Ultrastructural study of the intercellular bridges between female germinal cells in "Chirocephalus diaphanus" Prevost (Crustaceas: Branchiopoda)

S'ha efectuat un estudi en detall de la morfologia dels ponts intercel•lulars trobats entre les cèl•lules germinals femenines de Chirocephalus diaphanus. Sembla que provenen de citodièresis incompletes durant el procés de multiplicació de les oogònies. En l'interior dels ponts es pot observar una gran varietat d'orgànuls citoplasmàtics: mitocondris, reticle endoplasmàtic rugós, ribosomes lliures i vesícules que molt possiblement deriven dels dictiosomes, situats al voltant dels ponts. Cal destacar que en els ponts intercel•lulars que relacionen oòcits en estat de paquitè a la profase meiòtica, el nombre de vesícules és més abundant. En les zones properes als ponts intercel•lulars, l'espai intercel•lular presenta una dilatació en forma de canalicles, i es poden comptar un gran nombre d'unions cel•lulars del tipus macula adherens. Pel que fa al paper dels ponts intercel•lulars, sembla que concorren a la creació d'un tipus de sincronisme de la diferenciació cel•lular en el decurs de la gametogènesi

RBF neural net based classifier for the AIRIX accelerator fault diagnosis

The AIRIX facility is a high current linear accelerator (2-3.5kA) used for flash-radiography at the CEA of Moronvilliers France. The general background of this study is the diagnosis and the predictive maintenance of AIRIX. We will present a tool for fault diagnosis and monitoring based on pattern recognition using artificial neural network. Parameters extracted from the signals recorded on each shot are used to define a vector to be classified. The principal component analysis permits us to select the most pertinent information and reduce the redundancy. A three layer Radial Basis Function (RBF) neural network is used to classify the states of the accelerator. We initialize the network by applying an unsupervised fuzzy technique to the training base. This allows us to determine the number of clusters and real classes, which define the number of cells on the hidden and output layers of the network. The weights between the hidden and the output layers, realising the non-convex union of the clusters, are determined by a least square method. Membership and ambiguity rejection enable the network to learn unknown failures, and to monitor accelerator operations to predict future failures. We will present the first results obtained on the injector.Comment: 3 pages, 4 figures, LINAC'2000 conferenc

The solar differential rotation in the 18th century

The sunspot drawings of Johann Staudacher of 1749--1799 were used to determine the solar differential rotation in that period. These drawings of the full disk lack any indication of their orientation. We used a Bayesian estimator to obtain the position angles of the drawings, the corresponding heliographic spot positions, a time offset between the drawings and the differential rotation parameter \delta\Omega, assuming the equatorial rotation period is the same as today. The drawings are grouped in pairs, and the resulting marginal distributions for \delta\Omega were multiplied. We obtain \delta\Omega=-0.048 \pm 0.025 d^-1 (-2.75^o/d) for the entire period. There is no significant difference to the value of the present Sun. We find an (insignificant) indication for a change of \delta\Omega throughout the observing period from strong differential rotation, \delta\Omega\approx -0.07 d^-1, to weaker differential rotation, \delta\Omega\approx-0.04 d^-1.Comment: 6 pages, 6 figures, accepted for Astronomy and Astrophysic

The Dynamic Formation of Prominence Condensations

We present simulations of a model for the formation of a prominence condensation in a coronal loop. The key idea behind the model is that the spatial localization of loop heating near the chromosphere leads to a catastrophic cooling in the corona (Antiochos & Klimchuk 1991). Using a new adaptive grid code, we simulate the complete growth of a condensation, and find that after approx. 5,000 s it reaches a quasi-steady state. We show that the size and the growth time of the condensation are in good agreement with data, and discuss the implications of the model for coronal heating and SOHO/TRACE observations.Comment: Astrophysical Journal latex file, 20 pages, 7 b-w figures (gif files

Impaired hepatic drug and steroid metabolism in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency

Objective: Patients with congenital adrenal hyperplasia due to P450 oxidoreductase (POR) deficiency(ORD) present with disordered sex development and glucocorticoid deficiency. This is due to disruption of electron transfer from mutant POR to microsomal cytochrome P450 (CYP) enzymes that play a key role in glucocorticoid and sex steroid synthesis. POR also transfers electrons to all major drugmetabolizing CYP enzymes, including CYP3A4 that inactivates glucocorticoid and oestrogens. However, whether ORD results in impairment of in vivo drug metabolism has never been studied. Design:We studied an adult patient with ORD due to homozygous POR A287P, the most frequent POR mutation in Caucasians, and her clinically unaffected, heterozygous mother. The patient had received standard dose oestrogen replacement from 17 until 37 years of age when it was stopped after she developed breast cancer. Methods: Both subjects underwent in vivo cocktail phenotyping comprising the oral administration of caffeine, tolbutamide, omeprazole, dextromethorphan hydrobromide and midazolam to assess the five major drug-metabolizing CYP enzymes. We also performed genotyping for variant CYP alleles known to affect drug metabolism. Results: Though CYP enzyme genotyping predicted normal or high enzymatic activities in both subjects, in vivo assessment showed subnormal activities of CYP1A2, CYP2C9, CYP2D6 and CYP3A4 in the patient and of CYP1A2 and CYP2C9 in her mother. Conclusions: Our results provide in vivo evidence for an important role of POR in regulating drug metabolism and detoxification. In patients with ORD, in vivo assessment of drug-metabolizing activities with subsequent tailoring of drug therapy and steroid replacement should be considered

Biodegradation in soil effects on PLA/sisal and PHBV/sisal biocomposites

The use of bio-based composites like lignocellulosic fibres/polymer composites as an alternative materials are continuously increasing in several applications such as automobile manufacturing, packaging, construction or household and agricultural equipments. In order to warranty the durability on green biocomposites based on polymer matrixes like poly(hydroxy butyrate-co-valerate) (PHBV) and poly(lactide) (PLA), the previous knowledge about the influence of the ambient agents on their macromolecular properties is necessary. In this sense, biodegradation in soil normalised experiments are useful. In this work, two commercial PHBV and PLA were reinforced with sisal fibres at 10 %, 20% and 30% of weight, with the aid of maleic anhydride as coupling agent.the influence of the amount of sisal fiber and the effect of the coupling agent on the impact of the biodegradation in soil on the materiales, in terms of the variation of the physico-chemical properties of the biocomposites

Width of Sunspot Generating Zone and Reconstruction of Butterfly Diagram

Based on the extended Greenwich-NOAA/USAF catalogue of sunspot groups it is demonstrated that the parameters describing the latitudinal width of the sunspot generating zone (SGZ) are closely related to the current level of solar activity, and the growth of the activity leads to the expansion of SGZ. The ratio of the sunspot number to the width of SGZ shows saturation at a certain level of the sunspot number, and above this level the increase of the activity takes place mostly due to the expansion of SGZ. It is shown that the mean latitudes of sunspots can be reconstructed from the amplitudes of solar activity. Using the obtained relations and the group sunspot numbers by Hoyt and Schatten (1998), the latitude distribution of sunspot groups ("the Maunder butterfly diagram") for the 18th and the first half of the 19th centuries is reconstructed and compared with historical sunspot observations.Comment: 16 pages, 11 figures; accepted by Solar Physics; the final publication will be available at www.springerlink.co

Usefulness of the organ culture system in the in vitro diagnosis of coeliac disease: A multicentre study

Objective. Diagnosis of coeliac disease is based on the presence of villous atrophy which recovers following a gluten-free diet. The presence of circulating antiendomysial antibodies as well as their disappearance after a gluten-free diet supports the diagnosis. It has also been demonstrated that antiendomysial antibodies are detectable in supernatants of cultured intestinal biopsies from patients with coeliac disease. The objective of this study was to compare the histology and antiendomysial antibodies in culture supernatants of intestinal biopsies to validate the in vitro organ culture system as a future diagnostic tool for coeliac disease. Material and methods. Seventy-five antiendomysial serum-positive patients on a gluten-containing diet were evaluated. Patients underwent endoscopy with 5 biopsy fragments: 3 for histology, 1 cultured with and the other without gliadin-peptide activator. Antiendomysial antibodies were evaluated in all culture supernatants. Results. Sixty-eight patients had evidence of villous atrophy, while 73 out of 75 were positive to the organ culture system. The agreement rate between organ culture and histology results was 94%. Conclusions. As all the centres participating in the study obtained good agreement between organ culture and histology results, the new system could be considered a reliable tool for the diagnosis of coeliac disease. Nevertheless, it is possible to highlight cases with an organ culture-positive and -negative histology. This feature could be of considerable interest because, as the sensitivity of organ culture seems to be greater than the initial histology, the new system might be useful in uncertain cases where the risk of missing the diagnosis of coeliac disease is high

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency

Background Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited defect in the mitochondrial fatty acid oxidation pathway, resulting in significant morbidity and mortality in undiagnosed patients. Newborn screening (NBS) has considerably improved MCADD outcome, but the risk of complication remains in some patients. The aim of this study was to evaluate the relationship between genotype, biochemical parameters and clinical data at diagnosis and during follow-up, in order to optimize monitoring of these patients. Methods We carried out a multicenter study in southwest Europe, of MCADD patients detected by NBS. Evaluated NBS data included free carnitine (C0) and the acylcarnitines C8, C10, C10:1 together with C8/C2 and C8/C10 ratios, clinical presentation parameters and genotype, in 45 patients. Follow-up data included C0 levels, duration of carnitine supplementation and occurrence of metabolic crises. Results C8/C2 ratio and C8 were the most accurate biomarkers of MCADD in NBS. We found a high number of patients homozygous for the prevalent c.985A > G mutation (75%). Moreover, in these patients C8, C8/C10 and C8/C2 were higher than in patients with other genotypes, while median value of C0 was significantly lower (23 μmol/L vs 36 μmol/L). The average follow-up period was 43 months. To keep carnitine levels within the normal range, carnitine supplementation was required in 82% of patients, and for a longer period in patients homozygotes for the c.985A>G mutation than in patients with other genotypes (average 31 vs 18 months). Even with treatment, median C0 levels remained lower in homozygous patients than in those with other genotypes (14 μmol/L vs 22 μmol/L). Two patients died and another three suffered a metabolic crisis, all of whom were homozygous for the c.985 A>G mutation. Conclusions Our data show a direct association between homozygosity for c.985A>G and lower carnitine values at diagnosis, and a higher dose of carnitine supplementation for maintenance within the normal range. This study contributes to a better understanding of the relationship between genotype and phenotype in newborn patients with MCADD detected through screening which could be useful in improving follow-up strategies and clinical outcome