Modulatory role of lipoic acid on lipopolysaccharide-induced oxidative stress in adult rat Sertoli cells in vitro

被引:34
作者
Aly, Hamdy A. A. [3 ,4 ]
Lightfoot, David A. [5 ]
El-Shemy, Hany A. [1 ,2 ]
机构
[1] Cairo Univ, Fac Agr, FARP, Giza 12513, Egypt
[2] Cairo Univ, Fac Agr, Dept Biochem, Giza 12513, Egypt
[3] Al Azhar Univ, Fac Pharm, Dept Pharmacol & Toxicol, Nasr City, Cairo, Egypt
[4] Catholic Univ Louvain, Unit Cellular & Mol Pharmacol, B-1200 Brussels, Belgium
[5] SIUC, Dept Plant Soil & Agr Syst, Genom Core Facil, Carbondale, IL USA
关键词
Lipoic acid; Sertoli cells; Inflammation; LPS; Testicular toxicity; Lipid peroxidation; Antioxidants; LIPID-PEROXIDATION; GLUTATHIONE-REDUCTASE; INFLAMMATORY MEDIATORS; SUPEROXIDE-DISMUTASE; ANTIOXIDANT SYSTEM; FREE-RADICALS; LEYDIG-CELLS; TESTIS; METABOLISM; LACTATE;
D O I
10.1016/j.cbi.2009.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inflammatory reactions to microbial infections may cause male infertility. The mechanisms of inhibition of spermatogenesis can be studied in vitro using rat Sertoli cells. Bacterial lipopolysaccharides (LPS) induce acute inflammations. So LPS treated Sertoli cells can be used to test for new therapeutic compounds. The present study aimed to investigate the protective efficacy of DL-alpha-lipoic acid (LA) on lipopolysaccharide (LPS)-induced oxidative stress in adult rat Sertoli cells. Sertoli cells were divided into 4 groups. Group I served as a control incubated with water (vehicle). Groups II and IV were incubated with 100 mu M LA for 24 h before incubating Groups III and IV with 50 mu g/ml lipopolysaccharide (LPS) for 12 h. In Group III cells (LPS-treated, no LA) the lactate concentration was decreased whereas hydrogen peroxide production and lipid peroxidation were significantly increased. Moreover, the activities of antioxidant enzymes such as superoxide dismutase, glutathione peroxidase, catalase, glutathione-S-transferase, glutathione reductase were reduced. The concentrations of antioxidant molecules such as reduced glutathione and vitamin C were significantly decreased. The activities of enzymes normally elevated in Sertoli cells, gamma-glutamyl transpeptidase and beta-glucuronidase, were significantly decreased. Treatment with LA (100 mu M) for 24 h before LPS-treatment (Group IV), prevented these changes in enzyme activities and metabolite concentrations. Therefore, LA may have a cyto-protective role during LPS-induced inflammation in adult rat Sertoli cells. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:112 / 118
页数:7
相关论文
共 66 条
[1]   An antioxidative nutrient-rich enteral diet attenuates lethal activity and oxidative stress induced by lipopolysaccharide in mice [J].
Abe, Shizuko ;
Tanaka, Yoshiaki ;
Fujise, Nobuaki ;
Nakamura, Tsuyoshi ;
Masunaga, Hiroaki ;
Nagasawa, Takashi ;
Yagi, Minoru .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2007, 31 (03) :181-187
[2]   What an andrologist/urologist should know about free radicals and why [J].
Agarwal, A ;
Prabakaran, S ;
Allamaneni, S .
UROLOGY, 2006, 67 (01) :2-8
[3]   Clinical relevance of oxidative stress in male factor infertility: An update [J].
Agarwal, Ashok ;
Makker, Kartikeya ;
Sharma, Rakesh .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2008, 59 (01) :2-11
[5]   Ketoconazole-induced testicular damage in rats reduced by Gentiana extract [J].
Amin, Amr .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2008, 59 (06) :377-384
[6]   Antioxidant effects of sulfur-containing amino acids [J].
Atmaca, G .
YONSEI MEDICAL JOURNAL, 2004, 45 (05) :776-788
[7]   Biochemical effects of some pesticides on lipid peroxidation and free-radical scavengers [J].
Banerjee, BD ;
Seth, V ;
Bhattacharya, A ;
Pasha, ST ;
Chakraborty, AK .
TOXICOLOGY LETTERS, 1999, 107 (1-3) :33-47
[8]   ANTIOXIDANT SYSTEM IN RAT TESTICULAR CELLS [J].
BAUCHE, F ;
FOUCHARD, MH ;
JEGOU, B .
FEBS LETTERS, 1994, 349 (03) :392-396
[9]  
BELLVE AR, 1989, J REPROD FERTIL, V85, P771, DOI 10.1530/jrf.0.0850771
[10]   The pharmacology of the antioxidant lipoic acid [J].
Biewenga, GP ;
Haenen, GRMM ;
Bast, A .
GENERAL PHARMACOLOGY, 1997, 29 (03) :315-331