TOXICOPATHOLOGICAL STUDIES OF DI BUTYL PHTHALATE IN MALE WISTAR RATS


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Authors

  • Rina R. Patel Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.
  • B. P. Joshi Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.
  • D.J. Ghodasara Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.
  • J. H. Khorajiya Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.
  • Priya D. Ghodasara Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.
  • Sunanda Pandey Department of Veterinary Pathology, College of Veterinary Science & Animal Husbandry, Anand Agricultural University, Anand - 388 001. Gujarat.

https://doi.org/10.56093/ijvasr.v43i3.152918

Keywords:

Di butyl phthalate (DBP), toxicopathology, wistar rat

Abstract

Di butyl phthalate (DBP) is a most important plasticizer which is suspected as reproductive toxicant and exposure to it has the  potential effect on the human as well as animal reproductive system. The research work was conducted to evaluate the repeated dose toxicity of di butyl phthalate in male wistar rats. The animals were divided in four different groups with 12 male rats in each group.  Group I served as control and was administered corn oil (2 ml/kg body wt.) while groups II, III, and IV were administered DBP orally at  the dose rate of 500, 1000 and 2000 mg/kg respectively for consecutive seven days. Three rats from each group were sacrificed at 24 hrs, 7th day, 14th day and 21st day after initial dosing. There was gradual decrease in WBC count, RBC count, Hb, HCT, MCV, MCH, MCHC, gradual increase in albumin, gradual decrease in total protein, glucose values, gradual decrease in relative weights of the  testes, epididymis, prostate and seminal vesicles as well as increase in liver weight with increase in dose of DBP in group II, III and IV as compared to control group at different intervals of sacrifice. Grossly reductions in the size of testes were observed only in rats that belonged to high dose group IV on 21st day. The plasticizer DBP was found to produce histopathological lesions in male reproductive organs as well as in liver in dose dependent manner after oral administration. The finding suggested that DBP can cause toxicity  lesions in male reproductive organs especially in testes and epididymis at the dose rate of 500 to 2000 mg/kg body weight in wistar rats.

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References

Cater, B. R., Cook, M. W., Gangolli, S. D. and Grasso, P. (1977). Studies on dibutyl phthalate-induced testicular atrophy in the rat: Effect on zinc metabolism. Toxicology and Applied Pharmacology 41: 609-618.

Fukuoka, M., Kobayashi, T. and Zhou, Y. (1993). Mechanism of testicular atrophy induced by di-n-butyl phthalate in rats, Part 4.Changes in the activity of succinate dehydrogenase and the levels of transferring and ferritin in the sertoli and germ cells. Journal of Applied Toxicology, 13(4): 241-246.

Gray, T. J. and Gangolli, S. D. (1986). Aspects of the testicular toxicity of phthalate esters. Environmental Health 65: 229 - 235.

Gray, T., Rowland, I., Foster, P. and Gangolli, S. D.(1982). Species differences in the testicular toxicity of phthalate esters. Toxicology Letters, 11:141-147.

Kavlock, R., Boekelheide, K, and Chapin, R. (2002). NTP Center for the evaluation of risks to human reproduction: phthalate expert panel report on the reproductive and developmental toxicity of di-n-butyl phthalate. Reproductive Toxicology 16: 489-527.

Kembra, L.H., Cynthia, V. R., Vickie, S. W., L. and Earl, G. J. A (2008). Mechanisms of action of phthalate esters, individually and in combination, to induce abnormal reproductive development in male laboratory rats. Environmental Research. Volume 108(2): 168–176.

Kiran, S., Joshi, M. and Odd, G. N. (2009). Impact of Di butyl phthalate on haematology and biochemistry of albino rat. Toxicology International 16(2): 117-119.

Luna, L. G. (1968). Manual of histologic staining methods of the Armed forces institute of pathology. 3rdedn. Mc Graw Hill Book Co., New York.

Murakami, K., Nishiyama, K. and Higuti, T. (1986). Toxicity of dibutyl phthalate and its metabolites in rats. Japanese Journal of Hygiene, 41(4): 775-781.

NTP, (National Toxicology Program). (1995). Toxicity studies of dibutyl phthalate (CAS no. 84-74-2) administered in feed to F344/N and B6C3F1 mice. Oishi, S. and Hiraga, K. (1980). Testicular atrophy induced by phthalic acid esters: Effect on testosterone and zinc concentrations. Toxicology and Applied Pharmacology 53: 35-41.

Sandmeyer, E. E and Kirwin, C. J. (1981). Esters in: Clayton GD, Clayton FE, eds. Patty’s industrial hygiene and toxicology, 3(2): 2344-2412.

Smith, C. C. (1953). Toxicity of butyl stearate, dibutyl sebacate, di butyl phthalate, sand methoxyethyl oleate. A.M.A. Archives of Industrial Hygiene and Occupational Medicine, 7: 310-318.

Srivastava, S., Singh, G. B and Srivastava, S. P. (1990). Testicular toxicity of di-nbutyl phthalate in adult rats: Effect on marker enzymes of spermatogenesis. Indian Journal of Experimental Biology, 28: 67-70.

Wine, R. N., Li, L. H., Barnes, L. H., Gulati, D. K., and Chapin, R. E.(1997). Reproductive toxicity of di-n-butyl phthalate in a continuous breeding protocol in Sprague-Dawley rats. Environmental Health Perspectives, 105: 102–107.

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Submitted

19-06-2024

Published

08-08-2024

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How to Cite

Rina R. Patel, B. P. Joshi, D.J. Ghodasara, J. H. Khorajiya, Priya D. Ghodasara, & Sunanda Pandey. (2024). TOXICOPATHOLOGICAL STUDIES OF DI BUTYL PHTHALATE IN MALE WISTAR RATS. Indian Journal of Veterinary and Animal Sciences Research, 43(3), 211-220. https://doi.org/10.56093/ijvasr.v43i3.152918
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