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1.
Microbiology (Reading) ; 157(Pt 2): 459-472, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21071496

ABSTRACT

Forty fluorescent Pseudomonas strains isolated from white and red cocoyam roots were tested for their ability to synthesize N-acyl-l-homoserine lactones (acyl-HSLs). Remarkably, only isolates from the red cocoyam rhizosphere that were antagonistic against the cocoyam root rot pathogen Pythium myriotylum and synthesized phenazine antibiotics produced acyl-HSLs. This supports the assumption that acyl-HSL production is related to the antagonistic activity of the strains. After detection, the signal molecules were identified through TLC-overlay and liquid chromatography-multiple MS (LC-MS/MS) analysis. In our representative strain, Pseudomonas CMR12a, production of the signal molecules could be assigned to two quorum-sensing (QS) systems. The first one is the QS system for phenazine production, PhzI/PhzR, which seemed to be well conserved, since it was genetically organized in the same way as in the well-described phenazine-producing Pseudomonas strains Pseudomonas fluorescens 2-79, Pseudomonas chlororaphis PCL1391 and Pseudomonas aureofaciens 30-84. The newly characterized genes cmrI and cmrR make up the second QS system of CMR12a, under the control of the uncommon N-3-hydroxy-dodecanoyl-homoserine lactone (3-OH-C12-HSL) and with low similarity to other Pseudomonas QS systems. No clear function could yet be assigned to the CmrI/CmrR system, although it contributes to the biocontrol capability of CMR12a. Both the PhzI/PhzR and CmrI/CmrR systems are controlled by the GacS/GacA two-component regulatory system.


Subject(s)
Acyl-Butyrolactones/metabolism , Colocasia/microbiology , Phenazines/metabolism , Pseudomonas/metabolism , Quorum Sensing , Rhizosphere , Antibiosis , DNA, Bacterial/genetics , Genes, Bacterial , Mutation , Operon , Plant Roots/microbiology , Pseudomonas/genetics , Signal Transduction , Tandem Mass Spectrometry
2.
J Chromatogr A ; 1217(43): 6616-22, 2010 Oct 22.
Article in English | MEDLINE | ID: mdl-20483423

ABSTRACT

Perfluorinated compounds (PFCs), which are extensively used in a wide variety of applications because of their specific surfactant properties, have recently appeared as an important new class of global environmental pollutants. Quantitative analysis of PFCs in aqueous matrices remains, however, a challenging task. During this study, a new analytical method for the determination of 14 PFCs in surface-, sewage- and seawater was developed and validated. The target analytes were extracted using solid-phase extraction followed by liquid chromatography coupled to a time-of-flight mass spectrometer (LC-ToF-MS). The use of very narrow mass tolerance windows (< 10 ppm) resulted in a highly selective MS-technique for the detection of PFCs in complex aqueous matrices. Validation of this analytical method in surface-, sewage- and seawater resulted in limits of quantification (LOQs) varying from 2 to 200 ng L⁻¹, satisfying recoveries (92-134%), and good linearity (R²=0.99 for most analytes). Analysis of samples of the North Sea, the Scheldt estuary, and three harbours of the Belgian coastal region led to the detection of four different PFCs. Perfluorooctane sulfonate (PFOS) was found to be the most abundant PFC in levels up to 38.9 ng L⁻¹.


Subject(s)
Chromatography, Liquid/methods , Fluorocarbons/chemistry , Seawater/chemistry , Sewage/chemistry , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Belgium , Linear Models , North Sea , Reproducibility of Results , Sensitivity and Specificity
3.
J Steroid Biochem Mol Biol ; 119(3-5): 161-70, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20197090

ABSTRACT

Although beta-boldenone (bBol) used to be a marker of illegal steroid administration in calves, its endogenous formation has recently been demonstrated in these vertebrates. However, research on the pathway leading to bBol remains scarce. This study shows the usefulness of in vivo invertebrate models as alternatives to vertebrate animal experiments, using Neomysis integer and Lucilia sericata. In accordance with vertebrates, androstenedione (AED) was the main metabolite of beta-testosterone (bT) produced by these invertebrates, and bBol was also frequently detected. Moreover, in vitro experiments using feed-borne fungi and microsomes were useful to perform the pathway from bT to bBol. Even the conversion of phytosterols into steroids was shown in vitro. Both in vivo and in vitro, the conversion of bT into bBol could be demonstrated in this study. Metabolism of phytosterols by feed-borne fungi may be of particular importance to explain the endogenous bBol-formation by cattle. To the best of our knowledge, it is the first time the latter pathway is described in literature.


Subject(s)
Anabolic Agents/metabolism , Animal Feed/microbiology , Animal Use Alternatives/methods , Fungi/metabolism , Testosterone/analogs & derivatives , Androstenedione/metabolism , Animals , Biosynthetic Pathways , Cattle , Chromatography, High Pressure Liquid , Crustacea/metabolism , Diptera/metabolism , Larva/metabolism , Microsomes/metabolism , Phytosterols/metabolism , Pleurotus/metabolism , Substance Abuse Detection/veterinary , Tandem Mass Spectrometry , Testosterone/metabolism
4.
Anal Bioanal Chem ; 397(1): 345-355, 2010 May.
Article in English | MEDLINE | ID: mdl-20186540

ABSTRACT

Illegal steroid administration to enhance growth performance in veal calves has long been, and still is, a serious issue facing regulatory agencies. Over the last years, stating undisputable markers of illegal treatment has become complex because of the endogenous origin of several anabolic steroids. Knowledge on the origin of an analyte is therefore of paramount importance. The present study shows the presence of steroid analytes in wooden crates used for housing veal calves. For this purpose, an analytical procedure using accelerated solvent extraction (ASE(R)), solid-phase extraction (SPE) and ultra-high performance liquid chromatography coupled to triple quadrupole mass spectrometry (U-HPLC-MS-MS) is developed for the characterisation of androstadienedione (ADD), boldenone (bBol), androstenedione (AED), beta-testosterone (bT), alpha-testosterone (aT), progesterone (P) and 17alpha-hydroxy-progesterone (OH-P) in wood samples. In samples of wooden crates used for housing veal calves, ADD, AED, aT and P could be identified. Using the standard addition approach concentrations of these analytes were determined ranging from 20 +/- 4 ppb to 32 +/- 4 ppb for ADD, from 19 +/- 5 ppb to 44 +/- 17 ppb for AED, from 11 +/- 6 ppb to 30 +/- 2 ppb for aT and from 14 +/- 1 ppb to 42 +/- 27 ppb for P, depending on the sample type. As exposure of veal calves to steroid hormones in their housing facilities might complicate decision-making on illegal hormone administration, inequitable slaughter of animals remains possible. Therefore, complete prohibition of wooden calf accommodation should be considered.


Subject(s)
Anabolic Agents/analysis , Chromatography, High Pressure Liquid , Housing, Animal , Mass Spectrometry , Steroids/analysis , Wood , Animals , Cattle , Solid Phase Extraction , Substance Abuse Detection
5.
Article in English | MEDLINE | ID: mdl-19680866

ABSTRACT

The development of an analytical method that enables routine analysis of annatto dye, specifically bixin and norbixin, in meat tissue is described. Liquid-solid extraction was carried out using acetonitrile. Analysis was by HPLC with photodiode array detection using two fixed wavelengths (458 and 486 nm). The possibilities of ion trap mass spectrometry (MS) were also assessed. Method performance characteristics, according to Commission Decision 2002/657/EC, were determined, with recoveries between 99 and 102% and calibration curves being linear in the 0.5-10 mg kg(-1) range. The limit of quantification was 0.5 mg kg(-1).


Subject(s)
Carotenoids/analysis , Food Coloring Agents/analysis , Meat/analysis , Animals , Bixaceae , Chromatography, Liquid/methods , Food Analysis/methods , Mass Spectrometry/methods , Plant Extracts/analysis , Reproducibility of Results
6.
Anal Chim Acta ; 637(1-2): 2-12, 2009 Apr 01.
Article in English | MEDLINE | ID: mdl-19286005

ABSTRACT

Thyreostatic drugs (TS), illegally administrated to livestock for fattening purposes, are banned in the European Union since 1981 (Council Directive 81/602/EC). This paper reviews the trends in the analytical approaches for the determination of TS drugs in biological matrices. After a brief introduction on the different groups of compounds with a thyreostatic action, the most relevant legislation regarding the residue control of these compounds is presented. An overview of the analytical possibilities for the determination of TS in animal matrices, covering sample extraction, purification, separation techniques and detection methods is provided. Additionally, a brief outline of animal experiments is described that illustrates the excretion and distribution profiles of TS residues. Finally, the novel developments in TS analysis are highlighted. Also the possible semi-endogenous status of thiouracil is discussed.


Subject(s)
Antithyroid Agents/history , Animals , Antithyroid Agents/analysis , Antithyroid Agents/isolation & purification , Cattle , Chromatography, Gas , Chromatography, High Pressure Liquid , History, 20th Century , History, 21st Century , Inorganic Chemicals/analysis , Methylthiouracil/analysis , Oxazolidinones/analysis , Spectrometry, Mass, Electrospray Ionization , Swine , Tandem Mass Spectrometry
7.
J Chromatogr A ; 1216(46): 7964-76, 2009 Nov 13.
Article in English | MEDLINE | ID: mdl-19272610

ABSTRACT

A residue is a trace (microg kg(-1), ng kg(-1)) of a substance, present in a matrix. Residue analysis is a relatively young discipline and a very broad area, including banned (A) substances as well as registered veterinary medicinal products (B substances). The objective of this manuscript is to review future trends in the analysis of residues of veterinary drugs in meat producing animals out of historical perspectives. The analysis of residues in meat producing animals has known a tremendous evolution during the past 35-40 years. In the future, it can be foreseen that this evolution will proceed in the direction of the use of more and more sophisticated and expensive machines. These apparatus, and the necessary human resources for their use, will only be affordable for laboratories with sufficient financial resources and having guarantee for a sufficient throughput of samples.


Subject(s)
Chemistry Techniques, Analytical/history , Chemistry Techniques, Analytical/veterinary , Drug Residues/analysis , Veterinary Drugs/analysis , Animals , Chemistry Techniques, Analytical/methods , Chemistry Techniques, Analytical/trends , Drug Residues/history , Food Contamination/analysis , History, 20th Century , History, 21st Century , Humans , Veterinary Drugs/history
8.
Anal Chim Acta ; 611(1): 1-16, 2008 Mar 17.
Article in English | MEDLINE | ID: mdl-18298962

ABSTRACT

This paper reviews recently published multi-residue chromatographic methods for the determination of steroid hormones in edible matrices. After a brief introduction on steroid hormones and their use in animal fattening, the most relevant EU legislation regarding the residue control of these substances is presented. An overview of multi-residue analytical methods, covering sample extraction and purification as well as chromatographic separation and different detection methods, being in use for the determination of steroid hormones (estrogens, gestagens and androgens), is provided to illustrate common trends and method variability. Emphasis was laid on edible matrices and more specifically on meat, liver, kidney, fat and milk. Additionally, the possibilities of novel analytical approaches are discussed. The review also covers specific attention on the determination of natural steroids. Finally, the analytical possibilities for phytosterols, naturally occurring steroid analogues of vegetable origin and a specific group of steroid hormones with a hemi-endogenous status are highlighted.


Subject(s)
Food Analysis/methods , Hormones/analysis , Phytosterols/analysis , Steroids/analysis , Chromatography, Gas , Chromatography, Liquid , Mass Spectrometry
9.
Food Chem Toxicol ; 46(1): 140-8, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17766021

ABSTRACT

2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) is a carcinogenic heterocyclic amine formed in meats during cooking. Although the formation of PhIP metabolites by mammalian enzymes has been extensively reported, the involvement of the intestinal bacteria remains unclear. This study examined the urinary and fecal excretion of a newly identified microbial PhIP metabolite 7-hydroxy-5-methyl-3-phenyl-6,7,8,9-tetrahydropyrido[3',2':4,5]imidazo[1,2-a]pyrimidin-5-ium chloride (PhIP-M1) in humans. The subjects were fed 150 g of cooked chicken containing 0.88-4.7 microg PhIP, and urine and feces collections were obtained during 72 h after the meal. PhIP-M1 and its trideuterated derivate were synthesized and a LC/MS/MS method was developed for their quantification. The mutagenic activity of PhIP-M1, as analyzed using the Salmonella strains TA98, TA100 and TA102, yielded no significant response. Of the ingested PhIP dose, volunteers excreted 12-21% as PhIP and 1.2-15% as PhIP-M1 in urine, and 26-42% as PhIP and 0.9-11% as PhIP-M1 in feces. The rate of PhIP-M1 excretion varied among the subjects. Yet, an increase in urinary excretion was observed for successive time increments, whereas for PhIP the majority was excreted in the first 24h. These findings suggest that besides differences in digestion, metabolism and diet, the microbial composition of the gastrointestinal tract also strongly influences individual disposition and carcinogenic risk from PhIP.


Subject(s)
Bacteria/metabolism , Carcinogens/metabolism , Imidazoles/metabolism , Meat/analysis , Adult , Animals , Biotransformation , Chickens , Feces/chemistry , Humans , Imidazoles/blood , Imidazoles/urine , Mutagenicity Tests , Reproducibility of Results , Salmonella typhimurium/drug effects , Salmonella typhimurium/genetics , Spectrophotometry, Ultraviolet
10.
J Chromatogr A ; 1174(1-2): 132-7, 2007 Dec 07.
Article in English | MEDLINE | ID: mdl-17889887

ABSTRACT

Boar taint in entire male pigs remains a problem for fresh pork production. Since castration of pigs will be prohibited in the future on animal welfare reasons, attempts are made to detect boar taint pre and post mortem. Post mortem techniques focus on simultaneous quantification of the three boar taint substances by one simple and reliable method. In this study a liquid chromatographic multiple mass spectrometric (LC-MS(n)) method has been developed and validated for the simultaneous determination of indole (2,3-benzopyrrole, ID), skatole (3-methylindole, SK) and androstenone (5alpha-androst-16-en-3-one, AEON) in pig fat samples. Sample preparation was kept as short as possible, since a single extraction method for structurally different indols and steroids was seeked after. Analytes were extracted from the fat matrix by methanol and clean-up consisted of freezing the extract in liquid nitrogen followed by a filtration step. The analytes were chromatographically separated on a Symmetry C(18) column. Recoveries for ID, SK and AEON, as calculated from fortified fat samples using 2-methylindole (2-MID) as internal standard, were 96, 91 and 104%, respectively. However, matrix interferences were encountered determining the androstenone levels in fat. Linearity, determined in fat samples, was in the range of 50-1600 microg kg(-1) for the indolic compounds and 125-2000 microg kg(-1) for the steroid AEON. The correlation coefficients (R(2)) of the calibration curves were 0.998 for ID, 0.997 for SK and 0.810 for AEON.


Subject(s)
Androstenes/analysis , Chromatography, Liquid/methods , Indoles/analysis , Lipids/chemistry , Mass Spectrometry/methods , Skatole/analysis , Swine/metabolism , Animals , Calibration , Reproducibility of Results
11.
J Mass Spectrom ; 42(8): 983-98, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17657726

ABSTRACT

A residue is a trace (microg kg(-1), ng kg(-1)) of a substance, present in a matrix. Banned substances, such as growth promoters, which are abused in animal fattening and where this article is focused on, may be divided into four major groups: thyreostats, anabolics or anabolic steroids, corticosteroids and beta-agonists or repartitioning agents. The combination of chromatographic techniques with mass spectrometry (GC-MS(n), LC-MS(n), etc.) plays a key role in the production of specific results in residue analysis. In this review, the past, present and future of mass spectrometry in this area are discussed in the light of the impact of these substances on human health and the reliable production of analytical results, ready for challenge in a court.


Subject(s)
Drug Residues/analysis , Environmental Monitoring/methods , Food Contamination/prevention & control , Growth Substances/analysis , Mass Spectrometry/methods , Meat , Animals , Animals, Domestic , Environmental Monitoring/legislation & jurisprudence , Food Contamination/legislation & jurisprudence , Humans , Mass Spectrometry/trends
12.
Anal Chim Acta ; 586(1-2): 22-9, 2007 Mar 14.
Article in English | MEDLINE | ID: mdl-17386692

ABSTRACT

Since the 1970s, many analytical methods for the detection of illegal growth promoters, such as thyreostats, anabolics, beta-agonists and corticosteroids have been developed for a wide range of matrices of animal origin, including meat, fat, organ tissue, urine and faeces. The aim of this study was to develop an analytical method for the determination of ng L(-1) levels of estrogens, gestagens, androgens (EGAs) and corticosteroids in aqueous preparations (i.e. drinking water, drinking water supplements), commercially available on the 'black' market. For this, extraction was performed with Bakerbond C18 speedisk, a technique commonly used in environmental analysis. After fractionation, four fractions were collected using a methanol:water gradient program. Gas chromatography coupled to electron impact multiple mass spectrometry (GC-EI-MS2) screening for the EGAs was carried out on the derivatized extracts. For the detection of corticosteroids, gas chromatography coupled to negative chemical ionization mass spectrometry (GC-NCI-MS) was used after oxidation of the extracts. Confirmation was done by liquid chromatography coupled to electrospray ionization multiple mass spectrometry (LC-ESI-MS2). The combined use of GC and LC coupled to MS enabled the identification and quantification of anabolics and corticosteroids at the low ng L(-1) level. This study demonstrated the occurrence of both androgens and corticosteroids in different commercial aqueous samples.


Subject(s)
Adrenal Cortex Hormones/analysis , Drug Residues/analysis , Estrogens/analysis , Adipose Tissue/metabolism , Animals , Chromatography, Gas/methods , Feces , Mass Spectrometry/methods , Meat , Models, Chemical , Progestins/analysis , Spectrometry, Mass, Electrospray Ionization , Steroids/analysis , Urinalysis/methods , Water/analysis
13.
Anal Chim Acta ; 586(1-2): 49-56, 2007 Mar 14.
Article in English | MEDLINE | ID: mdl-17386696

ABSTRACT

Cholesterol is a well-known component in fats of animal origin and it also is the precursor of natural hormones. Phytosterols appear in plants and only differ slightly in structure from cholesterol. An important difference however is the low absorption in the gut of phytosterols and their saturated derivatives, the phytostanols. As a result, there is time for all kind of reactions in faecal material inside and outside of the gut. Determination of the abuse of natural hormones may be based on gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS). Abuse of natural hormones changes the 13C/12C ratio of some metabolites during a relatively long time. The formation of (natural) hormones in the gut may interfere with this method. Designer drugs are mainly known from sports doping. In animal fattening, designer drugs may be used as well. Small changes in the structure of (natural) hormones may lead to a new group of substances asking for new strategies for their detection and the constatation of their abuse.


Subject(s)
Anabolic Agents/analysis , Designer Drugs/analysis , Phytosterols/analysis , Substance Abuse Detection/methods , Animals , Cholesterol/analysis , Doping in Sports , Female , Gynecomastia/chemically induced , Hormones/chemistry , Humans , Male , Mass Spectrometry/methods , Phytosterols/chemistry , Testosterone/analogs & derivatives , Testosterone/analysis , Veterinary Medicine/methods
14.
Anal Chim Acta ; 586(1-2): 57-72, 2007 Mar 14.
Article in English | MEDLINE | ID: mdl-17386697

ABSTRACT

Regularly new anabolic steroids appear on the black market. In most cases these substances are marketed on websites or are confiscated during inspections. 1,(5alpha)-Androstene-17beta-ol-3-one, also known as 1-testosterone, is one of these substances presented to body-builders as a nutritional supplement or a pro-hormone. 1-Testosterone closely resembles the natural hormone testosterone except for a 1,2-double bound instead of a 4,5-double bound. 1-Androstene-3beta,17beta-diol is transformed into 1-testosterone after oral administration. 1-Testosterone, 1-androstene-3beta,17beta-diol and some other related 'new' anabolic steroids were studied with gas chromatography coupled to mass spectrometry (GC-MS) and Liquid chromatography coupled to tandem mass spectrometry (LC-MS2) methods. Similarities in spectra to known analytes, which may lead to pitfalls in the interpretation of the derivatised analytes, are discussed.


Subject(s)
Anabolic Agents/analysis , Androgens/analysis , Chromatography, Gas/methods , Chromatography, Liquid/methods , Mass Spectrometry/methods , Steroids/analysis , Testosterone/analogs & derivatives , Testosterone/analysis , Administration, Oral , Androstenediol/analysis , Chromatography, High Pressure Liquid/methods , Doping in Sports , Gas Chromatography-Mass Spectrometry , Models, Chemical , Substance Abuse Detection/methods , Testosterone/chemistry , Weight Lifting
15.
Anal Chim Acta ; 586(1-2): 163-70, 2007 Mar 14.
Article in English | MEDLINE | ID: mdl-17386708

ABSTRACT

Current evidence suggests that neo formation of the anabolic steroid boldenone (androsta-1,4-diene-17-ol-3-one) occurs in calves' faecal material, making it difficult to distinguish between illegally administered boldenone and its potential endogenous presence. This strengthens the urgent need to elucidate the pathway leading to boldenone formation. In our laboratory, the invertebrate Neomysis integer (Crustacea, Mysidacea) was used since 2004 as an alternative model for the partial replacement of vertebrate animals in metabolisation studies with illegal growth promotors and veterinary drugs, e.g. boldenone. The present study evaluates the metabolic capacity of other invertebrates, the brine shrimp Artemia franciscana and maggots of the greenbottle fly Lucilia sericata. The first results indicate that maggots of L. sericata are able to convert phytosterols and -stanols, nowadays in substantial amounts added to animal feed, into androsta-1,4-diene-3,17-dione (ADD), the precursor of boldenone, at a yield of 0.10-0.14% (p<0.001, significance compared to endogenous excretion of maggots) but not to boldenone itself. Furthermore, beta-testosterone, an endogenous hormone, was transformed into androst-4-ene-3,17-dione (AED), ADD and beta-boldenone at a significant (p<0.001, significance compared to endogenous excretion of maggots) yield of circa 13%, 0.80% and 2.2%, respectively. In future studies these results are of value to further evaluate the use of maggots of L. sericata as an invertebrate model in metabolisation studies.


Subject(s)
Anabolic Agents/analysis , Anabolic Agents/chemistry , Androstadienes/metabolism , Chemistry Techniques, Analytical/methods , Testosterone/analogs & derivatives , Animals , Artemia , Body Weight , Chromatography, Liquid , Diptera , Larva/metabolism , Mass Spectrometry , Models, Chemical , Phytosterols/analysis , Quality Control , Steroids/analysis , Steroids/chemistry , Testosterone/analysis , Testosterone/chemistry
16.
Vet Res Commun ; 31(3): 259-72, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17216314

ABSTRACT

The use of anabolic steroids has been banned in the European Union since 1981. In this study, the metabolism of the anabolic steroid methenolone acetate, was investigated in a male veal calf. After daily oral administration of methenolone acetate, three main metabolites were detected in both urine and faeces samples. Among these metabolites, alpha-methenolone was apparently the main one, but 1-methyl-5alpha-androstan-3,17-diol and 3alpha-hydroxy-1-methyl-5alpha-androstan-17-one were also observed. The parent compound was still detectable in faeces. As a consequence, abuse of methenolone acetate as growth promoter can be monitored by analysing urine and faeces samples. A few days after the last treatment, however, no metabolites were observed. Alpha-methenolone was detectable in urine until 5 days after the last treatment, but in faeces no metabolites were detectable after 3 days.


Subject(s)
Anabolic Agents/metabolism , Cattle/metabolism , Methenolone/analogs & derivatives , Anabolic Agents/urine , Animals , Feces/chemistry , Gas Chromatography-Mass Spectrometry/veterinary , Male , Methenolone/metabolism , Methenolone/urine
17.
Comp Biochem Physiol B Biochem Mol Biol ; 144(4): 405-12, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16815059

ABSTRACT

Cytochromes P450 (CYPs) are important enzymes involved in the regulation of hormone synthesis and in the detoxification and/or activation of xenobiotics. CYPs are found in virtually all organisms, from archae, and eubacteria to eukaryota. A number of endocrine disruptors are suspected of exerting their effects through disruption of normal CYP function. Consequently, alterations in steroid hormone metabolism through changes in CYP could provide an important tool to evaluate potential effects of endocrine disruptors. The aim of this study was to investigate the potential effects of the known CYP modulator, benzo(a)pyrene (BaP), on the testosterone metabolism in the invertebrate Neomysis integer (Crustacea; Mysidacea). N. integer were exposed for 96 h to 0.43, 2.39, 28.83, 339.00 and 1,682.86 microg BaP L(-1) and a solvent control, and subsequently their ability to metabolize testosterone was assessed. Identification and quantification of the produced phase I and phase II testosterone metabolites was performed using liquid chromatography coupled with multiple mass spectrometry (LC-MS2). Significant changes were observed in the overall ability of N. integer to metabolize testosterone when exposed to 2.39, 28.83, 339.00 and 1,682.86 microg BaP L(-1) as compared to the control animals.


Subject(s)
Benzo(a)pyrene/toxicity , Crustacea/drug effects , Cytochrome P-450 Enzyme System/metabolism , Endocrine Disruptors/toxicity , Testosterone/metabolism , Animals , Chromatography, Liquid , Crustacea/metabolism , Mass Spectrometry
18.
Vet Res Commun ; 30(6): 577-85, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16838200

ABSTRACT

The continuous introduction of new products used as growth promoters in animal husbandry, for sports doping and as products for body-building requires residue laboratories to initiate research on developing a strategy for the identification of 'unknown' components. In this study, a strategy is presented for elucidating the identity, the structure and the possible effects of illegal estrogenic compounds in an unidentified water-based solution. To obtain complete information on the composition and activity of the unidentified product, a multidisciplinary approach was needed. A case-study is described with a 'solution X' found during a raid. First, in vivo techniques (animal trials with mice, anatomical and histological research) were combined with in vitro techniques (the yeast estrogenic screen (YES)). In a later stage of the investigation, HPLC-fractionation, liquid chromatography-multiple mass spectrometry (LC-MSn) and gas chromatography-multiple mass spectrometry (GC-MSn) were used. Finally, the identity of 'solution X' was confirmed in a very low concentration range (10 ng/L estrone and 400 ng/l ethinyloestradiol).


Subject(s)
Drug Residues/analysis , Estrogens/analysis , Animal Husbandry/standards , Animals , Biological Assay/veterinary , Chromatography, High Pressure Liquid , Consumer Product Safety , Estrogens/administration & dosage , Female , Food Contamination/analysis , Gas Chromatography-Mass Spectrometry , Male , Mass Spectrometry , Meat/analysis , Mice , Random Allocation , Weight Gain
19.
Food Addit Contam ; 22(9): 798-807, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16192066

ABSTRACT

Boldenone (1,4-androstadiene-17-ol-3-one, Bol) has been the subject of a heated debate because of ongoing confusion about its endogenous or exogenous origin when detected in one of its forms in faecal or urine samples from cattle. An expert report was recently written on the presence and metabolism of Bol in various animal species. Androstadienedione (ADD) is a direct precursor of 17beta-boldenone (betaBol). It is a 3,17-dione; ssBol is a 17-ol-3-one. Not much is published on 1,4-androstadiene-3,17-diol, which is a 3,17-diol (ADL). If animals were exposed for a longer period to one of these analytes, a metabolic pathway would be initiated to eliminate these compounds. Similar to recent testosterone metabolism studies in the aquatic invertebrate Neomysis integer, ADD, ssBol and ADL could also be eliminated as hydroxymetabolites after exposure. The presence of 11-keto-steroids or 11-hydroxy-metabolites in faecal samples can interfere with a confirmation method by gas chromatography-negative chemical ionization mass spectrometry (GC-NCI-MS), after oxidation of corticosteroids with a double bond in the A-ring (e.g. prednisolone or its metabolite prednisone). The presence of androstadienetrione (ADT) in faecal samples of cattle has never been reported. The origin of its presence can be explained through different pathways, which are presented in this paper.


Subject(s)
Androstadienes/analysis , Cattle/metabolism , Feces/chemistry , Adrenal Cortex Hormones/metabolism , Animals , Chromatography, Liquid/methods , Gas Chromatography-Mass Spectrometry/methods , Mass Spectrometry/methods , Oxidation-Reduction
20.
Food Addit Contam ; 22(9): 808-15, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16192067

ABSTRACT

Following findings of 17beta-19-nortestosterone (150-200 microg kg(-1)) in pigs of unspecified gender imported into the European Union, a study to determine steroid and hormone levels in swine from six age/gender categories (uncastrated 'old' boars, cryptorchids, one intersex, barrows, gilts and sows) was initiated. Indeed, for some hormones there has been a discussion about their being endo- or exogenous. Tissue and urine samples from swine from each of the six categories were obtained in Belgium, France, the Netherlands and the USA. Samples were analysed in three laboratories. Quantitation was obtained for norandrostenedione, 19-nortestosterone and boldenone. The results give a well-documented overview of the status of the presence of these hormones in swine. The data illustrate that uncastrated 'old' boars produce the highest percentage of 'positive' matrices, followed by the cryptorchids. Concentrations in the matrices of the barrows and the gilts are lower. Also, sow matrices contain low amounts of nor-steroids. Furthermore, urine samples from an intersex pig contains a higher concentration of nortestosterone than sows and can therefore be suspected for illegal use of these hormones. Veterinarians taking samples in pig farms for the analysis of hormones need to be aware of the presence and concentrations of these substances in the different categories.


Subject(s)
Gonadal Steroid Hormones/analysis , Swine/metabolism , Androstenedione/analogs & derivatives , Androstenedione/analysis , Animals , Drug Residues/analysis , Female , Food Contamination/analysis , Gas Chromatography-Mass Spectrometry/methods , Gas Chromatography-Mass Spectrometry/veterinary , Male , Meat/analysis , Nandrolone/analysis , Orchiectomy/veterinary , Substance Abuse Detection/methods , Substance Abuse Detection/veterinary , Testosterone/analogs & derivatives , Testosterone/analysis , Tissue Distribution
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