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Ng G (ng + g)

Distribution by Scientific Domains
Life Sciences40%
Chemistry25%
Medical Sciences20%
Earth and Environmental Science15%

Selected Abstracts

Accumulation of tributyltin in Hyalella azteca as an indicator of chronic toxicity: Survival, growth, and reproduction

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2004
Adrienne J. Bartlett
Abstract The chronic toxicity of tributyltin (TBT) was examined by exposing two successive generations of the freshwater amphipod, Hyalella azteca, to sediments spiked with TBT. Survival was the most sensitive measure of effect, with lethal concentration resulting in 50% mortality (LC50) values on a water and body concentration basis ranging from 76 to 145 ng Sn/L and 2,790 to 4,300 ng Sn/g, respectively. Individual growth of amphipods was not negatively affected by TBT, and although reproduction might be more sensitive than survival, the data were too variable to use on a routine basis. There were no detectable TBT-induced differences in the response between first- and second-generation animals. The relationship between toxicity and bioaccumulation of TBT in H. azteca was determined and can be used as a tool to predict the toxicity of TBT in environmental samples. Body concentrations exceeding 2,000 ng Sn/g in H. azteca exposed to field-collected samples would indicate that chronic toxicity due to TBT is likely occurring in amphipod populations at those sites. [source]

Relationship between lysosomal membrane destabilization and chemical body burden in eastern oysters (Crassostrea virginica) from Galveston Bay, Texas, USA

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 6 2002
Hyun-Min Hwang
Abstract Lysosomal destabilization was measured by using hemocytes of eastern oysters (Crassostrea virginica) collected along a chemical concentration gradient in Galveston Bay, Texas, USA. Results of the lysosomal response were compared to concentrations of organic compounds and trace elements in oyster tissue. Concentrations (on a dry-wt basis) ranged from 288 to 2,390 ng/g for polycyclic aromatic hydrocarbons (PAHs), 38 to 877 ng Sn/g for tri- n -butyltin (TBT), 60 to 562 ng/g for polyclorinated biphenyls (PCBs), and 7 to 71 ng/g for total DDT. Trace element concentrations (on a dry-wt basis) ranged from 1.1 to 4.0 ,g/g for Cd, 105 to 229 ,g/g for Cu, 212 to 868 ,g/g for Al, and 1,200 to 8,180 ,g/g for Zn. The percentage of destabilized lysosomes ranged from 34 to 81%. A significant positive correlation (p < 0.05) was observed between lysosomal destabilization and body burden of organic compounds (PAHs, PCBs, TBT, and chlorinated pesticides). No significant correlation was found between metal concentrations and lysosomal destabilization. Based on lysosomal destabilization, the study sites in Galveston Bay can be placed in one of three groups: healthy (Hanna Reef and Confederate Bay), moderately damaged (Offats Bayou and Todd's Dump), and highly damaged (Yacht Club and Ship Channel). Lysosomal destabilization that is consistent with toxic chemical body burdens supports previous observations that lysosomal membranes are damaged by toxic chemicals and indicates that this method can serve as an early screening tool to assess overall ecosystem health by using oysters. [source]

Voltametric and Flow Injection Determination of Oxytetracycline Residues in Food Samples Using Carbon Fiber Microelectrodes

ELECTROANALYSIS, Issue 7 2003
L. Agüí
Abstract A voltammetric method for the determination of the antibiotic oxytetracycline (OTC) in food samples is reported. Carbon fiber microelectrodes (CFMEs), which allow voltammetric measurements to be performed in a small volume (1,mL) of the analyte extract from the samples, are employed. Repeatable electroanalytical responses were obtained with no need of applying cleaning treatments to the CFME. Under the optimized square-wave conditions, a linear calibration plot for OTC was obtained in the 1.0×10,6,1.0×10,4,mol,L,1 range, with a detection limit of 2.9×10,7,mol,L,1 (150,ng,mL,1) OTC. The determination of OTC by a flow-injection method with amperometric detection using a homemade flow cell specially designed to work with CFMEs, was also evaluated using pure acetonitrile as the carrier. The SW voltammetric method was applied to the determination of OTC in spiked milk and eggs samples, at 100,ng,mL,1 and 200,ng g,1 levels, respectively. The procedure involved the extraction of the analyte in ethyl acetate, evaporation of the solvent and reconstitution of the residue in acetonitrile ,5.0×10,4,mol,L,1 tetrabutylammonium perchlorate medium. Recoveries of 96±8 and 91±8% were obtained for milk and eggs, respectively, by applying the standard additions method. [source]

Butyltin compounds in sediments from the commercial harbor of Alexandria City, Egypt

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2001
Assem O. Barakat
Abstract Tributyltin (TBT), dibutyltin (DBT), and monobutyltin (MBT) compounds were quantitatively determined in surface-sediment samples collected from 23 sites in the commercial harbor of Alexandria City, Egypt. Butyltin concentrations in sediments varied widely depending on the sample location, ranging from less than 0.1 to 186 ng g,1 of Sn for MBT, less than 0.1 to 379 ng g,1 of Sn for DBT, and 1 to 2,067 ng g,1 of Sn for TBT. Elevated TBT concentrations, ranging from 727 to 2,067 ng g,1 of Sn were observed in harbors, marinas, and near ship-repair facilities, indicating that the butyltin-containing, antifouling paints of boats and vessels are the major source of butyltin contamination. The TBT concentration decreased rapidly away from potential source areas of boat docking and repair facilities. The high relative concentrations of TBT in the sediments indicated that degradation processes in the sediments are minor, probably due to the anoxic sedimentary conditions at the sampling sites and/or relatively fresh input of TBT to these sites. [source]

Linear alkylbenzenes in muscle tissues of white croaker near a large ocean outfall in southern California, USA

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2001
Charles R. Phillips
Abstract Muscle tissues of a bottom-dwelling marine fish, white croaker (Genyonemus lineatus), collected near a large wastewater outfall in southern California, USA, were analyzed for long-chain linear alkylbenzenes (LABs). Total LABs (summed concentrations of C11 through C14 isomers) were highest (166,748 ng g,1 wet wt) in individuals collected in the immediate vicinity of the Orange County Sanitation District (OCSD; Fountain Valley, CA, USA) outfall diffuser, whereas relatively lower concentrations occurred in fish from mid-shelf and inshore locations at distances of 2.5 and 5 km, respectively, from the outfall. Fish tissue LAB concentrations were roughly proportional to sediment LAB concentrations at the respective collection sites. The extent of LAB degradation, as determined by ratios of internal to external C12 isomers, did not appear to relate to LAB concentrations or sampling location. Tissue DDT and PCB concentrations were not significantly correlated with LABs and, thus, did not appear to relate to recent exposures to sewage residues from the OCSD discharge. Measurements of LAB concentrations in fish tissues may be widely applicable as a monitoring tool for interpreting exposures to sewage discharges. [source]

Routine Analyses of Trace Elements in Geological Samples using Flow Injection and Low Pressure On-Line Liquid Chromatography Coupled to ICP-MS: A Study of Geochemical Reference Materials BR, DR-N, UB-N, AN-G and GH

GEOSTANDARDS & GEOANALYTICAL RESEARCH, Issue 2-3 2001
Jean Carignan
géostandards; éléments traces; flow injection; chromatographie liquide; ICP-MS We describe analytical procedures for trace element determinations developed at the CNRS Service d'Analyse des Roches et des Minéraux (SARM) and report results obtained for five geochemical reference materials: basalt BR, diorite DR-N, serpentinite UB-N, anorthosite AN-G and granite GH. Results for rare earth elements, U and Th are also reported for other reference materials including dunite DTS-1, peridotite PCC-1 and basalt BIR-1. All rocks were decomposed using alkali fusion. Analyses were done by flow injection ICP-MS and by on-line low pressure liquid chromatography (LC)-ICP-MS for samples containing very low REE, U and Th concentrations. This latter method yielded limits of determination much lower than data by direct introduction and eliminated possible isobaric interference on these elements. Although results agree with most of the working values, when available, results for some elements differed slightly from the recommended concentrations. In these cases, we propose new values for Co, Y and Zn in basalt BR, Zr in diorite DR-N, Sr and U in granite GH, and Ga and Y in anorthosite AN-G. Furthermore, although the Sb concentration measured in AN-G was very close to our limit of determination, our value (0.3 ± 0.1 ,g g,1) is much lower than the reported working value of 1.4 ± 0.2 ,g g,1. These new values would need to be confirmed by a new inter-laboratory programme to further characterise these reference materials. Results obtained for REE, Th and U concentrations using the on-line low pressure LC-ICP-MS yielded good limits of determination (ng g,1to sub-ng g,1for rocks and ng l,1to sub-ng l,1for natural waters) and accurate results. The efficiency of the matrix separation allowed accurate measurements of Eu without the need to correct the BaO isobaric interference for samples having Ba/Eu ratios as high as 27700. For REE concentrations in PCC-1 and DTS-1, differences with values reported in the literature are interpreted as resulting from possible heterogeneity of the reference materials. Thorium and U values are proposed for these two samples, as well as for AN-G and UB-N. Nous rapportons les procédures d'analyse pour les éléments traces développées au Service d'Analyse des Roches et des Minéraux (SARM) du CNRS et les résultats obtenus pour 5 géostandards: le basalte BR, la diorite DR-N, la serpentinite UB-N, l'anorthosite AN-G et le granite GH. Des résultats obtenus pour les Terres Rares (REE), l'uranium et le thorium sont aussi rapportés pour d'autres matériaux de référence tels que la dunite DTS-1, la péridotite PCC-1 et le basalte BIR-1. Les roches ont été décomposées par fusion alcaline. Les analyses ont été faites par Flow Injection ICP-MS et par chromatographie liquide basse pression en ligne sur un ICP-MS pour les très faibles teneurs en REE, U et Th. Cette dernière méthode permet d'avoir une meilleure limite de détermination que celle par introduction directe et d'éliminer certaines interférences isobariques sur ces éléments. Bien que, dans la majorité des cas, nous ayons mesuré les valeurs de référence telles que rapportées dans la littérature, certaines concentrations mesurées diffèrent légèrement des valeurs recommandées. Ainsi, nous proposons de nouvelles valeurs de Co, Y et Zn pour le basalte BR, de Zr pour la diorite DR-N, de Sr et U pour le granite GH et de Ga et Y pour l'anorthosite AN-G. De plus, bien que la concentration en Sb mesurée pour AN-G soit très proche de notre limite de détermination, notre valeur (0.3 ± 0.1 ,g g,1) est bien inférieure à celle rapportée dans la littérature (1.4 ± 0.2 ,g g,1). Ces nouvelles valeurs devraient être confirmées par une nouvelle campagne de caractérisation inter laboratoire pour ces géostandards. Les résultats obtenus pour les REE, U et Th par chromatographie liquide basse pression en ligne sur un ICP-MS sont justes et livrent des limites de détermination faibles au niveau du ng g,1à sub-ng g,1pour les roches et ng l,1à sub-ng l,1pour les eaux naturelles. La séparation de la matrice est efficace et permet une mesure juste de Eu sans correction d'interférence générée par l'oxyde de Ba, et ce même pour des échantillons possédant des rapports Ba/Eu très élevés, de l'ordre de 27700. Les concentrations en REE mesurées pour les échantillons PCC-1 et DTS-1 peuvent être significativement différentes de celle rapportées dans la littérature, probablement à cause d'une hétérogénéité de ces échantillons. Des valeurs de concentrations en U et Th sont proposées pour ces deux échantillons ainsi que pour AN-G et UB-N. [source]

Dental pulp fibroblasts express neuropeptide Y Y1 receptor but not neuropeptide Y

INTERNATIONAL ENDODONTIC JOURNAL, Issue 10 2010
S. A. Killough
Killough SA, Lundy FT, Irwin CR. Dental pulp fibroblasts express neuropeptide Y Y1 receptor but not neuropeptide Y. International Endodontic Journal, 43, 835,842, 2010. Abstract Aim, To investigate whether dental pulp fibroblasts express neuropeptide Y (NPY) and NPY-Y1 in vitro and to determine the effects of the cytokines including interlukin-1, (IL-1,), TGF- ,1, substance P and NPY on the expression of NPY Y1. Methodology, Three primary fibroblast cell strains were obtained from freshly extracted human third molar teeth. RT-PCR was utilized to detect expression of NPY and mRNA expression. Membrane protein samples were isolated, and protein expression was determined by Western blotting. Radioimmunoassay was used to quantify NPY expression in healthy (n = 35) and carious (n = 39) whole pulp samples, and the student's t -test was used to test for statistical significance. In addition, the 3-(4,5-Dimethylthiazol,2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used to assay fibroblast cell growth. Results, mRNA transcripts were found in all three fibroblast cell populations with the cytokines having a stimulatory effect on its expression (P < 0.05). NPY mRNA was not detected in the cell strains. NPY-Y1 receptor protein expression was visualized by Western blotting, and there was no effect of IL-1, or TGF- ,1 on its expression. The mean concentration of NPY-Ir determined by radioimmunoassay in non-carious teeth was 19.40 ng g,1 (±17.03 SD) compared to 29.95 ng g,1 (±20.99 SD) in carious teeth (P < 0.05). Conclusion, Human dental pulp fibroblasts express, but do not synthesize, NPY, demonstrating that the fibroblast is a target cell for NPY. The effect of proinflammatory cytokines suggests that fibroblasts play a neuroimmunomodulatory role in the pulpal response to dental caries and injury. [source]

Fluorescence polarization immunoassay based on a monoclonal antibody for the detection of ochratoxin A

INTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 8 2004
Won-Bo Shim
Summary A fluorescence polarization immunoassay (FPIA) based on a monoclonal antibody for the determination of ochratoxin A (OTA) was developed. Fluorescein-labelled OTA derivative (tracer) was synthesized and purified by thin-layer chromatography. The optimized OTA FPIA had a dynamic range from 5 to 200 ng mL,1 with IC50 value of 30 ng mL,1 and a detection limit of 3 ng mL,1. The method developed was characterized by high specificity and reproducibility. Cross-reactivity with other mycotoxins (zearalenone, aflatoxins, patulin and T-2 toxin) was negligible (<0.1%). Methanol extracts of barley samples were used for the analysis. The results of OTA determination in barley were compared with those determined by indirect competitive enzyme-linked immunosorbent assay (ELISA). Recoveries for the samples spiked at 50, 100 and 500 ng g,1 levels were 91, 90 and 97%, respectively, for FPIA, and 98, 98 and 102%, for ELISA. Naturally contaminated barley samples were analysed by these methods but some disagreement was observed between the results. The FPIA method can be applied for screening of food samples for OTA residues without a complicated clean-up. [source]

Inhibition of Listeria monocytogenes in chicken cold cuts by addition of sakacin P and sakacin P-producing Lactobacillus sakei

JOURNAL OF APPLIED MICROBIOLOGY, Issue 2 2002
T. Katla
Aims: To evaluate the potential of sakacin P and sakacin P-producing Lactobacillus sakei for the inhibition of growth of Listeria monocytogenes in chicken cold cuts, by answering the following questions. (i) Is sakacin P actually produced in food? (ii) Is sakacin P produced in situ responsible for the inhibiting effect? (iii) How stable is sakacin P in food? Methods and Results:Listeria monocytogenes, a Lact. sakei strain and/or the bacteriocin sakacin P were added to chicken cold cuts, vacuum packed and incubated at 4 or 10°C for 4 weeks. Each of two isogenic Lact. sakei strains, one producing sakacin P and the other not, had an inhibiting effect on the growth of L. monocytogenes. The effect of these two isogenic strains on the growth of L. monocytogenes was indistinguishable, even though sakacin P was produced in the product by one of the two Lact. sakei strains. The addition of purified sakacin P had an inhibiting effect on the growth of L. monocytogenes. A high dosage of sakacin P (3·5 ,g g,1) had a bacteriostatic effect throughout the storage period of 4 weeks, while a low dosage (12 ng g,1) permitted initial growth, but at a slow rate. After 4 weeks of storage, the number of L. monocytogenes in the samples with a low dosage of sakacin P was 2 logs below that in the untreated control. When using a high dosage of sakacin P, the bacteriocin was detected in samples stored for up to 6 weeks. Conclusions: (i) Sakacin P is produced by a Lact. sakei strain when growing on vacuum-packed chicken cold cuts. (ii) Inhibiting effects of Lact. sakei, other than sakacin P, are active in inhibiting the growth of L. monocytogenes growing on chicken cold cuts. (iii) Sakacin P is stable on chicken cold cuts over a period of 4 weeks. Significance and Impact of the Study: Both sakacin P and Lact. sakei were found to have potential for use in the control of L. monocytogenes in chicken cold cuts. [source]

Cyclodextrin microparticles for drug delivery to the posterior segment of the eye: aqueous dexamethasone eye drops

JOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 5 2007
Thorsteinn Loftsson
Delivery of steroids to the retina is currently undertaken with invasive injections into the vitreous cavity. This paper describes a non-invasive method to deliver steroids in therapeutic levels to the retina in rabbits. Dexamethasone was formulated as somewhat water-soluble dexamethasone/,-cyclodextrin (,CD) microparticles in a low-viscosity aqueous eye drop suspension. The mean (± standard deviation) diameter of the particles was 20.4 ± 10.3 ,m, with no particles larger than 60 ,m. The aqueous suspension formulation was tested in rabbits and compared with an aqueous dexamethasone eye drop solution containing randomly methylated ,-cyclodextrin (RM,CD). The dexamethasone concentration was identical in both formulations (15 mg mL,1). The drug was administered to the left eye but determined in both eyes. The amount reaching different eye tissues via the topical route was determined by subtracting the amount found in the right eye from the amount found in the left eye. Two hours after single application of the dexamethasone/,CD eye drops to rabbits the mean (± s.d.) concentration in vitreous was 29 ± 16 ng g,1, 86% of which reached vitreous via the topical route and in retina the concentration was 57 ± 22 ng g,1 (49% via topical route). For the RM,CD the values were 22.6 ± 9 and 66 ± 49 ng g,1 (73 and 14% via topical route), respectively. These steroid levels are comparable with the dexamethasone concentration achieved 1 month after intravitreal injection. The aqueous dexamethasone/,CD eye drop formulation was chemically stable during 7 months storage and well tolerated with no visible short-term side effects. [source]

Sensitive enzyme-linked immunosorbent assay and rapid one-step immunochromatographic strip for fumonisin B1 in grain-based food and feed samples

JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 6 2010
Chang-Min Shiu
Abstract BACKGROUND: Maize contaminated with mycotoxin fumonisin B1 poses a global threat to agricultural production. In this study, polyclonal antibodies (pAb) specific to fumonisin B1 were generated from rabbits immunised with fumonisin B1,keyhole limpet haemocyanin (KLH). These antibodies were used to establish a sensitive competitive direct enzyme-linked immunosorbent assay (cdELISA) and gold nanoparticle immunochromatographic strip for detecting fumonisin B1 levels in maize-based foods and feeds. RESULTS: In cdELISA, fumonisins B1, B2 and B3 at concentrations of 0.42, 0.58 and 81.5 ng mL,1 respectively caused 50% inhibition (IC50) of binding of fumonisin B1,horseradish peroxidase (HRP) to the antibodies. Effective on-site detection of fumonisin B1 was achieved by developing a rapid and sensitive pAb-based gold nanoparticle immunochromatographic strip. This strip had a detection limit of 5 ng mL,1 for fumonisin B1 in maize-based samples. Additionally, the whole analytical process could be completed within 10 min. Close examination of 15 maize-based samples by cdELISA revealed that 11 were fumonisin-positive, with a mean concentration of 435 ± 20.1 ng g,1. These results correlated well with those obtained by immunochromatographic strip. CONCLUSION: Both cdELISA and immunochromatographic strip methods established in this study are sensitive for rapid detection of fumonisins in agricultural commodities. Copyright © 2010 Society of Chemical Industry [source]

Usefulness and pharmacokinetic study of oral terbinafine for hyperkeratotic type tinea pedis

MYCOSES, Issue 1 2008
Izumi Kikuchi
Summary To study and establish an optimal administration method of oral antifungal, terbinafine (TBF), for hyperkeratotic type tinea pedis, from the pharmacokinetic point of view, 20 patients with hyperkeratotic type tinea pedis were given TBF 125 mg once daily for 4 weeks and observed over time for improvement in dermatological symptoms and mycological efficacy. Targeting five of the patients, TBF concentration in the stratum corneum was measured using the liquid chromatography/tandem mass spectrometry (LC-MS/MS) method. TBF was detected in the stratum corneum of the sole 1 week after beginning the treatment in some cases and reached its peak 1 week after the completion of the treatment with a concentration of 247.8 ng g,1, which was approximately more than 50 times higher than its minimal inhibitory concentration against dermatophytes. TBF was not detected at 8 weeks post-treatment, although its concentration was 50.73 ng g,1 at 6 weeks post-treatment. Its effectiveness rate (effective + markedly effective) was 95% (19/20) with no adverse reactions, including abnormal changes in the laboratory test values, in any patient. These results suggest that TBF is a useful drug to treat hyperkeratotic tinea pedis from the pharmacokinetic point of view. [source]

Development of insect-resistant transgenic rice with Cry1C*-free endosperm

PEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 9 2009
Rongjian Ye
Abstract BACKGROUND: Yellow stem borer (Tryporyza incertulas Walker), striped stem borer (Chilo suppressalis Walker) and leaf folder (Cnaphalocrocis medinalis Guenec) are three lepidopteran pests that cause severe damage to rice in many areas of the world. In this study, novel insect-resistant transgenic rice was developed in which Bt protein expression was nearly absent in the endosperm. The resistant gene, cry1C*, driven by the rice rbcS promoter (small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase), was introduced into Zhonghua 11 (Oryza sativa L. ssp. japonica) by Agrobacterium -mediated transformation. RESULTS: A total of 83 independent transformants were obtained, 19 of which were characterised as single-copy foreign gene insertion. After preliminary screening of the T1 families of these 19 transformants in the field, six highly insect-resistant homozygous lines were selected. These six homozygous transgenic lines were field tested for resistance to leaf folders and stem borers, and for their agronomic performance. The Cry1C* protein levels in leaves and endosperm were measured by ELISA. Subsequently, the elite transgenic line RJ5 was selected; this line not only possessed high resistance to leaf folders and stem borers, normal agronomic performance, but also Cry1C* expression was only 2.6 ng g,1 in the endosperm. CONCLUSION: These results indicated that RJ5 has the potential for widespread utility in rice production. Copyright © 2009 Society of Chemical Industry [source]

Molecular analysis of resistance mechanisms to Orobanche cumana in sunflower

PLANT PATHOLOGY, Issue 3 2007
P. Letousey
Resistance to the dicotyledenous parasite Orobanche cumana in sunflower is characterized by a low number of parasitic attachments and a confinement of the parasite in host tissues leading to its necrosis. To help understand what determines such resistance mechanisms, molecular, biochemical and histological approaches were employed before (early response) and after (late response) attachment of the broomrape parasite to susceptible (2603) and resistant (LR1) sunflower genotypes. The expression patterns of 11 defence-related genes known to be involved in different metabolic pathways (phenylpropanoids, jasmonate, ethylene) and/or in resistance mechanisms against microorganisms were investigated. RT-PCR and cDNA blot experiments revealed that the resistant genotype exhibited a stronger overall defence response against O. cumana than the susceptible one, involving marker genes of the jasmonate (JA) and salicylic acid (SA) pathways. Among them, the SA-responsive gene, def. (defensin), appeared to be characteristic of LR1 sunflower resistance. However, no JA accumulation and similar SA contents (250,300 ng g,1 FW) were measured by GC/MS in both genotypes, parasitized or not. In addition, three cDNAs, isolated by a suppression-subtractive hybridization, were shown to be strongly induced only in the resistant genotype 8 days post-inoculation, when the first O. cumana attachments occurred. These genes, putatively encoding a methionine synthase, a glutathione S-transferase and a quinone oxidoreductase, might be involved in detoxification of reactive oxygen species, suggesting the occurrence of an oxidative burst during the incompatible interaction. Finally, host cell-wall modifications leading to parasite-confinement were correlated with more intense callose depositions in the resistant genotype, concomitant with over-expression of the callose synthase cDNA HaGSL1. [source]

Declining and low fecal corticoids are associated with distress, not acclimation to stress, during the translocation of African rhinoceros

ANIMAL CONSERVATION, Issue 1 2010
W. L. Linklater
Abstract Concentrations of adrenal steroid metabolites in feces are routinely used to assess the welfare of animals that are the subject of conservation efforts. The assumption that low and declining corticoid concentrations indicate the absence of stress and acclimation, respectively, is often made without experimental support or wild-animal comparisons, although intrinsic control of adrenal steroids might occur even under ongoing stress and distress. We adopted the capture and 11-week captivity of 18 black (Diceros bicornis: 11 males, seven females) and 52 white (Ceratotherium simum: 22 males, 30 females) rhinoceros as an experimental test of the relationship between corticoid concentrations and stress (translocation) and measured for suppressed gonad function as an indicator of distress , the biological cost of cumulative stressors. Fecal samples collected from the rectum at capture and during captivity were stored frozen and their corticoid, and androgen (in males) or progestin (in females), concentrations determined by radioimmunoassay. Corticoid profiles followed the expected pattern of being two to five times pre-capture levels (ng g,1: black rhino: female 24.5±3.7, male 23.9±2.2; white rhino: female 16.3±1.6, male 12.3±2.4) for up to 17 days after capture and declined with time in captivity. Black rhinoceros and male white rhinoceros corticoids declined below pre-capture values and were associated with suppressed levels of androgens and progestins with increased time in captivity. Declining corticoids could not be interpreted as acclimation or the absence of stressors, without also measuring for distress in African rhinoceros. White rhinoceros female corticoid values remained elevated, although their gonad steroid levels were also suppressed. We discuss our findings for the management of rhinoceros in the wild and captivity. [source]

Biochemical parameters of blood plasma and content of microcystins in tissues of common carp (Cyprinus carpio L.) from a hypertrophic pond with cyanobacterial water bloom

AQUACULTURE RESEARCH, Issue 15 2009
Radovan Kopp
Abstract The aim of this study was to evaluate the dynamics of the blood plasma parameters and the content of microcystins in the tissues of common carp (Cyprinus carpio L.) in relation to the toxic cyanobacterial water bloom. Fish (average body mass 2176±697 g) in the hypertrophic pond were exposed to natural water bloom (dominated by Planktothrix agardhii, Pseudanabaena limnetica and Limnothrix redekei), which contained microcystins (concentration in biomass 20,181 ,g g,1 dry wt, concentration in water 0.3,9.5 ,g L,1). Biochemical parameters in fish blood plasma were analysed in 89 fish at 14-day intervals during the whole season (nine sampling periods). Our results demonstrated high variability and fluctuations in the investigated parameters. The content of microcystins and density of cyanobacterial cells correlated with some haematological indices as lipase, alanine,aminotransferase, albumin, magnesium and chlorides. The concentrations of microcystins in the muscle and liver of the fish (determined by high-performance liquid chromatography with mass spectrometer) were below the limit of detection during the monitored period [0.31 ng g,1 fresh weight (f.w.) for the liver and 0.13 ng g,1 f.w. for muscle]. Our study demonstrates that although known cyanobacterial toxin microcystins were not detected in the fish tissues, several biochemical parameters important for the fish physiology were modulated by natural cyanobacterial bloom. [source]

Presence and distribution of PAHs, PCBs and DDE in feed and sediments under salmon aquaculture cages in the Bay of Fundy, New Brunswick, Canada

AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, Issue 4 2005
J. Hellou
Abstract 1.Wastes from feed and faeces can result in the deposition of contaminants in sediments around aquaculture sites. Five types of feed pellet, a commercial fish oil and 76 sediment samples collected under and up to 100 m away from salmon aquaculture cages in the south-western Bay of Fundy between 1998 and 2000 were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and chlorinated pesticides. 2.Five alkylated naphthalenes (aNAs) were consistently detected in fish oil (116,180 ng g,1, per aNA), in pellets (25,51 ng g,1, dry weight, per aNA), and sediments (<1,45 ng g,1, dry weight, per aNA). Other PAHs were detected at variable levels in feed or in sediments. 3.IUPAC congener 153 (a PCB) and p,p,-dichlorodiphenyldichloroethylene (p,p,-DDE) were detected more frequently than other chlorinated targets in oil (108 ng g,1 and 176 ng g,1 respectively), feed (<1,14 ng g,1 and 1.7,28.2 ng g,1 respectively) and sediments (<0.08,3 ng g,1 and <0.5,7 ng g,1 respectively). 4.Trends were observed during the first year of sediment sampling (1998), with higher organic carbon, PCBs and p,p,-DDE levels below the cages than 50 m away. The PAHs other than aNA showed an opposite trend with distance. In 1999, levels of p,p,-DDE and PCBs were somewhat reduced under the cages, but were detected up to 100 m away from the cages. 5.Levels of aNA tended to be higher at some sites in 1999 relative to 1998, reflecting variability in feed and/or differential transport or degradation of contaminants relative to the environmental background. When detected, mean levels of PCBs and DDE were 2,10 times lower in 2000 than in 1999, and PAHs were 30,40% lower in 2000 than in 1999. 6.Interpretation of the results is done cautiously, since the exact locations of the sites sampled is only known to an intermediate facilitating the work between farmers and scientists. Levels of contaminants are compared with international results, interpreted relative to potential toxicity, uptake from feed, from deposited sediments, and in the framework of an aquaculture decision-support system published recently. Copyright © 2005 John Wiley & Sons, Ltd. [source]

Simultaneous determination of quinolone antibacterials in bovine milk by liquid chromatography,mass spectrometry

BIOMEDICAL CHROMATOGRAPHY, Issue 11 2008
Alberto Zafra-Gómez
Abstract A new liquid chromatography,mass spectrometry (LC,MS) method has been developed and validated for the simultaneous determination of eight quinolone antibacterials for veterinary use in processed bovine milk samples. The quinolones studied included marbofloxacin, ciprofloxacin, danofloxacin, enrofloxacin, sarafloxacin, difloxacin, oxolinic acid and flumequine. Also, a new sample-treatment procedure was used for extraction and preconcentration of these compounds. It involved defatting by centrifugation, protein precipitation by adding a mixture of glacial acetic acid,acetonitrile and removing acetonitrile with dichloromethane; finally, the acidified aqueous layer was evaporated to dryness in a speed vac system, resuspended in the mobile phase and filtered prior to LC injection. The mobile phase was composed of a formic acid aqueous solution 0.1% (v/v) and acetonitrile, with an initial composition of water,acetonitrile 95: 5 (v/v) and using linear gradient elution. Norfloxacin was used as internal standard. The limits of quantification found (2,7 ng g,1) were in all cases lower than the maximum residue limits tolerated by the European Union for these compounds in milk. Copyright © 2008 John Wiley & Sons, Ltd. [source]

Inhibition of allergen-induced wheal and flare reactions by levocetirizine and desloratadine

BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, Issue 2 2008
Nelly Frossard
What is already known about this subject ,,The reproducible and standardized histamine-induced wheal and flare model helps identify the objective effectiveness of antihistamines in humans, as well as their differences in onset and duration of action. ,,Some of the newest antihistamines have already been compared in a head-to-head setting using this model. However, their objective action at inhibiting the allergen-induced wheal and flare response has not been reported yet. What this study adds ,,The time,response study presented here shows the objective activity of two of the newest generation of antihistamines, levocetirizine and desloratadine, at inhibiting the allergen-induced wheal and flare response in a randomized, cross over, placebo-controlled trial. ,,This model is interesting to the clinical setting since allergic subjects are recruited, and the response to allergen involves mast cell degranulation and release of numerous vasoactive and pro-inflammatory mediators additionally to histamine. ,,In addition, this study reports receptor occupancy for both antihistamines at therapeutic dosage, leading to analysis of potential differences in activity. ,,This study clearly shows the potential anti-inflammatory properties of desloratadine and levocetirizine in their skin activity when allergen is the challenging agent as occurs in the clinical situation. Aims To evaluate the inhibitory activity of the new-generation antihistamines levocetirizine and desloratadine at their therapeutic doses on the allergen-induced wheal and flare reaction at 1.5 h, 4 h, 7 h, 12 h and 24 h postdose, and to measure their plasma and skin concentrations. Methods A double-blind, randomized, cross-over, placebo-controlled study in 18 allergic subjects was carried out. The time,response of the wheal and flare reaction areas under the curve (AUC) were compared by anova. Results Both antihistamines significantly (P < 0.001) inhibited the allergen-induced wheal and flare reactions compared with placebo. Levocetirizine was significantly more potent than desloratadine. Mean ± SEM wheal AUC(0,24 h) was 506.4 ± 81.0 with levocetirizine and 995.5 ± 81.0 mm2 h with desloratadine as compared with placebo (1318.5 ± 361.0 mm2 h). Flare AUC(0,24 h) was 5927.3 ± 1686.5 and 15838.2 ± 1686.5 mm2 h, respectively [P < 0.001 for both compared with placebo (22508.2 ± 7437.1 mm2 h)]. Levocetirizine showed significant inhibition of wheal and flare already at 1.5 h postdose compared with placebo (P , 0.001); desloratadine achieved a significant effect only after 4 h. The mean total plasma concentration at 12 h and 24 h after intake was higher for levocetirizine (58.1 ± 13.4 and 20.0 ± 8.1 ng ml,1, respectively) as compared with desloratadine (0.82 ± 0.24 and 0.45 ± 0.16 ng ml,1). Similarly, higher mean unbound skin concentrations were observed for levocetirizine 24 h after intake (1.80 ng g,1) than for desloratadine (0.07 ng g,1). This was associated with greater receptor occupancy for levocetirizine (54%) than desloratadine (34%) at 24 h. Conclusions Levocetirizine suppressed the cutaneous allergic reactions with a higher potency than desloratadine, which correlated with its high receptor occupancy. Receptor occupancy rather than drug affinity or plasma half-life is more representative of antihistamine potency. [source]