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纸质出版日期:2017
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薛晓明, 王洋, 赵勤萍, 等. 宣肺平喘胶囊对慢性阻塞性肺疾病大鼠模型的影响[J]. 中国实验方剂学杂志, 2017,23(2):120-125.
XUE Xiao-ming, WANG Yang, ZHAO Qin-ping, et al. Effect of Xuanfei Pingchuan Capsules on Rat COPD Model[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(2): 120-125.
薛晓明, 王洋, 赵勤萍, 等. 宣肺平喘胶囊对慢性阻塞性肺疾病大鼠模型的影响[J]. 中国实验方剂学杂志, 2017,23(2):120-125. DOI: 10.13422/j.cnki.syfjx.2017020120.
XUE Xiao-ming, WANG Yang, ZHAO Qin-ping, et al. Effect of Xuanfei Pingchuan Capsules on Rat COPD Model[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(2): 120-125. DOI: 10.13422/j.cnki.syfjx.2017020120.
目的:研究宣肺平喘胶囊对慢性阻塞性肺疾病(COPD)的作用机制。方法: SD健康大鼠60只,除正常组10只外,其余大鼠采用香烟烟熏联合气管内注射脂多糖方法建立COPD大鼠模型,造模成功后,随机分为宣肺平喘胶囊低、中、高剂量组(0.38,0.75,1.5 g·kg-1),模型组,阳性药物组(地塞米松,0.09 mg·kg-1)。正常组和模型组以蒸馏水ig,阳性药物组以地塞米松混悬液ig,其余治疗组以宣肺平喘颗粒混悬液ig,时间30 d,每天1次。末次ig后,观测大鼠一般情况;取血清,酶连免疫吸附测定法(ELISA)检测血清中肿瘤坏死因子-α(TNF-α),血管内皮生长因子(VEGF),白细胞介素-8(IL-8),白细胞介素-1β(IL-1β)的含量,蛋白质免疫印迹(Western blot)检测大鼠肺组织血小板源生长因子-B(PDGF-B)蛋白的表达,检测大鼠支气管肺泡灌洗液(BALF)中白细胞计数和分类,同时进行苏木素-伊红(HE)染色,病理组织观察。结果:与正常组比较,模型组大鼠血清中TNF-α,IL-8,IL-1β含量增高,VEGF含量降低,肺组织PDGF-B含量增高,支气管肺泡灌洗液中白细胞总数增高,嗜中性粒细胞、淋巴细胞、肺泡巨噬细胞比例增高(P < 0.05,P < 0.01);与模型组比较,宣肺平喘胶囊各剂量组大鼠血清TNF-α,IL-8,IL-1β明显降低,VEGF明显增多,肺组织PDGF-B明显降低(P < 0.05,P < 0.01),支气管肺泡灌洗液中嗜中性粒细胞、淋巴细胞、肺泡巨噬细胞比例明显降低(P<0.05),宣肺平喘胶囊高剂量组和地塞米松组与模型组比较,支气管肺泡灌洗液中白细胞总数均明显降低(P < 0.05,P < 0.01)。结论:宣肺平喘胶囊能够降低COPD大鼠血清中的TNF-α,IL-8,IL-1β降低,降低肺组织中PDGF-B,增高血清中VEGF,高剂量组还可以降低BALF白细胞总数,作用机制有可能与减少炎症介质生成和释放,发挥抗炎作用,减轻气道表皮粘液分泌,抑制气道重塑有关。
Objective: To study the action mechanism of Xuanfei Pingchuan capsules in treating chronic obstructive pulmonary disease (COPD). Method: Totally 60 healthy SD rats were selected. Except for 10 rats in the normal group
all of the remaining rats were included in the COPD model by means of smoking mold and intratracheal injection with lipopolysaccharide. After the successful modeling
they were randomly divided into low-dose
middle-dose and high-dose Xuanfei Pingchuan capsules groups (0.38
0.75
1.5 g·kg-1)
the model group
and the positive drug group (dexamethasone
0.09 mg·kg-1). The normal group and the model group were given distilled water
ig
the positive drug group was given Dexamethasone suspension
ig
while the remaining treatment groups were given Xuanfei Pingchuan capsules suspension
ig
for 30 day
once a day. After the final ig
general conditions of the rats were observed. The content of tumor necrosis factor-α(TNF-α)
vascular endothelial growth factor (VEGF)
interleukin-8(IL-8) and interleukin-1β(IL-1β) in serum were detected by ELISA. Western blot was used to detect the expression of platelet deriwed growth factor-B(PDGF-B)
and the leukocyte count and the category of leukocytes in the bronchoalveolar lavage fluid (BALF) of rats. HE staining was adopted for the histopathological examination. Result: Compared with the normal group
in the model group
the content of TNF-α
IL-8 and IL-1β in serum was higher (P<0.01)
the content of VEGF was lower (P<0.01)
the PDGF-B content in lung tissues was higher
the total number of leukocytes in bronchoalveolar lavage fluid was higher (P<0.01)
the percentages of neutrogherphils
lymphocytes and alveolar macrophages were higher (P < 0.05
P < 0.01). Compared to the model group
in the Xuanfei Pingchuan capsules groups
the content of TNF-α
IL-8
IL-1β were lower (P < 0.05
P < 0.01)
the content of VEGF was significantly higher
PDGF-B in lung issues was remarkably lower (P < 0.05
P < 0.01)
the percentages of neutrogherphils
lymphocytes and alveolar macrophages were notably lower (P<0.05); compared with the dexamethasone group and model group
Xuanfei Pingchuan capsules high-dose group showed significant decrease in the total number of leukocytes in bronchoalveolar lavage fluid (P < 0.05
P < 0.01). Conclusion: Xuanfei Pingchuan capsules can lower the content of TNF-α
IL-8
IL-1β in the CORD rat serum and the PDGF-B in lung issues
and increase the VEGF in serum. In high-dose group
the number of BALF leukocytes was reduced. The action mechanism is probably related to reducing the generation and release of inflammatory mediators
exerting the anti-inflammatory effect
relieving airway mucus secretion epidermis
and inhibiting airway remodeling.
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