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1.
Gut Microbes ; 15(2): 2256045, 2023 12.
Article in English | MEDLINE | ID: mdl-37712629

ABSTRACT

Fabry disease (FD) is an X-linked metabolic disease caused by a deficiency in α-galactosidase A (α-Gal A) activity. This causes accumulation of glycosphingolipids, especially globotriaosylceramide (Gb3), in different cells and organs. Neuropathic pain and gastrointestinal (GI) symptoms, such as abdominal pain, nausea, diarrhea, constipation, and early satiety, are the most frequent symptoms reported by FD patients and severely affect their quality of life. It is generally accepted that Gb3 and lyso-Gb3 are involved in the symptoms; nevertheless, the origin of these symptoms is complex and multifactorial, and the exact mechanisms of pathogenesis are still poorly understood. Here, we used a murine model of FD, the male α-Gal A (-/0) mouse, to characterize functionality, behavior, and microbiota in an attempt to elucidate the microbiota-gut-brain axis at three different ages. We provided evidence of a diarrhea-like phenotype and visceral hypersensitivity in our FD model together with reduced locomotor activity and anxiety-like behavior. We also showed for the first time that symptomology was associated with early compositional and functional dysbiosis of the gut microbiota, paralleled by alterations in fecal short-chain fatty acid levels, which partly persisted with advancing age. Interestingly, most of the dysbiotic features suggested a disruption of gut homeostasis, possibly contributing to accelerated intestinal transit, visceral hypersensitivity, and impaired communication along the gut-brain axis.


Subject(s)
Fabry Disease , Gastrointestinal Microbiome , Male , Animals , Mice , Brain-Gut Axis , Disease Models, Animal , Quality of Life , Diarrhea , Dysbiosis
2.
J Chromatogr A ; 1585: 70-81, 2019 Jan 25.
Article in English | MEDLINE | ID: mdl-30482431

ABSTRACT

Bile acids (BAs) are endogenous steroids involved in the transport of lipids in bile, acting also as molecular signaling hormones. Primary BAs synthesized in the liver undergo several metabolic pathways in the intestine by gut microbiota to produce secondary BAs. Together with secondary BAs, other metabolites have been recovered from human faeces, including many oxo-BA analogues produced in the colon through oxidation of BA hydroxy groups. However, the complete oxo-BA characterization in biospecimens (particularly intestinal content and faeces) has not been reported yet, hampering the assessment of their potential physiological role. Herein, we have developed and validated a new RP-HPLC-ESI-MS/MS method in negative ionization mode for the simultaneous analysis of 21 oxo-BAs and their 7 metabolic BAs precursors in human faeces. The elution was performed in gradient mode and 28 compounds, including primary, secondary BAs, and their oxo-derivatives, were separated within 50 min at 40 °C column temperature. The method is accurate (bias% <13%), precise (CV% <10%), with limits of quantification (LOQ <30 ng/mLextract samples), similar for all the studied compounds. The matrix effect does not significantly affect the analysis accuracy, allowing the use of standard solutions for the quantifications, without matrix-matched protocols. Thanks to the high detectability and the relatively high concentration of oxo-BAs (about µg/gwet faeces), the method does not require a pre-analytical clean-up step. This method was used to identify and quantify oxo-BAs in human faecal samples from healthy subjects, serving as a proof of concept for application in patients with hepatobiliary disease and bacteria overgrowth.


Subject(s)
Bile Acids and Salts/analysis , Chromatography, Liquid , Clinical Laboratory Techniques/methods , Feces/chemistry , Keto Acids/analysis , Tandem Mass Spectrometry , Gastrointestinal Contents/chemistry , Humans , Limit of Detection , Reproducibility of Results
3.
Bone Marrow Transplant ; 50(7): 992-8, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25893458

ABSTRACT

Acute GvHD (aGvHD) is the main complication of hematopoietic SCT (HSCT) during the treatment of hematological disorders. We carried out the first longitudinal study to follow the gut microbiota trajectory, from both the phylogenetic and functional points of view, in pediatric patients undergoing HSCT. Gut microbiota trajectories and short-chain fatty acid production profiles were followed starting from before HSCT and through the 3-4 months after transplant in children developing and not developing aGvHD. According to our findings, HSCT procedures temporarily cause a structural and functional disruption of the gut microbial ecosystem, describing a trajectory of recovery during the following 100 days. The onset of aGvHD is associated with specific gut microbiota signatures both along the course of gut microbiota reconstruction immediately after transplant and, most interestingly, prior to HSCT. Indeed, in pre-HSCT samples, non-aGvHD patients showed higher abundances of propionate-producing Bacteroidetes, highly adaptable microbiome mutualists that showed to persist during the HSCT-induced ecosystem disruption. Our data indicate that structure and temporal dynamics of the gut microbial ecosystem can be a relevant factor for the success of HSCT and opens the perspective to the manipulation of the pre-HSCT gut microbiota configuration to favor mutualistic persisters with immunomodulatory properties in the gut.


Subject(s)
Gastrointestinal Microbiome/physiology , Graft vs Host Disease/complications , Hematopoietic Stem Cell Transplantation/adverse effects , Transplantation, Homologous/adverse effects , Acute Disease , Child , Female , Humans , Longitudinal Studies
4.
Eur J Mass Spectrom (Chichester) ; 19(6): 483-90, 2013.
Article in English | MEDLINE | ID: mdl-24378466

ABSTRACT

Amyloid beta 25-35 [Aß (25-35)], as a peptide model for full-length Aß in structural and functional investigations, has been chosen for aggregation studies. The complexity of the Aß (25-35) aggregation process required a multi-methodological analytical approach to obtain reliable and reproducible results. Here, we describe the results obtained by the use of mass spectrometry (MS) for the structural characterization of the self-assembly species during the aggregation process and for the definition of the self-assembly kinetics and myricetin inhibition patterns, comparing the results with those obtained by using the well-established spectroscopic method based on thioflavin T fluorescence. Flow injection electrospray ionization-ion trap-mass spectrometry (ESI-IT-MS) was applied to monitor the disappearance of the monomer specie in the first steps, whereas matrix-assisted laser desorption/ionization-time of flight-mass spectrometry (MALDI-ToF-MS) was used to follow monomer and small oligomer self-assembly trends in the early stages of the nucleating process.


Subject(s)
Amyloid beta-Peptides/chemistry , Amyloid beta-Peptides/metabolism , Models, Chemical , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/standards , Flavonoids/chemistry , Flavonoids/metabolism , Humans , Kinetics , Reproducibility of Results , Structure-Activity Relationship
5.
Br J Pharmacol ; 164(3): 1026-40, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21449913

ABSTRACT

BACKGROUND AND PURPOSE: AM251 is an inverse agonist of the cannabinoid 1 receptor (CB(1)R) that can exert 'off-target' effects in vitro and in CB(1)R knock-out mice. AM251 is also potent at modulating tumour cell growth, suggesting that growth factor-mediated oncogenic signalling could be regulated by AM251. Since dysregulation of the EGF receptor has been associated with carcinogenesis, we examined AM251 regulation of EGF receptor (EGFR) expression and function. EXPERIMENTAL APPROACH: The various biological functions of AM251 were measured in CB(1)R-negative human cancer cells. Pharmacological and genetic approaches were used to validate the data. KEY RESULTS: The mRNA levels for EGFR and its associated ligands, including HB-EGF, were induced several fold in PANC-1 and HCT116 cells in response to AM251. This event was associated with enhanced expression of EGFR on the cell surface with concomitant increase in EGF-induced cellular responses in AM251-treated cells. Exposure to XCT790, a synthetic inverse agonist of the orphan nuclear oestrogen-related receptor α (ERRα), also induced EGFR and HB-EGF expression to the same extent as AM251, whereas pretreatment with the ERRα-selective agonist, biochanin A, blunted AM251 actions. AM251 promoted the degradation of ERRα protein without loss of the corresponding mRNA. Knock-down of ERRα by siRNA-based approach led to constitutive induction of EGFR and HB-EGF levels, and eliminated the biological responses of AM251 and XCT790. Finally, AM251 displaced diethylstilbestrol prebound to the ligand-binding domain of ERRα. CONCLUSIONS AND IMPLICATIONS: AM251 up-regulates EGFR expression and signalling via a novel non-CB(1)R-mediated pathway involving destabilization of ERRα protein in selected cancer cell lines.


Subject(s)
ErbB Receptors/metabolism , Piperidines/pharmacology , Pyrazoles/pharmacology , Receptor, Cannabinoid, CB1/metabolism , Receptors, Estrogen/metabolism , Cell Line, Tumor , Epidermal Growth Factor/metabolism , ErbB Receptors/biosynthesis , ErbB Receptors/genetics , Genistein/pharmacology , HCT116 Cells , Heparin-binding EGF-like Growth Factor , Humans , Intercellular Signaling Peptides and Proteins/genetics , Intercellular Signaling Peptides and Proteins/metabolism , Ligands , Nitriles/pharmacology , Orphan Nuclear Receptors/metabolism , Protein Binding , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Receptors, Estrogen/agonists , Receptors, Estrogen/antagonists & inhibitors , Thiazoles/pharmacology , Up-Regulation/drug effects , ERRalpha Estrogen-Related Receptor
6.
Lett Appl Microbiol ; 51(6): 678-82, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21054446

ABSTRACT

AIMS: The bacteria-host molecular cross-talk is the matter of primary importance both in pathogenesis and in commensalism. Principally based on immunological methods, the methodologies commonly utilized for these studies are laborious and require specific antibodies. Here, we developed a new high-performance affinity chromatography (HPAC)-based approach that allows a direct measure of the interaction between whole bacterial cells and host molecules. METHODS AND RESULTS: Bifidobacterium lactis BI07 cells immobilized on amino-derivatized silica beads were utilized as stationary phase in a high-performance affinity chromatography approach. The analytes plasminogen, collagen I and collagen IV were injected, and interactions were evaluated by the insertion in an HPLC system with UV detection. According to our data, Bif. lactis BI07 is capable of interacting with plasminogen, while it does not exhibit any binding activity to collagen I and IV. CONCLUSIONS: In this study, we implemented a high-performance affinity chromatography-based method to characterize the biological interaction between whole micro-organisms and target proteins. SIGNIFICANCE AND IMPACT OF THE STUDY: With respect to the approaches commonly utilized to study the interaction between bacteria and host proteins, this HPAC-based approach is fast and cheaper than other methods and allows a direct measure of the interaction between bacterial cells and target molecules.


Subject(s)
Cells, Immobilized/metabolism , Chromatography, Affinity/methods , Proteins/metabolism , Bifidobacterium/metabolism , Chromatography, High Pressure Liquid/methods , Protein Binding , Proteins/analysis , Proteomics/methods , Silicon Dioxide
7.
Oncogene ; 29(1): 34-44, 2010 Jan 07.
Article in English | MEDLINE | ID: mdl-19802008

ABSTRACT

Tyrosine kinase receptors represent targets of great interest for cancer therapy. Here we show, for the first time, the importance of the orphan tyrosine kinase receptor, ROR2, in melanoma progression. Using melanoma tissue microarrays, we show that ROR2 is expressed predominantly in metastatic melanoma. As ROR2 has been shown to specifically interact with the non-canonical Wnt ligand, Wnt5A, this corroborates our earlier data implicating Wnt5A as a mediator of melanoma metastasis. We show here that increases in Wnt5A cause increases in ROR2 expression, as well as the PKC-dependent, clathrin-mediated internalization of ROR2. WNT5A knockdown by siRNA decreases ROR2 expression, but silencing of ROR2 has no effect on WNT5A levels. ROR2 knockdown does, however, result in a decrease in signaling downstream of Wnt5A. Using in vitro and in vivo metastasis assays, we show that ROR2 is necessary for the Wnt5A-mediated metastasis of melanoma cells. These data imply that ROR2 may represent a novel target for melanoma therapy.


Subject(s)
Melanoma/pathology , Proto-Oncogene Proteins/metabolism , Receptor Tyrosine Kinase-like Orphan Receptors/metabolism , Signal Transduction , Wnt Proteins/metabolism , Aged , Animals , Blotting, Western , Cell Line, Tumor , Cell Movement , Endocytosis/drug effects , Humans , Immunohistochemistry , Melanoma/genetics , Melanoma/metabolism , Melanoma, Experimental/genetics , Melanoma, Experimental/metabolism , Melanoma, Experimental/pathology , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Nude , Neoplasm Metastasis , Proto-Oncogene Proteins/genetics , RNA Interference , Receptor Tyrosine Kinase-like Orphan Receptors/genetics , Recombinant Proteins/pharmacology , Reverse Transcriptase Polymerase Chain Reaction , Tissue Array Analysis , Wnt Proteins/genetics , Wnt-5a Protein
8.
J Chromatogr A ; 1129(1): 73-81, 2006 Sep 29.
Article in English | MEDLINE | ID: mdl-16887128

ABSTRACT

The application of reversed-phase high-pressure liquid chromatography under gradient conditions and electrospray ion trap mass spectrometry (LC-ESI-MS) to the analysis of global modification levels of core histones is described. The optimised LC-ESI-MS method was applied for the first time to the characterisation of histones extracted from HT29, a human colon cancer cell line. Eight histones (H1-1, H1-2, H2A-1, H2A-2, H2B, H3-1, H3-2, H4) were separated on a C4 stationary phase with complete resolution, never reached in previous HPLC-MS methods, by using a gradient elution with the combined presence of heptafluorobutyric acid and formic acid as acidic modifiers in the mobile phase. Heptafluorobutyric acid was found to improve selectivity, whereas the presence of formic acid decreased ion suppression. Histones eluted from the column were detected with an ion trap mass spectrometer with an electrospray source. The peak averaged mass spectra were reconstructed by Mag Tran 1.0 software and the mass of the various isoforms of histones were derived. Method validation was conducted by performing the same sample analysis by coupling LC-ESI to a quadrupole-time-of-flight mass spectrometer (Q-TOF). The number of histone forms and their mass were found to differ not significantly from those obtained by ion trap mass spectrometer. Also the relative modifications abundance within the same histone type was found following the same trend as the two mass analysers. This method was then applied to the characterisation of changes in histone modification in HT29, never analysed by LC-MS before, treated with histone deacetylase inhibitors such as valproate and sodium butyrate, also used in preclinical trials as anticancer drugs. In particular, both the inhibitors produced a significant increase in H4 histone acetylated forms: 89% increase of the diacetyl dimethyl H4 form was observed with 1mM valproate supplementation, whereas 5 mM butyrate led to a 68% increase of the same form. Triacetyl monomethyl H4 (11,377 Da) and triacetyl dimethyl H4 (11,390 Da) were found only in cells treated with butyrate. Selective changes of H3 histone were detected with butyrate, in agreement with recently reported western blotting studies. Modifications in the H2A histone degree of acetylation were revealed by treatment of the cells with butyrate (H2A-1, H2A-2) and valproate (H2A-2). The results of the proposed methodology confirmed that inhibition of histone deacetylases caused histone hyperacetylation, responsible for decondensation and reorganization of interphase dynamic chromatin. This method resulted in selective and sensitive method to monitor variations in the acetylation and methylation state of histones after treatment of HT29 with inhibitors, and is therefore suitable for further application in new drug discovery for tumour therapy.


Subject(s)
Chromatography, High Pressure Liquid/methods , Colonic Neoplasms/metabolism , Histones/analysis , Spectrometry, Mass, Electrospray Ionization/methods , Acetylation/drug effects , Butyrates/pharmacology , HT29 Cells , Histone Deacetylase Inhibitors , Histone Deacetylases/metabolism , Histones/chemistry , Histones/metabolism , Humans , Reproducibility of Results , Valproic Acid/pharmacology
9.
J Pharm Biomed Anal ; 42(1): 17-24, 2006 Sep 11.
Article in English | MEDLINE | ID: mdl-16460902

ABSTRACT

Amaryllidaceae are known as ornamental plants, furthermore some species of this family contain galanthamine, an acetylcholinesterase inhibitor approved for the treatment of Alzheimer's disease, and other alkaloids with interesting pharmacological activity. In the present work, the quali- and quantitative analysis of Amaryllidaceae-type alkaloids in the bulbs of Narcissus species is presented using different analytical approaches. Extracts of Narcissus pseudonarcissus cv. Carlton and Narcissus jonquilla Quail, were first examined by GC-MS using a Rtx-5 MS (programmed temperature) and the major alkaloids were identified. Together with galanthamine, high contents of haemanthamine, were found. Galanthamine was reliably quantified by GC-MS, whereas haemanthamine partly decomposed under the GC conditions, thus alternative analytical methods were investigated. Firstly, reversed-phase HPLC-ESI-MS was applied to identify and isolate at semipreparative levels haemanthamine. The compound was fully characterized by MS/MS and (1)H NMR and then used as a reference substance. The quantitation of both galanthamine and haemanthamine was then accomplished by capillary electrophoresis with spectrophotometric detection. A non-aqueous (NACE) approach was selected in order to use a running buffer fully compatible with samples in organic solvent. In particular, a mixture methanol-acetonitrile (75:25, v/v) containing ammonium acetate (90 mM) was used as a background electrolyte. The same analytical sample was subjected to GC-MS and NACE analysis; the different selectivity displayed by these techniques allowed different separation profiles that can be useful in phytochemical characterization of the extracts. The GC-MS and NACE methods were validated and applied to the quantitation of galanthamine (GC-MS and NACE) and haemanthamine (NACE) in bulbs of N. jonquilla.


Subject(s)
Amaryllidaceae Alkaloids/analysis , Electrophoresis, Capillary/methods , Gas Chromatography-Mass Spectrometry/methods , Narcissus/chemistry , Chromatography, High Pressure Liquid , Sensitivity and Specificity
10.
J Chromatogr A ; 1099(1-2): 149-56, 2005 Dec 16.
Article in English | MEDLINE | ID: mdl-16188264

ABSTRACT

A previous GC/MS study highlighting the impurity profile of the synthetic pesticide d-allethrin is extended here to validate and confirm the impurities identity through the development of soft ionisation HPLC-MS methods. To accomplish this, we developed a reverse phase LC-MS analysis in gradient elution with two distinct soft ionisation techniques, the atmospheric pressure ionisation with electrospray source (API-ESI) and the chemical ionisation (APCI). A single quadrupole and an ion trap, which allowed the simultaneous determination of the molecular masses and structural information of the impurities by acquisition of collisionally induced (CID) product ions spectrum and in-source fragmentation, were employed as analysers. Single quadrupole and ion trap analysers resulted perfectly matching in the d-allethrin impurity fragmentation patterns. All the main impurities over 0.1% identified by GC/MS were confirmed. Results indicate that the proposed HPLC/MS method was found appropriate to confirm the presence of impurities such as chrysolactone, chloro allethrin derivatives, allethrolone and chrysanthemic acid, excluding their formation under GC/MS strong ionisation condition.


Subject(s)
Allethrins/analogs & derivatives , Allethrins/chemistry , Chromatography, High Pressure Liquid/methods , Mass Spectrometry/methods , Pesticides/chemistry , Calibration , Models, Theoretical , Spectrophotometry, Ultraviolet , Stereoisomerism
11.
J Pharm Biomed Anal ; 37(5): 979-85, 2005 Apr 29.
Article in English | MEDLINE | ID: mdl-15862676

ABSTRACT

HPLC-DAD and LC-ESI-MS methods have been developed for the analysis of doxycycline (DOX), including the identification of the related impurities metacycline (MTC) and 6-epidoxycycline (EDOX) and its determination in a medicated premix. The chromatographic separations have been performed on Luna C18 stationary phase and on Synergi (4 microm) Polar-RP 80A, using both acidic (pH 2.5) and basic (pH 8.0) mobile phases. The Synergi Polar-RP column, in combination with a mobile phase of oxalic acid (0.02 M; pH 2.5)-acetonitrile 82:18 (v/v), allowed the complete separation of MTC, EDOX and DOX. The same separation was also obtained using Luna C18 stationary phase with a pH 8 mobile phase. Application of a LC-ESI-MS system and MS/MS analysis, using both positive and negative polarity, allowed the peak identity to be confirmed. A method based on Luna C18 column and UV detection at 346 nm was validated for the determination of DOX in a medicated premix for incorporation in medicated feedstuff.


Subject(s)
Animal Feed , Doxycycline/analysis , Drug Contamination , Spectrometry, Mass, Electrospray Ionization/methods , Anti-Bacterial Agents/analysis , Chromatography, High Pressure Liquid/methods , Chromatography, Liquid/methods
12.
J Chromatogr A ; 1046(1-2): 67-73, 2004 Aug 13.
Article in English | MEDLINE | ID: mdl-15387172

ABSTRACT

A two-dimensional achiral/chiral HPLC method with circular dichroism (CD) detection was optimized for the stereochemical resolution and determination of the elution order of the eight stereoisomers of synthetic allethrin. A monolithic silica HPLC column (Chromolith, Merck, 100 mm x 4.6 mm i.d.) was put orthogonally to an enantioselective OJ Daicel column (250 mm x 4.6 mm i.d.) by means of a switching valve. The resolution of cis and trans diastereoisomers on the silica column was obtained by using a mobile phase consisting of n-hexane:tert-butyl methyl ether (96:4) (v/v) at a flow rate of 1 ml min(-1). The cis and trans peaks were then switched to the enantioselective OJ column separately in two subsequent injections. The resolution of the four trans stereoisomers was accomplished by using n-hexane:tert-butyl methyl ether (90:10) (v/v), while the mobile phase composition for the four cis stereoisomers consisted of n-hexane:isopropanol (99.3:0.7) (v/v). The CD based detection system allowed the determination of the elution order on the basis of the CD signals of the single stereoisomers, together with the injection of pure stereoisomers. Under the final conditions, the validated method was applied to the determination of stereoisomeric composition and absolute configuration of the prevailing stereoisomers of real samples, i.e. commercial batches of different sources of d-allethrin.


Subject(s)
Allethrins/analysis , Chromatography, High Pressure Liquid/methods , Circular Dichroism/methods , Spectrophotometry, Ultraviolet/methods , Stereoisomerism
13.
J Pharm Biomed Anal ; 35(2): 267-75, 2004 Apr 16.
Article in English | MEDLINE | ID: mdl-15063461

ABSTRACT

Nicardipine (NC)-cyclodextrin solid systems were prepared in equimolar ratios and their photostability in aqueous solution under exposure to UV(A)-UV(B) radiations was evaluated. The photodegradation process was monitored by a capillary electrophoresis (CE) method able to provide the enantioresolution of the rac-nicardipine. Enantioresolution was achieved using the mixture 3.0% sulfate-beta-cyclodextrin (SbetaCD) and 2.0% heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TMbetaCD) as chiral selector in 20mM triethanolammonium phosphate solution (pH 3.0). The photostability studies were carried out on inclusion complexes of rac-nicardipine with alpha-cyclodextrin (alphaCD), beta-cyclodextrin (betaCD), gamma-cyclodextrin (gammaCD), hydroxypropyl-alpha-cyclodextrin (HPalphaCD), hydroxypropyl-beta-cyclodextrin (HPbetaCD), hydroxypropyl-gamma-cyclodextrin (HPgammaCD), (2-hydroxyethyl)-beta-cyclodextrin (HEbetaCD) and methyl-beta-cyclodextrin (MbetaCD). A photoprotective effect was observed by betaCD, HPalphaCD, HEbetaCD, whereas gammaCD, MbetaCD, HPbetaCD and HPgammaCD did not affect the nicardipine photostability. Conversely, alphaCD was found to favour the drug photodegradation. Evidences for CDs-mediated stereoselective photodegradation of rac-nicardipine were observed only for the beta-CD complex. In this case, two distinct photodegradation profiles, with two different kinetic constants (k), were observed for the nicardipine enantiomers.


Subject(s)
Cyclodextrins/analysis , Cyclodextrins/radiation effects , Nicardipine/analysis , Nicardipine/radiation effects , Ultraviolet Rays , Biotransformation/radiation effects , Cyclodextrins/metabolism , Drug Stability , Electrophoresis, Capillary/methods , Nicardipine/metabolism
14.
Farmaco ; 58(9): 867-73, 2003 Sep.
Article in English | MEDLINE | ID: mdl-13679181

ABSTRACT

The photostability of the diuretic drugs triamterene and furosemide, individually and combined, was evaluated. Spectrophotometric, spectrofluorimetric and chromatographic (HPLC) methods were applied to monitor the drug photodegradation. Furosemide was confirmed to be highly photolable in both pH 7.4 solution and methanol. Differently triamterene proved to be highly fluorescent (emission quantum yield: 0.9 in methanol and 0.8 in pH 7.4 solution), but essentially photostable (photochemical reaction quantum yield: congruent with 5 x 10(-4)) under exposure at 365 and 313 nm radiations. When the combined drugs in pH 7.4 solutions were exposed to 365 nm radiations a significant photoprotective effect of triamterene on furosemide was observed. The photoreactivity of the drugs was exploited to develop an HPLC method involving a post-column on-line photochemical derivatization useful to confirm the analyte identity in a commercial dosage form (tablets). The commercial product, containing the combined drugs, proved to be photostable also after long (65 h) light exposure.


Subject(s)
Furosemide/radiation effects , Triamterene/radiation effects , Ultraviolet Rays , Chromatography, High Pressure Liquid , Drug Combinations , Drug Interactions , Drug Stability , Furosemide/chemistry , Kinetics , Pharmaceutical Solutions , Photochemistry , Solvents , Spectrometry, Fluorescence , Spectrophotometry/methods , Tablets , Time Factors , Triamterene/chemistry
15.
J Exp Biol ; 206(Pt 12): 2031-8, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12756285

ABSTRACT

In Drosophila flight muscles, glycolytic enzymes are co-localized along sarcomeres at M-lines and Z-discs and co-localization is required for normal flight. We have extended our analysis of this phenomenon to include a set of six glycolytic enzymes that catalyze consecutive reactions along the glycolytic pathway: aldolase, glycerol-3-phosphate dehydrogenase (GPDH), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), triose phosphate isomerase, phosphoglycerate kinase and phosphoglycerol mutase (PGLYM). Each of these enzymes has an identical pattern of localization. In mutants null for GPDH, localization of none of the other enzymes occurs and therefore is interdependent. In optimally fixed preparations of myofibrils, accumulation of the enzymes at M-lines is much greater than at Z-discs. However, localization at M-lines is more labile, as shown by loss of localization when fixation is delayed. We have begun to analyze the protein-protein interaction involved in glycolytic enzyme co-localization using the yeast two-hybrid system. We have identified two pair-wise interactions. One is between GPDH and GAPDH and another is between GPDH and PGLYM.


Subject(s)
Drosophila melanogaster/enzymology , Glycolysis/physiology , Myofibrils/enzymology , Animals , Codon, Nonsense , Enzymes/metabolism , Enzymes/physiology , Flight, Animal , Glycerol-3-Phosphate Dehydrogenase (NAD+) , Glycerolphosphate Dehydrogenase/deficiency , Microscopy, Fluorescence
16.
Photochem Photobiol ; 77(4): 356-61, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12733646

ABSTRACT

Administration of the second-generation antihistamine, terfenadine, is sometimes associated with photosensitivity and other skin reactions. To obtain information on its photoreactivity, we used a stepwise experimental approach involving tests for photostability, phototoxicity (PT) (mouse fibroblast cell line [3T3] neutral red uptake [NRU] test) and photomutagenicity (with standard Ames salmonella tester strains TA98, TA100 and TA102). Terfenadine was not phototoxic to cultured mammalian cells under the conditions used (i.e. 5000/161 mJ cm(-2) UVA-UVB). Natural sunlight and UV radiations caused considerable drug decomposition and formation of several photoproducts. Addition of the irradiated terfenadine solution (i.e. a mixture of photoproducts) to the tester did not significantly increase background mutation frequency. Irradiation of terfenadine coplated with the TA102 strain induced a clear-cut photomutagenic response, the magnitude of which was dependent upon the precursor compound concentration and the UV dose (212/7 to 339/11 mJ cm(-2) UVA-UVB). These findings demonstrate that in vitro terfenadine is photomutagenic in absence of PT. Further in vitro and in vivo studies are therefore needed to provide an adequate safety assessment of the photochemical genotoxicity--carcinogenicity potential of terfenadine. In the meantime, patients should be advised to avoid excessive exposure to sunlight.


Subject(s)
Mutagens/toxicity , Terfenadine/toxicity , 3T3 Cells , Animals , Mice , Mice, Inbred BALB C , Mutagenicity Tests , Mutagens/chemistry , Photochemistry , Salmonella/genetics , Terfenadine/chemistry
17.
Biochem Biophys Res Commun ; 293(5): 1502-7, 2002 May 24.
Article in English | MEDLINE | ID: mdl-12054686

ABSTRACT

Several studies point to the existence of an inverse correlation between cellular lipid peroxidation and both cell proliferation and neoplastic transformation. Furthermore, numerous results demonstrate that lipid peroxidation products affect central biochemical pathways and intracellular signalling at physiological concentrations. 4-Hydroxynonenal (HNE) is one of the most active products of lipid peroxidation. This work has focused on the evaluation of HNE nuclear content, so far never directly measured, by electrospray-ionization-mass-spectrometry (ESI/MS) and on the correlation between its concentration and the induced effects after exogenous administration. In a human osteosarcoma cell line (SaOS2), HNE exhibited an early cytotoxic effect characterized by apoptosis, cytostatic and differentiating effects characterized by slow growth, increase in alkaline phosphatase (ALP), and alpha5 integrin subunit content with decrease in tumorigenicity.


Subject(s)
Aldehydes/pharmacology , Cysteine Proteinase Inhibitors/pharmacology , Osteosarcoma/drug therapy , Aldehydes/toxicity , Antigens, CD/metabolism , Apoptosis , Cell Differentiation , Cell Division , Cell Line , Cell Nucleus/metabolism , Chromatin/metabolism , Chromatography, High Pressure Liquid , Cysteine Proteinase Inhibitors/toxicity , Cytoskeleton/metabolism , Humans , Integrin alpha5 , Kinetics , Lipid Peroxidation , Microscopy, Confocal , Osteosarcoma/metabolism , Oxidative Stress , Spectrometry, Mass, Electrospray Ionization , Time Factors , Tumor Cells, Cultured
18.
Farmaco ; 57(5): 369-72, 2002 May.
Article in English | MEDLINE | ID: mdl-12058811

ABSTRACT

An isocratic reversed-phase liquid chromatographic (HPLC) method is proposed for the practical and reliable determination of triclosan, an antimicrobic agent incorporated into a variety of personal heath care products. Chromatographic separations were performed on a C-18 column using acetonitrile-TEA phosphate (70 mM; pH 3.5) 55:45 (v/v) as mobile phase and UV detection at 230 and 280 nm. The selectivity of the method was assured by the on-line photodiode array detector. The identity of the triclosan peak was also confirmed by HPLC MS. The method was successfully applied to the determination of triclosan in commercially available health care products (deodorant stick, dentifrice gel, mouthrinse, toothpaste and handwash). All the products displayed triclosan concentrations in compliance with the EEC directive (< or = 0.3%,).


Subject(s)
Cosmetics/analysis , Triclosan/analysis , Anti-Infective Agents/analysis , Calibration , Chromatography, High Pressure Liquid/methods , Cosmetics/chemistry , Linear Models , Quality Control , Reproducibility of Results , Sensitivity and Specificity , Spectrometry, Mass, Electrospray Ionization , Triclosan/chemistry
19.
J Pharm Biomed Anal ; 27(5): 803-12, 2002 Feb 01.
Article in English | MEDLINE | ID: mdl-11814721

ABSTRACT

The photostability of Lacidipine, a dihydropyridine drug used in the treatment of mild and moderate hypertension, was studied in solutions exposed to UV-A radiations. The effects of the solvent (ethanol, acetone, dichloromethane), drug concentration and radiation wavelength on the drug photostability were evaluated. Lacidipine and its photoproducts were separated by a selective liquid chromatographic (HPLC) method, under normal phase conditions (CN-column), using n-hexane:ethanol 97:3 (v/v) as mobile phase, at a flow rate of 2.0 ml/min. The main photodegradation products were isolated and characterised and a photodegradation pathway was proposed for Lacidipine in solution. The cis-isomer and a photocyclic isomer proved to be the main photodegradation products.


Subject(s)
Calcium Channel Blockers/radiation effects , Dihydropyridines/radiation effects , Ultraviolet Rays , Calcium Channel Blockers/analysis , Calcium Channel Blockers/chemistry , Dihydropyridines/analysis , Dihydropyridines/chemistry , Drug Stability , Pharmaceutical Solutions/chemistry , Pharmaceutical Solutions/radiation effects , Photochemistry , Ultraviolet Rays/adverse effects
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