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[A comparative study of two chronic obstructive pulmonary disease mouse models established by different methods].
Zhou, F; Li, D F; Yuan, L; Fu, H Y; Ma, P; Zhang, K D; Lu, W J.
Afiliação
  • Zhou F; Ningxia Medical University, Yinchuan 750001, China.
  • Li DF; Department of Respiration, the Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou 510000, China.
  • Yuan L; Guangzhou Institute of Respiratory Health, State Key Lab of Respiratory Diseases, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510210, China.
  • Fu HY; Ningxia Medical University, Yinchuan 750001, China.
  • Ma P; Ningxia Medical University, Yinchuan 750001, China.
  • Zhang KD; Ningxia Medical University, Respiratory and Critical Care Medicine, the General Hospital of Ningxia Medical University, Yinchuan 750004, China.
  • Lu WJ; Guangzhou Institute of Respiratory Health, State Key Lab of Respiratory Diseases, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510210, China.
Zhonghua Jie He He Hu Xi Za Zhi ; 42(5): 367-371, 2019 May 12.
Article em Zh | MEDLINE | ID: mdl-31137113
ABSTRACT

Objective:

To compare chronic obstructive pulmonary disease (COPD) mouse models established by two different methods-cigarette smoke (CS) exposure alone and CS exposure combined with airway instillation of bacterial LPS.

Methods:

Male C57 mice were randomly divided into control group(CTL group), CS exposure group (CS group) and intra-tracheal LPS instillation combined with CS exposure group (LPS+CS group) according to the random number table, with 8 rats in each group. After the models were established, we measured the lung function and collected the bronchoalveolar lavage fluid (BALF) to detect the number of inflammatory cells and the expression of mucin and inflammatory mediators. HE and PAS staining were performed to observe the pathological changes in airway and lung tissue and to detect the goblet cells in airway, respectively.

Results:

Total lung capacity (TLC), functional residual capacity (FRC) and airway resistance (RI) of the CS and LPS+CS groups were higher than those of the CTL group, while the FEV(50)/FVC of these 2 groups was lower (P<0.05). Moreover, both RI and FEV(50)/FVC in the LPS+CS group were higher compared with the CS group (P<0.05). HE staining of lung tissue showed that the average alveolar intercept and thickness of small airway wall in the CS and LPS+CS groups were higher compared to the CTL group. In addition, the average alveolar intercept in the LPS+CS group was lower than that in the CS group [(47.86±2.82) µm and (61.94±7.68) µm respectively, P<0.05], but the area of bronchial inflammation of LPS+CS group was higher. The number of total white blood cells, neutrophils, lymphocytes, macrophages and the level of interleukin-6 (IL-6) in BALF of CS and LPS+CS groups were higher than those of CTL group (all P<0.05). Furthermore, the number of neutrophils and IL-6 level in BALF of LPS+CS group were higher in comparison with CS group, while the number of macrophages in BALF of LPS+CS group was lower (P<0.05). PAS staining of lung tissue indicated that the number of goblet cells in large airways of CS and LPS+CS groups increased more significantly compared to the CTL group, and the number of goblet cells in the LPS+CS group was higher than that in the CS group [(0.16±0.02) and (0.09±0.02) respectively, P<0.05]. The expression levels of Muc5ac and Muc5b in BALF of LPS+CS and CS groups were also higher than those of CTL group (P<0.05), and the level of Muc5ac in BALF of LPS+CS group was higher compared with CS group[(2.69±0.72) and (2.19±0.29) respectively, P<0.05].

Conclusions:

Combined exposure of LPS and CS for establishing a COPD mouse model could better simulate the pathological characteristics of human COPD during the acute exacerbation period. The COPD mouse model established by CS exposure alone was able to better imitate the basic features of human COPD in the stable period. Researchers could choose a more appropriate modeling method according to different purposes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poluição por Fumaça de Tabaco / Brônquios / Lipopolissacarídeos / Doença Pulmonar Obstrutiva Crônica / Pulmão Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poluição por Fumaça de Tabaco / Brônquios / Lipopolissacarídeos / Doença Pulmonar Obstrutiva Crônica / Pulmão Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article