Research Article
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Year 2021, Volume: 51 Issue: 2, 183 - 190, 31.08.2021

Abstract

Project Number

THD-2018-6548

References

  • Abdel-Daim, M., El-Bialy, B. E., Rahman, H. G., Radi, A. M., Hefny, H. A., & Hassan, A. M. (2016). Antagonistic effects of Spirulina platensis against sub-acute deltamethrin toxicity in mice: Biochemical and histopathological studies. Biomedicine & pharmacotherapy= Biomedecine & Pharmacotherapie, 77, 79–85
  • Abdollahi, M., Ranjbar, A., Shadnia, S., Nikfar, S., & Rezaie, A. (2004). Pesticides and oxidative stress: a review. Medical Science Monitor:International Medical Journal of Experimental and Clinical Research, 10(6), RA141–RA147.
  • Agrawal, A., Sharma, B., (2010). Pesticides induced oxidative stress in mammalian systems. Int J Biol Med Res, 1(3), 90-104.
  • Anogwih, J. A. (2014). Toxicity of pirimiphos methyl (Actellic 25EC) on Anopheles gambiae s.s., Culex quinquefasciatus (Diptera: Culicidae), and potential biocontrol agent, Poecilia reticulata (Pisces: Poeciliidae). Journal of Economic Entomology, 107(4), 1440–1446.
  • Bagherpour Shamloo, H., Golkari, S., Faghfoori, Z., Movassaghpour, A., Lotfi, H., Barzegari, A., & Yari Khosroushahi, A. (2016). “Lactobacillus Casei Decreases Organophosphorus Pesticide Diazinon Cytotoxicity in Human HUVEC Cell Line”. Advanced Pharmaceutical Bulletin, 6(2), 201–210.
  • Banaee, M., Akhlaghi, M., Soltanian, S., Gholamhosseini, A., Heidarieh, H., Fereidouni, M. S. (2019). “Acute exposure to chlorpyrifos and glyphosate induces changes in hemolymph biochemical parameters in the crayfish, Astacus leptodactylus (Eschscholtz, 1823)”. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 222, 145–155.
  • Ben Othmène, Y., Hamdi, H., Annabi, E., Amara, I., Ben Salem, I., Neffati, F., Najjar, M. F., Abid-Essefi, S. (2020). Tebuconazole induced cardiotoxicity in male adult rat. Food and chemical toxicology An international Journal Published for the British Industrial Biological Research Association, 137, 111134.
  • Benachour, N., and Séralini, G. E. (2009). Glyphosate formulations induce apoptosis and necrosis in human umbilical, embryonic, and placental cells. Chemical Research in Toxicology, 22(1), 97–105.
  • Berrouague, S., Rouag, M., Khaldi, T., Boumendjel, A., Boumendjel, M., Taibi, F., Messarah, M. (2019). Efficacy of Allium sativum oil to alleviate tebuconazol-induced oxidative stress in the liver of adult rats. Cellular and Molecular Biology (Noisy-le-Grand, France), 65(8), 23–31.
  • Bhattacharjee, P., Borah, A., Das, S. (2020). Quercetin-induced amelioration of deltamethrin stress in freshwater teleost, Channa punctata: Multiple biomarker analysis. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 227, 108626.
  • Cai, W., Yang, X., Li, X., Li, H., Wang, S., Wu, Z., Yu, M., Ma, S., Tang, S. (2020). Low-dose Roundup induces developmental toxicity in bovine preimplantation embryos in vitro. Environmental Science and Pollution Research International, 27(14), 16451–16459.
  • Cao, Y., Gong, Y., Liu, L., Zhou, Y., Fang, X., Zhang, C., Li, Y., Li, J. (2017). The use of human umbilical vein endothelial cells (HUVECs) as an in vitro model to assess the toxicity of nanoparticles to endothelium: a review. Journal of Applied Toxicology, 37(12), 1359–1369.
  • Deng, Y., Zhang, Y., Lu, Y., Zhao, Y., Ren, H. (2016). Hepatotoxicity and nephrotoxicity induced by the chlorpyrifos and chlorpyrifos-methyl metabolite, 3,5,6-trichloro-2-pyridinol, in orally exposed mice”. The Science of the Total Environment, 544, 507–514.
  • Dokuyucu, R., Bilgili, A., Hanedan, B., Dogan, H., Dokuyucu, A., Celik, M. M. (2016). Attenuating effects of caffeic acid phenethyl ester with intralipid on hepatotoxicity of chlorpyrifos in the case of rats. Medicina, 67(6), 743–749.
  • Ferreira, D., da Motta, A. C., Kreutz, L. C., Toni, C., Loro, V. L., Barcellos, L. J. (2010). Assessment of oxidative stress in Rhamdia quelen exposed to agrichemicals. Chemosphere, 79(9), 914–921.
  • Gholami-Seyedkolaei, S. J., Mirvaghefi, A., Farahmand, H., & Kosari, A. A. (2013). Effect of a glyphosate-based herbicide in Cyprinus carpio: assessment of acetylcholinesterase activity, hematological responses and serum biochemical parameters. Ecotoxicology and Environmental Safety, 98, 135–141.
  • Gündüz, E., Ülger, B. V., İbiloğlu, İ., Ekinci, A., Dursun, R., Zengin, Y., İçer, M., Uslukaya, Ö., Ekinci, C., Güloğlu, C. (2015). Glutamine provides effective protection against deltamethrin-induced acute hepatotoxicity in rats but not against nephrotoxicity. Medical Science Monitor:International Medical Journal of Experimental and Clinical Research, 21, 1107–1114.
  • Hatami, M., Banaee, M., Nematdoost Haghi, B. (2019). Sub-lethal toxicity of chlorpyrifos alone and in combination with polyethylene glycol to common carp (Cyprinus carpio). Chemosphere, 219, 981–988.
  • Jovanovic, P., Zoric, L., Stefanovic, I., Dzunic, B., Djordjevic-Jocic, J., Radenkovic, M., Jovanovic, M. (2010). Lactate dehydrogenase and oxidative stress activity in primary open-angle glaucoma aqueous humour. Bosnian Journal of Basic Medical Sciences, 10(1), 83–88.
  • Kim, K. H., Kabir, E., Jahan, S. A. (2017). Exposure to pesticides and the associated human health effects. The Science of the Total Environment, 575, 525–535.
  • Kumar, A., Sharma, R., Rana, D., Sharma, N. (2019). Protective Effect of Alpha-Tocopherol in Deltamethrin Induced Immunotoxicity, Endocr Metab Immune Disord Drug Targets, 19(2), 171-184.
  • Laetz, C. A., Baldwin, D. H., Collier, T. K., Hebert, V., Stark, J. D., Scholz, N. L. (2009). The synergistic toxicity of pesticide mixtures: implications for risk assessment and the conservation of endangered Pacific salmon. Environmental Health Perspectives, 117(3), 348–353.
  • Li, M. H., Ruan, L. Y., Zhou, J. W., Fu, Y. H., Jiang, L., Zhao, H., Wang, J. S. (2017). Metabolic profiling of goldfish (Carassius auratis) after long-term glyphosate-based herbicide exposure. Aquatic Toxicology (Amsterdam, Netherlands), 188, 159–169.
  • Li, S., Jiang, Y., Sun, Q., Coffin, S., Chen, L., Qiao, K., Gui, W., Zhu, G. (2020). Tebuconazole induced oxidative stress related hepatotoxicity in adult and larval zebrafish (Danio rerio). Chemosphere, 241, 125129.
  • Lu, Q., Sun, Y., Ares, I., Anadón, A., Martínez, M., Martínez-Larrañaga, M. R., Yuan, Z., Wang, X., Martínez, M. A. (2019). Deltamethrin toxicity: A review of oxidative stress and metabolism. Environmental Research, 170, 260–281.
  • Mansour, S. A., and Mossa, A. T. (2011). Adverse effects of exposure to low doses of chlorpyrifos in lactating rats. Toxicology and Industrial Health, 27(3), 213–224.
  • Martínez, M. A., Rodríguez, J. L., Lopez-Torres, B., Martínez, M., Martínez-Larrañaga, M. R., Maximiliano, J. E., Anadón, A., Ares, I. (2020). Use of human neuroblastoma SH-SY5Y cells to evaluate glyphosate-induced effects on oxidative stress, neuronal development and cell death signaling pathways. Environment International, 135, 105414.
  • Nasr, H. M., El-Demerdash, F. M., El-Nagar, W. A. (2016). Neuro and renal toxicity induced by chlorpyrifos and abamectin in rats: Toxicity of insecticide mixture. Environmental Science and Pollution Research International, 23(2), 1852–1859.
  • Ncir, M., Ben Salah, G., Kamoun, H., Makni Ayadi, F., Khabir, A., El Feki, A., Saoudi, M. (2016). Histopathological, oxidative damage, biochemical, and genotoxicity alterations in hepatic rats exposed to deltamethrin: modulatory effects of garlic (Allium sativum). Canadian journal of Physiology and Pharmacology, 94(6), 571–578.
  • Ndonwi, E. N., Atogho-Tiedeu, B., Lontchi-Yimagou, E., Shinkafi, T. S., Nanfa, D., Balti, E. V., Indusmita, R., Mahmood, A., Katte, J. C., Mbanya, A., Matsha, T., Mbanya, J. C., Shakir, A., Sobngwi, E. (2019). Gestational Exposure to Pesticides Induces Oxidative Stress and Lipid Peroxidation in Offspring that Persist at Adult Age in an Animal Model. Toxicological Research, 35(3), 241–248.
  • Odetti, L. M., López González, E. C., Romito, M. L., Simoniello, M. F., & Poletta, G. L. (2020). Genotoxicity and oxidative stress in Caiman latirostris hatchlings exposed to pesticide formulations and their mixtures during incubation period. Ecotoxicology and Environmental Safety, 193, 110312.
  • Olsvik, P. A., Berntssen, M., Søfteland, L. (2017). In vitro toxicity of pirimiphos-methyl in Atlantic salmon hepatocytes. Toxicology in Vitro, 39, 1–14.
  • Oyesola, T., Iranloye, B., & Adegoke, O. (2019). Implantation and pregnancy outcome of Sprague-Dawley rats exposed to pirimiphos-methyl. Endocrine Regulations, 53(3), 139–145.
  • Piatti, E., Marabini, L., & Chiesara, E. (1994). Increase of micronucleus frequency in cultured rat hepatocytes treated in vitro with benomyl and pirimiphos-methyl separately and in mixture. Mutation Research, 324(1-2), 59–64.
  • Roelofs, M., Temming, A. R., Piersma, A. H., van den Berg, M., & van Duursen, M. (2014). Conazole fungicides inhibit Leydig cell testosterone secretion and androgen receptor activation in vitro. Toxicology Reports, 1, 271–283.
  • Sai, L., Li, X., Liu, Y., Guo, Q., Xie, L., Yu, G., Bo, C., Zhang, Z., Li, L. (2014). Effects of chlorpyrifos on reproductive toxicology of male rats. Environmental Toxicology, 29(9), 1083–1088.
  • Staal, Y., Meijer, J., van der Kris, R., de Bruijn, A. C., Boersma, A. Y., Gremmer, E. R., Zwart, E. P., Beekhof, P. K., Slob, W., & van der Ven, L. (2018). Head skeleton malformations in zebrafish (Danio rerio) to assess adverse effects of mixtures of compounds. Archives of Toxicology, 92(12), 3549–3564
  • Tilak, K. S., Veeraiah, K., & Rao, D. K. (2005). Biochemical changes induced by chlorpyrifos, an organophosphate compound in sublethal concentrations to the freshwater fish Catla catla, Labeo rohita and Cirrhinus mrigala. Journal of Environmental Biology, 26(2 Suppl), 341–347.
  • Velki, M., Hackenberger, B. K. (2013). Different sensitivities of biomarker responses in two epigeic earthworm species after exposure to pyrethroid and organophosphate insecticides. Archives of Environmental Contamination and Toxicology, 65(3), 498–509.
  • Vijitharan, V., Warnasekare, J., Lokunarangoda, N. C., Farah, M. F., Siribaddana, S. H. (2016). Fatal poisoning with plant growth regulator - chlormequat. The Ceylon Medical Journal, 61(2), 89–90.
  • Wang, X., Shen, M., Zhou, J., & Jin, Y. (2019). Chlorpyrifos disturbs hepatic metabolism associated with oxidative stress and gut microbiota dysbiosis in adult zebrafish. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 216, 19–28.
  • Xiagedeer, B., Wu, S., Liu, Y., & Hao, W. (2016). Chlormequat chloride retards rat embryo growth in vitro. Toxicology in Vitro, 34, 274–282.
  • Yang, J., Gong, Y., Cai, J., Zheng, Y., Liu, H., Zhang, Z. (2020). “Chlorpyrifos induces redox imbalance-dependent inflammation in common carp lymphocyte through dysfunction of T-cell receptor γ”. Journal of Fish Diseases, 43(4), 423–430.
  • Yıldırım, E., Baydan, E., Kanbur, M., Kul, O., Cınar, M., Ekici, H., Atmaca, N. (2013). “The effect of chlorpyrifos on isolated thoracic aorta in rats.” BioMed Research International, 2013, 376051.
  • Zaki, S. M., Algaleel, W., Imam, R. A., Soliman, G. F., Ghoneim, F. M. (2020). Nano-curcumin versus curcumin in amelioration of deltamethrin-induced hippocampal damage. Histochemistry and Cell Biology, 154(2), 157–175
  • Zhang, H. C., Yang, Y. J., Ma, K. X., Shi, C. Y., Chen, G. W., & Liu, D. Z. (2020). “A novel sigma class glutathione S-transferase gene in freshwater planarian Dugesia japonica: cloning, characterization and protective effects in herbicide glyphosate stress”. Ecotoxicology (London, England), 29(3), 295–304

Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line

Year 2021, Volume: 51 Issue: 2, 183 - 190, 31.08.2021

Abstract

Background and Aims: Humans and animals have daily contact with various chemicals, including food additives, pesticides, antibiotics, other veterinary drugs, and other xenobiotics. Pesticide exposure causes many health disorders. Mixed exposure to pesticides is an important issue for human and environmental health. Methods: In this study, we have determined the cytotoxicity of chlormequat pirimiphos-methyl, glyphosate, tebuconazole, chlorpyrifos-methyl, deltamethrin, and the mixture of these six pesticides. We further investigated the role of oxidative stress, total oxidant status (TOS), lactate dehydrogenase (LDH) and antioxidant defense mechanism TOS, total glutathione (GSH) levels with the observed cytotoxicity. Results: In this study, the mixtures of pesticides reduced total antioxidant status (TAS) and GSH level one by one and increased the reactive oxygen species (ROS) generation in HUVECs, respectively. The results also showed a significant contribution of oxidative stress on cytotoxicity during pesticide mixture exposure. Conclusion: The findings are that pesticide mixture exposure might have an impact on human health risk at contaminated sites and under occupational exposure conditions.

Supporting Institution

Ataturk University Scientific Research Projects Fund

Project Number

THD-2018-6548

References

  • Abdel-Daim, M., El-Bialy, B. E., Rahman, H. G., Radi, A. M., Hefny, H. A., & Hassan, A. M. (2016). Antagonistic effects of Spirulina platensis against sub-acute deltamethrin toxicity in mice: Biochemical and histopathological studies. Biomedicine & pharmacotherapy= Biomedecine & Pharmacotherapie, 77, 79–85
  • Abdollahi, M., Ranjbar, A., Shadnia, S., Nikfar, S., & Rezaie, A. (2004). Pesticides and oxidative stress: a review. Medical Science Monitor:International Medical Journal of Experimental and Clinical Research, 10(6), RA141–RA147.
  • Agrawal, A., Sharma, B., (2010). Pesticides induced oxidative stress in mammalian systems. Int J Biol Med Res, 1(3), 90-104.
  • Anogwih, J. A. (2014). Toxicity of pirimiphos methyl (Actellic 25EC) on Anopheles gambiae s.s., Culex quinquefasciatus (Diptera: Culicidae), and potential biocontrol agent, Poecilia reticulata (Pisces: Poeciliidae). Journal of Economic Entomology, 107(4), 1440–1446.
  • Bagherpour Shamloo, H., Golkari, S., Faghfoori, Z., Movassaghpour, A., Lotfi, H., Barzegari, A., & Yari Khosroushahi, A. (2016). “Lactobacillus Casei Decreases Organophosphorus Pesticide Diazinon Cytotoxicity in Human HUVEC Cell Line”. Advanced Pharmaceutical Bulletin, 6(2), 201–210.
  • Banaee, M., Akhlaghi, M., Soltanian, S., Gholamhosseini, A., Heidarieh, H., Fereidouni, M. S. (2019). “Acute exposure to chlorpyrifos and glyphosate induces changes in hemolymph biochemical parameters in the crayfish, Astacus leptodactylus (Eschscholtz, 1823)”. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 222, 145–155.
  • Ben Othmène, Y., Hamdi, H., Annabi, E., Amara, I., Ben Salem, I., Neffati, F., Najjar, M. F., Abid-Essefi, S. (2020). Tebuconazole induced cardiotoxicity in male adult rat. Food and chemical toxicology An international Journal Published for the British Industrial Biological Research Association, 137, 111134.
  • Benachour, N., and Séralini, G. E. (2009). Glyphosate formulations induce apoptosis and necrosis in human umbilical, embryonic, and placental cells. Chemical Research in Toxicology, 22(1), 97–105.
  • Berrouague, S., Rouag, M., Khaldi, T., Boumendjel, A., Boumendjel, M., Taibi, F., Messarah, M. (2019). Efficacy of Allium sativum oil to alleviate tebuconazol-induced oxidative stress in the liver of adult rats. Cellular and Molecular Biology (Noisy-le-Grand, France), 65(8), 23–31.
  • Bhattacharjee, P., Borah, A., Das, S. (2020). Quercetin-induced amelioration of deltamethrin stress in freshwater teleost, Channa punctata: Multiple biomarker analysis. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 227, 108626.
  • Cai, W., Yang, X., Li, X., Li, H., Wang, S., Wu, Z., Yu, M., Ma, S., Tang, S. (2020). Low-dose Roundup induces developmental toxicity in bovine preimplantation embryos in vitro. Environmental Science and Pollution Research International, 27(14), 16451–16459.
  • Cao, Y., Gong, Y., Liu, L., Zhou, Y., Fang, X., Zhang, C., Li, Y., Li, J. (2017). The use of human umbilical vein endothelial cells (HUVECs) as an in vitro model to assess the toxicity of nanoparticles to endothelium: a review. Journal of Applied Toxicology, 37(12), 1359–1369.
  • Deng, Y., Zhang, Y., Lu, Y., Zhao, Y., Ren, H. (2016). Hepatotoxicity and nephrotoxicity induced by the chlorpyrifos and chlorpyrifos-methyl metabolite, 3,5,6-trichloro-2-pyridinol, in orally exposed mice”. The Science of the Total Environment, 544, 507–514.
  • Dokuyucu, R., Bilgili, A., Hanedan, B., Dogan, H., Dokuyucu, A., Celik, M. M. (2016). Attenuating effects of caffeic acid phenethyl ester with intralipid on hepatotoxicity of chlorpyrifos in the case of rats. Medicina, 67(6), 743–749.
  • Ferreira, D., da Motta, A. C., Kreutz, L. C., Toni, C., Loro, V. L., Barcellos, L. J. (2010). Assessment of oxidative stress in Rhamdia quelen exposed to agrichemicals. Chemosphere, 79(9), 914–921.
  • Gholami-Seyedkolaei, S. J., Mirvaghefi, A., Farahmand, H., & Kosari, A. A. (2013). Effect of a glyphosate-based herbicide in Cyprinus carpio: assessment of acetylcholinesterase activity, hematological responses and serum biochemical parameters. Ecotoxicology and Environmental Safety, 98, 135–141.
  • Gündüz, E., Ülger, B. V., İbiloğlu, İ., Ekinci, A., Dursun, R., Zengin, Y., İçer, M., Uslukaya, Ö., Ekinci, C., Güloğlu, C. (2015). Glutamine provides effective protection against deltamethrin-induced acute hepatotoxicity in rats but not against nephrotoxicity. Medical Science Monitor:International Medical Journal of Experimental and Clinical Research, 21, 1107–1114.
  • Hatami, M., Banaee, M., Nematdoost Haghi, B. (2019). Sub-lethal toxicity of chlorpyrifos alone and in combination with polyethylene glycol to common carp (Cyprinus carpio). Chemosphere, 219, 981–988.
  • Jovanovic, P., Zoric, L., Stefanovic, I., Dzunic, B., Djordjevic-Jocic, J., Radenkovic, M., Jovanovic, M. (2010). Lactate dehydrogenase and oxidative stress activity in primary open-angle glaucoma aqueous humour. Bosnian Journal of Basic Medical Sciences, 10(1), 83–88.
  • Kim, K. H., Kabir, E., Jahan, S. A. (2017). Exposure to pesticides and the associated human health effects. The Science of the Total Environment, 575, 525–535.
  • Kumar, A., Sharma, R., Rana, D., Sharma, N. (2019). Protective Effect of Alpha-Tocopherol in Deltamethrin Induced Immunotoxicity, Endocr Metab Immune Disord Drug Targets, 19(2), 171-184.
  • Laetz, C. A., Baldwin, D. H., Collier, T. K., Hebert, V., Stark, J. D., Scholz, N. L. (2009). The synergistic toxicity of pesticide mixtures: implications for risk assessment and the conservation of endangered Pacific salmon. Environmental Health Perspectives, 117(3), 348–353.
  • Li, M. H., Ruan, L. Y., Zhou, J. W., Fu, Y. H., Jiang, L., Zhao, H., Wang, J. S. (2017). Metabolic profiling of goldfish (Carassius auratis) after long-term glyphosate-based herbicide exposure. Aquatic Toxicology (Amsterdam, Netherlands), 188, 159–169.
  • Li, S., Jiang, Y., Sun, Q., Coffin, S., Chen, L., Qiao, K., Gui, W., Zhu, G. (2020). Tebuconazole induced oxidative stress related hepatotoxicity in adult and larval zebrafish (Danio rerio). Chemosphere, 241, 125129.
  • Lu, Q., Sun, Y., Ares, I., Anadón, A., Martínez, M., Martínez-Larrañaga, M. R., Yuan, Z., Wang, X., Martínez, M. A. (2019). Deltamethrin toxicity: A review of oxidative stress and metabolism. Environmental Research, 170, 260–281.
  • Mansour, S. A., and Mossa, A. T. (2011). Adverse effects of exposure to low doses of chlorpyrifos in lactating rats. Toxicology and Industrial Health, 27(3), 213–224.
  • Martínez, M. A., Rodríguez, J. L., Lopez-Torres, B., Martínez, M., Martínez-Larrañaga, M. R., Maximiliano, J. E., Anadón, A., Ares, I. (2020). Use of human neuroblastoma SH-SY5Y cells to evaluate glyphosate-induced effects on oxidative stress, neuronal development and cell death signaling pathways. Environment International, 135, 105414.
  • Nasr, H. M., El-Demerdash, F. M., El-Nagar, W. A. (2016). Neuro and renal toxicity induced by chlorpyrifos and abamectin in rats: Toxicity of insecticide mixture. Environmental Science and Pollution Research International, 23(2), 1852–1859.
  • Ncir, M., Ben Salah, G., Kamoun, H., Makni Ayadi, F., Khabir, A., El Feki, A., Saoudi, M. (2016). Histopathological, oxidative damage, biochemical, and genotoxicity alterations in hepatic rats exposed to deltamethrin: modulatory effects of garlic (Allium sativum). Canadian journal of Physiology and Pharmacology, 94(6), 571–578.
  • Ndonwi, E. N., Atogho-Tiedeu, B., Lontchi-Yimagou, E., Shinkafi, T. S., Nanfa, D., Balti, E. V., Indusmita, R., Mahmood, A., Katte, J. C., Mbanya, A., Matsha, T., Mbanya, J. C., Shakir, A., Sobngwi, E. (2019). Gestational Exposure to Pesticides Induces Oxidative Stress and Lipid Peroxidation in Offspring that Persist at Adult Age in an Animal Model. Toxicological Research, 35(3), 241–248.
  • Odetti, L. M., López González, E. C., Romito, M. L., Simoniello, M. F., & Poletta, G. L. (2020). Genotoxicity and oxidative stress in Caiman latirostris hatchlings exposed to pesticide formulations and their mixtures during incubation period. Ecotoxicology and Environmental Safety, 193, 110312.
  • Olsvik, P. A., Berntssen, M., Søfteland, L. (2017). In vitro toxicity of pirimiphos-methyl in Atlantic salmon hepatocytes. Toxicology in Vitro, 39, 1–14.
  • Oyesola, T., Iranloye, B., & Adegoke, O. (2019). Implantation and pregnancy outcome of Sprague-Dawley rats exposed to pirimiphos-methyl. Endocrine Regulations, 53(3), 139–145.
  • Piatti, E., Marabini, L., & Chiesara, E. (1994). Increase of micronucleus frequency in cultured rat hepatocytes treated in vitro with benomyl and pirimiphos-methyl separately and in mixture. Mutation Research, 324(1-2), 59–64.
  • Roelofs, M., Temming, A. R., Piersma, A. H., van den Berg, M., & van Duursen, M. (2014). Conazole fungicides inhibit Leydig cell testosterone secretion and androgen receptor activation in vitro. Toxicology Reports, 1, 271–283.
  • Sai, L., Li, X., Liu, Y., Guo, Q., Xie, L., Yu, G., Bo, C., Zhang, Z., Li, L. (2014). Effects of chlorpyrifos on reproductive toxicology of male rats. Environmental Toxicology, 29(9), 1083–1088.
  • Staal, Y., Meijer, J., van der Kris, R., de Bruijn, A. C., Boersma, A. Y., Gremmer, E. R., Zwart, E. P., Beekhof, P. K., Slob, W., & van der Ven, L. (2018). Head skeleton malformations in zebrafish (Danio rerio) to assess adverse effects of mixtures of compounds. Archives of Toxicology, 92(12), 3549–3564
  • Tilak, K. S., Veeraiah, K., & Rao, D. K. (2005). Biochemical changes induced by chlorpyrifos, an organophosphate compound in sublethal concentrations to the freshwater fish Catla catla, Labeo rohita and Cirrhinus mrigala. Journal of Environmental Biology, 26(2 Suppl), 341–347.
  • Velki, M., Hackenberger, B. K. (2013). Different sensitivities of biomarker responses in two epigeic earthworm species after exposure to pyrethroid and organophosphate insecticides. Archives of Environmental Contamination and Toxicology, 65(3), 498–509.
  • Vijitharan, V., Warnasekare, J., Lokunarangoda, N. C., Farah, M. F., Siribaddana, S. H. (2016). Fatal poisoning with plant growth regulator - chlormequat. The Ceylon Medical Journal, 61(2), 89–90.
  • Wang, X., Shen, M., Zhou, J., & Jin, Y. (2019). Chlorpyrifos disturbs hepatic metabolism associated with oxidative stress and gut microbiota dysbiosis in adult zebrafish. Comparative Biochemistry and Physiology. Toxicology & Pharmacology, 216, 19–28.
  • Xiagedeer, B., Wu, S., Liu, Y., & Hao, W. (2016). Chlormequat chloride retards rat embryo growth in vitro. Toxicology in Vitro, 34, 274–282.
  • Yang, J., Gong, Y., Cai, J., Zheng, Y., Liu, H., Zhang, Z. (2020). “Chlorpyrifos induces redox imbalance-dependent inflammation in common carp lymphocyte through dysfunction of T-cell receptor γ”. Journal of Fish Diseases, 43(4), 423–430.
  • Yıldırım, E., Baydan, E., Kanbur, M., Kul, O., Cınar, M., Ekici, H., Atmaca, N. (2013). “The effect of chlorpyrifos on isolated thoracic aorta in rats.” BioMed Research International, 2013, 376051.
  • Zaki, S. M., Algaleel, W., Imam, R. A., Soliman, G. F., Ghoneim, F. M. (2020). Nano-curcumin versus curcumin in amelioration of deltamethrin-induced hippocampal damage. Histochemistry and Cell Biology, 154(2), 157–175
  • Zhang, H. C., Yang, Y. J., Ma, K. X., Shi, C. Y., Chen, G. W., & Liu, D. Z. (2020). “A novel sigma class glutathione S-transferase gene in freshwater planarian Dugesia japonica: cloning, characterization and protective effects in herbicide glyphosate stress”. Ecotoxicology (London, England), 29(3), 295–304
There are 46 citations in total.

Details

Primary Language English
Subjects Pharmacology and Pharmaceutical Sciences
Journal Section Original Article
Authors

Çiğdem Sevim 0000-0002-0575-3090

Ali Taghizadehghalehjoughi 0000-0002-3506-0324

Mehtap Kara 0000-0001-7764-5593

Project Number THD-2018-6548
Publication Date August 31, 2021
Submission Date February 16, 2021
Published in Issue Year 2021 Volume: 51 Issue: 2

Cite

APA Sevim, Ç., Taghizadehghalehjoughi, A., & Kara, M. (2021). Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line. İstanbul Journal of Pharmacy, 51(2), 183-190.
AMA Sevim Ç, Taghizadehghalehjoughi A, Kara M. Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line. iujp. August 2021;51(2):183-190.
Chicago Sevim, Çiğdem, Ali Taghizadehghalehjoughi, and Mehtap Kara. “Effects of Chlorpyrifos-Methyl, Chlormequat, Deltamethrin, Glyphosate, Pirimiphos-Methyl, Tebuconazole and Their Mixture on Oxidative Stress and Toxicity in HUVEC Cell Line”. İstanbul Journal of Pharmacy 51, no. 2 (August 2021): 183-90.
EndNote Sevim Ç, Taghizadehghalehjoughi A, Kara M (August 1, 2021) Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line. İstanbul Journal of Pharmacy 51 2 183–190.
IEEE Ç. Sevim, A. Taghizadehghalehjoughi, and M. Kara, “Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line”, iujp, vol. 51, no. 2, pp. 183–190, 2021.
ISNAD Sevim, Çiğdem et al. “Effects of Chlorpyrifos-Methyl, Chlormequat, Deltamethrin, Glyphosate, Pirimiphos-Methyl, Tebuconazole and Their Mixture on Oxidative Stress and Toxicity in HUVEC Cell Line”. İstanbul Journal of Pharmacy 51/2 (August 2021), 183-190.
JAMA Sevim Ç, Taghizadehghalehjoughi A, Kara M. Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line. iujp. 2021;51:183–190.
MLA Sevim, Çiğdem et al. “Effects of Chlorpyrifos-Methyl, Chlormequat, Deltamethrin, Glyphosate, Pirimiphos-Methyl, Tebuconazole and Their Mixture on Oxidative Stress and Toxicity in HUVEC Cell Line”. İstanbul Journal of Pharmacy, vol. 51, no. 2, 2021, pp. 183-90.
Vancouver Sevim Ç, Taghizadehghalehjoughi A, Kara M. Effects of chlorpyrifos-methyl, chlormequat, deltamethrin, glyphosate, pirimiphos-methyl, tebuconazole and their mixture on oxidative stress and toxicity in HUVEC cell line. iujp. 2021;51(2):183-90.