sprague-Dawley rats were randomly divided into blank
model
acupuncture and moxibustion groups
n=10 in each group. Ovalbumin sensitization via intraperitoneal injection was performed to establish a model of asthma. The rats in the acupuncture group and the moxibustion group were given acupuncture for 20 min or circling moxibustion for 10 min at BL13
GV14 and BL12
once a day for 7 days. H.E. staining was used to observe the morphological changes of lung tissue. Real-time fluorescence quantitative PCR was used to measure the mRNA expression of signal transducer and activator of transcription 6(STAT6) in lung tissue and immunohistochemistry was used to measure the protein expression of CCL1 and CCR8 in lung tissue. Results H.E. staining showed that the rats in the blank group had regular bronchial lumens and alveolar arrangement
with no inflammatory cell infiltration and aggregation around the bronchi; the rats in the model group had the infiltration and aggregation of a large number of inflammatory cells around the bronchi
stenosis of bronchial lumens
wall thickening
and alveolar structural disorder; compared with the model group
the acupuncture group and the moxibustion group had lower degrees of inflammatory cell infiltration and aggregation around the bronchi
stenosis of bronchial lumens
and wall thickening
as well as regular alveolar arrangement. The model group had significantly higher protein expression of CCL1 and CCR8 and mRNA expression of STAT6 than the blank group(P<0.05)
and the acupuncture group and the moxibustion group had significantly lower protein expression of CCL1 and CCR8 and mRNA expression of STAT6(P<0.05). Conclusion Acupuncture and moxibustion can intervene against airway inflammation by inhibiting the protein expression of CCL1 and CCR8 and STAT6 signal transduction in lung tissue
which may be one of the mechanisms of acupuncture and moxibustion in the treatment of asthma.
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