Involvement of different protein kinases and phospholipases A2 in phorbol ester (TPA)-induced arachidonic acid liberation in bovine platelets.

The effect of various phospholipase A2 and protein kinase inhibitors on the arachidonic acid liberation in bovine platelets induced by the protein kinase activator 12-O-tetradecanoylphorbol-13-acetate (TPA) was studied. TPA stimulates arachidonic acid release mainly by activating group IV cytosolic PLA2 (cPLA2), since inhibitors of this enzyme markedly inhibited arachidonic acid formation. However, group VI Ca2+-independent PLA2 (iPLA2) seems to contribute to the arachidonic acid liberation too, since the relatively specific iPLA2 inhibitor bromoenol lactone (BEL) decreased arachidonic acid generation in part. The pronounced inhibition of the TPA-induced arachidonic acid release by the protein kinase C (PKC) inhibitors GF 109203X and Ro 31-82220, respectively, and by the p38 MAP kinase inhibitor SB 202190 suggests that the activation of the PLA2s by TPA is mediated via PKC and p38 MAP kinase

Transport study of charged current interactions in neutrino-nucleus reactions

Within a dynamical transport approach we investigate charged current interactions in neutrino-nucleus reactions for neutrino energies of 0.3 - 1.5 GeV with particular emphasis on resonant pion production channels via the $\Delta_{33}(1232)$ resonance. The final-state-interactions of the resonance as well as of the emitted pions are calculated explicitly for $^{12}C$ and $^{56}Fe$ nuclei and show a dominance of pion suppression at moderate momenta $p_\pi >$ 0.2 GeV/c. A comparison to integrated $\pi^+$ spectra for $\nu_\mu + ^{12}C$ reactions with the available (preliminary) data demonstrates a reasonable agreement.Comment: 13 pages incl. 6 eps-figures; computational error in final state interactions corrected; to be published in Phys. Lett.

Total Synthesis of Tulearin C

With the help of the smaller brother: Although alkyne metathesis will always be the little brother of alkene metathesis, it allows problems to be solved that are currently beyond reach of the more famous sibling. This notion is exemplified by the tulearin macrolides, which could only be selectively forged by ring-closing alkyne metathesis (RCAM)/trans reduction using the latest generation of alkyne metathesis catalysts

Vanadium centers in ZnTe crystals. II. Electron paramagnetic resonance

Four V-related electron-paramagnetic-resonance (EPR) spectra are observed in Bridgman-grown ZnTe doped with vanadium. Two of them are attributed to the charge states VZn3+(A+) and VZn2+(A0) of the isolated V impurity. For the ionized donor, VZn3+(A+), the spectrum reveals the typical behavior of the expected 3A2(F) ground state in tetrahedral symmetry. The incorporation on a cation lattice site could be proved by the resolved superhyperfine interaction with four Te ions. The second spectrum showing triclinic symmetry and S=3/2 is interpreted as the neutral donor state VZn2+(A0). The origin of the triclinic distortion of the cubic (Td) crystal field could be a static Jahn-Teller effect. The two additionally observed EPR spectra are attributed to nearest-neighbor V-related defect pairs. The spectrum of the first one, V2+Zn-YTe, shows trigonal symmetry and can be explained by the S=3/2 manifold of an orbital singlet ground state. An associated defect "YTe" is responsible for the trigonal distortion of the tetrahedral crystal field of V2+Zn. The spectrum of the second pair defect also shows trigonal symmetry and can be described by S=1/2. The ground-state manifold implies a VZn3+−XTe pair as the most probable origin of this spectrum. The S=1/2 ground state is produced by a dominating isotropic exchange interaction coupling the S=1 ground-state manifold of V3+Zn to an assumed S=1/2 ground state of "XTe" in antiferromagnetic orientation. The nature of the associated defects "YTe" and "XTe" remains unknown for both pairs since no hyperfine structure has been observed, but most probably acceptorlike defects are involved

Vanadium centers in ZnTe crystals. I. Optical properties

In ZnTe:V bulk crystals with nominal vanadium concentrations between 1000 and 7000 ppm three vanadium-ion states V+, V2+, and V3+ were found in low-temperature optical measurements. No-phonon lines of the internal emissions were detected for the 5E(D)→5T2(D) transition of V+(d4) at 3401 cm−1 (0.422 eV), for 4T2(F)→4T1(F) of V2+(d3) at 4056 cm−1 (0.503 eV), and for 3T2(F)→3A2(F) of V3+(d2) at 4726 cm−1 (0.586 eV). The energies of the internal transitions are reduced with respect to the corresponding transitions in ZnS:V and ZnSe:V. The respective excitation spectra display, in addition to broad charge-transfer bands, higher excited levels of the individual charge states. Crystal-field calculations of the detected transition energies based on the Tanabe-Sugano scheme are presented. With the help of sensitization experiments, a one-electron model is designed, in which the donor level (V2+/V3+) is situated 12 500 cm−1 (1.55 eV) below the conduction-band edge and the acceptor level (V2+/V+) 9400 cm−1 (1.17 eV) above the valence-band edge. The dynamical behavior of the three infrared lurainescence bands was measured. Decay time constants of 43 μs (V+), 120 μs (V2+), and 420 μs (V3+) were found. Electron-paramagnetic-resonance (EPR) results measured on the same samples are presented in an accompanying paper and confirm the optical detection of isolated substitutional V2+(d3) and V3+(d2) ions. Relations between the EPR and optical results are discussed

Spectral Function of Quarks in Quark Matter

We investigate the spectral function of light quarks in infinite quark matter using a simple, albeit self-consistent model. The interactions between the quarks are described by the SU(2) Nambu--Jona-Lasinio model. Currently mean field effects are neglected and all calculations are performed in the chirally restored phase at zero temperature. Relations between correlation functions and collision rates are used to calculate the spectral function in an iterative process.Comment: final version, published in PRC; 15 pages, RevTeX

A New Method for the Preparation of Non-Terminal Alkynes: Application to the Total Syntheses of Tulearin A and C

Lactones are known to react with the reagent generated in situ from CCl4 and PPh3 in a Wittig-type fashion to give gem-dichloro-olefin derivatives. Such compounds are now shown to undergo reductive alkylation on treatment with organolithium reagents RLi to furnish acetylene derivatives bearing the substituent R at their termini (R=Me, n-, sec-, tert-alkyl, silyl); the reaction can be catalyzed with either Cu(acac)2 or Fe(acac)3/1,2-diaminobenzene. Two alkynol derivatives prepared in this way from readily accessible lactone precursors served as the key building blocks for the total syntheses of the cytotoxic marine macrolides tulearin A (1) and C (2). The assembly of these fragile targets hinged upon ring closing alkyne metathesis (RCAM) followed by a formal trans-reduction of the resulting cycloalkynes via trans-hydrosilylation/protodesilylation