Gastrointestinal and neurotoxic effects of cypermethrin in rats
By: Remya R Nair.
Contributor(s): Mammen J Abraham(Guide).
Material type:
BookPublisher: Mannuthy Centre For Excellence In Pathology, College of Veterinary and Animal Sciences 2008DDC classification: 636.0896 Online resources: Click here to access online Dissertation note: MVSc Abstract: The present study entitled ‘Gastrointestinal and neurotoxic effects of cypermethrin in rats’ was undertaken to investigate the potential toxic effects of cypermethrin in rats with particular emphasis on its effect on the nervous and digestive system.The clinical signs, gross pathology, histopathology, haematology and biochemical parameters were analysed to study the effects.
Cypermethrin was found to be neurotoxic and gastroenterotoxic at the given dose levels. Oral administration of cypermethrin in medium and high doses produced nervous signs in animals. However cypermethrin did not cause any significant variation in the body weight of animals.
All haematological parameters evaluated showed a dose dependent reduction in its value. Biochemical parameters assessed revealed hepatotoxic and multisystemic effects of cypermethrin.
Gross lesions observed in the intoxicated groups were bloat, congestion of lungs, heart, brain, pulmonary haemorrhage and degenerative changes in liver and kidneys.
On histopathological examination, cypermethrin was found to be neurotoxic, hepatotoxic, enterotoxic, pneumotoxic, cardiotoxic and nephrotoxic as evidenced by varying degrees of degeneration and necrosis in various organs examined. Effects on all organs were mild to moderate degenerative changes at the low dose level. Medium and high dose intoxicated groups revealed necrotic changes, extensive haemorrhages, congestion in organs like liver, kidney and lungs apart from the changes observed in low dose group animals. Haemodynamic disturbances were manifested in the forms of congestion and haemorhages in lungs, heart, liver and kidneys. The histopathological evaluation revealed no cypermethrin induced toxic effects on the oesophagus. Spinal cord lesions were observed only in the lowest dose group. Brain lesions were only degenerative changes. These findings suggested that biochemical effects rather than structural changes were involved in toxicity.
| Item type | Current location | Call number | Status | Date due | Barcode |
|---|---|---|---|---|---|
Theses
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KAU Central Library, Thrissur Theses | 636.0896 REM/GA (Browse shelf) | Available | 172782 |
MVSc
The present study entitled ‘Gastrointestinal and neurotoxic effects of cypermethrin in rats’ was undertaken to investigate the potential toxic effects of cypermethrin in rats with particular emphasis on its effect on the nervous and digestive system.The clinical signs, gross pathology, histopathology, haematology and biochemical parameters were analysed to study the effects.
Cypermethrin was found to be neurotoxic and gastroenterotoxic at the given dose levels. Oral administration of cypermethrin in medium and high doses produced nervous signs in animals. However cypermethrin did not cause any significant variation in the body weight of animals.
All haematological parameters evaluated showed a dose dependent reduction in its value. Biochemical parameters assessed revealed hepatotoxic and multisystemic effects of cypermethrin.
Gross lesions observed in the intoxicated groups were bloat, congestion of lungs, heart, brain, pulmonary haemorrhage and degenerative changes in liver and kidneys.
On histopathological examination, cypermethrin was found to be neurotoxic, hepatotoxic, enterotoxic, pneumotoxic, cardiotoxic and nephrotoxic as evidenced by varying degrees of degeneration and necrosis in various organs examined. Effects on all organs were mild to moderate degenerative changes at the low dose level. Medium and high dose intoxicated groups revealed necrotic changes, extensive haemorrhages, congestion in organs like liver, kidney and lungs apart from the changes observed in low dose group animals. Haemodynamic disturbances were manifested in the forms of congestion and haemorhages in lungs, heart, liver and kidneys. The histopathological evaluation revealed no cypermethrin induced toxic effects on the oesophagus. Spinal cord lesions were observed only in the lowest dose group. Brain lesions were only degenerative changes. These findings suggested that biochemical effects rather than structural changes were involved in toxicity.
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