Phenols animal metabolism

Examples of PLC with autoradiography detection include the published studies on labeling of l- H-PAF-aceter [25] diazinon and related compounds from plant material [26] metabolic fate of triamcinolone acetonide in laboratory animals [27] synthesis of 4-S-cysteaminyl-[U- " C]phenol antimelanoma agent [28] radiolabeled... 

Comparative Toxicokinetics. The metabolism and excretion of orally administered phenol in 18 animal species have been compared to metabolism and excretion in humans (Capel et al. 1972). The rat was the most similar to the human with respect to the fraction of administered dose excreted in urine in 24 hours (95%) and the number and relative abundance of the 4 principal metabolites excreted in urine (sulfate and glucuronide conjugates of phenol and 1,4-dihydroxybenzene). The rat excreted a larger fraction of the orally administered dose than the guinea pig or the rabbit (Capel et al. 1972) and appears to be the least susceptible of the three species to respiratory, cardiovascular, hepatic, renal, and neurological effects of inhaled phenol (Deichmann et al. 1944). More rapid metabolism and excretion of absorbed phenol may account for the lower sensitivity of the rat to systemic effects of phenol. More information on the relative rates of metabolism of phenol in various species is needed to identify the most appropriate animal model for studying potential health effects in humans. 

The nutritional value of the diet influences the ability of herbivores to detoxify plant secondary metabolites (Schwass and Finley, 1985). For instance, voles in winter have to consume the bark of birch Betula sp.). This causes stress and leads to poor growth and high mortality among young animals. Birch bark contains phenolics and terpenoids. Both are metabolized by cytochrome P450 monooxidases in phase I and conjugated with glucuronic acid in phase II. 

The thyroid hormone thyroxine (tetraiodo-thyronine, T4) and its active form triiodothyronine (T3) are derived from the amino acid tyrosine. The iodine atoms at positions 3 and 5 of the two phenol rings are characteristic of them. Post-translational synthesis of thyroxine takes place in the thyroid gland from tyrosine residues of the protein thyro-globulin, from which it is proteolytically cleaved before being released, iodothyronines are the only organic molecules in the animal organism that contain iodine. They increase the basal metabolic rate, partly by regulating mitochondrial ATP synthesis, in addition, they promote embryonic development. 

Phenol is produced through both natural and anthropogenic processes. It is naturally occurring in some foods, human and animal wastes, and decomposing organic material, and is produced endogenously in the gut from the metabolism of aromatic amino acids. Phenol has been isolated from coal tar, but it is now synthetically manufactured (EPA, 2002). Currently, the largest use of phenol is as an intermediate in the production of phenolic resins, which are used in the plywood, adhesive, construction, automotive, and appliance industries. Phenol is also used in the production of synthetic fibers such as nylon and for epoxy resin precursors such as bisphenol-A. 

Numerous studies on the metabolism of 2,1t-dichlorophenoxy-acetic acid (2,1+-D) and related herbicides in animals have shown that these chemicals are absorbed and distributed rapidly in the body, and are excreted, undegraded, relatively quantitatively in the urine within a week after administration (M Pharmacokinetic studies with 2,1+,5-T in rats and dogs (5.) and in humans (6J supported these findings, and demonstrated that rates of clearance from plasma and elimination in urine depend on dosage level, animal species, and chemical structure of the phenoxy acid being studied ( + ). Corresponding chlorinated phenol metabolites were detected only in ruminants (M or in trace amounts in urine of rats fed very high doses of phenoxy herbicides (7.) ... 

Animals. Rapidly absorbed, extensively metabolised and rapidly excreted. No evidence of accumulation, even on repeated dosing. Metabolism proceeds by oxidation to phenolic derivatives which are excreted as glucuronide or sulfate conjugates Plants. Little metabolism occurs in fruit Soil. Rapid degradation, DT50 7-54 days. Low potential for leaching... 

The metabolic fate of benzene can be altered in fasted animals. In nonfasted rats that received an intraperitoneal injection of 88 mg of benzene, the major metabolites present in urine were total conjugated phenols (14-19% of dose), glucuronides (3-4% of dose), and free phenol (2-3% of dose). However, in rats fasted for 24 hours preceding the same exposure, glucuronide conjugation increased markedly (18-21% of dose) (Cornish and Ryan 1965). Free phenol excretion (8-10% of dose) was also increased in... 

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