Observation of dynamic atom-atom correlation in liquid helium in real space.

Liquid 4He becomes superfluid and flows without resistance below temperature 2.17 K. Superfluidity has been a subject of intense studies and notable advances were made in elucidating the phenomenon by experiment and theory. Nevertheless, details of the microscopic state, including dynamic atom-atom correlations in the superfluid state, are not fully understood. Here using a technique of neutron dynamic pair-density function (DPDF) analysis we show that 4He atoms in the Bose-Einstein condensate have environment significantly different from uncondensed atoms, with the interatomic distance larger than the average by about 10%, whereas the average structure changes little through the superfluid transition. DPDF peak not seen in the snap-shot pair-density function is found at 2.3 Å, and is interpreted in terms of atomic tunnelling. The real space picture of dynamic atom-atom correlations presented here reveal characteristics of atomic dynamics not recognized so far, compelling yet another look at the phenomenon.

Influence of a gonadotropin-releasing hormone agonist on circulating concentrations of luteinizing hormone and testosterone and tissue concentrations of compounds associated with boar taint.

Twenty-four Yorkshire boars and six barrows approximately 8 mo of age were used to evaluate the effects of a GnRH agonist (GnRH-A) on circulating concentrations of LH and testosterone (T), concentrations of skatole in fat, and concentrations of 16-androstene steroids in fat and salivary glands. Pigs were assigned to five groups of six pigs each: L200, boars injected with 200 micrograms of GnRH-A/kg BW; L50, boars injected with 50 micrograms of GnRH-A/kg BW; Boar, boars treated with vehicle; Castrate, males castrated on the same day that Groups 1 to 3 received injections; and Barrow, males castrated as neonates. Pigs in L200, L50, and Boar were only given one injection. Blood samples were taken twice daily from d -2 to 28 for determinations of T and LH concentrations and at 15-min intervals for 6 h on d -1, 1, 7, 14, 21, and 28 for characterization of pulsatile LH release. Pigs were slaughtered on d 30, and samples of backfat and salivary glands were collected for quantification of skatole and 16-androstene steroid concentrations. The LH concentrations increased immediately following GnRH-A injection in L200 and L50 (P < .001) and then declined to pretreatment values by approximately 29 h after treatment. Serum T concentrations in L200 and L50 increased after GnRH-A treatment (P < .0001) and then decreased to less than pretreatment concentrations by d 5 in L200 (P < .001) and by d 8 in L50 (P < .01). Concentrations of 16-androstene steroids in fat were less (P < .05) in L200 and Barrow than in Boar.(ABSTRACT TRUNCATED AT 250 WORDS)

Culture of human preovulatory granulosa cells: effect of extracellular matrix on steroidogenesis.

Human luteal granulosa cells, harvested from preovulatory follicles during in vitro fertilization attempts, were cultured in a serum-precoated substratum ('serum cells') or on a collagen matrix ('collagen cells'). Concerning the 'serum cell' model, E2 secretion was very low in the absence of androgen; when androstenedione was added to the culture medium, cells secreted 180 +/- 52 pmol/ml/24 h of estradiol, 440 +/- 78 pmol/ml/24 h of testosterone and lower quantities of estrone and estriol. Follicle stimulating hormone induced a significant increase in estradiol and estriol, while the secretion of the other steroids was not altered. The secretion of progesterone was 3.15 +/- 1 nmol/ml/24 h and significantly enhanced by luteinizing hormone (+ 95%; P < 0.01). The secretions of 17 alpha-hydroxyprogesterone and 20 alpha-dihydroprogesterone were low and not modified by luteinizing hormone. 'Collagen cells', in basal conditions, showed an increased secretion of estradiol (+ 50%, P < 0.05), became rounded and were less responsive to gonadotropins when compared with 'serum cells'. Thus, the use of a collagen matrix, similarly to gonadotropins, stimulated granulosa cell steroidogenesis in relation to modifications of cell shape. The higher responsiveness of serum cells to gonadotropins makes this model more suitable for physiological and pharmacological studies than the collagen one.

[The G.E.R.U. retrospective study of 400 cases of urticaria]. / G.E.R.U. étude rétrospective de 400 cas d'urticaire.

The authors report on a study with computerised results of 400 urticaria and/or angioedema cases, which were explored in single dermatology center (Pr. J. SAYAG) by the members of GERU. The study was managed with a computerised file and was processed with Sesame software. The figures achieved are related to semilogic and paraclinical data and to etiological factors.

[Chronic urticaria--an inventory proposed by the Urticaria Study and Research Group]. / Urticaires chroniques--proposition d'inventaire du G.E.R.U.

The Urticaria Study and Research Group (Groupe d'Etudes et de Researches de l'Urticaria, G.E.R.U.) was formed in the Dermatology Department of the Hôpital Michel Levy in 1983 and now it continues to operate in the new Dermatology Department of the C.H.U. Timone Adultes. This has been possible because in four years 400 cases of urticaria have been seen and computerized information on these will appear in the next issue. As a result of this experience, we have been able to lay out a prospective study and develop a rigorous methodology.

Glutaryl phosphatidylcholine effects on pH and composition dependent behavior of liposomes studied by spin-labeling method.

The influence of glutaryl phosphatidylcholine on the molecular organization of phosphatidylcholine liposomes was studied by spin-labeling technique. The ESR signals given by the 5-nitroxide stearic acid label showed that the presence of glutaryl lecithin (i) significantly increased the negative charge density of the polar liposome surface with increasing proton concentration depending on the bulk solution pH, and (ii) apparently decreased the packing (order) of the hydrophobic region close to the surface, essentially in the presence of saturated phospholipids. The spectral information--S (order parameter) and alpha N (isotropic nitrogen coupling constant)--resulted in the location of the probe near or in the polar zone of the membrane or in the hydrophobic region, depending on the protonation/deprotonation of the fatty acid carboxyl group of the probe. The microviscosity of the inner region of the membrane monitored by the 12- and 16-probes was not significantly altered by glutaryl lecithin. On the other hand, glutaryl lecithin has a lesser effect on liposomes containing anionic polar head groups, such as dipalmitoyl phosphatidylglycerol or phosphatidylinositol, the anionic charge of which already had the same effect on protonation of the polar surface. The temperature dependence of dipalmitoyl phosphatidylcholine liposome dynamic behavior indicates that the glutaryl lecithin effect is completely different above and below the gel-to-liquid crystalline phase transition point.