702 research outputs found
Radiative Capture of Protons by Be9
The gamma rays from the capture in Be9 of protons of energy between 0.27 and 1.2 Mev have been studied using large scintillation crystals. Excitation functions of the gamma rays leading to the 0-, 0.72-, 1.74-, 2.15-, 3.58-, and 5.16-Mev states of B10 were computed from the measured gamma-ray spectra. In addition to the resonances previously known to exist at 0.33-, 0.99-, and 1.086-Mev proton energy [corresponding to (1-) 6.88-, (2-) 7.48-, and (0+) 7.56-Mev states in B10], evidence was found only for the p-wave resonance near 1 Mev [(2+) 7.5-Mev state in B10] postulated by Mozer and by Dearnaly and for the influence of higher lying states. This work leaves unexplained the large isotopic-spin impurity of the 6.88-Mev level. Appreciable nonresonant capture was found for the transitions to the 0-, 0.72-, 3.58-, and 5.16-Mev states, which is probably not s-wave for the latter two transitions. Accurate energy measurements and coincidence work showed that the 5.16-Mev level of B10 is populated in preference to the 5.11-Mev level, contradicting earlier work of Clegg. Also, experimental evidence has been found which appears to be in contradiction to the 0+ spin assignment for the 7.56-Mev level of B10 and raises doubts about the 2+ spin assignment of the 5.16-Mev level
Primary structure and evolutionary relationship between the adult alpha-globin genes and their 5'-flanking regions of Xenopus laevis and Xenopus tropicalis
To investigate the evolution of globin genes in the genus Xenopus, we have determined the primary structure of the related adult alpha I- and alpha II-globin genes of X. laevis and of the adult alpha-globin gene of X. tropicalis, including their 5'-flanking regions. All three genes are comprised of three exons and two introns at homologous positions. The exons are highly conserved and code for 141 amino acids. By contrast, the corresponding introns vary in length and show considerable divergence. Comparison of 900 bp of the 5'-flanking region revealed that the X. tropicalis gene contains a conserved proximal 310-bp promoter sequence, comprised of the canonical TATA and CCAAT motifs at homologous positions, and five conserved elements in the same order and at similar positions as previously shown for the corresponding genes of X. laevis. We therefore conclude that these conserved upstream elements may represent regulatory sequences for cell-specific regulation of the adult Xenopus globin genes
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Agonist-induced endocytosis of rat somatostatin receptor 1
Somatostatin-receptor 1 (sst1) is an autoreceptor in the central nervous system that regulates the release of somatostatin. Sst1 is present intracellularly and at the cell surface. To investigate sst1 trafficking, rat sst1 tagged with epitope was expressed in rat insulinoma cells 1046-38 (RIN-1046-38) and tracked by antibody labeling. Confocal microscopic analysis revealed colocalization of intracellularly localized rat sst1-human simplex virus (HSV) with Rab5a-green fluorescent protein and Rab11a-green fluorescent protein, indicating the distribution of the receptor in endocytotic and recycling organelles. Somatostatin-14 induced internalization of cell surface receptors and reduction of binding sites on the cell surface. It also stimulated recruitment of intracellular sst1-HSV to the plasma membrane. Confocal analysis of sst1-HSV revealed that the receptor was initially transported within superficial vesicles. Prolonged stimulation of the cells with the peptide agonist induced intracellular accumulation of somatostatin-14. Because the number of cell surface binding sites did not change during prolonged stimulation, somatostatin-14 was internalized through a dynamic process of continuous endocytosis, recycling, and recruitment of intracellularly present sst1-HSV. Accumulated somatostatin-14 bypassed degradation via the endosomal-lysosomal route and was instead rapidly released as intact and biologically active somatostatin-14. Our results show for the first time that sst1 mediates a dynamic process of endocytosis, recycling, and re-endocytosis of its cognate ligand
Density effect in Cu K-shell ionization by 5.1-GeV electrons
We have made an absolute measurement of the Cu K-shell impact ionization cross section by 5.1-GeV electrons, which demonstrates directly a density effect predicted by Fermi in 1940. By determining the ratio of the K x-ray yield from a thin front and back layer of the target by a novel grazing emission method, we have verified the effect of transition radiation on the x-ray production, suggested by Sorensen and reported by Bak et al
Effects of intraduodenal infusion of the bitter tastant, quinine, on antropyloroduodenal motility, plasma cholecystokinin, and energy intake in healthy men
Background/Aims:Nutrient-induced gut hormone release (eg, cholecystokinin [CCK]) and the modulation of gut motility (particularly pyloric stimulation) contribute to the regulation of acute energy intake. Non-caloric bitter compounds, including quinine, have recently been shown in cell-line and animal studies to stimulate the release of gastrointestinal hormones by activating bitter taste receptors expressed throughout the gastrointestinal tract, and thus, may potentially suppress energy intake without providing additional calories. This study aims to evaluate the effects of intraduodenally administered quinine on antropyloroduodenal pressures, plasma CCK and energy intake. Methods:Fourteen healthy, lean men (25 ± 5 years; BMI: 22.5 ± 2.0 kg/m2) received on 4 separate occasions, in randomized, double-blind fashion, 60-minute intraduodenal infusions of quinine hydrochloride at doses totaling 37.5 mg ("Q37.5"), 75 mg ("Q75") or 225 mg ("Q225"), or control (all 300 mOsmol). Antropyloroduodenal pressures (high-resolution manometry), plasma CCK (radioimmunoassay), and appetite perceptions/gastrointestinal symptoms (visual analog questionnaires) were measured. Ad libitum energy intake (buffet-meal) was quantified immediately post-infusion. Oral quinine taste-thresholds were assessed on a separate occasion using 3-alternative forced-choice procedure. Results:All participants detected quinine orally (detection-threshold: 0.19 ± 0.07 mmol/L). Intraduodenal quinine did not affect antral, pyloric or duodenal pressures, plasma CCK (pmol/L [peak]; control: 3.6 ± 0.4, Q37.5: 3.6 ± 0.4, Q75: 3.7 ± 0.3, Q225: 3.9 ± 0.4), appetite perceptions, gastrointestinal symptoms or energy intake (kcal; control: 1088 ± 90, Q37.5: 1057 ± 69, Q75: 1029 ±7 0, Q225: 1077 ± 88). Conclusions:Quinine, administered intraduodenally over 60 minutes, even at moderately high doses, but low infusion rates, does not modulate appetite-related gastrointestinal functions or energy intake.Vida Bitarafan, Penelope C E Fitzgerald, Tanya J Little, Wolfgang Meyerhof, Tongzhi Wu, Michael Horowitz and Christine Feinle-Bisse
Continuum Coupling and Single-Nucleon Overlap Integrals
The presence of a particle continuum, both of a resonant and non-resonant
character, can significantly impact spectroscopic properties of weakly bound
nuclei and excited nuclear states close to, and above, the particle emission
threshold. In the framework of the continuum shell model in the complex
momentum-plane, the so-called Gamow Shell Model, we discuss salient effects of
the continuum coupling on the one-neutron overlap integrals and the associated
spectroscopic factors in neutron-rich helium and oxygen nuclei. In particular,
we demonstrate a characteristic near-threshold energy dependence of the
spectroscopic factors for different l-waves. We show also that the realistic
radial overlap functions, which are needed for the description of transfer
reactions, can be generated by single-particle wave functions of the
appropriately chosen complex potential.Comment: 9 figures; 23 pages; corrected version; accepted in Nuclear Physics
Two-body Photodisintegration of He with Full Final State Interaction
The cross sections of the processes He()H and
He()He are calculated taking into account the full final
state interaction via the Lorentz integral transform (LIT) method. This is the
first consistent microscopic calculation beyond the three--body breakup
threshold. The results are obtained with a semirealistic central NN potential
including also the Coulomb force. The cross sections show a pronounced dipole
peak at 27 MeV which lies within the rather broad experimental band. At higher
energies, where experimental uncertainties are considerably smaller, one finds
a good agreement between theory and experiment. The calculated sum of three--
and four--body photodisintegration cross sections is also listed and is in fair
agreement with the data.Comment: 18 pages, 6 figure
The Lymnaea cardioexcitatory peptide (LyCEP) receptor: A G-protein-couplex receptor for a novel member of the RFamide neuropeptide family.
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