Bifenthrin exerts proatherogenic effects via arterial accumulation of native and oxidized LDL in rats: the beneficial role of vitamin E and selenium
The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targete...
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| Vydáno v: | Environmental science and pollution research international Ročník 27; číslo 6; s. 5651 - 5660 |
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| Hlavní autoři: | , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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Berlin/Heidelberg
Springer Berlin Heidelberg
01.02.2020
Springer Nature B.V |
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| ISSN: | 0944-1344, 1614-7499, 1614-7499 |
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| Abstract | The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targeted. Thus, rats were treated by gastric gavage with combination of Vit E (100 mg/kg/bw) and Se (0.25 mg/kg/bw) in alone and co-treated groups for 90 days. Apart from control and Vit E-Se groups, all the groups were subjected to Bif (3 mg/kg, via gavage) toxicity. Results showed that Bif increased markedly plasmatic and aortic total cholesterol, LDL-cholesterol, native LDL-apoB-100, and oxidized-LDL, compared to the control. Moreover, Bif treatment significantly increased the plasmatic levels of the pro-inflammatory cytokines TNF-α, IL-2, and IL-6. In addition, the densitometric quantification of protein bands showed that the amount of hepatic native LDL-receptor protein decreased significantly in the intoxicated rats compared to the control group. The expression of arterial LDL receptors (LDLRs) and scavenger receptors (CD36) was amplified owing to Bif toxicity. This harmful effect was confirmed by histological study using Oil-Red-O staining. Owing to their antioxidant capacities, Vit E and Se have maintained all the changes in plasma and aorta lipids and prevented the pro-atherogenic effect observed in Bif-treated animals. |
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| AbstractList | The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targeted. Thus, rats were treated by gastric gavage with combination of Vit E (100 mg/kg/bw) and Se (0.25 mg/kg/bw) in alone and co-treated groups for 90 days. Apart from control and Vit E-Se groups, all the groups were subjected to Bif (3 mg/kg, via gavage) toxicity. Results showed that Bif increased markedly plasmatic and aortic total cholesterol, LDL-cholesterol, native LDL-apoB-100, and oxidized-LDL, compared to the control. Moreover, Bif treatment significantly increased the plasmatic levels of the pro-inflammatory cytokines TNF-α, IL-2, and IL-6. In addition, the densitometric quantification of protein bands showed that the amount of hepatic native LDL-receptor protein decreased significantly in the intoxicated rats compared to the control group. The expression of arterial LDL receptors (LDLRs) and scavenger receptors (CD36) was amplified owing to Bif toxicity. This harmful effect was confirmed by histological study using Oil-Red-O staining. Owing to their antioxidant capacities, Vit E and Se have maintained all the changes in plasma and aorta lipids and prevented the pro-atherogenic effect observed in Bif-treated animals. The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targeted. Thus, rats were treated by gastric gavage with combination of Vit E (100 mg/kg/bw) and Se (0.25 mg/kg/bw) in alone and co-treated groups for 90 days. Apart from control and Vit E-Se groups, all the groups were subjected to Bif (3 mg/kg, via gavage) toxicity. Results showed that Bif increased markedly plasmatic and aortic total cholesterol, LDL-cholesterol, native LDL-apoB-100, and oxidized-LDL, compared to the control. Moreover, Bif treatment significantly increased the plasmatic levels of the pro-inflammatory cytokines TNF-α, IL-2, and IL-6. In addition, the densitometric quantification of protein bands showed that the amount of hepatic native LDL-receptor protein decreased significantly in the intoxicated rats compared to the control group. The expression of arterial LDL receptors (LDLRs) and scavenger receptors (CD36) was amplified owing to Bif toxicity. This harmful effect was confirmed by histological study using Oil-Red-O staining. Owing to their antioxidant capacities, Vit E and Se have maintained all the changes in plasma and aorta lipids and prevented the pro-atherogenic effect observed in Bif-treated animals. The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targeted. Thus, rats were treated by gastric gavage with combination of Vit E (100 mg/kg/bw) and Se (0.25 mg/kg/bw) in alone and co-treated groups for 90 days. Apart from control and Vit E-Se groups, all the groups were subjected to Bif (3 mg/kg, via gavage) toxicity. Results showed that Bif increased markedly plasmatic and aortic total cholesterol, LDL-cholesterol, native LDL-apoB-100, and oxidized-LDL, compared to the control. Moreover, Bif treatment significantly increased the plasmatic levels of the pro-inflammatory cytokines TNF-α, IL-2, and IL-6. In addition, the densitometric quantification of protein bands showed that the amount of hepatic native LDL-receptor protein decreased significantly in the intoxicated rats compared to the control group. The expression of arterial LDL receptors (LDLRs) and scavenger receptors (CD36) was amplified owing to Bif toxicity. This harmful effect was confirmed by histological study using Oil-Red-O staining. Owing to their antioxidant capacities, Vit E and Se have maintained all the changes in plasma and aorta lipids and prevented the pro-atherogenic effect observed in Bif-treated animals.The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters disturbance and their pro-atherogenic possibility in Wistar rats. The ameliorative role of vitamin E (Vit E) and selenium (Se) were also targeted. Thus, rats were treated by gastric gavage with combination of Vit E (100 mg/kg/bw) and Se (0.25 mg/kg/bw) in alone and co-treated groups for 90 days. Apart from control and Vit E-Se groups, all the groups were subjected to Bif (3 mg/kg, via gavage) toxicity. Results showed that Bif increased markedly plasmatic and aortic total cholesterol, LDL-cholesterol, native LDL-apoB-100, and oxidized-LDL, compared to the control. Moreover, Bif treatment significantly increased the plasmatic levels of the pro-inflammatory cytokines TNF-α, IL-2, and IL-6. In addition, the densitometric quantification of protein bands showed that the amount of hepatic native LDL-receptor protein decreased significantly in the intoxicated rats compared to the control group. The expression of arterial LDL receptors (LDLRs) and scavenger receptors (CD36) was amplified owing to Bif toxicity. This harmful effect was confirmed by histological study using Oil-Red-O staining. Owing to their antioxidant capacities, Vit E and Se have maintained all the changes in plasma and aorta lipids and prevented the pro-atherogenic effect observed in Bif-treated animals. |
| Author | Hachani, Rafik Tir, Meriam Borgi, Mohamed Ali Ghazouani, Lakhdar Mufti, Afoua Feriani, Anouar Allagui, Mohamed Salah |
| Author_xml | – sequence: 1 givenname: Anouar surname: Feriani fullname: Feriani, Anouar email: ferianianwer@yahoo.fr organization: Unité de Biochimie Macromoléculaire et Génétique, Faculté des Sciences de Gafsa, cité Zarroug, Université de Gafsa – sequence: 2 givenname: Rafik surname: Hachani fullname: Hachani, Rafik organization: Unité de Physiologie Intégrée, Laboratoire de Pathologies Vasculaires, Faculté des Sciences de Bizerte, Université de Carthage, Laboratoire d’Etude de la Microcirculation (EA 3509), Faculté de Médecine Lariboisière-St. Louis, Université Paris VII – sequence: 3 givenname: Meriam surname: Tir fullname: Tir, Meriam organization: Unité de Physiologie et Environnement Aquatique, Faculté des Sciences de Tunis, Université Tunis EL Manar – sequence: 4 givenname: Lakhdar surname: Ghazouani fullname: Ghazouani, Lakhdar organization: Unité de Biochimie Macromoléculaire et Génétique, Faculté des Sciences de Gafsa, cité Zarroug, Université de Gafsa – sequence: 5 givenname: Afoua surname: Mufti fullname: Mufti, Afoua organization: Unité de Biochimie Macromoléculaire et Génétique, Faculté des Sciences de Gafsa, cité Zarroug, Université de Gafsa – sequence: 6 givenname: Mohamed Ali surname: Borgi fullname: Borgi, Mohamed Ali organization: Unité de Biochimie Macromoléculaire et Génétique, Faculté des Sciences de Gafsa, cité Zarroug, Université de Gafsa – sequence: 7 givenname: Mohamed Salah surname: Allagui fullname: Allagui, Mohamed Salah organization: Laboratoire d’Ecophysiologie Animale, Faculté des Sciences de Sfax |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30465240$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_jhazmat_2024_136603 crossref_primary_10_1080_26395940_2025_2470219 crossref_primary_10_1111_and_14456 crossref_primary_10_1016_j_ecoenv_2023_115365 crossref_primary_10_1038_s41598_024_56494_4 crossref_primary_10_3390_antiox11091785 crossref_primary_10_2478_phr_2021_0005 crossref_primary_10_1016_j_ecoenv_2021_112461 crossref_primary_10_3390_biomedicines11072010 crossref_primary_10_1002_jbt_22747 crossref_primary_10_1039_D2FO00888B crossref_primary_10_3390_biom10050753 |
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| Copyright | Springer-Verlag GmbH Germany, part of Springer Nature 2018 Environmental Science and Pollution Research is a copyright of Springer, (2018). All Rights Reserved. |
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| Keywords | Pro-atherogenic Vit E-Se Aorta LDL Bifenthrin Lipid |
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| Snippet | The purpose of this study was to investigate, for the first time, the effects of Bifenthrin (Bif) chronic exposure on plasmatic and aortic lipid parameters... |
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| SubjectTerms | Animals antioxidant activity Antioxidants Aorta Aorta - drug effects Aorta - pathology Aquatic Pollution Atmospheric Protection/Air Quality Control/Air Pollution bifenthrin CD36 antigen Cholesterol Cholesterol, LDL Chronic exposure Cytokines Densitometers densitometry Earth and Environmental Science Ecotoxicology Environment Environmental Chemistry Environmental Health Environmental Pollution Environmental science Food Contamination histology Inflammation Insecticides Interleukin 2 Interleukin 6 laboratory animals Lipids Lipoproteins, LDL Low density lipoprotein low density lipoprotein cholesterol low density lipoprotein receptors Male oxidation Proteins Pyrethrins - toxicity Rats Rats, Wistar Receptors Risk Assessment and Remediation Rodents Scavenger receptors Selenium Selenium - pharmacology staining Tocopherol Toxicity tumor necrosis factor-alpha Tumor necrosis factor-α Vitamin E Vitamin E - pharmacology Waste Water Technology Water Management Water Pollution Control |
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| Title | Bifenthrin exerts proatherogenic effects via arterial accumulation of native and oxidized LDL in rats: the beneficial role of vitamin E and selenium |
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| Volume | 27 |
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