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R.K. Singh
(Corresponding
author)
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Division of Toxicology, Central Drug Research Institute, Chattar
Manzil,
Lucknow - 226 001,
India
e-mail:
rktox@yahoo.com
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F.W. Bansode
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Division of Endocrinology, Central Drug Research
Institute, Chattar Manzil, Lucknow
- 226 001,
India
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Publication Data
Paper received:
18
March 2010
Revised
received:
28
September 2010
Re-revised
received:
16
November 2010
Accepted:
20 November 2010
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Abstract
Benzene has been considered as
an occupational hematotoxin and leukemogen.
The present study was conducted to determine the effects of oral
administration of benzene on reproductive organs and testicular
spermatogenesis in rats. Adult rats were divided into three weight matched
groups (Gr. I-III) containing 6 each. Gr. I rats received vehicle only and
served as control. Rats in Gr. II and III were fed orally with 0.5 and 1 ml
kg-1 dose of benzene for 14 and 9 days, respectively and autopsy
was done on 15th and 10th day. Food and water intake and gross
behavioral changes were recorded daily during the entire treatment. Results
showed no significant change in reproductive organ weights viz. testis, epididymis and ventral prostate in benzene-treated (0.5
or 1 ml kg-1) rats than that in controls. But, caused a
significant decrease (p<0.005) in weights of seminal vesicles in rats
treated with both 0.5 and 1 ml kg-1 doses compared to control. In
contrast, at higher dose (1 ml kg-1) of benzene, significant
(p<0.001) decline in body weight and 100% mortality was observed on day 10
of autopsy. In treated rats, testicular cytotoxicity
was marked by multinucleated giant cells formation, cytoplasmic
vacuolization, pyknosis of
nuclei, chromatolysis, desquamation and dissolution
of germ cells in tubular lumen. The quantitative analysis of spermatogenesis
showed a significant (p<0.001) decrease in number of A-spermatogonia
(in 1 ml kg-1 dose only), primary spermatocytes
(non-pachytene and pachytene)
and spermatids (round and elongated) in treated as
compared to control rats. The diameters of testicular tubules and Leydig cells nuclei were also significantly (p<0.001)
reduced in treated rats. A steady loss in food and water intake recorded and
signs of ill health were observed in treated (0.5 or 1 ml kg-1)
rats.? Results of the study indicated antitesticular /antispermatogenic
effects of benzene at 0.5 and 1 ml kg-1 dose in rats.
Key words
Spermatogenesis, Population dynamics, Leydig cell, Histology, Benzene
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