Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats

To contribute new information to the pyrethroid pesticide α-cypermethrin toxicity profile, we evaluated its effects after oral administration to Wistar rats at daily doses of 2.186, 0.015, 0.157, and 0.786 mg/kg bw for 28 days. Evaluations were performed using markers of oxidative stress, cholineste...

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Main Authors: Vilena Kašuba, Blanka Tariba Lovaković, Ana Lucić Vrdoljak, Anja Katić, Nevenka Kopjar, Vedran Micek, Mirta Milić, Alica Pizent, Davor Želježić, Suzana Žunec
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Toxics
Subjects:
Online Access:https://www.mdpi.com/2305-6304/10/12/717
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author Vilena Kašuba
Blanka Tariba Lovaković
Ana Lucić Vrdoljak
Anja Katić
Nevenka Kopjar
Vedran Micek
Mirta Milić
Alica Pizent
Davor Želježić
Suzana Žunec
author_facet Vilena Kašuba
Blanka Tariba Lovaković
Ana Lucić Vrdoljak
Anja Katić
Nevenka Kopjar
Vedran Micek
Mirta Milić
Alica Pizent
Davor Želježić
Suzana Žunec
author_sort Vilena Kašuba
collection DOAJ
description To contribute new information to the pyrethroid pesticide α-cypermethrin toxicity profile, we evaluated its effects after oral administration to Wistar rats at daily doses of 2.186, 0.015, 0.157, and 0.786 mg/kg bw for 28 days. Evaluations were performed using markers of oxidative stress, cholinesterase (ChE) activities, and levels of primary DNA damage in plasma/whole blood and liver, kidney, and brain tissue. Consecutive exposure to α-cypermethrin affected the kidney, liver, and brain weight of rats. A significant increase in concentration of the thiobarbituric acid reactive species was observed in the brain, accompanied by a significant increase in glutathione peroxidase (GPx) activity. An increase in GPx activity was also observed in the liver of all α-cypermethrin-treated groups, while GPx activity in the blood was significantly lower than in controls. A decrease in ChE activities was observed in the kidney and liver. Treatment with α-cypermethrin induced DNA damage in the studied cell types at almost all of the applied doses, indicating the highest susceptibility in the brain. The present study showed that, even at very low doses, exposure to α-cypermethrin exerts genotoxic effects and sets in motion the antioxidative mechanisms of cell defense, indicating the potential hazards posed by this insecticide.
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spelling doaj.art-2887624df5e1443f8864e15215ae3e552023-11-24T18:24:38ZengMDPI AGToxics2305-63042022-11-01101271710.3390/toxics10120717Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male RatsVilena Kašuba0Blanka Tariba Lovaković1Ana Lucić Vrdoljak2Anja Katić3Nevenka Kopjar4Vedran Micek5Mirta Milić6Alica Pizent7Davor Želježić8Suzana Žunec9Institute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaInstitute for Medical Research and Occupational Health, 10000 Zagreb, CroatiaTo contribute new information to the pyrethroid pesticide α-cypermethrin toxicity profile, we evaluated its effects after oral administration to Wistar rats at daily doses of 2.186, 0.015, 0.157, and 0.786 mg/kg bw for 28 days. Evaluations were performed using markers of oxidative stress, cholinesterase (ChE) activities, and levels of primary DNA damage in plasma/whole blood and liver, kidney, and brain tissue. Consecutive exposure to α-cypermethrin affected the kidney, liver, and brain weight of rats. A significant increase in concentration of the thiobarbituric acid reactive species was observed in the brain, accompanied by a significant increase in glutathione peroxidase (GPx) activity. An increase in GPx activity was also observed in the liver of all α-cypermethrin-treated groups, while GPx activity in the blood was significantly lower than in controls. A decrease in ChE activities was observed in the kidney and liver. Treatment with α-cypermethrin induced DNA damage in the studied cell types at almost all of the applied doses, indicating the highest susceptibility in the brain. The present study showed that, even at very low doses, exposure to α-cypermethrin exerts genotoxic effects and sets in motion the antioxidative mechanisms of cell defense, indicating the potential hazards posed by this insecticide.https://www.mdpi.com/2305-6304/10/12/717cholinesterasegenotoxicityoxidative damagesubacute exposuresynthetic pyrethroids
spellingShingle Vilena Kašuba
Blanka Tariba Lovaković
Ana Lucić Vrdoljak
Anja Katić
Nevenka Kopjar
Vedran Micek
Mirta Milić
Alica Pizent
Davor Želježić
Suzana Žunec
Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
Toxics
cholinesterase
genotoxicity
oxidative damage
subacute exposure
synthetic pyrethroids
title Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
title_full Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
title_fullStr Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
title_full_unstemmed Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
title_short Evaluation of Toxic Effects Induced by Sub-Acute Exposure to Low Doses of α-Cypermethrin in Adult Male Rats
title_sort evaluation of toxic effects induced by sub acute exposure to low doses of α cypermethrin in adult male rats
topic cholinesterase
genotoxicity
oxidative damage
subacute exposure
synthetic pyrethroids
url https://www.mdpi.com/2305-6304/10/12/717
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