Volume 14 Issue 4
Dec.  2001
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Article Navigation >  Biomedical and Environmental Sciences  > 2001  >  14(4): 333-340

FAKRUL ISLAM, U.MANI, A.K.PRASAD, P.KUMAR, B.K.MAJI, K.K.DUTTA. Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days[J]. Biomedical and Environmental Sciences, 2001, 14(4): 333-340.
Citation: FAKRUL ISLAM, U.MANI, A.K.PRASAD, P.KUMAR, B.K.MAJI, K.K.DUTTA. Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days[J]. Biomedical and Environmental Sciences, 2001, 14(4): 333-340.
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Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days

  • Department of Medical Elementology Toxicology, Hamdard University,

  • Inhalation Toxicology Laboratory, Industrial Toxicology Research Centre, M. G. Marg, P. Box. No. 80, M. G. Marg,

  • Objective　The pulmonary toxicity of a commercially available formulated preparation of Fenvalerate (Fen), a synthetic pyrethroid has been studied in rats following subchronic nose only inhalation exposure route. Method　 Adult male rats were exposed to Fen for 4h/day, 5 days a week for 90 days by using Flow Past Dynamic Nose only Inhalation Chamber. Results　Fen exposed rats showed a significant increase in enzymatic activities of lactate dehydrogenase (LDH), acid phosphatase (ACP), alkaline phosphatase (ALP) and γ-glutamyl transferase (γ-GT) which are considered as biochemical indicators of pulmonary damage. The concomitant histopathological examination of Fen exposed rats' lung revealed inflammatory changes viz., influx of mononuclear cells admixed with a few giant cells in alveolar lumen, hypetrophied bronchiolar and alveolar epithelial lining cells and presence of edematous fluid in alveolar lumen alongwith congested parenchymatous blood vessels. Conclusion　These results for the first time indicate the pulmonary toxic effects of a commonly used formulated Fen preparation by using rat model and nose only inhalation as the route of exposure.
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Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days

  • Department of Medical Elementology Toxicology, Hamdard University,
  • Inhalation Toxicology Laboratory, Industrial Toxicology Research Centre, M. G. Marg, P. Box. No. 80, M. G. Marg,

Abstract: Objective　The pulmonary toxicity of a commercially available formulated preparation of Fenvalerate (Fen), a synthetic pyrethroid has been studied in rats following subchronic nose only inhalation exposure route. Method　 Adult male rats were exposed to Fen for 4h/day, 5 days a week for 90 days by using Flow Past Dynamic Nose only Inhalation Chamber. Results　Fen exposed rats showed a significant increase in enzymatic activities of lactate dehydrogenase (LDH), acid phosphatase (ACP), alkaline phosphatase (ALP) and γ-glutamyl transferase (γ-GT) which are considered as biochemical indicators of pulmonary damage. The concomitant histopathological examination of Fen exposed rats' lung revealed inflammatory changes viz., influx of mononuclear cells admixed with a few giant cells in alveolar lumen, hypetrophied bronchiolar and alveolar epithelial lining cells and presence of edematous fluid in alveolar lumen alongwith congested parenchymatous blood vessels. Conclusion　These results for the first time indicate the pulmonary toxic effects of a commonly used formulated Fen preparation by using rat model and nose only inhalation as the route of exposure.

FAKRUL ISLAM, U.MANI, A.K.PRASAD, P.KUMAR, B.K.MAJI, K.K.DUTTA. Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days[J]. Biomedical and Environmental Sciences, 2001, 14(4): 333-340.
Citation: FAKRUL ISLAM, U.MANI, A.K.PRASAD, P.KUMAR, B.K.MAJI, K.K.DUTTA. Pulmonary Toxicity of a Formulated Preparation of Fenvalerate in Rats Subchronically Exposed by Nose Only Inhalation for 90 Days[J]. Biomedical and Environmental Sciences, 2001, 14(4): 333-340.
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