The effects of α-tocopherol on oxidative damage and serum levels of Clara cell protein 16 in aspiration pneumonitis induced by bile acids

被引:9
作者
Alacam, H. [1 ]
Karli, R. [2 ]
Alici, O. [3 ]
Avci, B. [1 ]
Guzel, A. [4 ,8 ]
Kozan, A. [1 ]
Mertoglu, C. [5 ]
Murat, N. [6 ]
Salis, O. [7 ]
Guzel, A. [4 ,8 ]
Sahin, M. [5 ]
机构
[1] Ondokuz Mayis Univ, Dept Med Biochem, Fac Med, TR-55139 Kurupelit, Samsun, Turkey
[2] Ondokuz Mayis Univ, Dept Otorhinolaryngol, Fac Med, TR-55139 Kurupelit, Samsun, Turkey
[3] Samsun Educ & Res Hosp, Dept Pathol, Samsun, Turkey
[4] Ondokuz Mayis Univ, Dept Chest Dis, Fac Med, TR-55139 Kurupelit, Samsun, Turkey
[5] Gaziosmanpasa Univ, Dept Med Biochem, Fac Med, Tokat, Turkey
[6] Ondokuz Mayis Univ, Dept Stat, TR-55139 Kurupelit, Samsun, Turkey
[7] Mental Hlth & Dis Hosp, Samsun, Turkey
[8] Ondokuz Mayis Univ, Dept Pediat, Fac Med, TR-55139 Kurupelit, Samsun, Turkey
关键词
Aspiration pneumonitis; alpha-tocopherol; bile acids; Clara cell protein 16; malondialdehyde; LUNG INJURY; VITAMIN-E; PATHOGENESIS; ANTIOXIDANT; NEUTROPHILS; INHIBITION; CLEARANCE; ADHESION; MARKERS; STRESS;
D O I
10.1177/0960327112459531
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Our aim in this study is to examine the effects of alpha-tocopherol (AT) on rats with aspiration pneumonitis induced with bile acids (BAs). The animals were divided in to four groups, namely saline group (n = 7), saline + AT group (n = 7), BA group (n = 7), and BA + AT group (n = 7). Saline and BA groups aspirated intratracheally with 1 ml/kg saline and 1 ml/kg bile acids, respectively. AT was given at 20 mg/kg/day dosage for 7 days to the groups. AT group was given 20 mg/kg/day AT for 7 days. Malondialdehyde (MDA), Clara cell protein 16 (CC-16), catalase (CAT), superoxide dismutase (SOD), as well as peribronchial inflammatory cell infiltration, alveolar septal infiltration, alveolar edema, alveolar exudate, alveolar histiocytes, and necrosis were evaluated. The CAT activity of the BA group was significantly lower than the saline group. In the BA + AT group, there was a significant increase in SOD and CAT activities when compared with that of the BA group. The CC-16 and MDA contents in the BA group were significantly higher than in the saline group. The CC-16 and MDA levels of the BA + AT group were significantly lower than BA group. Histopathologic changes were seen in BA group, and there was a significant decrease in the BA + AT group. In conclusion, AT might be beneficial in the treatment of aspiration pneumonitis induced by BAs because AT decreased oxidative damage and resulted in a decrease in CC-16 levels.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 59 条
  • [1] Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins
    Abuja, PM
    Albertini, R
    [J]. CLINICA CHIMICA ACTA, 2001, 306 (1-2) : 1 - 17
  • [2] HETEROGENEITY OF ERYTHROCYTE CATALASE .2. ISOLATION AND CHARACTERIZATION OF NORMAL AND VARIANT ERYTHROCYTE CATALASE AND THEIR SUBUNITS
    AEBI, H
    WYSS, SR
    SCHERZ, B
    SKVARIL, F
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1974, 48 (01): : 137 - 145
  • [3] The Role of Asymmetric Dimethyl Arginine and Oxidant/Antioxidant System in Preeclampsia
    Alacam, Hasan
    Dikmen, Gunnur
    Yaman, Halil
    Cakir, Erdinc
    Deren, Ozgur
    Akgul, E. Ozgur
    Aydin, Ibrahim
    Kurt, Yasemin Gulcan
    Keskin, Ugur
    Akalin, Sukran
    Polat, Belgin
    Danisman, Nuri
    Dogan, Pakize
    [J]. FETAL AND PEDIATRIC PATHOLOGY, 2011, 30 (06) : 387 - 393
  • [4] Fluticasone propionate protects against ozone-induced airway inflammation and modified immune cell activation markers in healthy volunteers
    Alexis, Neil E.
    Lay, John C.
    Haczku, Angela
    Gong, Henry
    Linn, William
    Hazucha, Milan J.
    Harris, Brad
    Tal-Singer, Ruth
    Peden, David B.
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2008, 116 (06) : 799 - 805
  • [5] [Anonymous], 2002, JPEN J PARENTER ENTE, DOI [10.1177/014860710202600602, DOI 10.1177/014860710202600602]
  • [6] BATZRI S, 1991, P SOC EXP BIOL MED, V197, P393
  • [7] BOSCOBOINIK D, 1991, J BIOL CHEM, V266, P6188
  • [8] Broeckaert F, 2000, CLIN EXP ALLERGY, V30, P469
  • [9] Chitra K. C., 2004, Indian Journal of Experimental Biology, V42, P220
  • [10] CHOW CK, 1991, FREE RADICAL BIO MED, V11, P215