[
1. Saillenfait AM, Ndiaye D, Sabaté JP. Pyrethroids: exposure and health effects--an update. Int J Hyg Environ Health. 2015;218(3):281-92;10.1016/j.ijheh.2015.01.00225648288
]Search in Google Scholar
[
2. Hill N, Zhou HN, Wang P, Guo X, Carneiro I, Moore SJ. A household randomized, controlled trial of the efficacy of 0.03% transfluthrin coils alone and in combination with long-lasting insecticidal nets on the incidence of Plasmodium falciparum and Plasmodium vivax malaria in Western Yunnan Province, China. Malar J. 2014; 13:208;10.1186/1475-2875-13-208405759824885993
]Search in Google Scholar
[
3. Tang W, Wang D, Wang J, Wu Z, Li L, Huang M, Xu S, Yan D. Pyrethroid pesticide residues in the global environment: An overview. Chemosphere. 2018 Jan;191:990-1007. doi: 10.1016/j.chemosphere.2017.10.115. Epub 2017 Oct 23. PMID: 29145144;29145144
]Open DOISearch in Google Scholar
[
4. Morgan MK. Children’s exposures to pyrethroid insecticides at home: a review of data collected in published exposure measurement studies conducted in the United States. Int J Environ Res Public Health. 2012;9(8):2964-85;10.3390/ijerph9082964344759923066409
]Search in Google Scholar
[
5. Al-Omar MS, Naz M, Mohammed SAA, Mansha M, Ansari MN, Rehman NU, Kamal M, Mohammed HA, Yusuf M, Hamad AM, Akhtar N, Khan RA. Pyrethroid-Induced Organ Toxicity and Anti-Oxidant-Supplemented Amelioration of Toxicity and Organ Damage: The Protective Roles of Ascorbic Acid and α-Tocopherol. Int J Environ Res Public Health. 2020 25;17(17):6177;10.3390/ijerph17176177750332732854455
]Search in Google Scholar
[
6. Nieradko-Iwanicka B, Borzęcki A. Subacute poisoning of mice with deltamethrin produces memory impairment, reduced locomotor activity, liver damage and changes in blood morphology in the mechanism of oxidative stress. Pharmacol Rep. 2015;67(3):535-41;10.1016/j.pharep.2014.12.01225933966
]Search in Google Scholar
[
7. Skolarczyk J, Pekar J, Nieradko-Iwanicka B. Immune disorders induced by exposure to pyrethroid insecticides. Postepy Hig Med Dosw (Online). 2017;71(0):446-453;10.5604/01.3001.0010.382728665275
]Search in Google Scholar
[
8. Amin KA, Hashem KS. Deltamethrin-induced oxidative stress and biochemical changes in tissues and blood of catfish (Clarias gariepinus): antioxidant defense and role of alpha-tocopherol. BMC Vet Res. 2012; 8:45;10.1186/1746-6148-8-45348214522537979
]Search in Google Scholar
[
9. Jaremek M, Nieradko-Iwanicka B. The effect of subacute poisoning with fenpropathrin on mice kidney function and the level of interleukin 1β and tumor necrosis factor α. Mol Biol Rep. 2020;47(6):4861-4865;10.1007/s11033-020-05480-w729584532385770
]Search in Google Scholar
[
10. Burns CJ, Pastoor TP. Pyrethroid epidemiology: a quality-based review. Crit Rev Toxicol. 2018; 48(4):297-311;10.1080/10408444.2017.142346329389244
]Search in Google Scholar
[
11. Glorennec P, Serrano T, Fravallo M, Warembourg C, Monfort C, Cordier S, Viel JF, Le Gléau F, Le Bot B, Chevrier C. Determinants of children’s exposure to pyrethroid insecticides in western France. Environ Int. 2017; 104:76-82;10.1016/j.envint.2017.04.00728453973
]Search in Google Scholar
[
12. Abdel-Daim MM, Abdelkhalek NK, Hassan AM. Antagonistic activity of dietary allicin against deltamethrin-induced oxidative damage in freshwater Nile tilapia; Oreochromis niloticus. Ecotoxicol Environ Saf. 2015; 111:146-52;10.1016/j.ecoenv.2014.10.01925450927
]Search in Google Scholar
[
13. Dubey N, Khan AM, Raina R. Sub-acute deltamethrin and fluoride toxicity induced hepatic oxidative stress and biochemical alterations in rats. Bull Environ Contam Toxicol. 2013; 91(3):334-8;10.1007/s00128-013-1052-123820696
]Search in Google Scholar
[
14. Abdou RH, Abdel-Daim MM. Alpha-lipoic acid improves acute deltamethrin-induced toxicity in rats. Can J Physiol Pharmacol. 2014;92(9):773-9;10.1139/cjpp-2014-028025167376
]Search in Google Scholar
[
15. Lu Q, Sun Y, Ares I, Anadón A, Martínez M, Martínez-Larrañaga MR, Yuan Z, Wang X, Martínez MA. Deltamethrin toxicity: A review of oxidative stress and metabolism. Environ Res. 2019; 170:260-28110.1016/j.envres.2018.12.04530599291
]Search in Google Scholar
[
16. Zhong YF, Huang XW, Shi N. [Role of interleukin-1 beta in deltamethrin neurotoxicity]. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2009; 27(4):244-6;
]Search in Google Scholar
[
17. Han B, Lv Z, Zhang X, Lv Y, Li S, Wu P, Yang Q, Li J, Qu B, Zhang Z. Deltamethrin induces liver fibrosis in quails via activation of the TGF-β1/Smad signaling pathway. Environ Pollut. 2020; 259:113870;10.1016/j.envpol.2019.11387031918140
]Search in Google Scholar
[
18. Feriani A, Hachani R, Tir M, Ghazouani L, Mufti A, Borgi MA, Allagui MS. Bifenthrin exerts proatherogenic effects via arterial accumulation of native and oxidized LDL in rats: the beneficial role of vitamin E and selenium. Environ Sci Pollut Res Int. 2020; 27(6):5651-5660;10.1007/s11356-018-3771-730465240
]Search in Google Scholar
[
19. Aouey B, Derbali M, Chtourou Y, Bouchard M, Khabir A, Fetoui H. Pyrethroid insecticide lambda-cyhalothrin and its metabolites induce liver injury through the activation of oxidative stress and proinflammatory gene expression in rats following acute and subchronic exposure. Environ Sci Pollut Res Int. 2017;24(6):5841-5856;10.1007/s11356-016-8323-428058584
]Search in Google Scholar
[
20. Gargouri B, Bhatia HS, Bouchard M, Fiebich BL, Fetoui H. Inflammatory and oxidative mechanisms potentiate bifenthrin-induced neurological alterations and anxiety-like behavior in adult rats. Toxicol Lett. 2018; 294:73-86;10.1016/j.toxlet.2018.05.02029775722
]Search in Google Scholar
[
21. Piłat D, Mika J. The role of interleukin-1 family of cytokines in nociceptive transmission. Ból 2014;15(4): 39-47;10.5604/1640324x.1132019
]Search in Google Scholar
[
22. Nieradko-Iwanicka B, Konopelko M. Effect of Lambdacyhalothrin on Locomotor Activity, Memory, Selected Biochemical Parameters, Tumor Necrosis Factor α, and Interleukin 1ß in a Mouse Model. Int J Environ Res Public Health. 2020; 17(24):9240;10.3390/ijerph17249240776478333321891
]Search in Google Scholar
[
23. Abdel-Daim MM, El-Ghoneimy A. Synergistic protective effects of ceftriaxone and ascorbic acid against subacute deltamethrin-induced nephrotoxicity in rats. Ren Fail. 2015; 37(2):297-304;10.3109/0886022X.2014.98301725691087
]Search in Google Scholar
[
24. Klimowska A, Amenda K, Rodzaj W, Wileńska M, Jurewicz J, Wielgomas B. Evaluation of 1-year urinary excretion of eight metabolites of synthetic pyrethroids, chlorpyrifos, and neonicotinoids. Environ Int. 2020; 145:106119;10.1016/j.envint.2020.10611932950790
]Search in Google Scholar
[
25. Radwan M, Jurewicz J, Wielgomas B, Piskunowicz M, Sobala W, Radwan P, Jakubowski L, Hawuła W, Hanke W. The association between environmental exposure to pyrethroids and sperm aneuploidy. Chemosphere. 2015;128:42-8;10.1016/j.chemosphere.2014.12.07725655817
]Search in Google Scholar
[
26. Dziewirska E, Radwan M, Wielgomas B, Klimowska A, Radwan P, Kałużny P, Hanke W, Słodki M, Jurewicz J. Human Semen Quality, Sperm DNA Damage, and the Level of Urinary Concentrations of 1N and TCPY, the Biomarkers of Nonpersistent Insecticides. Am J Mens Health. 2019; 13(1):1557988318816598;10.1177/1557988318816598677554630813854
]Search in Google Scholar
[
27. Radwan M, Jurewicz J, Wielgomas B, Sobala W, Piskunowicz M, Radwan P, Hanke W. Semen quality and the level of reproductive hormones after environmental exposure to pyrethroids. J Occup Environ Med. 2014; 56(11):1113-9;10.1097/JOM.000000000000029725376404
]Search in Google Scholar
[
28. Wielgomas B, Nahorski W, Czarnowski W. Urinary concentrations of pyrethroid metabolites in the convenience sample of an urban population of Northern Poland. Int J Hyg Environ Health. 2013; 216(3):295-300;10.1016/j.ijheh.2012.09.00123021951
]Search in Google Scholar
[
29. Klimowska A, Wielgomas B. Off-line microextraction by packed sorbent combined with on solid support derivatization and GC-MS: Application for the analysis of five pyrethroid metabolites in urine samples. Talanta. 2018;176:165-171;10.1016/j.talanta.2017.08.01128917736
]Search in Google Scholar
[
30. Wielgomas B, Piskunowicz M. Biomonitoring of pyrethroid exposure among rural and urban populations in northern Poland. Chemosphere. 2013; 93(10):2547-53;10.1016/j.chemosphere.2013.09.07024156982
]Search in Google Scholar
[
31. Rodzaj W, Wileńska M, Klimowska A, Dziewirska E, Jurewicz J, Walczak-Jędrzejowska R, Słowikowska-Hilczer J, Hanke W, Wielgomas B. Concentrations of urinary biomarkers and predictors of exposure to pyrethroid insecticides in young, Polish, urban-dwelling men. Sci Total Environ. 2021; 773:145666;10.1016/j.scitotenv.2021.14566633596511
]Search in Google Scholar
[
32. Jurewicz J, Radwan M, Wielgomas B, Sobala W, Piskunowicz M, Radwan P, Bochenek M, Hanke W. The effect of environmental exposure to pyrethroids and DNA damage in human sperm. Syst Biol Reprod Med. 2015; 61(1):37-43.10.3109/19396368.2014.98188625376306
]Search in Google Scholar
