Effects of N-acetylcysteine on Clara cells in rats with cigarette smoke exposure

被引:13
|
作者
Liao Ji-ping [1 ]
Chi Chun-hua [1 ]
Li Hai-chao [1 ]
Tang Xiu-ying [2 ]
机构
[1] Peking Univ, Hosp 1, Dept Resp Med, Beijing 100034, Peoples R China
[2] Peking Univ, Hosp 1, Dept Pathol, Beijing 100034, Peoples R China
关键词
tobacco smoke pollution; Clara cells; N-acetylcysteine; glutathion; OBSTRUCTIVE PULMONARY-DISEASE; ALVEOLAR EPITHELIAL-CELLS; SMALL AIRWAYS; KDA PROTEIN; INFLAMMATION; GLUTATHIONE; EXPRESSION; STRESS; FLUID;
D O I
10.3760/cma.j.issn.0366-6999.2010.04.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The number of Clara cells and the Clara cell 16-kDa protein (CC16) levels of the lung decrease inpatients with chronic obstructive pulmonary disease (COPD) N-acetylcysteine (NAC) is a powerful antioxidant and can reduce the frequency of acute exacerbations of COPD But the exact mechanism is unclear The present study was designed to investigate the effects of NAC on Clara cells in rats with cigarette smoke exposure Methods Eighteen adult male Wistar rats were randomly divided into 3 groups, 12 exposed to cigarette smoke (CS) thrice a day, 10 cigarettes for 30 minutes each time for 1 week, without (CS group) or with (CS+NAC group) oral intake of NAC 80 mg kg(-1) d(-1), and another 6 rats exposed to fresh air (control group) Clara cells were observed by an electron microscope. The mRNA expression of CC16 and CC16 protein in lungs were determined by reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemistry respectively The glutathion (GSH) level in plasma and lung tissue were tested by fluorimetry assay Results Compared with the controls, the pathologic score of small airways significantly increased in the CS exposed rats (20 3 +/- 14 7 vs 53.7 +/- 11.5, P <0 05). The Clara cell particles in cytoplasm decreased in the CS group (P <0.05) The percentage of CC16-positive cells in bronchioles in the CS group (27 8 +/- 4.3 and 29 5 +/- 2 4 in terminal bronchioles and respiratory bronchioles, respectively) significantly decreased as compared with the control group (37 1 +/- 3.8 and 43 8 +/- 5.8 in terminal bronchioles and respiratory bronchioles, respectively) (P <0 05) No significant difference was observed in GSH level ((18 +/- 26) nmol/L in the control group vs (170 +/- 18) nmol/L in the CS group) between the two groups After treatment with NAC, the pathologic score of small airways (24 1 +/- 17.5) decreased (P <0 05). Clara cell particles in cytoplasm of Clara cells increased and GSH level in plasma ((213 +/- 40) nmol/L vs (170 +/- 18) nmol/L in the CS group) increased too (P <0.05), while the increase in the proportions of CC16 positive cells in bronchioles (30 1 +/- 6.4 and 34 3 +/- 6.3 in terminal bronchioles and respiratory bronchioles, respectively) did not reach the statistical significance (P >0 05) No significant difference was found in the expression of CC16 mRNA among the three groups Correlation analysis indicated that the percentage of CC16-positive cells in bronchioles negatively correlated with the pathologic score of small airways (r = -0 592, P <0.05), but not with GSH level Conclusions One-week CS exposure decreased the number of Clara cells and the expression of CC16 in bronchiciles in rats NAC might provide protection of the Clara cells from oxidative damage and possibly through the elevation of the synthesis and secretion of CC16. These data indicate that NAC decreases airway inflammation induced by CS via induction of CC16 Chin Med J 2010,-123(4).412-417
引用
收藏
页码:412 / 417
页数:6
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