Predicting the start of the birch pollen season at London, Derby and Cardiff, United Kingdom, using a multiple regression model, based on data from 1987 to 1997

Recent changes in weather in North-West Europehave been reflected in the start dates ofpollen seasons. It is therefore necessary toupdate previous models, such as the oneproduced by Jones (1995), so that the modelwill be weighted by current weather patterns. Birch pollen data, collected over a period ofeleven years (1987 to 1997 inclusive) fromthree pollen counting stations in the UK,London, Derby and Cardiff, were analysed todetermine the start dates using the Sum75method. The start dates of the birch pollenseasons of the eleven-year period were thentested for significance against ten-dayaggregated variables of temperature andrainfall for each site. The significantvariables were entered into multiple regressionmodels until the most valid equation for eachsite was found. The models were then tested onthree years not included in their data sets. The models showed mean differences betweenactual and predicted start dates, for theeleven years used, of 1.5, 3 and 5 days atDerby, Cardiff and London respectively. Forthe test years the mean difference was 1, 4.5and 7.5 days at Derby, Cardiff and Londonrespectively. The most powerful model was forDerby where the corresponding meteorologicalstation is at 0.5 km distance and the weakestwas for London where the correspondingmeteorological station is much further away at21 km distance. Weather variables from earlyFebruary to mid March were found to be the mostinfluential on the start dates of the birchpollen season at the three sites.     

Analysis of a glucose tetrasaccharide elevated in Pompe disease by stable isotope dilution-electrospray ionization tandem mass spectrometry

Patients with glycogen storage disease type II (GSD II) typically excrete increased amounts of a glycogen-derived glucose tetrasaccharide, Glcalpha1-6Glcalpha1-4Glcalpha1-4Glc (Glc(4)), in the urine. With the advent of a new enzyme replacement therapy for GSD II, there is a need for early identification of patients with this disease and for monitoring the efficacy of treatment. Glc(4) is a good candidate biomarker for GSD II. A simple and robust method using stable isotope dilution-electrospray ionization-tandem mass spectrometry for the analysis of Glc(4) in biological samples was developed. A 13C(6)-labeled stable isotope internal standard was synthesized by transglycosylation using a recombinant alpha-amylase. Butyl 4-aminobenzoate derivatives of Glc(4) and the internal standard were analyzed using multiple reaction monitoring. This method was shown to be accurate and precise by the repeated analysis of calibrators and quality control samples in urine and plasma. There was good agreement with a high-performance liquid chromatography-UV method for urine samples, whereas there was less agreement with plasma samples. Accurate determination from dried urine spot samples was also demonstrated. This method is amenable to high-throughput analysis, a necessary prerequisite for mass screening for GSD II.     

Robustness of MetaNet graph models: predicting control of urea production in humans

Urea production in human liver was described by a MetaNet graph, a flowchart-like representation of metabolic pathways that includes parameters for the kinetic constants of the constituent enzymes. Formal operations on the graph facilitate the identification of ligand-binding equilibria that participate in feedback regulation in the network of biochemical reactions. The state of the biochemical network is specified by the concentrations of the intermediates. At any particular time, the influence of an identified locus of regulation is proportional to the respective fractional saturation of the corresponding binding site. Enzymes that make or consume the feedback chemicals share in the control of the strength of the feedback signal in proportion to their fractional saturation. This model predicts control of urea production by the processes that deliver amino groups to the urea cycle enzymes more than by the cycle enzymes themselves. Mitochondrial membrane transport processes are important for transmission of information through the network, but irreversible enzymes and processes far from equilibrium control the strength of the feedback signal. Systematic variation of the parameter values by amounts comparable to the expected variability of their measured values indicated a high probability of invariance in the identities of the predicted control points. The properties of the model are consistent with those of error-tolerant scale-free networks. These results demonstrate the robustness of a MetaNet model's predictions with respect to uncertainties in the values of its parameters.     

UK regional variations in Betula pollen (1993–1997)

Betula pollen is known to be an importantaeroallergen in Europe and the UK, with very largequantities of pollen released into the air at theheight of the season, making it the most abundant treepollen present in the UK spring air.There has been long term pollen monitoring in Cardiff,Derby and London but in recent years the number ofregional sites has increased.Seven sites throughout the UK have monitoredBetula pollen using Burkard samplers for the period1993–1997 and for this study regionaldifferences in Betula pollen and climate wereinvestigated.Detailed analysis revealed considerable variation inthe start dates, duration and quantityof Betula pollen for the seven UK sitesthroughout the five year period.These regional variations in Betula pollenduration and intensity of season, indicate theimportance of maintaining sites throughout the UK asan aid to clinicians, researchers and the generalpublic.     

Quantitative changes in alkaline phosphatase in epithelial cells of rat small intestine from birth to weaning

Synopsis Alkaline phosphatase activity has been measured in mucosal scrapings of rat small intestine from birth to weaning. The levels of activity were then compared with those found in brush border fractions and cell residues over the same period. The amount of activity found in the residues was too high and variable to be accounted for in terms of diffusion, and it was concluded that during the developmental period considerable quantities of enzyme were present in the cytoplasm.The duodenal changes were similar, in form, in both mucosal scrapings and brush border, but the changes in the ileal brush borders were markedly different from those found in the ileal mucosal scrapings. A peak in the activity measured in the brush border fraction was observed during the weaning period. A partial explanation for the observed changes is suggested but a detailed analysis was not possible at the present stage in the work.     

Endogenous steroid concentrations in human breast tumours determined by high-resolution mass fragmentography (Short Communication)

A pilot study of the endogenous steroid concentrations in human breast tumours was performed. The technique of high-resolution molecular-ion monitoring during combined g.l.c.-mass spectrometry was used to determine oestrone, oestradiol-17beta and oestriol in concentrations above 1ng/g wet wt. of tissue, and dehydroepiandrosterone, testosterone, androsterone (3alpha-hydroxy-5alpha-androstan-17-one) and 3beta-hydroxy-5alpha-androstan-17-one in concentrations exceeding 5ng/g, in extracts of five primary breast tumours.     

Kinetics of Na(+) transport in necturus proximal tubule

The dependence of proximal tubular sodium and fluid readsorption on the Na(+) concentration of the luminal and peritubular fluid was studied in the perfused necturus kidney. Fluid droplets, separated by oil from the tubular contents and identical in composition to the vascular perfusate, were introduced into proximal tubules, reaspirated, and analyzed for Na(+) and [(14)C]mannitol. In addition, fluid transport was measured in short-circuited fluid samples by observing the rate of change in length of the split droplets in the tubular lumen. Both reabsorptive fluid and calculated Na fluxes were simple, storable functions of the perfusate Na(+) concentration (K(m) = 35-39 mM/liter, V(max) = 1.37 control value). Intracellular Na(+), determined by tissue analysis, and open-circuit transepithelial electrical potential differences were also saturable functions of extracellular Na(+). In contrast, net reabsorptive fluid and Na(+) fluxes were linearly dependent on intracellular Na(+) and showed no saturation, even at sharply elevated cellular sodium concentrations. These concentrations were achieved by addition of amphotericin B to the luminal perfusate, a maneuver which increased the rate of Na(+) entry into the tubule cells and caused a proportionate rise in net Na(+) flux. It is concluded that active peritubular sodium transport in proximal tubule cells of necturus is normally unsaturated and remains so even after amphotericin-induced enhancement of luminal Na(+) entry. Transepithelial movement of NaCl may be described by a model with a saturable luminal entry step of Na(+) or NaCl into the cell and a second, unsaturated active transport step of Na(+) across the peritubular cell boundary.