The impact of Triton WR-1339 induced hyperlipidemia on the effects of benzo(a)pyrene or guaiacol on α- and γ-tocopherol pools and selected markers of pro-/antioxidative balance in rat plasma and erythrocytes
► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ► Tocopherol pools and pro-/antioxidative balance markers in blood were measured. ► In normolipemic groups malondialdehyde (MDA) increased and erythrocyte tocoph...
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Published in | Environmental toxicology and pharmacology Vol. 33; no. 3; pp. 386 - 393 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.05.2012
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Online Access | Get full text |
ISSN | 1382-6689 1872-7077 1872-7077 |
DOI | 10.1016/j.etap.2012.01.004 |
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Abstract | ► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ► Tocopherol pools and pro-/antioxidative balance markers in blood were measured. ► In normolipemic groups malondialdehyde (MDA) increased and erythrocyte tocopherol decrease after BaP or guaiacol short-lasting treatment. ► Pro-oxidative effects of BaP and guaiacol were not increased in hyperlipemic animals.
The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can be formed during enzymatic biotransformation or in the process of co-oxygenation with lipid peroxidation. This study assesses if the acute hyperlipidemia can increase pro-oxidative effects of BaP as a factor intensifying processes of lipid peroxidation and co-oxygenation. After three days of i.p. administration of BaP or guaiacol (equimolar dose 10mg/kg b.w.) without or with the hyperlipidemia inducer-Triton WR-1339 to male Wistar rats, the levels of α- and γ-tocopherol were measured in erythrocytes and plasma together with the level of lipid peroxidation as malonyldialdehyde (MDA) concentration. Guaiacol was chosen as a reference substance due to its high ability to co-oxygenate. Additionally, the activity of superoxide dismutase (Cu,ZnSOD) in erythrocytes and plasma was monitored. In normolipaemic groups the significant decrease in erythrocyte α-tocopherol pool and the increase in lipid peroxidation level were observed after BaP or guaiacol administration. In hyperlipaemic groups, despite the increase in the level of lipid peroxidation, there were no additional effects in tocopherol pools compared to the normolipaemic groups which could be attributed to co-oxygenation. Decrease of α-tocopherol in erythrocytes was proportional to the reduction in normolipemic subjects when accounting for the migration to hyperlipemic plasma. There was no co-oxygenation effect on the activity of superoxide dismutase (Cu,ZnSOD) in blood. |
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AbstractList | The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can be formed during enzymatic biotransformation or in the process of co-oxygenation with lipid peroxidation. This study assesses if the acute hyperlipidemia can increase pro-oxidative effects of BaP as a factor intensifying processes of lipid peroxidation and co-oxygenation. After three days of i.p. administration of BaP or guaiacol (equimolar dose 10mg/kg b.w.) without or with the hyperlipidemia inducer-Triton WR-1339 to male Wistar rats, the levels of α- and γ-tocopherol were measured in erythrocytes and plasma together with the level of lipid peroxidation as malonyldialdehyde (MDA) concentration. Guaiacol was chosen as a reference substance due to its high ability to co-oxygenate. Additionally, the activity of superoxide dismutase (Cu,ZnSOD) in erythrocytes and plasma was monitored. In normolipaemic groups the significant decrease in erythrocyte α-tocopherol pool and the increase in lipid peroxidation level were observed after BaP or guaiacol administration. In hyperlipaemic groups, despite the increase in the level of lipid peroxidation, there were no additional effects in tocopherol pools compared to the normolipaemic groups which could be attributed to co-oxygenation. Decrease of α-tocopherol in erythrocytes was proportional to the reduction in normolipemic subjects when accounting for the migration to hyperlipemic plasma. There was no co-oxygenation effect on the activity of superoxide dismutase (Cu,ZnSOD) in blood. The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can be formed during enzymatic biotransformation or in the process of co-oxygenation with lipid peroxidation. This study assesses if the acute hyperlipidemia can increase pro-oxidative effects of BaP as a factor intensifying processes of lipid peroxidation and co-oxygenation. After three days of i.p. administration of BaP or guaiacol (equimolar dose 10mg/kg b.w.) without or with the hyperlipidemia inducer-Triton WR-1339 to male Wistar rats, the levels of α- and γ-tocopherol were measured in erythrocytes and plasma together with the level of lipid peroxidation as malonyldialdehyde (MDA) concentration. Guaiacol was chosen as a reference substance due to its high ability to co-oxygenate. Additionally, the activity of superoxide dismutase (Cu,ZnSOD) in erythrocytes and plasma was monitored. In normolipaemic groups the significant decrease in erythrocyte α-tocopherol pool and the increase in lipid peroxidation level were observed after BaP or guaiacol administration. In hyperlipaemic groups, despite the increase in the level of lipid peroxidation, there were no additional effects in tocopherol pools compared to the normolipaemic groups which could be attributed to co-oxygenation. Decrease of α-tocopherol in erythrocytes was proportional to the reduction in normolipemic subjects when accounting for the migration to hyperlipemic plasma. There was no co-oxygenation effect on the activity of superoxide dismutase (Cu,ZnSOD) in blood.The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can be formed during enzymatic biotransformation or in the process of co-oxygenation with lipid peroxidation. This study assesses if the acute hyperlipidemia can increase pro-oxidative effects of BaP as a factor intensifying processes of lipid peroxidation and co-oxygenation. After three days of i.p. administration of BaP or guaiacol (equimolar dose 10mg/kg b.w.) without or with the hyperlipidemia inducer-Triton WR-1339 to male Wistar rats, the levels of α- and γ-tocopherol were measured in erythrocytes and plasma together with the level of lipid peroxidation as malonyldialdehyde (MDA) concentration. Guaiacol was chosen as a reference substance due to its high ability to co-oxygenate. Additionally, the activity of superoxide dismutase (Cu,ZnSOD) in erythrocytes and plasma was monitored. In normolipaemic groups the significant decrease in erythrocyte α-tocopherol pool and the increase in lipid peroxidation level were observed after BaP or guaiacol administration. In hyperlipaemic groups, despite the increase in the level of lipid peroxidation, there were no additional effects in tocopherol pools compared to the normolipaemic groups which could be attributed to co-oxygenation. Decrease of α-tocopherol in erythrocytes was proportional to the reduction in normolipemic subjects when accounting for the migration to hyperlipemic plasma. There was no co-oxygenation effect on the activity of superoxide dismutase (Cu,ZnSOD) in blood. ► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ► Tocopherol pools and pro-/antioxidative balance markers in blood were measured. ► In normolipemic groups malondialdehyde (MDA) increased and erythrocyte tocopherol decrease after BaP or guaiacol short-lasting treatment. ► Pro-oxidative effects of BaP and guaiacol were not increased in hyperlipemic animals. The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can be formed during enzymatic biotransformation or in the process of co-oxygenation with lipid peroxidation. This study assesses if the acute hyperlipidemia can increase pro-oxidative effects of BaP as a factor intensifying processes of lipid peroxidation and co-oxygenation. After three days of i.p. administration of BaP or guaiacol (equimolar dose 10mg/kg b.w.) without or with the hyperlipidemia inducer-Triton WR-1339 to male Wistar rats, the levels of α- and γ-tocopherol were measured in erythrocytes and plasma together with the level of lipid peroxidation as malonyldialdehyde (MDA) concentration. Guaiacol was chosen as a reference substance due to its high ability to co-oxygenate. Additionally, the activity of superoxide dismutase (Cu,ZnSOD) in erythrocytes and plasma was monitored. In normolipaemic groups the significant decrease in erythrocyte α-tocopherol pool and the increase in lipid peroxidation level were observed after BaP or guaiacol administration. In hyperlipaemic groups, despite the increase in the level of lipid peroxidation, there were no additional effects in tocopherol pools compared to the normolipaemic groups which could be attributed to co-oxygenation. Decrease of α-tocopherol in erythrocytes was proportional to the reduction in normolipemic subjects when accounting for the migration to hyperlipemic plasma. There was no co-oxygenation effect on the activity of superoxide dismutase (Cu,ZnSOD) in blood. Highlights ► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ► Tocopherol pools and pro-/antioxidative balance markers in blood were measured. ► In normolipemic groups malondialdehyde (MDA) increased and erythrocyte tocopherol decrease after BaP or guaiacol short-lasting treatment. ► Pro-oxidative effects of BaP and guaiacol were not increased in hyperlipemic animals. |
Author | Gawlik, Małgorzata B. Gawlik, Maciej Brandys, Jerzy |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22387351$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1002_lipd_12217 crossref_primary_10_1016_j_scitotenv_2020_138944 crossref_primary_10_1016_S1875_5364_16_30076_0 |
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Keywords | Co-oxygenation Guaiacol Benzo(a)pyrene Tocopherol Rat blood Hyperlipidemia |
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Snippet | ► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ► Tocopherol pools... Highlights ► The impact of hyperlipidemia induced by Triton WR-1339 on co-oxygenation effects of benzo(a)pyrene (BaP) or guaiacol was studied in rat. ►... The toxicity of carcinogenic benzo(a)pyrene (BaP) can be intensified by the pro-oxidative effects of metabolic activation. The oxidatively active products can... |
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SubjectTerms | alpha-tocopherol alpha-Tocopherol - blood Animals Benzo(a)pyrene Benzo(a)pyrene - toxicity biotransformation carcinogenicity Carcinogens - toxicity Co-oxygenation Emergency Erythrocytes gamma-tocopherol gamma-Tocopherol - blood Guaiacol Guaiacol - toxicity Hyperlipidemia Hyperlipidemias - blood Hyperlipidemias - chemically induced lipid peroxidation Lipid Peroxidation - drug effects Lipids - blood Male males Malondialdehyde - blood Polyethylene Glycols Rat blood Rats Rats, Wistar superoxide dismutase Superoxide Dismutase - blood Surface-Active Agents Tocopherol |
Title | The impact of Triton WR-1339 induced hyperlipidemia on the effects of benzo(a)pyrene or guaiacol on α- and γ-tocopherol pools and selected markers of pro-/antioxidative balance in rat plasma and erythrocytes |
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