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Metabolism PCBs resistance

Another entry point for accumulation of organic in animal tissue and animal food products is direct ingestion of contaminated soil by grazing animals [44]. The compounds of main concern are the halogenated aromatics, including PCBs, organochlorine pesticides, PCDDs and PCDFs, which are resistant to metabolization and tend to accumulate in animal fat. The bioaccumulation factor (the ratio of the concentration of animal tissue or produce to the concentration in the diet) can be as high as 5-6 [43]. Compounds such as PAHs and phthalate esters are readily metabolised and excreted by the animals and thus do not accumulate in animal tissue or products. [Pg.486]

The polychlorinated biphenyls (PCBs, coplanar biphenyls) have been used in a large variety of applications as dielectric and heat transfer fluids, lubricating oils, plasticizers, wax extenders, and flame retardants. Their industrial use and manufacture in the USA were terminated by 1977. Unfortunately, PCBs persist in the environment. The products used commercially were actually mixtures of PCB isomers and homologs containing 12-68% chlorine. These chemicals are highly stable and highly lipophilic, poorly metabolized, and very resistant to environmental degradation they bioaccumulate in food chains. Food is the major source of PCB residues in humans. [Pg.1223]

Like PCBs, these chemicals are very stable and highly lipophilic. They are poorly metabolized and very resistant to environmental degradation. [Pg.1223]

These PCDFs were stiU detectable in victims of the poisoning more than eleven years after the exposure, and they seemed to be retained more than PCBs. They have been detected in the livers of victims of Yusho disease some years after the exposure occurred. Furthermore, the isomers and congeners (see box) retained in the livers were the most toxic, it would seem because these are more resistant to metabolism and so are more persistent. [Pg.129]

Polychlorinated diphenyl ethers (PCDE) are common impurities in chlorophenol formulations, which were earlier used as fungicides, slimicides, and as wood preservatives. PCDEs are structurally and by physical properties similar to polychlorinated biphenyls (PCB). They have low water solubility and are lipophilic. PCDEs are quite resistant to degradation and are persistent in the environment. In the aquatic environment, PCDEs bioaccumulate. These compounds are found in sediment, mussel, fish, bird, and seal. PCDEs show biomagnification potential, since levels of PCDEs increase in species at higher trophic levels. PCDEs are also detected in human tissue. Despite the persistence and bio accumulation, the significance of PCDEs as environmental contaminants is uncertain. The acute toxicity and Ah-receptor-me-diated (aryl hydrocarbon) activity of PCDEs is low compared to those of polychlorinated di-benzo-p-dioxins (PCDD) and dibenzofurans (PCDF). Due to structural similarity to thyroid hormone, PCDEs could bind to thyroid hormone receptor and alter thyroid function. Furthermore, PCDEs might be metabolized to toxic metabolites. In the environment, it is possible that photolysis converts PCDEs to toxic PCDDs and PCDFs. [Pg.157]

Polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), polychlorobiphenyls (PCBs), and polychlorophenols (PCPs) are well-known artifacts ubiquitous in the present environment. Due to their lipophilic-ity and resistance to metabolism or chemical degradation these have the potential to accumulate in the food chain and cause toxic effects [1, 2]. Polycyclic aromatic sulfur heterocycles (PASHs) along with different kinds of polycyclic aromatic compounds (PACs) also occur widely in the environment [3,4]. In particular, alkylated dibenzothiophenes have previously been found to be persistent residues in the marine environment after oil spills. Dibenzothiophene and its alkylated derivatives have been found to accumulate in fish and other marine organisms [5-7]. [Pg.290]

The PBDEs are of particular concern. They are incorporated into polymer matrices, but are not covalently bonded and readily leach out of substrates holding them. These compounds are similar in structure to PCBs, are persistent organic polluters (POPs), and are resistant to environmental degradation and metabolism. They can be absorbed via inhalation, ingestion, and dermal contact. The less-brominated PBDE species (tetra-, penta-, and hexa- moieties) have been found in human blood, adipose tissue, and breast milk. These bioaccumulate in human adipose tissues. 16 ... [Pg.165]

In that study, muscle of treated quails had increased loadings of congeners chlorinated in the 2,4,5 position (such as PCBs 138,153,170, and 180), and these are comparatively toxic and resistant to metabolic degradation. More research is needed on variables known to modify PCB uptake, retention, translocation, and toxicity. [Pg.636]


See other pages where Metabolism PCBs resistance is mentioned: [Pg.26]    [Pg.28]    [Pg.98]    [Pg.1306]    [Pg.374]    [Pg.92]    [Pg.1306]    [Pg.21]    [Pg.1377]    [Pg.161]    [Pg.92]    [Pg.320]    [Pg.330]    [Pg.1799]    [Pg.2094]    [Pg.56]    [Pg.366]    [Pg.129]    [Pg.275]    [Pg.441]    [Pg.543]    [Pg.52]    [Pg.9]    [Pg.354]    [Pg.414]    [Pg.628]    [Pg.25]    [Pg.555]    [Pg.70]    [Pg.403]    [Pg.404]    [Pg.107]    [Pg.48]    [Pg.311]    [Pg.671]   
See also in sourсe #XX -- [ Pg.129 ]




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