Role of vitamin C on lead acetate induced spermatogenesis in swiss mice

被引:41
作者
Acharya, UR [1 ]
Rathore, RM [1 ]
Mishra, M [1 ]
机构
[1] Berhampur Univ, Dept Zool, Berhampur 760007, Orissa, India
关键词
Swiss mice; testes; lead acetate; Vit C; lipid peroxidation; sperm count; sperm abnormalities; chromosomal abnormalities;
D O I
10.1016/S1382-6689(02)00107-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In the present study significantly increased lipid peroxidation value (LPP) after a single intraperitioneal injection of lead acetate (LA) (100 mg/kg b.w.) indicated enormous generation of Reactive Oxygen Species (ROS). Lead-induced ROS has a direct inhibitory effect on the growth and differentiation of the spermatogonial cells showing a significant decline in sperm count. Chromosomal analysis of the primary spermatocytes at week 4 post-treatment in lead-treated mice revealed significantly higher no of aberrant cells including chromosomal deficiency, autosomal and XY-asynapsis plates compared to untreated control mice. Sperm morphology studies at week 1-4 and at week 8 post-treatment, indicated higher percentage of deformed sperm population compared to vehicle injected groups of mice. Supplementation of vitamin C (Vit C) at a dose of 10 mg/kg body weight to lead-treated mice groups., however, significantly reduced the LPP with a concomitant increase in sperm count, marked decrease in the no of aberrant cells and significant decline in the percentage of morphologically abnormal sperm population, Protective role of Vit C in combating lead-induced oxidative stress in mice testicular cells, has been discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:9 / 14
页数:6
相关论文
共 50 条
[1]  
ABULNASAR SM, 2001, B NCR EGYPT, V26, P111
[2]   In vivo lipid peroxidation responses of tissues in lead-treated Swiss mice [J].
Acharya, S ;
Acharya, UR .
INDUSTRIAL HEALTH, 1997, 35 (04) :542-544
[3]  
Acharya U. R., 1997, Cytologia, V62, P231, DOI 10.1508/cytologia.62.231
[4]  
AITKEN RJ, 1989, BIOL REPROD, V40, P143
[5]   SYNAPTONEMAL COMPLEX DAMAGE AS A MEASURE OF GENOTOXICITY AT MEIOSIS [J].
ALLEN, JW ;
POORMAN, PA ;
BACKER, LC ;
GIBSON, JB ;
WESTBROOKCOLLINS, B ;
MOSES, MJ .
CELL BIOLOGY AND TOXICOLOGY, 1988, 4 (04) :487-493
[6]  
Aly Fawzia A. E., 2002, Cytologia (Tokyo), V67, P1, DOI 10.1508/cytologia.67.1
[7]  
[Anonymous], 1991, OXIDATIVE STRESS OXI
[8]   SYNAPTONEMAL COMPLEX DAMAGE IN RELATION TO MEIOTIC CHROMOSOME-ABERRATIONS AFTER EXPOSURE OF MALE-MICE TO CYCLOPHOSPHAMIDE [J].
BACKER, LC ;
GIBSON, JB ;
MOSES, MJ ;
ALLEN, JW .
MUTATION RESEARCH, 1988, 203 (04) :317-330
[9]  
BECK B, 1974, EXPERIENTIA, V30, P1007
[10]   THE ANTIOXIDANT ROLE OF VITAMIN-C [J].
BENDICH, A ;
MACHLIN, LJ ;
SCANDURRA, O ;
BURTON, GW ;
WAYNER, DDM .
ADVANCES IN FREE RADICAL BIOLOGY AND MEDICINE, 1986, 2 (02) :419-444