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1.
Int J Food Sci Nutr ; 65(8): 942-7, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25156359

RESUMEN

Tomatoes, members of the Solanaceae plant family, produce biologically active secondary metabolites, including glycoalkaloids and aglycons, which may have both adverse and beneficial biological effects. A new liquid chromatography method that utilized LTQ-Orbitrap MS was developed for the analysis of tomatidine, the main aglycon in tomatoes. Recoveries of tomatidine were >98.3% with the relative standard deviations (RSDs) below 6.1%. The limit of detection (LODs) was 0.0003 mg kg(-1). The limit of quantitation (LOQs) is 0.001 mg kg(-1). The linear range was between with 0.0025 and 1 mg kg(-1) with an excellent correlation coefficient (R(2)) equal to 0.9990. Various tomato samples were analyzed and the level of tomatidine in the 11 samples analysed was higher in normal respect to organic tomatoes. The capability of the set-up Full Scan LTQ-Orbitrap MS method allowed us to quantified two non-target analytes. The m/z 1032 was identified as dehydrotomatine, confirmed through accurate mass studies (mass error in ppm equal to 1.5017) meanwhile m/z 902 as (Glc)2-Gal-Tomatidine (ß1-Tomatine) (mass error in ppm equal to 2.0719).


Asunto(s)
Frutas/química , Solanum lycopersicum/química , Tomatina/análogos & derivados , Cromatografía Líquida de Alta Presión , Límite de Detección , Espectrometría de Masas , Tomatina/análisis
2.
Rapid Commun Mass Spectrom ; 26(16): 1793-802, 2012 Aug 30.
Artículo en Inglés | MEDLINE | ID: mdl-22777781

RESUMEN

RATIONALE: Most of the liquid chromatography/mass spectrometry (LC/MS) methods that have been developed for the analysis of Diarrhetic Shellfish Poisoning (DSP) toxins in shellfish and algae samples have been unable to differentiate the isomers okadaic acid (OA) and dinophysistoxin-2 (DTX2), unless separated by chromatography. Since there are many bioconversion products of these compounds it is imperative to determine characteristic product ions, which can provide unequivocal identification of OA and DTX2 and their analogs. METHODS: Using electrospray ionization, the fragmentation processes for two types of precursor ions, [M+Na](+) and [M-H](-), of the polyether marine toxins, dinophysistoxins (DTXs), were studied using a hybrid linear ion trap Orbitrap mass spectrometer which provided high mass accuracy data in combination with multiple tandem mass (MS(n)) spectra. Three structurally related toxins were compared; okadaic acid (OA), dinophysistoxin-2 (DTX2) and dinophysistoxin-1 (DTX1). A quick multiple reaction monitoring (MRM) LC/MS/MS method was developed utilizing the characteristic precursor/product ion mass transitions. RESULTS: Comparison of the high-resolution product ion, [M-H](-), spectra of these toxins featured dominant signals that resulted from two six-centered rearrangements and previously proposed fragmentation pathways for the ion of m/z 321 and 293 have been corrected and identified. By contrast, the [M+Na](+) product ion spectra only revealed distinctive ions for the isomers, OA (m/z 595, 443 and 151) and DTX2 (m/z 581, 429 and 165). To illustrate the benefits of this study, a mass selective LC/MS/MS method was developed in which the isomers OA and DTX2 co-eluted but were distinguished using the mass transitions, m/z 827/595, 827/443 (OA) and m/z 827/581, 827/429 (DTX2). CONCLUSIONS: Comparison of OA, DTX2 and DTX1 led to the correction of proposed negative ion mode fragmentation pathways. Through extensive study and comparison of the [M+Na](+) product ion spectra, distinctive product ions were identified which allowed for these compounds to be identified and distinguished without separation for the first time.


Asunto(s)
Dinoflagelados/química , Toxinas Marinas/química , Piranos/química , Espectrometría de Masa por Ionización de Electrospray/métodos , Cromatografía Liquida , Iones/química , Isomerismo , Ácido Ocadaico , Espectrometría de Masas en Tándem
3.
J Integr Complement Med ; 28(3): 241-249, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-35294299

RESUMEN

Objectives: The prevalence of inpatient integrative medicine (IM) consult services is increasing among academic health care institutions. The diversity of services between institutions, as well as the novel nature of such interventions, makes it challenging for health care administrators to determine the cost/benefit of adding such a program to their institution. The main purpose of this study was to examine the performance of the new University of California, Los Angeles (UCLA) East-West (EW) consult service as measured by 30-day readmission rates and lengths of stay. Design: This is a retrospective observational case-control study with participants matched to themselves. Setting: UCLA Santa Monica Hospital, a 281-bed academic tertiary care hospital near Los Angeles, California. Subjects: Patients who had received an EW consultation during the inaugural 20 months of the program (2018-2020), and who had been hospitalized in the prior 2 years from the date of their first EW consult. Intervention: Inpatient East-West consultation, which may include counseling, acupuncture and/or trigger point injections depending on medical necessity. Outcome Measures: Thirty-day readmission rates and lengths of hospital admission were compared between the hospitalization that included an EW consult (which included the use of acupuncture and/or trigger point injections when appropriate) and any prior admissions during the 2 years before that EW consult. Secondary outcomes included quantitative analysis of average number of treatments and qualitative assessment of integrative treatment(s) received, conditions treated, and reasons that EW treatment may have been deferred during a consult. Results: One hundred sixty-five unique patients met the study criteria. The EW consultation was associated with clinically relevant, statistically significant decreased 30-day readmission rates (33.0% vs. 4.6%, p < 0.001, odds ratio [OR] 0.10, 95% confidence interval [CI] 0.06-0.17). This effect was similar when limiting the analysis to pain-related admissions (32.3% vs. 3.4%, p < 0.001, OR = 0.07, 95% CI 0.03-0.16). Hospital admissions with EW consults were found to have a statistically significant increased length of stay (7.03 days vs. 5.40 days, p < 0.001). Conclusion: The EW medicine, an example of IM, correlates with a reduced risk of 30-day readmission and with modestly increased lengths of stay.


Asunto(s)
Medicina Integrativa , Readmisión del Paciente , Estudios de Casos y Controles , Hospitales , Humanos , Pacientes Internos , Tiempo de Internación , Derivación y Consulta
4.
Environ Sci Technol ; 45(7): 3102-8, 2011 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-21401083

RESUMEN

Azaspiracid Poisoning (AZP) is a human toxic syndrome which is associated with the consumption of bivalve shellfish. Unlike other shellfish, mussels contain a large array of azaspiracid analogs, many of which are suspected bioconversion products. These studies were conducted to elucidate the metabolic pathways of azaspiracid (AZA1) in the blue mussel (Mytilus edulis) and revealed that the main biotransformation product was the more toxic demethyl analog, AZA3. To elucidate the mechanism of this C-demethylation, an unprecedented xenobiotic bioconversion step in shellfish, AZA1 was fed to mussels that contained no detectable azaspiracids. Triple quadrupole mass spectrometry (MS) and high resolution Orbitrap MS were used to determine the uptake of AZA1 and the toxin profiles in three tissue compartments of mussels. The second most abundant bioconversion product was identified as AZA17, a carboxyl analog of AZA3, which is a key intermediate in the formation of AZA3. Also, two pairs of isomeric hydroxyl analogs, AZA4/AZA5 and AZA7/AZA8, have been confirmed as bioconversion products for the first time. Ultra high resolution (100 k) MS studies showed that the most probable structural assignment for AZA17 is 22-carboxy-AZA3 and a mechanism for its facile decarboxylation to form AZA3 has been proposed.


Asunto(s)
Toxinas Marinas/toxicidad , Mytilus edulis/metabolismo , Compuestos de Espiro/toxicidad , Xenobióticos/toxicidad , Animales , Biotransformación , Cromatografía Liquida , Toxinas Marinas/química , Toxinas Marinas/metabolismo , Compuestos de Espiro/química , Compuestos de Espiro/metabolismo , Espectrometría de Masas en Tándem , Xenobióticos/química , Xenobióticos/metabolismo
5.
Anal Bioanal Chem ; 400(2): 587-94, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21359575

RESUMEN

Effluent from wastewater treatment plants have been identified as an important source of micro-organic contaminants in the environment. An online high-performance liquid chromatography-heated electrospray ionization tandem mass spectrometric method was developed and validated for the determination of basic pesticides in effluent wastewaters. Most available methods for pesticide analysis of wastewater samples are time-consuming, require complex clean-up steps and are difficult to automate. The method developed used a simple solid-phase extraction clean-up for salt and lipid reduction. On-line sample pre-concentration was performed using a reversed phase (C(18)) column, and analytes were separated by back-flushing onto an analytical column (C(8)) with detection using QqQ MS. An option to increase MS resolution was exploited to minimize interference from endogenous compounds in the matrix. A better than unit mass resolution was used (Q1 full width half maximum (FWHM) = 0.2 Da and Q3 FWHM = 0.7 Da), which was as rugged as a unit resolution method, and improved signal/noise and better detection limits were achieved for the targeted basic pesticides. This method was applied to the determination of 11 pesticides, including methoxytriazine, chlorotriazines, chloroacetanilides, phenylurea and carbamate pesticides. The percentage recovery values for these pesticides using the online trapping column were within the range, 73-95%, with relative standard deviation (RSD) values <8.9%. The highest concentrations of these pesticides in wastewater effluents in County Cork, Ireland, were simazine (0.51 µg/L), prometon (0.14 µg/L), diuron (0.21 µg/L) and atrazine (0.19 µg/L).


Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Plaguicidas/análisis , Aguas del Alcantarillado/análisis , Espectrometría de Masas en Tándem/métodos , Contaminantes Químicos del Agua/análisis
6.
Rapid Commun Mass Spectrom ; 24(20): 2966-74, 2010 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-20872629

RESUMEN

The biotoxins, azaspiracids (AZAs), from marine phytoplankton accumulate in shellfish and affect human health by causing severe gastrointestinal disturbance, diarrhea, nausea and vomiting. Specific and sensitive methods have been developed and validated for the determination of the most commonly occurring azaspiracid analogs. An LTQ Orbitrap mass spectrometer is a hybrid instrument that combines linear ion trap (LIT) mass spectrometry (MS) with high-resolution Fourier transform (FT) MS and this was exploited to perform simultaneous ultra-high-resolution full-scan MS analysis and collision-induced dissociation (CID) tandem mass spectrometry (MS/MS). Using the highest mass resolution setting (100,000 FWHM) in full-scan mode, the methodology was validated for the determination of six AZAs in mussel (Mytilus galloprovincialis) tissue extracts. Ultra-high mass resolution, together with a narrow mass tolerance window of ±2 mDa, dramatically improved detection sensitivity. In addition to employing chromatographic resolution to distinguish between the isomeric azaspiracid analogs, AZA1/AZA6 and AZA4/AZA5, higher energy collisionally induced dissociation (HCD) fragmentation on selected precursor ions were performed in parallel with full-scan FTMS. Using HCD MS/MS, most precursor and product ion masses were determined within 1 ppm of the theoretical m/z values throughout the mass spectral range and this enhanced the reliability of analyte identity.For the analysis of mussels (M. galloprovincialis), the method limit of quantitation (LOQ) was 0.010 µg/g using full-scan FTMS and this was comparable with the LOQ (0.007 µg/g) using CID MS/MS. The repeatability data were; intra-day RSD% (1.8-4.4%; n = 6) and inter-day RSD% (4.7-8.6%; n = 3). Application of these methods to the analysis of mussels (M. edulis) that were naturally contaminated with azaspiracids, using high-resolution full-scan Orbitrap MS and low-resolution CID MS/MS, produced equivalent quantitative data.


Asunto(s)
Contaminación de Alimentos/análisis , Toxinas Marinas/análisis , Mariscos/análisis , Compuestos de Espiro/análisis , Espectrometría de Masas en Tándem/métodos , Animales , Toxinas Marinas/química , Mytilus/química , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Compuestos de Espiro/química
7.
Anal Bioanal Chem ; 398(3): 1477-91, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-20694458

RESUMEN

The azaspiracids are a family of lipophilic polyether marine biotoxins that have caused a number of human intoxication incidents in Europe since 1995 after consumption of contaminated shellfish (Mytilus edulis). Levels of azaspiracids in shellfish for human consumption are monitored in accordance with EU guidelines: only shellfish with less than 160 microg kg(-1) are deemed safe. The limited availability of commercially available standards for azaspiracids is a serious problem, because validated LC-MS methods are required for routine analysis of these toxins in shellfish tissues. The procedure described herein has been used for the separation and the isolation of four azaspiracid (AZA) toxins from shellfish, for use as LC-MS-MS reference materials. Five separation steps have been used to isolate azaspiracids 1, 2, 3, and 6. The purity of the toxins obtained has been confirmed by multiple mass spectrometric methods using authentic azaspiracid standards. The same techniques have been used for quantification of the toxins extracted. The isolation procedure involves several chromatographic purification techniques: solid-phase extraction (diol sorbent, 90% mass reduction, and 95 +/- 1% toxin recovery); Sephadex size-exclusion chromatography (87% mass reduction and up to 95 +/- 2% toxin recovery), Toyopearl HW size-exclusion chromatography (90% mass reduction and up to 92.5 +/- 2.5% toxin recovery), and semi-preparative LC (78 +/- 3% toxin recovery). The procedure effectively separates the toxins from the sample matrix and furnishes azaspiracid toxins (AZA1, AZA2, AZA3 and AZA6) of sufficient purity with an average yield of 65% (n = 5). Triple-quadrupole mass spectrometry was used for qualitative and quantitative monitoring of the isolation efficiency after each stage of the process. High-resolution mass spectrometric evaluation of the toxic isolated material in both positive and negative modes suggests high purity.


Asunto(s)
Cromatografía en Gel/métodos , Toxinas Marinas/aislamiento & purificación , Compuestos de Espiro/aislamiento & purificación , Espectrometría de Masas en Tándem/métodos , Animales , Bivalvos , Estándares de Referencia
8.
NPJ Regen Med ; 5: 1, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31934351

RESUMEN

Formation of a perfusable microvascular network (µVN) is critical for tissue engineering of solid organs. Stromal cells can support endothelial cell (EC) self-assembly into a µVN, but distinct stromal cell populations may play different roles in this process. Here we describe the differential effects that two widely used stromal cell populations, fibroblasts (FBs) and pericytes (PCs), have on µVN formation. We examined the effects of adding defined stromal cell populations on the self-assembly of ECs derived from human endothelial colony forming cells (ECFCs) into perfusable µVNs in fibrin gels cast within a microfluidic chamber. ECs alone failed to fully assemble a perfusable µVN. Human lung FBs stimulated the formation of EC-lined µVNs within microfluidic devices. RNA-seq analysis suggested that FBs produce high levels of hepatocyte growth factor (HGF). Addition of recombinant HGF improved while the c-MET inhibitor, Capmatinib (INCB28060), reduced µVN formation within devices. Human placental PCs could not substitute for FBs, but in the presence of FBs, PCs closely associated with ECs, formed a common basement membrane, extended microfilaments intercellularly, and reduced microvessel diameters. Different stromal cell types provide different functions in microvessel assembly by ECs. FBs support µVN formation by providing paracrine growth factors whereas PCs directly interact with ECs to modify microvascular morphology.

10.
Toxicon ; 46(8): 852-8, 2005 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-16289180

RESUMEN

In December 1999, domoic acid (DA) a potent neurotoxin, responsible for the syndrome Amnesic Shellfish Poisoning (ASP) was detected for the first time in shellfish harvested in Ireland. Two liquid chromatography (LC) methods were applied to quantify DA in shellfish after sample clean-up using solid-phase extraction (SPE) with strong anion exchange (SAX) cartridges. Toxin detection was achieved using photodiode array ultraviolet (LC-UV) and multiple tandem mass spectrometry (LC-MS(n)). DA was identified in four species of bivalve shellfish collected along the west and south coastal regions of the Republic of Ireland. The amount of DA that was present in three species was within EU guideline limits for sale of shellfish (20 microg DA/g); mussels (Mytilus edulis), <1.0 microg DA/g; oysters (Crassostrea edulis), <5.0 microg DA/g and razor clams (Ensis siliqua), <0.3 microg DA/g. However, king scallops (Pecten maximus) posed a significant human health hazard with levels up to 240 microg DA/g total tissues. Most scallop samples (55%) contained DA at levels greater than the regulatory limit. The DA levels in the digestive glands of some samples of scallops were among the highest that have ever been recorded (2,820 microg DA/g).


Asunto(s)
Bivalvos/química , Monitoreo del Ambiente/estadística & datos numéricos , Ácido Kaínico/análogos & derivados , Toxinas Marinas/análisis , Mariscos , Animales , Cromatografía Liquida , Irlanda , Ácido Kaínico/análisis , Ácido Kaínico/química , Espectrometría de Masas
11.
J Chromatogr A ; 1082(1): 91-7, 2005 Jul 29.
Artículo en Inglés | MEDLINE | ID: mdl-16038198

RESUMEN

Anatoxin-a (AN) is a potent neurotoxin, produced by a number of cyanobacterial species, and consumption of freshwater contaminated with this toxin has led to animal deaths. Forensic investigations of suspected AN poisonings are frequently hampered by difficulties in detecting this toxin in biological matrices due to its rapid decay. In addition, detection of AN using single quadrupole mass spectrometry (MS) is suspect due to the presence of the amino acid, phenylalanine (Phe), since these compounds are isobaric and elute similarly in reversed phase liquid chromatography (LC). Approaches to prevent the misidentification of AN that have been explored in these studies included: (a) fluorimetric LC following derivatisation using 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F); (b) methylation using diazomethane prior to LC-MS determination; (c) multiple tandem MS using a quadrupole ion-trap (LC-MS3); and (d) hybrid quadrupole time-of-flight (QqTOF). Interference from Phe was not observed in any of procedures, (a)-(c), and the high mass accuracy obtained in method (d), readily distinguished between AN (165.11536) and Phe (165.07898). LC-MSn was also employed to study the fragmentation pathway of Phe and multi-stage MS spectra provided characteristic fragmentation information that clearly distinguished between AN and Phe. The difficulties associated with the over reliance on low resolution MS without MS/MS data in forensic toxicology are discussed.


Asunto(s)
Toxinas Bacterianas/análisis , Cromatografía Liquida/métodos , Errores Diagnósticos/prevención & control , Toxinas Marinas/análisis , Espectrometría de Masas/métodos , Neurotoxinas/envenenamiento , 4-Cloro-7-nitrobenzofurazano/análogos & derivados , 4-Cloro-7-nitrobenzofurazano/química , Animales , Cianobacterias , Toxinas de Cianobacterias , Medicina Legal/métodos , Humanos , Metilación , Microcistinas , Fenilalanina/análisis , Tropanos
12.
Mar Environ Res ; 60(3): 397-401, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-15769507

RESUMEN

The change in concentration of the disulfated polyether yessotoxin (YTX) produced by a culture of the marine dinoflagellate Protoceratium reticulatum was measured in laboratory experiments under light and dark conditions. Experimental cultures were inoculated and grew at a growth rate of 0.14 d(-1) until stationary phase was reached, after approximately 21 days. Cultures were maintained in the stationary phase until 31 days after inoculation. Cells of P. reticulatum contained a concentration of approximately 10-15 pg YTX cell(-1) during stationary phase but this was considerably lower (<5 pg cell-1) during the growth phase. Low amounts of 45-hydroxy-YTX were also detected. At day 32, P. reticulatum was killed by cooling to 1 degrees C (confirmed microscopically) and YTX concentrations were measured periodically under light and dark conditions. YTX concentrations decreased rapidly to approximately 10% of the initial concentration within the first 3 days and depleted to near zero within a week in the light treatment. In the dark environment, YTX persisted longer with approximately 10% of the initial YTX concentration still remaining after 18 days.


Asunto(s)
Dinoflagelados/metabolismo , Éteres Cíclicos/análisis , Toxinas Marinas/análisis , Animales , Cromatografía Liquida , Oscuridad , Dinoflagelados/crecimiento & desarrollo , Éteres Cíclicos/metabolismo , Modelos Lineales , Toxinas Marinas/metabolismo , Espectrometría de Masas , Factores de Tiempo
13.
J Mass Spectrom ; 50(1): 112-6, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25601682

RESUMEN

Isoflavones and coumestranes are the most important classes of compounds among phytoestrogens; by binding to estrogen receptors, they mimic or modulate the effect on the endogenous receptors. Little information can be found in literature about the presence of isoflavones and coumestrol in the environment, even if it is known that this may have significance, being these substances classified as endocrine disrupting compounds. In this research, we aim to explore the capabilities of the LTQ Orbitrap Discovery hybrid MS in full-scan acquisition mode, with high resolution, to validate an analytical method for the quantification of nine isoflavones (genistein, genistin, glycitein, daidzein, daidzin, (R,S)-equol, biochanin A, formononetin and coumestrol) in wastewater samples. The correlation coefficients of calibration curves of the nine analyzed compounds were in a range of 0.996-0.999; recoveries at two different levels of concentration (0.05 and 0.5 µg/l) were in the range 73-98%, and the limits of detection ranged between 0.0014 and 0.017 µg/l, proving that this method is sensitive enough in comparison with other methods available in literature. This method has been applied for the analysis of 20 wastewater treatment plants in County Cork, Ireland.


Asunto(s)
Isoflavonas/análisis , Espectrometría de Masas/métodos , Aguas Residuales/análisis , Cromatografía Líquida de Alta Presión/métodos , Irlanda , Isoflavonas/química , Límite de Detección , Espectrometría de Masas/instrumentación , Fitoestrógenos/análisis , Aguas Residuales/química , Contaminantes Químicos del Agua/análisis
14.
J Mass Spectrom ; 38(11): 1178-86, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-14648825

RESUMEN

Collision-induced dissociation (CID) mass spectra were generated for azaspiracids using electrospray ionisation (ESI), and hydrogen/deuterium (H/D) exchange was used to ascertain the number and type of replaceable hydrogens in the three predominant azaspiracid toxins. H/D exchange was conveniently achieved using deuterated solvents for liquid chromatography (LC). Using ion-trap mass spectrometry, multiple-stage CID experiments (MS(n)) on the protonated and fully exchanged ions were performed to decipher characteristic fragmentation pathways. The precursor and product ions from azaspiracids lost up to five water molecules from different regions during MS(n) experiments and it was possible to distinguish between the water losses from different molecular regions. These studies confirmed that the first water-loss ion in the spectra of azaspiracids resulted from dehydration at the vicinal diol at C20-C21. Five MS dissociation pathways were identified that resulted from fragmentation of the carbon skeleton of azaspiracids producing nitrogen-containing ions. Two pathways, involving cleavage of the E-ring and C27-C28, gave ions that were found in all azaspiracids. Three pathways, A-ring, C-ring and C19-C20 cleavages, were useful for distinguishing between azaspiracid analogues. The same product ions from backbone fragmentation were also observed using hybrid quadrupole time-of-flight mass spectrometry (QqTOFMS). The fragmentation of the A-ring was the most facile and was exploited in the development of LC/MS(n) methods for the analysis of azaspiracids.


Asunto(s)
Medición de Intercambio de Deuterio , Toxinas Marinas/química , Toxinas Marinas/metabolismo , Espectrometría de Masa por Ionización de Electrospray/métodos , Compuestos de Espiro/química , Compuestos de Espiro/metabolismo , Animales , Bivalvos , Irlanda , Estructura Molecular
15.
Toxicol Sci ; 80(1): 74-82, 2004 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15141105

RESUMEN

Diarrhetic shellfish poisoning (DSP) toxins of algal origin are frequent contaminants of coastal waters and seafood. The potential risk for human health due to the continuous presence of these toxins in food has not been clearly established. We have used cerebellar primary cultures to investigate the effects of the DSP toxin dinophysistoxin-2 (DTX-2) on central nervous system neurons and glial cells. Exposure to DTX-2 produced neurotoxicity at concentrations starting at 2.5 nM, characterized first by disintegration of neurites and later by cell death. DTX-2-induced neurodegeneration required long exposures (at least 20 h), involved DNA fragmentation and condensation and fragmentation of chromatin, typical hallmarks of apoptosis, and required the synthesis of new proteins. The concentration that reduced by 50% the maximum neuronal survival after 24 h exposure to DTX-2 (EC50(24)) was approximately 8 nM. Morphology and viability of glial cells remained unaffected up to at least 15 nM DTX-2. Higher concentrations of the toxin caused strong shrinkage of glial cell bodies and retraction of processes, and a significant reduction of glial cell viability. Glial toxicity by DTX-2 involved typical apoptotic condensation and fragmentation of chromatin. Compared to neurons, the effect on glial cells was a much shorter process, and extensive glial degeneration and death occurred after 7 h exposure to DTX-2 (EC50(7) approximately 50 nM; EC50(24) approximately 30 nM). Although further experiments are needed to confirm these toxic actions in vivo, our in vitro data suggest that chronic exposure to amounts of DSP toxins below the current safety regulatory limits may represent a risk for human health that should be taken into consideration.


Asunto(s)
Apoptosis , Astrocitos/efectos de los fármacos , Cerebelo/citología , Toxinas Marinas/toxicidad , Neuronas/efectos de los fármacos , Piranos/toxicidad , Animales , Astrocitos/patología , Astrocitos/ultraestructura , Bivalvos , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Fragmentación del ADN/efectos de los fármacos , Electroforesis en Gel de Agar , Neuritas/efectos de los fármacos , Neuronas/patología , Neuronas/ultraestructura , Síndromes de Neurotoxicidad/patología , Ácido Ocadaico/análogos & derivados , Estrés Oxidativo/efectos de los fármacos , Ratas
16.
Toxicon ; 44(8): 919-26, 2004 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-15530974

RESUMEN

Diarretic shellfish poisoning (DSP) is a toxic syndrome associated with the consumption of bivalve molluscs. The DSP toxins are polyether compounds, which include okadaic acid (OA), dinophysistoxins (DTXs), pectenotoxins (PTXs) and pectenotoxin seco acids (PTX2SAs). These toxins originate in marine dinoflagellates, including Dinophysis spp. Phytoplankton samples were collected from the southwest coast of Ireland and D. acuta was the predominant species. Monocultures of D. acuta cells were prepared by hand picking from microscope slides in order to confirm their toxin profiles. There was a remarkable consistency in the toxin profiles in all of the phytoplankton samples collected during the summer months, irrespective of location, depth or mesh size. Analysis using liquid chromatography-multiple tandem mass spectrometry (LC-MS/MS) revealed that DTX2 and OA were the predominant toxins at a consistent ratio. The average toxin composition was: DTX2 (53+/-5%), OA (26.5+/-2.3%) and total pectenotoxins (20.8+/-4.7%). Toxin profiles in D. acuta from Europe were distinctly different from those found in New Zealand, where PTX2 was the predominant toxin and DTX2 was absent.


Asunto(s)
Dinoflagelados/química , Éteres Cíclicos/análisis , Toxinas Marinas/análisis , Espectrometría de Masas/métodos , Animales , Cromatografía Liquida , Éteres Cíclicos/química , Enfermedades Transmitidas por los Alimentos/prevención & control , Irlanda , Toxinas Marinas/química , Estructura Molecular
17.
Toxicon ; 41(2): 145-51, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12565733

RESUMEN

A new human toxic syndrome, azaspiracid poisoning (AZP), was identified following illness from the consumption of contaminated mussels (Mytilus edulis). To discover the aetiology of AZP, sensitive analytical protocols involving liquid chromatography-mass spectrometry (LC-MS) were used to screen marine phytoplankton for azaspiracids. Collections of single species were prepared by manually separating phytoplankton for LC-MS analysis. A dinoflagellate species of the genus, Protoperidinium, has been identified as the progenitor of azaspiracids. Azaspiracid-1, and its analogues, AZA2 and AZA3, were identified in extracts of 200 cells using electrospray multiple tandem MS. This discovery has significant implications for both human health and the aquaculture industry since this phytoplankton genus was previously considered to be toxicologically benign. The average toxin content was 1.8 fmol of total AZA toxins per cell with AZA1 as the predominant toxin, accounting for 82% of the total.


Asunto(s)
Bivalvos/metabolismo , Dinoflagelados/metabolismo , Enfermedades Transmitidas por los Alimentos/etiología , Toxinas Marinas/envenenamiento , Fitoplancton/metabolismo , Mariscos , Compuestos de Espiro/envenenamiento , Animales , Bivalvos/química , Cromatografía Líquida de Alta Presión , Dinoflagelados/química , Dinoflagelados/citología , Enfermedades Transmitidas por los Alimentos/metabolismo , Humanos , Toxinas Marinas/análisis , Toxinas Marinas/metabolismo , Fitoplancton/química , Espectrometría de Masa por Ionización de Electrospray , Compuestos de Espiro/análisis , Compuestos de Espiro/metabolismo
18.
Toxicon ; 41(3): 277-83, 2003 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-12565749

RESUMEN

The polyether dinoflagellate toxins, azaspiracids, are responsible for azaspiracid poisoning (AZP), a new human toxic syndrome arising from the consumption of shellfish. To date, five azaspiracids have been isolated and fully structurally elucidated, including, AZA1, its 8-methyl and 22-demethyl analogues, AZA2 and AZA3, respectively, and two hydroxyl derivatives of AZA3, named AZA4 and AZA5. Using a recently developed method involving liquid chromatography with multiple tandem mass spectrometry (LC-MS(n)), five new azaspiracids, AZA7-AZA11, have been found in mussels (Mytilus edulis). AZA6 is a positional isomer of AZA1 and four of the new compounds are isomers with a mass of 857.5 amu. AZA7 and AZA8 are hydroxyl analogues of AZA1 while AZA9 and AZA10 are hydroxyl analogues of AZA6. AZA11 is a hydroxyl analogue of AZA2. The separation of all 11 azaspiracids was achieved using isocratic reversed phase liquid chromatography using a combination of eluent additives, trifluoroacetic acid and ammonium acetate. The ion-trap MS experiments, with electrospray ionisation, involved the fragmentation of the protonated molecule [M+H](+), trapping and fragmenting the product ions due to the loss of a water molecule [M+H-H(2)O](+), together with mass spectral data analysis that included the characteristic A-ring fragmentation for each compound.


Asunto(s)
Cromatografía Liquida/métodos , Enfermedades Transmitidas por los Alimentos , Toxinas Marinas/análisis , Mariscos/análisis , Espectrometría de Masa por Ionización de Electrospray/métodos , Compuestos de Espiro/análisis , Animales , Toxinas Marinas/clasificación , Compuestos de Espiro/clasificación
19.
Toxicon ; 41(3): 297-303, 2003 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-12565752

RESUMEN

The first identification of the rare cyanobacterial neurotoxin, homoanatoxin-a, in Ireland is reported. A sensitive fluorimetric liquid chromatographic (LC) method was applied to the analysis of homoanatoxin-a in the low microg/l range. The analysis of the anatoxins in water samples required weak cation exchange solid phase extraction, fluorimetric derivatisation with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and isocratic reversed-phase LC. Confirmation of toxin identity was made using LC with electrospray mass spectrometry (MS) of the NBD-derivatised homoanatoxin-a as well as LC-MS/MS of the free toxin. Application of the fluorimetric LC protocol to examine cyanotoxins in 20 Irish lakes resulted in the detection of homoanatoxin-a at four locations, Lough Sillan (24 microg/l), Inniscarra Reservoir (34 microg/l), Lough Key (12 microg/l), Caragh Lake (1.4 microg/l). An improved procedure for the isolation of homoanatoxin-a from cyanobacteria was also developed and confirmation of homoanatoxin-a was achieved by chromatographic and mass spectral comparison with authentic toxin isolated from a laboratory clone culture of Planktothrix (formerly Oscillatoria) formosa.


Asunto(s)
Compuestos Bicíclicos Heterocíclicos con Puentes/aislamiento & purificación , Cromatografía Liquida/métodos , Agua Dulce/química , Irlanda , Espectrometría de Masa por Ionización de Electrospray/métodos
20.
Toxicon ; 42(1): 105-8, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12893067

RESUMEN

Incidents of human intoxications throughout Europe, following the consumption of mussels have been attributed to Azaspiracid Poisoning (AZP). Although first discovered in Ireland, the search for the causative toxins, named azaspiracids, in other European countries has now led to the first discovery of these toxins in shellfish from France and Spain. Separation of the toxins, azaspiracid (AZA1) and analogues, AZA2 and AZA3, was achieved using isocratic reversed-phase liquid chromatography coupled, via an electrospray ionisation source, to an ion-trap mass spectrometer. Azaspiracids were identified in mussels (Mytilus galloprovincialis), 0.24 microg/g, from Galicia, Spain, and scallops (Pecten maximus), 0.32 microg/g, from Brittany, France. Toxin profiles were similar to those found in the equivalent shellfish in Ireland in which AZA1 was the predominant toxin.


Asunto(s)
Toxinas Marinas/aislamiento & purificación , Moluscos/metabolismo , Mariscos , Compuestos de Espiro/aislamiento & purificación , Animales , Cromatografía Líquida de Alta Presión , Brotes de Enfermedades , Enfermedades Transmitidas por los Alimentos/epidemiología , Enfermedades Transmitidas por los Alimentos/etiología , Francia , Toxinas Marinas/envenenamiento , Mariscos/análisis , Intoxicación por Mariscos , España , Espectrometría de Masa por Ionización de Electrospray , Compuestos de Espiro/envenenamiento
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