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Laser scanning cytometer-based assays for measuring host cell attachment and invasion by the human pathogen Toxoplasma gondii.

BACKGROUND: Toxoplasma gondii is among the most common protozoan parasites of humans. Both attachment to and invasion of host cells by T. gondii are necessary for infection, yet little is known about the molecular mechanisms underlying these processes. T. gondii's etiological importance and its role as a model organism for studying invasion in related parasites necessitate a means to quantitatively assay host cell attachment and invasion. METHODS: We present here Laser Scanning Cytometer (LSC)-based assays of T. gondii invasion and attachment. The invasion assay involves automated counting of invaded and non-invaded parasites, differentially labeled with distinct fluorochromes. The attachment assay compares the relative binding of differentially labeled parasites. The assays were evaluated using treatments known to decrease invasion or attachment. RESULTS: The LSC-based assays are robust and reproducible, remove operator bias, and significantly increase the sample size that can be feasibly counted compared to other currently available microscope-based methods. In the first application of the new assays, we have shown that parasites attach to fixed and unfixed host cells using different mechanisms. CONCLUSIONS: The LSC-based assays represent useful new methods for quantitatively measuring attachment and invasion by T. gondii, and can be readily adapted to study similar processes in other host-pathogen systems.

Animals↗

An index technique to monitor broadcast calibration and bait pick up, plus rodent and avian sign under arid conditions.

As part of product-performance and wildlife-hazards studies of 2% zinc phosphide (Zn3P2) steam-rolled-oat baits (11.2 kg ha-1) to reduce vole populations (Microtus spp) in alfalfa (Medicago sativa), we used randomly located, brushed-dirt plots (eight approximately 930-cm2 plots per 0.2-ha enclosure) to monitor bait-broadcast and -removal patterns, as well as to index vole and avian sign. Research was conducted in 18 x 0.2-ha enclosures containing 2.5-year-old stands of alfalfa; a 2-day pre-bait (placebo baits broadcast in all enclosures) period followed by a 14-day test-bait period (placebo and 2% Zn3P2 baits in nine enclosures each) characterized the bait exposures. Baits were broadcast manually by two certified pesticide applicators (CPAs) using Spyker Model-75 spreaders. Baits that fell onto plots were counted < 30 min later to assess the uniformity of bait distribution. The main statistical design was a 2 (placebo or Zn3P2 baits) x 3 (vole-only, vole-pheasant, vole-quail exposures) x 14 (days) factorial, with days considered repeated measurements. In the six vole-only enclosures, baits were removed from the brushed-dirt plots and replaced with four 0% or 2% Zn3P2 baits (one per 232.6-cm2 quadrant; 32 per enclosure); these 'placed' baits were then monitored daily for removal, while the surfaces of all plots were monitored daily for the presence:absence of animal/bird sign. Key results were: (a) 3.51 (+/- 2.66) and 3.39 (+/- 3.52) mean (+/- SD) baits were found on plots after pre-bait and test-bait broadcasts, respectively--less than the predicted 4.52 particles per 930-cm2 plot; (b) baits 'placed' on plots in placebo-baited enclosures were removed earlier than those in Zn3P2-baited enclosures--data in agreement with observed vole mortality; and (c) species x bait interactions occurred for both the vole- and pheasant-sign counts, but not quail-sign counts--data also indirectly confirming Zn3P2-induced mortality effects on voles and pheasants. This technique has utility for a variety of wildlife biology and chemical registration studies; although limited to arid conditions, the technique affords useful indices of broadcast calibration, bait pick-up, as well as target and non-target species mortality.

Animals↗

Mean square error of estimates of HIV prevalence and short-term AIDS projections derived by backcalculation.

We simulated multinomial AIDS incidence counts from 27 'representative' AIDS epidemics that spanned a period corresponding to previous applications of backcalculation (1 January 1977 to 1 July 1987) and assessed mean square error for several back-calculated estimators of HIV prevalence and short-term AIDS projections. Estimators were based on flexible model selection procedures that chose the best-fitting non-negatively constrained model of the infection curve from a family of possible step-function models. Selection of the best-fitting model from a family of four-step models each with a long last step of width of 4 or 4.5 years offered a favourable tradeoff between bias and variance when compared with selection from families of models with three steps or from families with a short last step. Five-step models performed as well as four-step models. Three-step models had substantially larger mean square error in some epidemic situations. Percentage root mean square error (PRMSE) for estimates of cumulative HIV prevalence as of 1 January 1985 was less than 14 per cent over a range of hypothetical epidemics of N = 50,000 infected individuals. PRMSE for short-term projections was less than 18 per cent. Estimates of cumulative HIV prevalence as of 1 July 1987 were substantially more uncertain and had a PRMSE of 33 per cent in the unfavourable case of a rapidly rising HIV epidemic. Estimates of cumulative HIV prevalence as of 1 July 1987 were positively biased in HIV epidemics with a rapidly decreasing recent HIV incidence rate and negatively biased in rapidly increasing HIV epidemics. Despite these uncertainties, we obtained useful estimates even for HIV epidemics with as few as 5000 infected individuals.

Acquired Immunodeficiency Syndrome↗

Immune response in infants undergoing application of cast: comparison of halothane and balanced anesthesia.

PURPOSE: To study the immunological effects of two types of anesthesia on the immune response in infants during a minimally stressful surgical procedure. METHODS: The effects of inhalational halothane (halothane + N2O + O2, spontaneous breathing, n = 12) and conventional balanced anesthesia (thiopental + N2O + O2 + fentanyl + vecuronium, mechanical ventilation, n = 12) on immune function were measured in a crossover study in 12 infants undergoing application of casts to the lower extremity or hip joint. Leukocyte and differential counts, lymphocyte subpopulations, spontaneous lymphocyte proliferative responses as well as responses to phytohemagglutinin (PHA), concavalin A (ConA) and pokeweed mitogen (PWM), and serum cortisol concentration were measured before, immediately after and four hours after the end of anesthesia. RESULTS: Halothane anesthesia was associated with a higher percentage of T helper cells than conventional balanced anesthesia [47.1+/-1.8 (SEM)%, 48.1+/-2.3% and 50.7+/-1.9% before, immediately and four hours after anesthesia vs. 45.7+/-1.7%, 44.0+/-2.3% and 45.1+/-1.9%, respectively, by groups, P<0.05]. Leukocyte count and the percentages of activated T cells, natural killer cells and B cells showed similar alterations in both groups, and no alterations were observed in the percentages of T lymphocytes or T cytotoxic cells. Lymphocyte transformation response to PWM was decreased four hours after anesthesia in the halothane but not in the balanced anesthesia group. CONCLUSION: Anesthesia of short duration during minimal surgical stress alters lymphocyte subpopulations and lymphoproliferative responses in infants and, furthermore, halothane anesthesia and balanced anesthesia have different effects.

Anesthesia↗

Comparison of processing four and five times the patients' blood volume during peripheral blood stem cell collection and analysis of CD34+38--and CD34+49d+ subsets during apheresis.

PURPOSE: We investigated whether increasing the patients' processed blood volume (BV) during peripheral blood stem cell collection (PBSCC) from four to five times leads to a greater yield of CD34+ cells. We also studied the kinetics of CD34+38- and CD34+49d+ subsets and compared the amount of transfused cells with engraftment. METHODS: All patients ( n=20) received chemotherapy followed by G-CSF for PBSC mobilization. Samples from the patients' peripheral blood and the PBSC harvests were taken after processing 1-, 4-, and 5 times the patients' calculated BV. RESULTS: The mean total yields of CD34+, CD34+38-, and CD34+49d+ cells were 15.69-, 1.13- and 4.17 x 10(6)/kg body weight, respectively. The mean increase for these subsets between 4- and 5 BV was 10%, 8%, and 21%, respectively. Based on the mean number of 2.25 (range 2-3) planned courses of high-dose chemotherapy (HDC) per patient, the mean yield of CD34+ cells per kg body weight and intended course of HDC after 4- and 5 BV was 6.31- and 6.97 x 10(6) ( P=0.014). Twenty HDC were evaluable for engraftment. There was some correlation between the number of transfused CD34+ and CD34+38- cells and WBC engraftment ( r = -0.66 and --0.69; P<0.01) and CD34+ cells and platelet engraftment ( r = -0.56; P= 0.013). No toxicity occurred during PBSCC, although the mean platelet count dropped by 50% which must be kept in mind regarding the additional application of anti-coagulants and the fact that most patients had large indwelling catheters. CONCLUSION: Processing 4 BV is sufficient to collect >5 x 10(6) CD34+ cells/kg body weight and intended course of HDC in most patients, although extension to 5 BV further increases the total yield of CD34+ cells.

ADP-ribosyl Cyclase↗

Developmental and neurochemical specificity of neuronal deficits produced by electrical impulse blockade in dissociated spinal cord cultures.

Blockade of spontaneous electrical activity in dissociated fetal spinal cord cultures produced neuronal deficits as measured by biochemical and morphological techniques. Spinal cord cultures exhibited an age-dependent vulnerability to impulse blockade with tetrodotoxin (TTX) or xylocaine. Neuronal cell counts, [125I]tetanus toxin fixation and [125I]scorpion toxin binding indicated that TTX application produced neuronal deficits during the second or third week in culture. Application of TTX during the first or fourth week did not produce a difference in tetanus toxin fixation from controls. Radioautography of [125I]tetanus toxin revealed no obvious change in the label distribution after TTX treatment. Suppression of electrical activity during the first 6 days in culture had no effect on choline acetyltransferase (CAT) activity and no apparent effect on the appearance of the cultures. Application of TTX during the seventh day in culture decreased CAT activity to 68% of control. Chronic electrical blockade produced a progressively greater loss of CAT activity through 21 days in culture. GABAergic neurons, as indicated by high-affinity GABA uptake, glutamic acid decarboxylase activity and [3H]GABA radioautography, were not affected by electrical blockade. These data indicate that there is developmental and neurochemical specificity in the neuronal death produced by blocking spontaneous electrical activity in dissociated spinal cord cultures.

Animals↗

Analysis of synaptic bodies in the Sprague-Dawley rat pineal gland under extreme photoperiods.

Synaptic bodies (SBs) are small, prominent organelles in pinealocytes, most probably involved in signal transduction processes. To check the influence of the photoperiod on their shape plasticity and number we chose two extreme lighting conditions, i.e. 20h of illumination followed by 4h of darkness (LD 20:4) versus (LD 4:20). Pineal glands were assessed at 0, 4 and 13h after dark onset. Under both conditions reconstructed SBs were plates or ribbons but never spheres and there were no obvious differences in morphology. Photoperiodic changes in SB profile size and number were investigated: application of the established method for SB quantification based on single section profile counts (SSPC) of areas showed a significant increase of SB profiles under LD 20:4. However, it has to be noted that SSPC depend on both, number and size of the structures. In contrast to this, modification of the disector counting method, also applied for unbiased quantification of whole SBs, revealed that rat pinealocytes show insignificantly more SBs under LD 20:4 than under 4:20 conditions. The lengths of the SB profiles, which were first measured under different conditions in this study, depend on SB size. They increased significantly under LD 20:4. In conclusion, we detected only an increase in SB size but not in their number. We further prove that, at least for SBs, it is of no value to calculate disector levels from SSPCs.

Animals↗

Evaluation of anthelmintic properties of extracts from some plants used as livestock dewormers by pastoralist and smallholder farmers in Kenya against Heligmosomoides polygyrus infections in mice.

Parasitic nematodes are among the most common and economically important infectious diseases of grazing livestock, especially in small ruminants in the tropics and subtropics in Kenya the control of gastrointestinal nematode infections in sheep and goats is usually made with synthetic anthelmintics but substantial levels of anthelmintic resistance have been recorded. A number of medicinal plants, that may provide possible alternatives, and are used by pastoralists and smallholder farmers in Kenya as deworming agents for their livestock and equines, namely Aframomum sanguineum, Dodonea angustifolia, Hildebrandtia sepalosa, Myrsine africana, Rapanea melanophloeos from Kenya, and Azadirachta indica from Kenya and Malaysia, together with the chemicals embelin and santonin that occur in some of these plants, were evaluated against Heligmosomoides polygyrus in mice. Commercial anthelmintics, namely ivermectin, pyrantel and piperazine, were also investigated, both to validate the mouse model system and to assess efficacy of these drugs against H. polygyrus. Pyrantel and ivermectin were highly effective in reducing the numbers of H. polygyrus worms as well as eggs in faeces of the mice, but piperazine had a lower activity. Application of santonin and M. africana significantly reduced the number of total worm counts (TWC) but not faecal egg counts (FEC). The use of embelin, R. melanophloeos and A. indica reduced FEC but not TWC. In all cases, however, reductions were well below the a priori level of 70% required for biological significance. A. sanguineum, D. angustifolia and H. sepalosa had no effect on either TWC or FEC. In conclusion, none of the plant preparations had any biologically significant anthelmintic effect in this monogastric host-parasite model system.

Animals↗

Effect of biological control through the daily application of spores of Duddingtonia flagrans in lambs kept under an evasive grazing system in the Netherlands.

In 2004, an experiment was carried out to evaluate the effect of biological control through feeding spores of Duddingtonia flagrans on parasitic gastroenteritis in lambs, kept under an evasive grazing system. In total 66 lambs were used. Forty naturally infected 3-month old ram lambs were weaned in mid June, and divided into four groups of 10 lambs. On 21 June, G1-G4 were moved to four separate virtually clean plots, they were moved after 4 and 8 weeks to similar plots, and housed after 12 weeks to be necropsied 16 days later. The other 26 lambs had been raised helminth-free, and were used as pairs of tracer lambs. All but one of these pairs, were grazed during the last 2 weeks on each plot. The remaining pair (TA) was grazed during the last 2 weeks on pasture (30 August to 13 September) on the plot that had been grazed by G3 between 19 July and 16 August, to study inhibited development in Haemonchus contortus. All lambs were fed 200 g of concentrates daily throughout the whole period, and those of G1 and G2 were also fed 500,000 spores of D. flagrans/kg bodyweight daily. The faecal cultures demonstrated a high reduction in yield as a result of fungal application. However, no differences between groups were seen in weight gain, faecal egg counts, pasture larval counts, worm counts and tracer worm counts. H. contortus was the dominant species, and it is obvious that the moves at 4-week intervals prevented the development of severe haemonchosis. This is in particular demonstrated by the much higher worm counts in the two TA tracer lambs grazed. Nevertheless, increases to high faecal egg counts 3 weeks after the first and second moves, indicated acquisition of infection before these moves and at least subclinical haemonchosis. This was supported with the worm counts of lambs and tracer lambs. A higher proportion of inhibited early L4 than in other tracers and than in the permanent lambs were found in the pair of TA tracer lambs. This indicates that moves to new pastures in late summer and autumn delays the onset of inhibition.

Analysis of Variance↗

Preliminary results using pentoxifylline in a pronuclear stage tubal transfer (PROST) program for severe male factor infertility.

In vitro trials with washed spermatozoa incubated in medium containing 1 mg/ml of the methyl xanthine phosphodiesterase inhibitor PF showed improved counts of total motile and total progressively motile spermatozoa in cases of oligospermia/asthenospermia. Application of this agent in a PROST program for a series of nine couples presenting for treatment with histories of failed fertilization in vitro resulted in five pregnancies (four singleton, one triplet) and the subsequent delivery of normal infants. The results warrant further evaluation of this sperm treatment for cases of severe male factor infertility.

Embryo Transfer↗

Immortalized hypothalamic luteinizing hormone-releasing hormone (LHRH) neurons induce a functional switch in the growth factor responsiveness of astroglia: involvement of basic fibroblast growth factor.

Recent evidence indicates that astroglial-derived growth factors (GFs) participate in the development of luteinizing hormone-releasing hormone (LHRH) neurons, but it is still unknown whether LHRH neurons may exert a reciprocal modulation of glial cell function. Using immortalized hypothalamic LHRH (GT1-1) neurons in co-culture with glial cells, we have recently shown that basic fibroblast growth factor (bFGF) plays a prominent role in the glial-induced acquisition of the mature LHRH phenotype by GT1-1 cells. We have resorted to this model and combined biochemical and morphological approaches to study whether the response of glial cells to a number of GFs (including bFGF, insulin-like growth factor I, IGF-I, epidermal growth factor, EGF and insulin) expressed during LHRH neuron differentiation, is modulated by co-culture with pure LHRH neurons. Pre-treatment of hypothalamic astrocytes with an inactive ('priming') dose of bFGF for 12 h powerfully increased astroglia proliferative response to IGF-I (10 ng/ml), EGF (10 g/ml) and insulin (10 microg/ml), inducing a 65-100% increase in the [3H]thymidine incorporation compared to untreated cultures. When astroglial cells and developing GT1-1 neurons were co-cultured for 5 days in vitro (DIV), the [3H]thymidine incorporation was significantly higher than in astroglial cells cultured without neurons. Application of the different GFs to the co-culture for either 12 or 24 h further stimulated DNA synthesis to various extent according to the GF applied and the time of application. Localization of the proliferating cells by dual immunohistochemical staining, followed by cell counting and bromodeoxiuridine (BrdU) labeling index calculation, revealed that the incorporation of BrdU was restricted to the nuclei of LHRH-immunopositive neurons. Such changes were accompanied by extensive morphological alterations of astroglial and LHRH fiber networks, whereas neutralization of bFGF activity in GT1-1 neuron-glial co-cultures by a bFGF-antibody, dramatically counteracted the observed effects. The functional switch of astroglia proliferative response to GFs coupled to the potent morphological and functional modifications of developing glia and pure LHRH neurons observed in vitro, support a bidirectional interaction between immortalized LHRH neurons and astroglial cells and identify bFGF as a key player in this crosstalk.

Animals↗

[The course of pregnancy in lupus anticoagulant syndrome].

More than 95 per cent of the pregnancies with circulating lupus anticoagulant (LA) without therapy lead to abortion or intrauterine death. We report on the course of a pregnancy in a patient, who developed deep venous thrombosis and circulating LA. One of the rare cases of successful pregnancy management without the common prednisolone-aspirin therapy, but with heparin-monotherapy associated with intensive medical and obstetrical surveillance under clinical conditions is reported. In spite of intermittent corticosteroid and immunoglobulin application, a healthy child was born, although normalisation of the aPTT and platelet count was not achieved. It seems, that an alternative concept of therapy may have been established.

Autoantibodies↗

Sources of variance in daily physical activity levels as measured by an accelerometer.

PURPOSE: To examine sources of variance in objective measures of physical activity in a group of healthy adults (N = 92) participating in a physical activity measurement study. METHODS: Physical activity was assessed for up to 21 consecutive days using the Computer Science Applications (CSA) accelerometer. Day-of-the-week effects were evaluated for activity counts (ct.min(-1).d(-1), ct.d(-1)) and time (min.d(-1)) spent in inactivity (0-499 ct), moderate-1 (500-1951 ct), and moderate-2-vigorous activity (> or =1952 ct). Random effects models were employed to estimate variance components for subject, day of the week, and residual error from which the number of days of assessment required to achieve 80% reliability were estimated. RESULTS: Physical inactivity was lower on weekend days, and Saturday was the least inactive day of the week for both men and women. Inter-individual variation, or differences between subjects, was proportionally the largest source of variance (55-60% of total) in accelerometer counts and time spent in moderate to vigorous activity. Differences within subjects (intra-individual variation) accounted for 30-45% of the overall variance, and day-of-the-week effects accounted for 1-8%. For activity counts, and time spent in moderate to vigorous activity, at least 3-4 d of monitoring were required to achieve 80% reliability. Reliable measures of physical inactivity required at least 7 d of monitoring. CONCLUSION: These findings provide insight for understanding the behavioral variability in the activity patterns of adults and suggest that reliable measures of activity behaviors require at least 7 d of monitoring.

Acceleration↗

Sandalwood oil prevent skin tumour development in CD1 mice.

Sandalwood oil (SW oil) has been used for the treatment of inflammatory and eruptive skin diseases. In the present study, the chemopreventive effects of SW oil on 7,12-dimethylbenz(a)-anthracene (DMBA)-initiated and 12-O-tetradecanoylphorbol-13-acetate(TPA)-promoted skin tumour development and TPA-induced ornithine decarboxylase (ODC) activity in CD1 mice were investigated. Female CD1 mice (5-6 weeks old) were divided in different groups, having 30 mice in each group. One week after topical application of DMBA (200 nmole in 100 microl acetone) alone or with SW oil at different concentrations (100 microl, 1.25, 2.5, 3.75, 5% in acetone), at different times (0.5, 1, 2 h) before DMBA, the mice were treated topically with TPA (5 nmole in 100 microl acetone) alone or with SW oil at different concentrations (100 microl, 1.25, 2.5, 3.75, 5% in acetone) at different times (0.5, 1, 2 h) before TPA applications twice a week for 20 weeks. The mice were weighed and papillomas counted weekly. The results indicate that SW oil pre-treatment decreased the papilloma incidence and multiplicity in a concentration and time-dependent manner. The pre-treatment with 5% SW oil (100 microl) 1 h before DMBA and TPA treatments provided a maximum of 67% and 96% decrease in papilloma incidence and multiplicity, respectively, after 20 weeks of promotion. The mice pre-treated with SW oil at all concentrations and time period before TPA had significantly lower ODC activity than the group treated with TPA alone. The data suggest that SW oil could be an effective chemopreventive agent against chemically-induced skin cancer.

9,10-Dimethyl-1,2-benzanthracene↗

A high-throughput structural biology/proteomics beamline at the SRS on a new multipole wiggler.

The North West Structural Genomics Centre's beamline, MAD10, at the SRS receives the central part of the radiation fan (0.5 mrad vertically, 4 mrad horizontally) produced by a new 2.46 T ten-pole wiggler. The optical arrangement of the beamline consists of a Rh-coated collimating Si mirror, a fixed-exit-beam double-crystal monochromator with sagittal bending for horizontal focusing and a second Rh-coated Si mirror for vertical focusing. The double-crystal Si (111) monochromator allows data collection in the 5-13.5 keV photon energy range with rapid (subsecond) tunability and high energy resolution. The monochromatic beam is optimized through a 200 microm collimator. The beamline end station has been designed around a Mar desktop beamline with high-throughput cryogenic sample changer, Mar225 CCD detector, liquid-N(2) autofill system and an ORTEC C-TRAIN-04 energy-resolving high-count-rate X-ray fluorescence detector. The instrument is optimized for MAD/SAD applications in protein crystallography with the additional mode of operation of online single-crystal EXAFS studies on the same crystals. Thus, screening of metals/Se in the crystal can be performed quickly prior to MAD/SAD data collection by exciting the crystal with X-rays of appropriate energy and recording an energy-dispersive fluorescence spectrum. In addition, this experimental set-up allows for parallel XAFS measurements on the same crystal to monitor 'radiation-induced' changes, if any, in e.g. the redox state of metal centres to be detected for a 'metallic' functional group during crystallographic data collection. Moreover, careful minimization of the thickness of the Be window maximizes the intensity performance for the 2.0-2.5 A softer wavelength range. This range also covers the K-edges of a number of important 3d transition metals as well as the L-edges of xenon and iodine and enhanced sulfur f ''.

Algorithms↗

Elimination of extracranial blood flow during dynamic cerebral perfusion studies using diffusible and non-diffusible radioisotope.

The extracranial blood flow seriously complicates the interpretation of dynamic cerebral studies. To eliminate this, we used a blood pressure cuff placed around the head in 50 patients with no evidence of cerebrovascular disease. The pressure in the headband was increased to 30 mmHg above the patient's systolic pressure, and the first 60 sec static scintigram was taken exactly 3 min after the injection of 99mTc-pertechnetate. A second 60 sec static scintigram was taken without pressure in the headband at 6 min after injection. After correction for diffusion of tracer into extravascular compartments we could still show 13% reduction in counting rates over the hemispheric regions and 30% over the convexity regions during application of the pressure headband. With the Xenon method, the application of the headband appears to have insignificant influence on the results of cerebral perfusion. We thus recommend that a headband should be used for dynamic 99mTc-isotope cerebral circulation studies.

Cerebrovascular Circulation↗

A simple model combining quantum noise and anatomical variation in radiographs.

A model is presented for the detection of uniform lesions by means of an ideal photon detector. The difference of observed photons between an area overlaying the embedded lesion and an adjacent reference area of equal size constitutes the signal to be detected. Application of ROC analysis reveals that the exact probability distribution of this photon count difference can be approximated well by a Gaussian, on condition that modulation less than 0.1 and signal-to-noise ratio (SNR) greater than 1. Moreover, within these constraints, SNR emerged as the more salient parameter characterizing detection performance. It is shown that in the absence of anatomical variation, lesions of arbitrarily small size may be detected at any prescribed level of confidence, provided one is willing to accept the required high photon exposure. The effect of anatomical variation on detection performance is conveniently demonstrated in a graph of SNR versus exposure. There, two global regions are identified, each characterized by an asymptote, corresponding to either photon-limited or photon-saturated imaging. Under the first condition, quantum fluctuations are dominating the noise, and thus, detection performance is influenced by the photon exposure. Under the second, anatomical variations limit the SNR to an upper value, irrespective of exposure magnitude. Data obtained from dental radiographs demonstrate that anatomical variation is amenable to experimental measurement, and that it sets the upper limit for the SNR achievable in the diagnostic task of detecting incipient carious lesions.

Elementary Particles↗

Characteristics of the cellular response of the rat conjunctiva to topically applied leukotriene B4.

Cellular events in the rat conjunctiva were studied at 1, 6 and 24 h following the topical application of leukotriene B4. A significant increase was noted in the number of eosinophils (p less than 0.01) and neutrophils (p less than 0.05) at 1 h and only in eosinophils at 6 h after leukotriene B4 application at the 2-micrograms dose. At the 200-ng dose, the eosinophil count was significantly elevated at 1 h only, and the number of neutrophils was not significantly changed at any time point. No significant increase in cell counts was observed at the 20-ng dose. In conclusion, certain doses of topically applied leukotriene B4 significantly increased the number of eosinophils and neutrophils in the rat conjunctiva.

Administration, Topical↗