1. 长江大学医学院
2. 长江大学附属荆州临床医学院
3. 湖北中医药大学
4. 三峡大学
纸质出版:2016
移动端阅览
[1]丁建中,倪圣,张六通,黄江荣,肖长义.桑杏汤对温燥模型小鼠肺呼吸膜超微结构、表面活性物质及炎性细胞因子的影响[J].中医杂志,2016,57(12):1057-1060.
DING Jianzhong, NI Sheng, ZHANG Liutong, et al. Impact of Sangxing Decoction (桑杏汤) on Ultra Microstructure,Surface Active Substance and Inflammatory Cytokines of Pulmonary Respiratory Membrane of Mice Model of Warm Dryness[J]. Journal of Traditional Chinese Medicine2016, 57(12): 1057-1060.
[1]丁建中,倪圣,张六通,黄江荣,肖长义.桑杏汤对温燥模型小鼠肺呼吸膜超微结构、表面活性物质及炎性细胞因子的影响[J].中医杂志,2016,57(12):1057-1060. DOI: 10.13288/j.11-2166/r.2016.12.017.
DING Jianzhong, NI Sheng, ZHANG Liutong, et al. Impact of Sangxing Decoction (桑杏汤) on Ultra Microstructure,Surface Active Substance and Inflammatory Cytokines of Pulmonary Respiratory Membrane of Mice Model of Warm Dryness[J]. Journal of Traditional Chinese Medicine2016, 57(12): 1057-1060. DOI: 10.13288/j.11-2166/r.2016.12.017.
目的探讨桑杏汤"生津润燥"的可能分子机制。方法 110只小鼠随机分为常温常湿组、温燥模型组、温燥阴性治疗组和桑杏汤低、高剂量组
每组22只。采用"温度-相对湿度-风"综合条件建立温燥小鼠模型。造模6天后桑杏汤低、高剂量组分别给予桑杏汤0.009、0.018 g/(kg·d)灌胃
常温常湿组、温燥阴性治疗照组用等量无菌生理盐水灌胃
连续6天。观察各组小鼠气道与肺组织学变化并观察左肺中叶超微结构
检测肺组织水通道蛋白5(AQP5)mRNA和蛋白表达水平及气管肺泡灌洗液中黏多糖、无机磷、中性粒细胞弹性蛋白酶(NE)、a1-抗胰蛋白酶(a1-AT)、白细胞介素10(IL-10)和血小板活化因子(PAF)水平。结果与常温常湿组比较
温燥模型组小鼠气管及肺组织病理及超微组织均出现损伤
呼吸膜增厚
肺泡灌洗液黏多糖、无机磷、IL-10水平降低
PAF水平增高
AQP5 mRNA和蛋白表达降低(P<0.05或P<0.01)。与温燥模型组比较
桑杏汤低剂量组小鼠气管上皮化生、纤毛缺损与黏膜腺体化生减轻
呼吸膜平均厚度降低
肺泡灌洗液黏多糖、无机磷、a1-AT、IL-10水平增高但NE、PAF水平下降
肺组织AQP5 mRNA和蛋白表达升高(P<0.05或P<0.01)。结论桑杏汤"生津"可能与增加气道液和肺泡表面活性物质分泌、上调AQP5基因表达相关
"润燥"可能是抑制炎性细胞因子"级联反应"
以改善气道病理损伤。
Objective To explore the possible molecular mechanism of Sangxing Decoction in "promoting production of fluid and moistening dryness". Methods One hundred and ten mice were randomized into the normal temperature and humidity group
the warm dryness model group
the warm dryness negative treatment group
and the low and high dose Sangxing Decoction groups
with 22 mice in each group. Warm dryness mice were modeled by synthetic condition of "temperature-relative humidity-wind". After mice were modeled for 6 days
the low and high dose Sangxing Decoction groups were given Sangxing Decoction 0. 009
or 0. 018 g /( kg·d) by gavage
respectively
and the normal temperature and humidity group and the warm dryness negative treatment group were given equivalent sterile normal saline by gavage
all once daily for 6 days. Changes of mice’s airway and lung histology in each group were examined. Ultra microstructure of middle lobe of left lung was observed. The expressions of aquaporin 5( AQP5)mRNA and proteins in lung tissue
and the levels of mucoitin
inorganic phosphorus
neutrophil elastase( NE)
a1-antitrypsin( a1-AT)
interleukin 10( IL-10) and platelet activating factors( PAF) in bronchoalveolar lavage fluid were detected. Results Compared with the normal temperature and humidity group
there were pathological and ultrastructural damage in trachea and lung tissue of mice in the warm dryness model group. The respiratory membrane thickened. The levels of mucoitin
inorganic phosphorus and IL-10 in bronchoalveolar lavage fluid decreased. PAF increased. The expressions of AQP5 mRNA and proteins decreased( P < 0. 05 or P < 0. 01). Compared with the warm dryness model group
mice’s tracheal metaplasia
cilium defect and mucous membrane gland metaplasia in the low dose Sangxing Decoction group were improved. Average thickness of respiratory membrane decreased. The levels of mucoitin
inorganic phosphorus
a1-AT and IL-10 in bronchoalveolar lavage fluid increased; while the levels of NE and PAF decreased. The expressions of AQP5 mRNA and proteins in lung tissue increased( P < 0. 05 or P < 0. 01).Conclusion Sangxing Decoction "promoting production of fluid"might relate to increasing the secretion of airway fluid and alveolar surfactant
as well as up-regulating the gene expression of AQP5. "Moistening dryness"might be inhibiting the "cascade"of inflammatory cytokines. Thus airway pathological injury might be improved.
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