ABSTRACT
In this study, the effect of environmental toxins such as pentachlorophenol (PCP), tetrachlorocatechol (TeCC) and tetrachloroguaiacol (TeCG) on human peripheral blood lymphocytes was investigated. All the compounds studied increased the size and granularity of the lymphocytes in the concentrations range from 5 to 600 ppm. The PCP caused the strongest increase in the size of the cells, whereas lymphocytes granularity was more strongly increased by TeCC and PCP than by TeCG. The PCP and its derivatives in the concentrations range from 1 to 125 ppm significantly depleted ATP level. It was also observed that PCP most strongly decreased ATP content at its highest concentration of 125 ppm. Moreover, PCP caused the highest loss of lymphocytes viability in the concentrations range from 125 to 600 ppm. The TeCC in the concentrations of 1 and 5 ppm significantly increased the level of strand breaks in DNA, whereas lower damage was noted for PCP, and particularly for TeCG. The increase in carbonyl groups content was more strongly induced by TeCG and TeCC than by PCP in the concentrations range from 0.04 to 1 ppm; however, in a concentration of 5 ppm, all the compounds studied increased this parameter to a similar degree. DNA and protein damage was the most probably induced by free radical formation, as it was observed that all the compounds examined, and TeCC, in particular, were able of oxidize a fluorescent probe 6-carboxy-2',7'-dichlorodihydrofluorescein in the concentrations range from 0.01 to 1 ppm.
Subject(s)
Lymphocytes/drug effects , Pentachlorophenol/toxicity , Adenosine Triphosphate/analysis , DNA Damage , Dose-Response Relationship, Drug , Humans , Lymphocytes/metabolism , Lymphocytes/pathology , Oxidation-Reduction , Pentachlorophenol/analogs & derivatives , Protein Carbonylation/drug effects , Reactive Oxygen Species/metabolismABSTRACT
Pentachlorophenol (PCP) is a persistent chemical contaminant that has been extensively investigated in terms of its toxicology and metabolism. Similar to PCP, other chlorinated phenol derivatives are also widely present in the environment from various sources. Even though some of the chlorine-substituted phenols, and particularly PCP, are well-known inhibitors of phenol sulfotransferases (SULTs), these compounds have been shown to undergo sulfation in humans. To investigate the enzymatic basis for sulfation of PCP in humans, we have studied the potential for PCP as well as the mono-, di-, tri-, and tetra-chlorinated phenols to serve as substrates for human hydroxysteroid sulfotransferase, hSULT2A1. Our results show that all of these compounds are substrates for this isoform of sulfotransferase, and the highest rates of sulfation are obtained with PCP, trichlorophenols, and tetrachlorophenols. Much lower rates of sulfation were obtained with isomers of monochlorophenol and dichlorophenol as substrates for hSULT2A1. Thus, the sulfation of polychlorinated phenols catalyzed by hSULT2A1 may be a significant component of their metabolism in humans.
Subject(s)
Environmental Pollutants/metabolism , Pentachlorophenol/metabolism , Sulfotransferases/metabolism , Environmental Pollutants/chemistry , Humans , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/chemistry , Substrate SpecificityABSTRACT
A relationship between formation of methylsulfonyl (MeSO2) metabolites of 2,2',4,5,5'-pentachlorobiphenyl (PentaCB) and decrease in serum thyroxine (T4) level was examined in the rats and mice after a single i.p. injection of PentaCB (342 micromol/kg body weight). In either rats or mice, levels of the 3- and 4-MeSO2 metabolites of PentaCB in the liver and feces increased in a time-dependent fashion up to 8 days after PentaCB-treatment. However, there was a marked difference between rats and mice in the amount of the metabolites formed, and the cumulative amount of the either MeSO2 metabolite for 8 days after PentaCB treatment in the liver was 4 to 15 times higher in mice than in rats. On the other hand, a 40 to 60% decrease in level of serum total T4 occurred in both rats and mice at 1 day after PentaCB treatment, and the decrease was retained up to 8 days after PentaCB treatment. Thus, there was a marked difference between rats and mice in the formation of MeSO2 metabolites from PentaCB but not a significant difference between rats and mice in PentaCB-induced decrease in the level of serum total T4, indicating that PentaCB-induced decrease in the level of serum total T4 is not necessarily dependent on the MeSO2 metabolites formed.
Subject(s)
Polychlorinated Biphenyls/pharmacology , Thyroxine/blood , Animals , Feces/chemistry , Glucuronosyltransferase/metabolism , Liver/enzymology , Male , Mice , Monosaccharide Transport Proteins/metabolism , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/metabolism , Polychlorinated Biphenyls/pharmacokinetics , Rats , Rats, Wistar , Species Specificity , Sulfones/metabolism , Time FactorsABSTRACT
The purpose of this study was to investigate the degree of chlorination of catechol (CAT) derivatives of pentachlorophenol (PCP) on the induction of cytotoxicity and DNA damaging effects in calf thymus DNA (ct-DNA) and in two human breast carcinoma cell lines. Results indicated that with the addition of the transition metal copper(II), increases in the amount of aldehydic DNA lesions (ADL) were detected in ct-DNA exposed to PCP-derived CATs over the corresponding control. The DNA lesions induced by various degrees of chlorination of PCP-derived CATs decrease in the rank order CAT congruent with 4-chlorocatechol (4-ClCAT) > 4,5-dichlorocatechol (4,5-Cl2CAT) > 3,4,5-trichlorocatechol (3,4,5-Cl3CAT) > tetrachlorocatechol (Cl4CAT). In contrast, Cl4CAT was the only congeneric form of PCP-derived catechols that induced a significant increase in the number of ADL in human MCF-7 cells, and this only occurred when glutathione was depleted. Pretreatment with copper(I) and iron(II) chelators significantly reduced the formation of ADL in cells exposed to Cl4CAT. The data also indicated that the ADL induced by Cl4CAT in MCF-7 cells contain approximately 70% putrescine excisable ADL. This evidence confirmed that the ADL induced by Cl4CAT in MCF-7 cells were derived from oxidative events. In addition, we demonstrated that the depletion of NAD(P)H in human T47D cells exposed to chlorinated CATs decreased in the rank order Cl4CAT >> 4-ClCAT congruent with CAT. The depletion of NAD(P)H induced by Cl4CAT in T47D cells was partially blocked by catalase, superoxide dismutase, dimethyl sulfoxide, and copper(I) and iron(II) specific chelators. Additionally, the depletion of NAD(P)H in T47D cells exposed to Cl4CAT (1-10 microM) was completely blocked by three types of poly(ADP-ribose) polymerase-1 inhibitors. This evidence suggests that Cl4CAT induces an imbalance in DNA repair and the subsequent accumulation of DNA strand breaks in human cultured cells. Overall, these findings indicate that dechlorination may decrease the potentials of chlorinated catechols to induce oxidative DNA lesions and cytotoxic effects in living cells.
Subject(s)
Breast Neoplasms/metabolism , Catechols , DNA Damage , DNA/drug effects , Pentachlorophenol , Poly(ADP-ribose) Polymerases/drug effects , Animals , Breast Neoplasms/drug therapy , Catechols/chemistry , Catechols/pharmacology , Catechols/toxicity , Cattle , Cell Line, Tumor , Cell Survival/drug effects , DNA/chemistry , Enzyme Activation/drug effects , Enzyme Inhibitors/pharmacology , Ethylmaleimide/pharmacology , Female , Glutathione/drug effects , Humans , NADP/metabolism , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/pharmacology , Pentachlorophenol/toxicity , Poly (ADP-Ribose) Polymerase-1 , Poly(ADP-ribose) Polymerases/metabolismABSTRACT
The complex formed between 4-methylpyridine and pentachlorophenol (4MPPCP) crystallizes in a triclinic space group. If the same complex is synthesized from deuterated pentachlorophenol (4MPPCP-d1), it crystallizes in an entirely different monoclinic polymorph. Solid-state NMR of samples synthesized with a full range of deuteration levels, crystallized from solution or the melt, and in the presence or absence of seeds confirms that the isotopomers indeed have different thermodynamically stable crystal structures. The phenomenon is apparently due to very different hydrogen bond strengths between the two polymorphs.
Subject(s)
Pentachlorophenol/analogs & derivatives , Pyridines/chemistry , Deuterium , Hydrogen Bonding , Kinetics , Magnetic Resonance Spectroscopy/methods , Pentachlorophenol/chemistry , ThermodynamicsABSTRACT
Pentachlorophenol (PCP), a fungicide and insecticide, leaves behind considerable residue in the environment in the form of unreacted molecule, metabolites and photoreduction products. Most of the previously reported photoproducts have resulted from dechlorination of the parent molecule. We have shown that photoreduction of PCP also proceeds by photoreduction of the parent molecule at carbons 2 and 4. These products were identified and characterized as 2-dehydro-2,3,4,5,6-pentachlorocyclohexanone (II) and 2,3,4,5,6-pentachlorocyclohexanone (IV). Both of them display keto-enol tautomerism. Identification and characterization of new photoproducts of PCP is significant for determining its overall environmental impact in the ecosystem.
Subject(s)
Environmental Pollutants/analysis , Pentachlorophenol/analysis , Environmental Monitoring , Isomerism , Oxidation-Reduction , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/chemistry , PhotochemistryABSTRACT
1. Pentachlorophenyl methyl sulphoxide and pentachlorophenyl methyl sulphone were found to be substrates for microsomal and cytosolic glutathione-S-transferase of rabbit, monkey, chicken and human liver, covalently immobilized on beaded sepharose. 2. Protein was immobilized with greater than 95% transferase activity, measured by dinitrochlorobenzene. Immobilized rabbit liver microsomal transferase activity was more stable than immobilized cytosolic activity. 3. The sulphoxide moiety was displayed by glutathione in the presence of chicken liver microsomal protein. The sulphone moiety was displayed by glutathione in the formation of a diglutathione under catalysis by rhesus monkey liver cytosolic and microsomal protein. 4. Chlorine was displaced by transferases from all species to form regioisomeric monoglutathiones. 5. Qualitative and quantitative differences were observed in product distributions between species and between microsomal and cytosolic protein.
Subject(s)
Chlorobenzenes/metabolism , Glutathione/metabolism , Pentachlorophenol/analogs & derivatives , Sulfones/metabolism , Sulfoxides/metabolism , Agriculture , Animals , Chickens , Cytosol/metabolism , Glutathione Transferase/metabolism , Humans , In Vitro Techniques , Macaca mulatta , Microsomes, Liver/metabolism , Pentachlorophenol/metabolism , Rabbits , Xenobiotics/metabolismABSTRACT
Effects of hexachlorobenzene (HCB) and its sulfur-containing metabolites on the heme metabolic enzymes in rat liver were investigated. A single injection of HCB caused the increase in activities of delta-aminolevulinic acid (ALA) synthetase and heme oxygenase, and contents of cytochrome P-450 and total heme. After a single injection of pentachlorothioanisol (PCTA) or pentachlorophenyl methyl sulfore (PCPSO2Me), ALA synthetase activity was enhanced. Heme oxygenase activity was increased by PCPSO2Me treatment. Cytochrome P-450 and total heme contents were increased by PCPSO2Me or 1,4-bis(methylthio)tetrachlorobenzene (MTTCB). When HCB was injected once daily for 5 weeks, a marked increase in ALA synthetase activity, a significant decrease in ALA dehydratase, almost complete inhibition of uroporphyrinogen decarboxylase activity, and an increased excretion of total porphyrin in the urine were shown. After chronic treatment with its sulfur-containing compounds, PCPSO2Me and MTTCB produced a significant increase in ALA synthetase activity. However, activities of ALA dehydratase and uroporphyrinogen decarboxylase, and excretion of total porphyrin in the urine were unaltered. At this time, the concentrations of the corresponding sulfur-containing compound and related metabolite(s) in blood, liver and kidney were nearly the same as those observed in HCB-treated rats. It is suggested that PCPSO2Me and MTTCB could induce the hepatic ALA synthetase, but, these metabolites, and also PCTA, were not able to induce the porphyria in female rats, and the induction of porphyria by HCB is not attributable to the action of its sulfur-containing compound.
Subject(s)
5-Aminolevulinate Synthetase/biosynthesis , Heme/metabolism , Hexachlorobenzene/pharmacology , Liver/enzymology , Sulfur/pharmacology , Animals , Chlorobenzenes/administration & dosage , Chlorobenzenes/pharmacology , Drug Administration Schedule , Female , Hexachlorobenzene/administration & dosage , Hexachlorobenzene/metabolism , Pentachlorophenol/administration & dosage , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/pharmacology , Porphyrins/urine , Rats , Rats, Inbred Strains , Sulfones/administration & dosage , Sulfones/pharmacology , Sulfur/administration & dosage , Sulfur/pharmacokinetics , Tissue DistributionABSTRACT
Palmitoylpentachlorophenol (PPCP), which is a lipid conjugate of a xenobiotic compound, has been found in human fat. To study the toxicity associated with PPCP, rats were given 100 mg/kg PPCP and sacrificed at 4, 8 and 12 days. The target organ identified was the exocrine pancreas; no other major organs examined showed any gross or histopathological abnormality. At 4 and 8 days after treatment, focal, spotty vacuolation, and loss of pancreatic acini was observed. Acute inflammatory infiltrate was also observed in parenchyma at all time points and the loss of acinar tissue was resolved through fibrous tissue formation by 12 days. The present study indicates that PPCP has a specific target organ toxicity.
Subject(s)
Chlorophenols/toxicity , Palmitates/toxicity , Palmitic Acids/toxicity , Pancreas/drug effects , Pentachlorophenol/toxicity , Animals , Fatty Acids/metabolism , Male , Pancreas/pathology , Pentachlorophenol/analogs & derivatives , Rats , Rats, Inbred Strains , Vacuoles/drug effectsSubject(s)
Adipose Tissue/analysis , Chlorophenols/isolation & purification , Environmental Pollutants/analysis , Palmitates/isolation & purification , Palmitic Acids/isolation & purification , Pentachlorophenol/isolation & purification , Humans , Palmitic Acid , Palmitic Acids/metabolism , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/analysis , Pentachlorophenol/metabolismSubject(s)
Chlorophenols/biosynthesis , Chlorophenols/metabolism , Glucuronates/biosynthesis , Microsomes, Liver/metabolism , Pentachlorophenol/biosynthesis , Pentachlorophenol/metabolism , Animals , Humans , In Vitro Techniques , Male , Pentachlorophenol/analogs & derivatives , Rats , Rats, Inbred Strains , Species SpecificityABSTRACT
The DNA-damaging potential of pentachlorophenol (PCP) and its metabolite tetrachlorohydroquinone (TCH) was investigated. TCH was found to bind covalently to calf-thymus DNA and to cause single-strand breaks in PM2 DNA. No DNA-damaging effects were observed for PCP. Exposure of human fibroblasts to PCP and TCH showed that TCH is more toxic, when colony-forming ability after exposure to the agent is used as a measure of toxicity. In the evaluation of the mutagenic and carcinogenic potential of PCP the metabolite TCH should be taken into consideration.
Subject(s)
Chlorophenols/toxicity , Hydroquinones/toxicity , Mutagens , Pentachlorophenol/toxicity , Biotransformation , Cell Survival/drug effects , Cells, Cultured , Humans , Pentachlorophenol/analogs & derivatives , Structure-Activity RelationshipABSTRACT
The distribution of methylsulphonylpentachloro-[14C]benzene (I), methylthiopentachloro-[14C]benzene (II), 1,4-bis(methylthio)tetrachloro-[14C]benzene (III) and 1,2,4-tris(methylthio)trichloro[14C]benzene (IV) was studied after intravenous injection in mice. The administration of I resulted in a rapid and selective accumulation of radioactivity in the gray matter of the brain, the lung and the zona reticularis of the adrenal cortex. In mice pretreated with metyrapone, or with high dose of unlabelled I, the radioactivity in the tissues was increased, whereas pretreatment with diethyl maleate did not change the disposition of I. In mice injected with II-IV no site of selective accumulation in the tissues was observed. Similarly to I, compounds II-IV were rapidly excreted in bile/faeces and urine. It is proposed that the sulphone group is essential for the high affinity of I for the brain, lung and adrenal cortex.
Subject(s)
Adrenal Cortex/metabolism , Brain/metabolism , Chlorobenzenes/metabolism , Hexachlorobenzene/metabolism , Lung/metabolism , Pentachlorophenol/analogs & derivatives , Sulfones , Animals , Autoradiography , Bile/metabolism , Biotransformation , Feces/analysis , Metyrapone/pharmacology , Mice , Mice, Inbred C57BLABSTRACT
Laboratory trials of sodium 2.5 dichloro-4-bromophenol named B-2 for the molluscicidal effect against Oncomelania nasophora were carried out by Komiya's immersion technique. The values of LC50 of B-2 varied from 0.38 ppm to 0.54 ppm depending on the collection time of the snail. They were almost equal to those of NaPCP, but lower than those of Niclosamide. In the tests of toxicity to carp, rainbow trout and killifish, B-2 showed lower toxicity than NaPCP. Some aspects of mollusciciding application of the chemical were discussed.
Subject(s)
Fishes , Molluscacides/toxicity , Animals , Female , Lethal Dose 50 , Male , Niclosamide/toxicity , Pentachlorophenol/analogs & derivatives , Pentachlorophenol/toxicity , Rats , SnailsABSTRACT
Analogues of the potent uncoupler of oxidative phosphorylation pentachlorophenol were tested as inhibitors of proline and glycine transport by Bacillus subtilis. These analogues included less highly substituted chlorophenols and pentachlorothiophenol. Like pentachlorophenol, they are non-competitive inhibitors of proline transport and uncompetitive inhibitors of glycine transport. However, the less highly substituted chlorophenols are weaker acids than pentachlorophenol and also weaker inhibitors. Analysis indicated that the anionic form of the uncouplers is the inhibiting species. Pentachlorothiophenol, a water-insoluble anion, is also a potent inhibitor. These results support previous studies that concluded that uncouplers of oxidative phosphorylation inhibit amino acid transport by binding at specific sites on proteins, the free energy of interaction stabilizing 'unproductive' conformations. Such specific interactions of uncoupler with protein are probably commonplace.