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Various Time Intervals (various + time_interval)
Selected AbstractsIntrastriatal administration of human immunodeficiency virus-1 glycoprotein 120 reduces glial cell-line derived neurotrophic factor levels and causes apoptosis in the substantia nigraDEVELOPMENTAL NEUROBIOLOGY, Issue 12 2006Rachel L. Nosheny Abstract Uninfected neurons of the substantia nigra (SN) degenerate in human immunodeficiency virus (HIV)-positive patients through an unknown etiology. The HIV envelope glycoprotein 120 (gp120) causes apoptotic neuronal cell death in the rodent striatum, but its primary neurotoxic mechanism is still under investigation. Previous studies have shown that gp120 causes neurotoxicity in the rat striatum by reducing brain-derived neurotrophic factor (BDNF). Because glial cell line-derived neurotrophic factor (GDNF) and BDNF are neurotrophic factors crucial for the survival of dopaminergic neurons of the SN, we investigated whether gp120 reduces GDNF and BDNF levels concomitantly to induce apoptosis. Rats received a microinjection of gp120 or vehicle into the striatum and were sacrificed at various time intervals. GDNF but not BDNF immunoreactivity was decreased in the SN by 4 days in gp120-treated rats. In these animals, a significant increase in the number of caspase-3- positive neurons, both tyrosine hydroxylase (TH)-positive and -negative, was observed. Analysis of TH immunoreactivity revealed fewer TH-positive neurons and fibers in a medial and lateral portion of cell group A9 of the SN, an area that projects to the striatum, suggesting that gp120 induces retrograde degeneration of nigrostriatal neurons. We propose that dysfunction of the nigrostriatal dopaminergic system associated with HIV may be caused by a reduction of neurotrophic factor expression by gp120. © 2006 Wiley Periodicals, Inc. J Neurobiol, 2006 [source] Interspecific competition between the ichneumonid Campoletis chlorideae and the braconid Microplitis mediator in their host Helicoverpa armigeraENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 1 2008Shen-Peng Tian Abstract We investigated interspecific competition between Campoletis chlorideae Uchida (Hymenoptera: Ichneumonidae) and Microplitis mediator (Haliday) (Hymenoptera: Braconidae) in their host, the cotton bollworm, Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) under laboratory conditions. Cotton bollworm larvae were allowed to be parasitized by both wasp species simultaneously or sequentially at different time intervals. When host larvae were parasitized simultaneously by both parasitoids, the majority of the cocoons produced were of M. mediator. When host larvae were parasitized initially by M. mediator followed by C. chlorideae at 12 or 24 h, parasitoids emerging from the multiparasitized hosts were mainly M. mediator. In contrast, when host larvae were parasitized initially by C. chlorideae, followed by M. mediator 12 or 24 h later, parasitoids emerging from the multiparasitized hosts were mainly C. chlorideae. Dissections of host larvae at various time intervals after parasitization by the two parasitoids showed that first instars of M. mediator could physically attack the larvae of C. chlorideae, but not the eggs of C. chlorideae. When a host was parasitized by both wasp species sequentially, more host larvae died and the number of wasp offspring was significantly reduced compared to a host parasitized by only one wasp. Conversely, in simultaneous multiparasitism, the host mortality and wasp offspring production were not significantly different from those parasitized by single wasp species. [source] Protein degradation, as with protein synthesis, is required during not only long-term spatial memory consolidation but also reconsolidationEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 11 2008Julien Artinian Abstract The formation of long-term memory requires protein synthesis, particularly during initial memory consolidation. This process also seems to be dependant upon protein degradation, particularly degradation by the ubiquitin-proteasome system. The aim of this study was to investigate the temporal requirement of protein synthesis and degradation during the initial consolidation of allocentric spatial learning. As memory returns to a labile state during reactivation, we also focus on the role of protein synthesis and degradation during memory reconsolidation of this spatial learning. Male CD1 mice were submitted to massed training in the spatial version of the Morris water maze. At various time intervals after initial acquisition or after a reactivation trial taking place 24 h after acquisition, mice received an injection of either the protein synthesis inhibitor anisomycin or the protein degradation inhibitor lactacystin. This injection was performed into the hippocampal CA3 region, which is specifically implicated in the processing of spatial information. Results show that, in the CA3 hippocampal region, consolidation of an allocentric spatial learning task requires two waves of protein synthesis taking place immediately and 4 h after acquisition, whereas reconsolidation requires only the first wave. However, for protein degradation, both consolidation and reconsolidation require only one wave, taking place immediately after acquisition or reactivation, respectively. These findings suggest that protein degradation is a key step for memory reconsolidation, as for consolidation. Moreover, as protein synthesis-dependent reconsolidation occurred faster than consolidation, reconsolidation did not consist of a simple repetition of the initial consolidation. [source] Postnatal handling alters the activation of stress-related neuronal circuitriesEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 8 2000István M. Ábrahám Abstract Postnatal handling, as a crucial early life experience, plays an essential role in the development of hypothalamo-pituitary,adrenal axis responses to stress. The impact of postnatal handling on the reactivity of stress-related neuronal circuitries was investigated in animals that were handled for the first 21 days of life and as adults they were exposed to physical (ether) or emotional (restraint) challenge. To assess neuronal activation we relied on the induction of immediate-early gene product c-Fos and analysed its spatial and temporal distribution at various time intervals after stress. Ether and restraint commonly activated parvocellular neurons in the hypothalamic paraventricular nucleus, and resulted in activation of brain areas providing stress-related information to the hypothalamic effector neurons and/or in regions governing autonomic and behavioural responses to stress. Beyond these areas, the strength and timing of c-Fos induction showed stressor specificity in olfactory and septal region, basal ganglia, hypothalamus, hippocampal formation, amygdala and brainstem. Handled rats displayed a lower number of c-Fos-positive cell nuclei and weaker staining intensity than non-handled controls in the hypothalamic paraventricular nucleus, bed nucleus of stria terminalis, central nucleus of amygdala, hippocampus, piriform cortex and posterior division of the cingulum. Significant differences were revealed in timing of c-Fos induction as a function of stressor and early life experience. Together, these data provide functional anatomical evidence that environmental enrichment in the early postnatal period attenuates the reactivity of stress-related neuronal circuitries in the adult rat brain. [source] Factors Associated with the Income Distribution of Full-Time Physicians: A Quantile Regression ApproachHEALTH SERVICES RESEARCH, Issue 5 2007Ya-Chen Tina Shih Objective. Physician income is generally high, but quite variable; hence, physicians have divergent perspectives regarding health policy initiatives and market reforms that could affect their incomes. We investigated factors underlying the distribution of income within the physician population. Data Sources. Full-time physicians (N=10,777) from the restricted version of the 1996,1997 Community Tracking Study Physician Survey (CTS-PS), 1996 Area Resource File, and 1996 health maintenance organization penetration data. Study Design. We conducted separate analyses for primary care physicians (PCPs) and specialists. We employed least square and quantile regression models to examine factors associated with physician incomes at the mean and at various points of the income distribution, respectively. We accounted for the complex survey design for the CTS-PS data using appropriate weighted procedures and explored endogeneity using an instrumental variables method. Principal Findings. We detected widespread and subtle effects of many variables on physician incomes at different points (10th, 25th, 75th, and 90th percentiles) in the distribution that were undetected when employing regression estimations focusing on only the means or medians. Our findings show that the effects of managed care penetration are demonstrable at the mean of specialist incomes, but are more pronounced at higher levels. Conversely, a gender gap in earnings occurs at all levels of income of both PCPs and specialists, but is more pronounced at lower income levels. Conclusions. The quantile regression technique offers an analytical tool to evaluate policy effects beyond the means. A longitudinal application of this approach may enable health policy makers to identify winners and losers among segments of the physician workforce and assess how market dynamics and health policy initiatives affect the overall physician income distribution over various time intervals. [source] Development of hydrogel patch for controlled release of alpha-hydroxy acid contained in tamarind fruit pulp extractINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 2 2005J. Viyoch Synopsis The aim of this study was to develop hydrogel patch using crosslinked chitosan,starch as polymeric matrix for controlling the release of the natural alpha-hydroxy acid (AHA) contained in the extract of tamarind's fruit pulp. The chitosan (MW 100 000) was blended with corn, tapioca or rice starch in various ratios and then crosslinked with glutaraldehyde. The physical characteristics, mechanical resistance, bio-adhesion property and surface morphology of the prepared hydrogel patches with and without the extract were investigated. The release patterns of the hydrogel patches containing the extract were investigated by measuring the amount of tartaric acid, a major AHA present in the tamarind's fruit pulp extract, accumulated in the receptor medium of the vertical diffusion cell at various time intervals over a period of 6 h. The results indicated that the formulations of chitosan : corn starch 4.5 : 0.5 with glutaraldehyde 0.02% w/w (C4.5C0.5G0.02) or 0.04% w/w (C4.5C0.5G0.04), chitosan : tapioca starch 4.5 : 0.5 with glutaraldehyde 0.04% w/w (C4.5T0.5G0.04) or 0.05% w/w (C4.5T0.5G0.05), and chitosan : rice starch 4.5 : 0.5 with glutaraldehyde 0.04% w/w (C4.5R0.5G0.04) and chitosan : rice starch 4.0 : 1.0 with glutaraldehyde 0.03% w/w (C4.0R1.0G0.03) provided the flexible and elastic patches with good bio-adhesive property. The tensile strength values ranged from 5 to15 N mm,2 and the elasticity ranged from 30 to 60%. The addition of the extract in these formulations significantly increased the tensile strength values of the obtained patches. The patch of C4.0R1.0G0.03 formulation containing the extract showed relatively highest porosity, corresponding to its highest amount (12.02 ± 0.33 mg) and rate (0.452 ± 0.012 mg mm,2 min,1/2) of tartaric acid released. The amounts of tartaric acid released from the developed hydrogel patches were proportional to a square root of time (Higuchi's model), particularly the release from C4.0R1.0G0.03 (R2, 0.9978 ± 0.0020) and C4.5R0.5G0.04 (R2, 0.9961 ± 0.0024) patches. Résumé Le but de cette étude était de développer un patch hydrogel en utilisant, en tant que matrice polymère, un mélange chitosane/amidon réticulé pour le contrôle du relargage d', -hydroxyacide naturel contenu dans l'extrait de la pulpe du fruit du tamarinier. Du chitosane (MW 100 000) a été mélangéà des farines de maïs, de tapioca ou de riz dans différentes proportions, les mélanges ont été réticulés avec du glutaraldéhyde. Les caractéristiques physiques, résistance mécanique, propriétés de bio adhésion et morphologie de surface des patchs hydrogels préparés avec et sans extrait ont étéétudiées. Le profil de relargage des patchs hydrogels contenant l'extrait a étéétudié en mesurant la quantité d'acide tartarique, , -aminoacide majoritaire présent dans l'extrait, accumulé dans le milieu récepteur d'une cellule à diffusion verticale en fonction du temps sur une période de 6 heures. Les résultats ont montré que les formulations contenant: ,,un mélange chitosane/amidon de maïs dans un rapport 4.5 : 0.5 réticulé avec 0.02% ou 0.04% poids/poids de glutaraldéhyde (respectivement C4.5C0.5G0.02 et C4.5 C0.5 G0.04) ou ,,un mélange de chitosane/amidon de tapioca dans un rapport 4.5 : 0.5 réticulé avec 0.04% ou 0.05% poids/poids de glutaraldéhyde (C4.5T0.5 G0.04ou C4.5 T0.5 G0.05) ,,ainsi que le mélange chitosane/amidon de riz dans un rapport 4.5 : 0.5 réticulé avec 0.04% poids/poids de glutaraldehyde (C4.5R0.5 G0.04) ,,et le mélange chitosane/amidon de riz dans un rapport 4.0 : 1.0 réticulé avec 0,03% poids/poids de glutaraldehyde (C4.0 R1.0 G0.03) conduisaient à des patchs flexibles et élastiques avec de bonnes propriétés bio adhésives. Leur résistance mécanique varie de 5 à 15 N/m2 et leur élasticité de 30 à 60%. L'addition de l'extrait de fruit à ces formules augmente significativement la résistance mécanique des patchs. Le patch C4.0R1.0 G0.03 contenant l'extrait montre la plus grande porosité correspondant à la quantité d'acide tartarique relargué la plus élevée (12.02 ± 0.33 mg), ainsi qu'à la plus grande vitesse de relargage (0.452 ± 0.012 mg mm- 2 mn- 1/2). Les quantités d'acide tartarique relarguées à partir de patchs hydrogels développés sont proportionnelles à la racine carrée du temps (modèle d'Higuchi), en particulier pour les patchs C4.0 R1.0G0.03 (R2, 0.9978 ± 0.0020) et C4.5R0.5 C0.004 (R2, 0.9061 ± 0.0024). [source] Degradation behavior of nanoreinforced epoxy systems under pulse laserJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2009M. Calhoun Abstract Nanocomposites using EPON 824 as their matrix were exposed to pulse laser at 532 nm for various time intervals. The developed nanomaterials used for this study were manufactured using EPON 824 with multiwalled carbon nanotubes (MWCNTs) at a loading rate of 0.15% by weight and nanoclays at a loading rate of 2% by weight as reinforcements. The effect of laser irradiation on polymer composites has been investigated. The degradation mechanism for the epoxy was of a laser induced burning nature. Of all specimens tested, the ultimate strength of the MWCNT-reinforced specimens decreased the most as a function of radiation time; the nanoclay-reinforced epoxy retained the most strength after 2 min of laser radiation. In addition, the threshold fluence for decomposition indicated that less energy was required to initiate decomposition in the MWCNT-reinforced epoxy than in the nanoclay-reinforced epoxy. This can be attributed to the high thermal conductivity of the carbon nanotubes. Measurement of surface damage in the material was observed via electron microscopy. Fourier transform infrared spectroscopy was used to investigate changes to the molecular structure as a function of exposure time. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] ESR and FTIR studies on electron beam-irradiated low-density polyethylene blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Z. I. Ali Abstract Low-density polyethylene (LDPE) composites modified with a resin based on ethylene/methacrylic acid copolymer (surlyn) and/or citric acid were electron beam-irradiated and investigated by electron spin resonance (ESR) at room temperature. ESR studies were carried out directly after irradiation and after various time intervals up to 72 h postirradiation. The irradiated samples showed the ESR spectrum of seven lines that was assigned to the formation of allyl radical. The nature and yield of the allyl radical of the different LDPE samples were analyzed as a function of time after irradiation. Also, the radical concentration, decay, decay rate, and kinetics of radical decay were evaluated. Fourier transform infrared (FTIR) analysis at a series of different temperatures upon cooling from room temperature to ,175°C and the reverse heating to +125°C was also carried out. The structural changes while cooling and heating of LDPE samples were investigated using FTIR spectrometry. The results showed that cooling of unirradiated LDPE samples to ,175°C results in a decrease of the intensities of IR bands. However, heating the samples from ,175°C up to +125°C led to a consequence increase in the intensities of the IR bands. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3461,3469, 2007 [source] Oral mucosa alterations induced by cyclosporin in mice: morphological featuresJOURNAL OF PERIODONTAL RESEARCH, Issue 6 2002A. T. Meller Background and objective:, The mechanisms involved in the pathogenesis of cyclosporin A-induced gingival hyperplasia are not well understood. The present work aimed at developing a mouse model with the characteristics of the human process, i.e. time of appearance, dose dependency and the capacity of developing in a variety of genetic backgrounds. This model would present the advantages of using a very well known animal species, small and easy to handle, with a number of experimental reagents (antibodies, etc.) already available against its products. Methods:, Three different strains of mice were used: CBA, F1(C57Bl × DBA), Balb/c. Groups of mice received different concentrations of cyclosporin A (CSA) (10 mg/kg, 25 mg/kg and 40 mg/kg body weight) intraperitoneally five times a week. Anatomical and histological alterations were recorded at various time intervals. Results:, All strains of mice presented gingival hyperplasia after 8 weeks of CSA treatment. A dose-dependency was observed with regard to the time of first appearance of alterations. Increased redness was seen in all animals at the sixth week, independent of the dosage used. Histologic examination exhibited increased vascularization, epithelial and connective tissue thickening, edema and a mononuclear infiltrate. Conclusions:, It was possible to develop CSA-induced gingival hyperplasia in mice with the characteristics described in humans and other species. The use of this animal model may help in the elucidation of the process involved in CSA-induced gingival overgrowth. [source] Ethanol Blocks Adenosine Uptake via Inhibiting the Nucleoside Transport System in Bronchial Epithelial CellsALCOHOLISM, Issue 5 2009Diane S. Allen-Gipson Background:, Adenosine uptake into cells by nucleoside transporters plays a significant role in governing extracellular adenosine concentration. Extracellular adenosine is an important signaling molecule that modulates many cellular functions via 4 G-protein-coupled receptor subtypes (A1, A2A, A2B, and A3). Previously, we demonstrated that adenosine is critical in maintaining airway homeostasis and airway repair and that airway host defenses are impaired by alcohol. Taken together, we hypothesized that ethanol impairs adenosine uptake via the nucleoside transport system. Methods:, To examine ethanol-induced alteration on adenosine transport, we used a human bronchial epithelial cell line (BEAS-2B). Cells were preincubated for 10 minutes in the presence and absence of varying concentrations of ethanol (EtOH). In addition, some cells were pretreated with S-(4-Nitrobenzyl)-6-thioinosine (100 ,M: NBT), a potent adenosine uptake inhibitor. Uptake was then determined by addition of [3H]-adenosine at various time intervals. Results:, Increasing EtOH concentrations resulted in increasing inhibition of adenosine uptake when measured at 1 minute. Cells pretreated with NBT effectively blocked adenosine uptake. In addition, short-term EtOH revealed increased extracellular adenosine concentration. Conversely, adenosine transport became desensitized in cells exposed to EtOH (100 mM) for 24 hours. To determine the mechanism of EtOH-induced desensitization of adenosine transport, cAMP activity was assessed in response to EtOH. Short-term EtOH exposure (10 minutes) had little or no effect on adenosine-mediated cAMP activation, whereas long-term EtOH exposure (24 hours) blocked adenosine-mediated cAMP activation. Western blot analysis of lysates from unstimulated BEAS-2B cells detected a single 55 kDa band indicating the presence of hENT1 and hENT2, respectively. Real-time RT-PCR of RNA from BEAS-2B revealed transcriptional expression of ENT1 and ENT2. Conclusions:, Collectively, these data reveal that acute exposure of cells to EtOH inhibits adenosine uptake via a nucleoside transporter, and chronic exposure of cells to EtOH desensitizes the adenosine transporter to these inhibitory effects of ethanol. Furthermore, our data suggest that inhibition of adenosine uptake by EtOH leads to an increased extracellular adenosine accumulation, influencing the effect of adenosine at the epithelial cell surface, which may alter airway homeostasis. [source] The ripening and aging of noni fruits (Morinda citrifolia L.): microbiological flora and antioxidant compoundsJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 9 2007Yanine Chan-Blanco Abstract The juice of noni fruit (Morinda citrifolia L.) is claimed to be a natural functional beverage with a growing market both in the USA and Europe. It is traditionally produced by keeping harvested fruit in closed containers for several weeks as the fruit senesces or ages. Little is known about the changes that occur in the juice's microbiological, physicochemical, and functional characteristics during this treatment. Traditional processing was simulated in the laboratory, with samples being recovered and analyzed at various time intervals. At first, fermentation occurred and populations of molds, yeasts, and mesophilic bacteria increased significantly. After 2 weeks, microbial growth changed abruptly, stopping for yeasts, molds, and mesophilic bacteria, and decreasing suddenly for lactic bacteria. Analyses of pH, soluble solids, ethanol, and lactic acid in the fruits confirmed the microbial analyses, indicating initial sensitive variations, followed by values remaining comparatively steady during aging. Vitamin C and total phenol contents also remained constant at 300 ± 60 mg and 50 ± 20 mg GAE, respectively, per 100 g of pulp. Antioxidant capacity likewise remained relatively high at 8 ± 1.5 µmol Trolox® g,1. All phenolic compounds, including scopoletin and rutin, varied significantly immediately after harvest but remained more or less steady during aging. Copyright © 2007 Society of Chemical Industry [source] Development of Gelatin Hydrogel Pads as Antibacterial Wound DressingsMACROMOLECULAR BIOSCIENCE, Issue 10 2009Vichayarat Rattanaruengsrikul Abstract Gelatin hydrogel pads have been prepared from a 10,wt.-% gelatin solution that contained 2.5,wt.-% AgNO3 in 70% v/v acetic acid by a solvent-casting technique. The AgNO3 -containing gelatin solution was aged under mechanical stirring for various time intervals to allow for the formation of silver nanoparticles (nAgs). The formation of nAgs was monitored by a UV-vis spectrophotometer. The morphology and size of the nAgs were characterized by transmission electron microscopy (TEM). To improve the water resistance of the hydrogels, various contents of glutaraldehyde (GTA) were added to the AgNO3 -containing gelatin solution to cross-link the obtained gelatin hydrogels. These hydrogels were tested for their water retention and weight loss behavior, release characteristics of the as-loaded silver, and antibacterial activity against Gram-negative Escherichiacoli and Gram-positive Staphylococcusaureus. The AgNO3 -containing gelatin solution that had been aged for 5 d showed the greatest number of nAgs formed. The size of these particles, based on TEM results, was 10,11,nm. With an increase in the GTA content used to cross-link the hydrogels, the water retention, the weight loss, and the cumulative amount of silver released were found to decrease. Finally, all of the nAg-loaded gelatin hydrogels could inhibit the growth of the tested pathogens, which confirmed their applicability as antibacterial wound dressings. [source] Quantitative microscopy reveals 3D organization and kinetics of endocytosis in rat hepatocytesMICROSCOPY RESEARCH AND TECHNIQUE, Issue 9 2006Permsin Marbet Abstract In order to demonstrate the power of quantitative microscopy, the endocytic apparatus of rat hepatocytes was reexamined using in situ liver and short term cultured hepatocyte couplets that were allowed to internalize endocytic markers for various time intervals. Correlative confocal light and electron microscopy demonstrate a tubulovesicular reticulum representing the endocytic apparatus. Volume and membrane area account for 2% of cell volume and 30% plasma membrane surface. Colocalization analysis demonstrated that pathway-specific ligands and fluid-phase markers enter EEA1-positive vesicles, the early endosomal compartment, immediately after internalization. These vesicles are translocated rapidly from basolateral to perinuclear and apical locations. Ligands are sorted within 5 min to their respective pathways. Sequential colocalization of an asialoglycoprotein-pulse with rab7 and lamp3 demonstrates that early endosomes change into or fuse with late endosomes and lysosomes. Alternatively, markers are sequestered into the common endosome consisting of rab11-positive, long tubules that originate from early endosomes and show an affinity for the transcytotic marker pIgA and its receptor. This compartment mediates transcytosis by delivering the receptor,ligand complex to the subapical compartment, a set of apical, rab11-positive vesicles, which are connected to the tubular reticulum. We conclude that vesicular traffic between preexisting compartments, maturation or fusion of endocytic organelles, and transport in tubules act in concert and together mediate transport between compartments of a tubulovesicular endocytic apparatus. In addition, we show that quantitative microscopy using high resolution data sets can detect and characterize kinetics of various parameters thus adding a dynamic component to 3D information. Microsc. Res. Tech., 2006. © 2006 Wiley-Liss, Inc. [source] A combined agar-absorption and BIO-PCR assay for rapid, sensitive detection of Xylella fastidiosa in grape and citrusPLANT PATHOLOGY, Issue 1 2005M. Fatmi Application of the polymerase chain reaction (PCR) to disease diagnosis is limited in part by the presence of PCR inhibitors. Inhibition can be overcome and sensitivity increased by culturing bacteria on agar media prior to PCR (termed BIO-PCR). However, Xylella fastidiosa grows slowly, requiring 10,14 days for visible colonies to appear. In this study an agar-absorption BIO-PCR method for detecting X. fastidiosa in grape and citrus plants was developed. Optimum lengths of time for absorption of inhibitors by the agar medium or enrichment of bacteria on the medium were determined for Pierce's disease of grape and citrus variegated chlorosis. When petioles of grape and citrus leaves with symptoms were spotted onto agar media, the spots washed after various time intervals and assayed for X. fastidiosa by real-time PCR, 97% (31 out of 32) and 100% (six out of six) of spots were positive after 2 days and 4 h for grape and citrus, respectively. With direct PCR, only 12·5% (four out of 32) and 33% (two out of six) of spots were positive, respectively, and visible X. fastidiosa colonies were evident after 10 and 14 days, respectively. In a separate experiment with samples from a different vineyard, 46% (13 out of 28) of the grape samples (agar spots) were positive after 1 day and 93% (26 out of 28) after 5 days using agar-absorption PCR. In contrast, all samples were negative by direct PCR. Viable X. fastidiosa were recovered from all samples after 14 days. Further tests with eight randomly selected grape petioles from three Texas vineyards known to have Pierce's disease resulted in 50% being positive by a simple 24 h agar-absorption PCR assay, whereas none was positive by direct PCR. Overall, 10 out of 16 (63%) vines from five vineyards (two in California and three in Texas) were positive after the 24 h agar-absorption PCR assay. In contrast, only one vine was positive by direct PCR. This simple agar absorption-based PCR assay protocol should prove useful for the routine detection of X. fastidiosa and other slow-growing bacteria in the presence of PCR inhibitors. [source] Impact damage detection and degradation monitoring of wet GFRP composites using noncontact ultrasonicsPOLYMER COMPOSITES, Issue 8 2009K. Berketis Two different non-crimp glass fabrics with a polyester resin were used to produce laminated plates that were subjected to low velocity impact testing using three impact energy levels. The plates were immersed in water at 65°C for up to 24 months. The effectiveness of a traditional water coupled and an air-coupled ultrasonic C-Scan system was assessed in terms of damage size evaluation at various time intervals. The conditioned impacted plates were retested statically in compression to determine the residual strength for evaluation of damage tolerance. Weight change measurements revealed an initial increase due to water diffusion, followed by an extended decrease due to matrix dissolution at long-term immersion times. The use of water coupled pulse-echo ultrasonics proved ineffective after long-term water immersion as damaged areas became ultrasound-invisible. The contrast between impact damaged areas and water diffused areas was restored with the air-coupled C-scan. The macroscopic damage size was not affected by the long-term water immersion and the overall weight change while the residual compression strength was seemed to be dependent on the time of immersion and the size of the pre-existing impact damage. Calibrating the air-coupled system to a dry condition specimen, a good qualitative and quantitative indication of the degraded state of water immersed plates was obtained. This monitoring system for the degradation process seems to be very promising. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Hepatopancreatic and muscular distribution of oxytetracycline antibiotics in farmed pacific white shrimp (Penaeus vannamei): a physiological-based pharmacokinetic model approachAQUACULTURE RESEARCH, Issue 1 2009Damrongsak Faroongsarng Abstract Oxytetracycline (OTC) pharmacokinetic models previously used to investigate Penaeus vannamei have not addressed the specific problems related to drug distribution/disposition in particular tissues. This study aimed to provide an insight into OTC kinetics in the hepatopancreas and muscle based on a physiological model approach. Adult male P. vannamei at the C-D0 inter-moulting stage were randomly assigned to intra-sinus and oral administrations. In the intra-sinus group, shrimps were dosed via the ventral sinus at an OTC level of 10.0 ,g g,1 body weight, while in the oral one, they were force fed at a dose level of 50.2 ,g g,1. The medicated animals were sampled at various time intervals until 170 h after dosing. Haemolymph, muscle and hepatopancreas samples were taken and OTC levels were determined using the validated HPLC method. A model focused on the hepatopancreas and muscle was developed. Oxytetracycline pharmacokinetic profiles in particular tissues were fitted into the model with an R2 of between 0.6568 and 0.9904. Oxytetracycline muscular distributions were essentially identical for both groups and the drug did not accumulate in muscle. The distributions in the hepatopancreas for both groups were extensive, whereas that for oral administration was approximately 2.3 times greater than that for the intra-sinus one. It was demonstrated that hepatopancreatic OTC may undergo significant first-pass elimination with non-linear kinetics. [source] Preventive effect of preoperative portal vein ligation on endotoxin-induced hepatic failure in hepatectomized rats is associated with reduced tumour necrosis factor , productionBRITISH JOURNAL OF SURGERY (NOW INCLUDES EUROPEAN JOURNAL OF SURGERY), Issue 10 2000Dr S. Yachida Background Preoperative portal vein embolization successfully reduces the incidence of postoperative hepatic failure in which endotoxin is postulated to be involved. To identify the mechanism of this preventive effect, the relationship of endotoxin-induced liver injury with tumour necrosis factor (TNF) , and nitric oxide production in the peripheral blood, liver and spleen of rats subjected to preoperative portal vein branch ligation (PVL) was compared with that in rats undergoing sham operation. Methods Rats with PVL and those that underwent sham operation were subjected to resection of ligated liver lobes (PVL-Hx rats) and two-thirds hepatectomy (noPVL-Hx rats) respectively at day 5, followed by intravenous administration of endotoxin 200 ,g/kg body-weight at day 7. At various time intervals after endotoxin injection, the peripheral blood, liver and spleen tissues were harvested and analysed for TNF-, and nitric oxide production. Results The survival rates of noPVL-Hx and PVL-Hx rats at 48 h after endotoxin administration were 40 and 100 per cent respectively. The former rats showed more extensive liver injury as represented by higher serum aminotransferase and hyaluronate levels than the latter. Plasma concentrations of TNF-, at 1·5 h after endotoxin treatment were significantly higher in noPVL-Hx rats (mean(s.e.m.) 22 125(2175) pg/ml; n = 6) than PVL-Hx rats (8344(4076) pg/ml; n = 6) (P < 0·01). Consistent with this, expression of TNF-, messenger RNA in the liver and spleen was suppressed in PVL-Hx rats. In two-thirds hepatectomized rats, plasma TNF-, concentrations after endotoxin administration at 1, 2 and 3 days (14 350(2186), 26 375(2478) and 23 000(3745) pg/ml respectively; n = 6 each) were significantly higher than that before operation (9067(1559) pg/ml; n = 6) (P < 0·05), whereas those at 5 and 7 days (10 102(3616) and 8580(1427) pg/ml respectively; n = 6 each) showed no significant increase. Furthermore, nitric oxide production in peripheral blood and liver was suppressed by preoperative PVL. Conclusion Prevention of endotoxin-induced liver failure by preoperative PVL is associated with reduced production of TNF-, in the later phase of liver regeneration. © 2000 British Journal of Surgery Society Ltd [source] Enalaprilat and enalapril maleate eyedrops lower intraocular pressure in rabbitsACTA OPHTHALMOLOGICA, Issue 3 2010Thorsteinn Loftsson Abstract. Purpose:, This study aimed to develop low-viscosity aqueous eyedrops containing enalaprilat and its prodrug enalapril maleate in solution, and to evaluate the eyedrops in rabbits. Methods:, Aqueous eyedrops with hydroxypropyl-,-cyclodextrin containing 0.01,2.9% (w/v) enalaprilat, 1.0% (w/v) enalapril maleate with cyclodextrin or 0.5% (w/v) timolol were prepared. The eyedrops were administered to rabbits and intraocular pressure (IOP) was measured at various time intervals after the administration and the results (mean of 10 experiments ± standard error of the mean) are expressed as the change from baseline (24.7 ± 3.3 mmHg). Results:, Enalaprilat possessed sufficient stability to be formulated as an aqueous eyedrop solution with a shelf-life of several years at room temperature. The maximum decline in IOP after topical administration of one drop of 2.9% enalaprilat solution was 6.2 ± 0.7 mmHg at 4 hours after administration. Duration of activity exceeded 10 hours. A 1% enalaprilat solution lowered IOP by 4.4 ± 0.8 mmHg at 4 hours after administration and had similar duration, and was more potent than 0.5% timolol. The enalapril maleate eyedrops resulted in delayed action, showing maximum potency at 10,22 hours after administration and duration of up to 32 hours. Conclusions:, Enalaprilat eyedrops lower IOP in rabbits. The decline in IOP is proportional to the concentration of dissolved enalaprilat in low-viscosity aqueous eyedrop formulations. [source] | ||||||||||||||||