RESUMEN
Selenium-binding protein 1 (SELENBP1) has been associated with several cancers, although its exact role is unknown. We show that SELENBP1 is a methanethiol oxidase (MTO), related to the MTO in methylotrophic bacteria, that converts methanethiol to H2O2, formaldehyde, and H2S, an activity not previously known to exist in humans. We identified mutations in SELENBP1 in five patients with cabbage-like breath odor. The malodor was attributable to high levels of methanethiol and dimethylsulfide, the main odorous compounds in their breath. Elevated urinary excretion of dimethylsulfoxide was associated with MTO deficiency. Patient fibroblasts had low SELENBP1 protein levels and were deficient in MTO enzymatic activity; these effects were reversed by lentivirus-mediated expression of wild-type SELENBP1. Selenbp1-knockout mice showed biochemical characteristics similar to those in humans. Our data reveal a potentially frequent inborn error of metabolism that results from MTO deficiency and leads to a malodor syndrome.
Asunto(s)
Halitosis/genética , Oxidorreductasas/genética , Proteínas de Unión al Selenio/genética , Animales , Pruebas Respiratorias , Línea Celular , Células Cultivadas , Dimetilsulfóxido/sangre , Dimetilsulfóxido/líquido cefalorraquídeo , Dimetilsulfóxido/orina , Halitosis/enzimología , Humanos , Ratones Endogámicos C57BL , Ratones Noqueados , Mutación , Proteínas de Unión al Selenio/deficiencia , Proteínas de Unión al Selenio/metabolismoRESUMEN
This paper describes quantitative methods for the determination of dimethylsulfoxide (DMSO) in equine plasma and urine based on simple precipitation and dilution followed by hydrophilic interaction liquid chromatography coupled to tandem mass spectrometry (HILIC-MS/MS). DMSO is a polar solvent with analgesic and anti-inflammatory properties. Its pharmacological features make it prohibited in horse racing. However, since DMSO is naturally present in the horses' environment, international threshold values have been implemented for plasma and urine (1 and 15 µg/mL, respectively). Previously presented quantitative methods for the determination of DMSO are based on gas chromatography, thus demanding a tedious extraction step to transfer the analyte from the aqueous bodily fluid to an injectable organic solvent. The column used in the presented method was an Acquity BEH HILIC and the mobile phase was a mixture of ammonium acetate buffer and acetonitrile delivered as a gradient. Hexadeuterated DMSO (2 H6 -DMSO) was used as the internal standard. Validation was performed in the range of the international thresholds concerning selectivity, carry-over, linearity, precision, accuracy, stability and inter-individual matrix variation. The results fulfilled the predefined criteria and the methods were considered fit for purpose. Successful applications on real equine doping control samples were carried out with determined DMSO concentrations exceeding the international thresholds. Copyright © 2016 John Wiley & Sons, Ltd.
Asunto(s)
Dimetilsulfóxido/sangre , Dimetilsulfóxido/orina , Caballos/sangre , Caballos/orina , Detección de Abuso de Sustancias/métodos , Espectrometría de Masas en Tándem/métodos , Animales , Antiinflamatorios/sangre , Antiinflamatorios/orina , Cromatografía Líquida de Alta Presión/métodos , Doping en los Deportes , Límite de DetecciónRESUMEN
Olfactory cues play a vital role in kin recognition and mate choice of the rat. Here, using 2 inbred strains of rats, Brown Norway (BN) and Lewis, as models to simulate kinship via genetic distance, we examined whether urine-derived volatiles are genetically determined, and, if so, how they code for olfactory information and the degree of genetic relatedness in mate choice. Binary choice tests showed that BN females preferred the urine odor of Lewis males over that of BN males, suggesting that they avoided males genetically similar to themselves and were able to assess this olfactorily. Gas chromatography-mass spectrometry analysis revealed that the composition of urine-derived volatiles was more similar within strains than between strains and suggests that odortypes may reflect genetic relatedness. Our data further show that BN males had lower ratios of 2-heptanone and 4-heptanone and higher ratios of dimethyl sulfone and 4-ethyl phenol than Lewis males. When we supplemented BN and Lewis male urine to make each similar, the preferences of BN females were reversed. We conclude that some urine-derived volatiles covary in relative abundance with degree of genetic relatedness, and this relationship may play a key role in chemical signaling and genetic identity in this species.
Asunto(s)
Filogenia , Reconocimiento en Psicología , Atractivos Sexuales/genética , Atractivos Sexuales/orina , Animales , Dimetilsulfóxido/orina , Femenino , Cromatografía de Gases y Espectrometría de Masas , Cetonas/orina , Masculino , Percepción Olfatoria , Fenoles/orina , Ratas , Ratas Endogámicas BN , Ratas Endogámicas Lew , Especificidad de la Especie , Sulfonas/orina , VolatilizaciónRESUMEN
A method for routinely determination of dimethyl sulfoxide (DMSO) and dimethyl sulfone (DMSO(2)) in human urine was developed using gas chromatography-mass spectrometry. The urine sample was treated with 2,2-dimethoxypropane (DMP) and hydrochloric acid for efficient removal of water, which causes degradation of the vacuum level in mass spectrometer and shortens the life-time of the column. Experimental DMP reaction parameters, such as hydrochloric acid concentration, DMP-urine ratio, reaction temperature and reaction time, were optimized for urine. Hexadeuterated DMSO was used as an internal standard. The recoveries of DMSO and DMSO(2) from urine were 97-104 and 98-116%, respectively. The calibration curves showed linearity in the range of 0.15-54.45 mg/L for DMSO and 0.19-50.10 mg/L for DMSO(2). The limits of detection of DMSO and DMSO(2) were 0.04 and 0.06 mg/L, respectively. The relative standard deviations of intra-day and inter-day were 0.2-3.4% for DMSO and 0.4-2.4% for DMSO(2). The proposed method may be useful for the biological monitoring of workers exposed to DMSO in their occupational environment.
Asunto(s)
Dimetilsulfóxido/orina , Cromatografía de Gases y Espectrometría de Masas/métodos , Sulfonas/orina , Adulto , Humanos , Límite de Detección , PropanolesRESUMEN
The metabolome following intake of onion by-products is evaluated. Thirty-two rats were fed a diet containing an onion by-product or one of the two derived onion by-product fractions: an ethanol extract and the residue. A 24 hour urine sample was analyzed using (1)H NMR spectroscopy in order to investigate the effects of onion intake on the rat metabolism. Application of interval extended canonical variates analysis (ECVA) proved to be able to distinguish between the metabolomic profiles from rats consuming normal feed and rats fed with an onion diet. Two dietary biomarkers for onion intake were identified as dimethyl sulfone and 3-hydroxyphenylacetic acid. The same two dietary biomarkers were subsequently revealed by interval partial least squares regression (PLS) to be perfect quantitative markers for onion intake. The best PLS calibration model yielded a root mean square error of cross-validation (RMSECV) of 0.97% (w/w) with only 1 latent variable and a squared correlation coefficient of 0.94. This indicates that urine from rats on the by-product diet, the extract diet, and the residue diet all contain the same dietary biomarkers and it is concluded that dimethyl sulfone and 3-hydroxyphenylacetic acid are dietary biomarkers for onion intake. Being able to detect specific dietary biomarkers is highly beneficial in the control of nutritionally enhanced functional foods.
Asunto(s)
Dieta , Dimetilsulfóxido/metabolismo , Ingestión de Alimentos , Metabolómica , Fenómenos Fisiológicos de la Nutrición , Cebollas , Sulfonas/metabolismo , Animales , Antioxidantes/química , Antioxidantes/metabolismo , Antioxidantes/farmacología , Biomarcadores/química , Biomarcadores/metabolismo , Biomarcadores/orina , Dimetilsulfóxido/química , Dimetilsulfóxido/orina , Etanol/química , Espectroscopía de Resonancia Magnética , Masculino , Cebollas/química , Fenilacetatos/química , Fenilacetatos/metabolismo , Fenilacetatos/orina , Extractos Vegetales/química , Extractos Vegetales/metabolismo , Extractos Vegetales/farmacología , Extractos Vegetales/orina , Análisis de Componente Principal , Ratas , Solubilidad , Sulfonas/química , Sulfonas/orinaRESUMEN
We present a highly sensitive, rapid method for the determination of ruthenium originating from the investigational anti-cancer drug NAMI-A in human plasma ultrafiltrate, plasma, and urine. The method is based on the quantification of ruthenium by inductively coupled plasma mass spectrometry and allows quantification of 30 ng L(-1) ruthenium in plasma ultrafiltrate and urine, and 75 ng L(-1) ruthenium in human plasma, in 150 microL of matrix. The sample pretreatment procedure is straightforward and only involves dilution with appropriate diluents. The performance of the method, in terms of accuracy and precision, fulfilled the most recent FDA guidelines for bioanalytical method validation. Validated ranges of quantification were 30.0 to 1 x 10(4) ng L(-1) for ruthenium in plasma ultrafiltrate and urine and 75.0 to 1 x 10(4) ng L(-1) for ruthenium in plasma. The applicability of the method and its superiority to atomic-absorption spectrometry were demonstrated in two patients who were treated with intravenous NAMI-A in a phase I trial. The assay is now successfully used to support pharmacokinetic studies in cancer patients treated with NAMI-A.
Asunto(s)
Antineoplásicos/sangre , Antineoplásicos/orina , Dimetilsulfóxido/análogos & derivados , Espectrometría de Masas/métodos , Compuestos Organometálicos/sangre , Compuestos Organometálicos/orina , Rutenio/análisis , Antineoplásicos/farmacocinética , Área Bajo la Curva , Dimetilsulfóxido/sangre , Dimetilsulfóxido/farmacocinética , Dimetilsulfóxido/orina , Semivida , Humanos , Compuestos Organometálicos/farmacocinética , Reproducibilidad de los Resultados , Compuestos de RutenioRESUMEN
NAMI-A is a novel ruthenium-containing experimental anticancer agent. We have developed and validated a rapid and sensitive analytical method to determine NAMI-A in human plasma, plasma ultrafiltrate and urine using atomic absorption spectrometry with Zeeman correction. The sample pretreatment procedure is straightforward, involving only dilution with an appropriate hydrochloric acid buffer-solution. Because the response signal of the spectrometer depended on the composition of the sample matrix, in particular on the amount of human plasma in the sample, all unknown samples were diluted to match the matrix composition in which the standard line was prepared (plasma-buffer 1:10 v/v). This procedure enabled the measurement of samples of different biological matrices in a single run. The validated range of determination was 1.1-220 microM NAMI-A for plasma and urine, and 0.22-44 microM for plasma ultrafiltrate. The lower limit of detection was 0.85 microM in plasma and urine and 0.17 microM in plasma ultrafiltrate. The lower limit of quantitation was 1.1 and 0.22 microM, respectively. The performance of the method, in terms of precision and accuracy was according to the generally accepted criteria for validation of analytical methodologies. The applicability of the method was demonstrated in a patient who was treated in a pharmacokinetic phase I trial with intravenous NAMI-A.
Asunto(s)
Antineoplásicos/farmacocinética , Dimetilsulfóxido/farmacocinética , Compuestos Organometálicos/farmacocinética , Espectrofotometría Atómica , Antineoplásicos/sangre , Antineoplásicos/orina , Tampones (Química) , Dimetilsulfóxido/análogos & derivados , Dimetilsulfóxido/sangre , Dimetilsulfóxido/orina , Humanos , Ácido Clorhídrico , Compuestos Organometálicos/sangre , Compuestos Organometálicos/orina , Rutenio/farmacocinética , Compuestos de RutenioRESUMEN
The on-line determination of volatile and semivolatile organic compounds (SVOCs) is reported using membrane inlet mass spectrometry with in-membrane preconcentration (IMP-MIMS). Semivolatile organic compounds in aqueous samples are preconcentrated in a flow-through silicone hollow-fiber membrane inlet held in a GC oven. The sample stream is replaced with air, and the SVOCs are thermally desorbed into the mass spectrometer by rapid heating of the membrane. The method is evaluated for the on-line determination of 4-fluorobenzoic acid, 3,5-difluorobenzoic acid, 2-chlorophenol, p-tert-butylphenol, and dimethyl sulfoxide (DMSO) in water. The selectivity of the IMP-MIMS technique for SVOCs in the presence of VOCs is demonstrated. Cryotrapping and a rapid gas chromatographic separation step were added between the membrane and the mass spectrometer ion source for the determination of SVOCs in complex mixtures. The procedure is demonstrated for the determination of dimethyl sulfoxide (DMSO) in equine urine, using internal standardization with DMSO-d6. Full-scan electron ionization (EI) mass spectrometric detection showed good linearity (R = 0.998) and RSDs, relative to the internal standard, of 2.2% for desorption only and 4.6% for desorption and cryotrapping.
Asunto(s)
Compuestos Orgánicos/análisis , Animales , Cromatografía de Gases , Dimetilsulfóxido/orina , Caballos , Indicadores y Reactivos , Espectrometría de Masas , Membranas Artificiales , Compuestos Orgánicos/orinaRESUMEN
Dimethyl sulfoxide (DMSO) had been postulated to be a 'masking agent' when used concurrently with therapeutic or prohibited drugs in racing animals. Eight drugs (flunixin, furosemide, caffeine, apomorphine, phenylbutazone, lidocaine, cocaine, and acepromazine maleate) were administered to six horses singly and with concurrent intravenous DMSO. Urine samples were analyzed for the presence of the drugs and/or their metabolites by thin layer chromatography. Direct comparison of thin layer chromatograms of extracts of positive urine samples with and without DMSO verified that DMSO did not interfere with the detection of these drugs.
Asunto(s)
Dimetilsulfóxido/orina , Caballos/orina , Preparaciones Farmacéuticas/orina , Acepromazina/orina , Animales , Apomorfina/orina , Cafeína/orina , Cromatografía en Capa Delgada , Clonixina/análogos & derivados , Clonixina/orina , Cocaína/orina , Interacciones Farmacológicas , Femenino , Furosemida/orina , Lidocaína/orina , Fenilbutazona/orinaRESUMEN
The absorption and excretion of dimethyl sulfoxide (DMSO) were studied in Rhesus monkeys (Macaca mulatta) given daily oral doses of 3 gms DMSO/kg B.W. for 14 days. DMSO and its major metabolite, dimethyl sulfone (DMSO2), were measured in serum, urine and feces by gas-liquid chromatography. DMSO was absorbed rapidly, reached a steady state blood level after 1 day and then was cleared from blood within 72 hrs after ending treatment. Serum DMSO declined in a linear fashion on semilogarithmic coordinates as described by second order kinetics. It had a half-life of 16 hrs. DMSO2 appeared in blood within 2 hrs and reached a steady state concentration after 4 days of treatment. DMSO2 was cleared from blood about 120 hrs after DMSO administration was stopped. Its half-life in blood was calculated to be 38 hrs. Urinary excretion of unmetabolized DMSO and DMSO2 accounted for about 60% and 16%, respectively, of the total ingested dose. Neither DMSO nor DMSO2 was detected in fecal samples. However, when added to fecal samples, DMSO was degraded rapidly. Although dimethyl sulfide (DMS) was not measured, some DMSO was metabolized to this compound because of the particular sweetness of breath of the monkeys. We conclude that the absorption of DMSO by monkeys is similar to that for humans, but that its conversion to DMSO2 and urinary elimination are more rapid in monkeys.
Asunto(s)
Dimetilsulfóxido/metabolismo , Absorción , Animales , Cromatografía de Gases , Dimetilsulfóxido/sangre , Dimetilsulfóxido/orina , Heces/análisis , Semivida , Cinética , Macaca mulatta , Sulfonas/sangre , Sulfonas/orinaRESUMEN
A gas chromatographic procedure for the determination of dimethyl sulfoxide in serum, plasma, urine, and CSF is described. Features of the method include simple sample preparation, excellent accuracy, linearity, and precision. Results obtained on patient samples following intravenous administration are presented.