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

Background The number of Clara cells and the Clara cell 16-kDa protein (CC16) levels of the lung decrease in patients 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 mechani...

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Veröffentlicht in:Chinese medical journal 2010-02, Vol.123 (4), p.412-417
Hauptverfasser: Liao, Ji-ping, Chi, Chun-hua, Li, Hai-chao, Tang, Xiu-ying
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Sprache:eng
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Zusammenfassung:Background The number of Clara cells and the Clara cell 16-kDa protein (CC16) levels of the lung decrease in patients 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 ((181±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.
ISSN:0366-6999
2542-5641
DOI:10.3760/cma.j.issn.0366-6999.2010.04.006