Molecular particle-core model and its application to 13C-13C scattering

On the basis of the two-center shell model a theory is developed for the excitation of loosely bound nucleons in heavy ion collisions. These nucleons move in the two-center shell model potential generated by all the nucleons and are described by molecular wave functions. The model is applied to calculate the cross sections for the elastic and inelastic 13C-13C scattering. The cross sections show intermediate structures caused by the excitation of quasibound resonances in the molecular nucleus-nucleus potential. NUCLEAR REACTIONS 13C(13C,13C) molecular wave functions, dynamical two-center shell model, quasimolecular resonances, radial and Coriolis coupling, coupled channel calculations for σ(θ)

Inelastic excitation and neutron transfer in the 13-13C scattering with the molecular particle-core model

The molecular particle-core model is applied to the scattering of 13C on 13C. The model divides the 13C+ 13C system into two 12C cores and two valence neutrons. The valence neutrons are described with molecular eigenfunctions of the symmetric two-center shell model. Coupled channel calculations are carried out for the inelastic single and mutual excitation of the first (1/2+ state of 13C and the neutron transfer to the 12C+14C system. The results reproduce the experimental data. The analysis of the S matrix shows that the gross structure of the transfer excitation function is related to resonances in the relative motion of the elastic and transfer channels

In vivo detection of γ-glutamyl-transferase up-regulation in glioma using hyperpolarized γ-glutamyl-[1-13C]glycine.

Glutathione (GSH) is often upregulated in cancer, where it serves to mitigate oxidative stress. γ-glutamyl-transferase (GGT) is a key enzyme in GSH homeostasis, and compared to normal brain its expression is elevated in tumors, including in primary glioblastoma. GGT is therefore an attractive imaging target for detection of glioblastoma. The goal of our study was to assess the value of hyperpolarized (HP) γ-glutamyl-[1-13C]glycine for non-invasive imaging of glioblastoma. Nude rats bearing orthotopic U87 glioblastoma and healthy controls were investigated. Imaging was performed by injecting HP γ-glutamyl-[1-13C]glycine and acquiring dynamic 13C data on a preclinical 3T MR scanner. The signal-to-noise (SNR) ratios of γ-glutamyl-[1-13C]glycine and its product [1-13C]glycine were evaluated. Comparison of control and tumor-bearing rats showed no difference in γ-glutamyl-[1-13C]glycine SNR, pointing to similar delivery to tumor and normal brain. In contrast, [1-13C]glycine SNR was significantly higher in tumor-bearing rats compared to controls, and in tumor regions compared to normal-appearing brain. Importantly, higher [1-13C]glycine was associated with higher GGT expression and higher GSH levels in tumor tissue compared to normal brain. Collectively, this study demonstrates, to our knowledge for the first time, the feasibility of using HP γ-glutamyl-[1-13C]glycine to monitor GGT expression in the brain and thus to detect glioblastoma

Systemic availability and metabolism of colonic-derived short-chain fatty acids in healthy subjects: a stable isotope study

The short-chain fatty acids (SCFAs), acetate, propionate and butyrate, are bacterial metabolites that mediate the interaction between the diet, the microbiota and the host. In the present study, the systemic availability of SCFAs and their incorporation into biologically relevant molecules was quantified. Known amounts of 13C-labelled acetate, propionate and butyrate were introduced in the colon of 12 healthy subjects using colon delivery capsules and plasma levels of 13C-SCFAs 13C-glucose, 13C-cholesterol and 13C-fatty acids were measured. The butyrate-producing capacity of the intestinal microbiota was also quantified. Systemic availability of colonic-administered acetate, propionate and butyrate was 36%, 9% and 2%, respectively. Conversion of acetate into butyrate (24%) was the most prevalent interconversion by the colonic microbiota and was not related to the butyrate-producing capacity in the faecal samples. Less than 1% of administered acetate was incorporated into cholesterol and <15% in fatty acids. On average, 6% of colonic propionate was incorporated into glucose. The SCFAs were mainly excreted via the lungs after oxidation to 13CO2, whereas less than 0.05% of the SCFAs were excreted into urine. These results will allow future evaluation and quantification of SCFA production from 13C-labelled fibres in the human colon by measurement of 13C-labelled SCFA concentrations in blood

Coupling and higher-order effects in the 12C(d,p)13C and 13C(p,d)12C reactions

Coupled channels calculations are performed for the 12C(d,p)13C and 13C(p,d)12C reactions between 7 and 60 MeV to study the effect of inelastic couplings in transfer reactions. The effect of treating transfer beyond Born approximation is also addressed. The coupling to the 12C 2+ state is found to change the peak cross-section by up to 15 %. Effects beyond Born approximation lead to a significant renormalization of the cross-sections, between 5 and 10 % for deuteron energies above 10 MeV, and larger than 10 % for lower energies. We also performed calculations including the remnant term in the transfer operator, which has a small impact on the 12C(d,p)13C(g.s.) and 13C(p,d)12C(g.s.) reactions. Above 30 MeV deuteron energy, the effect of the remnant term is larger than 10 % for the 12C(d,p)13C(3.09 MeV) reaction and is found to increase with decreasing neutron separation energy for the 3.09 MeV state of 13C. This is of importance for transfer reactions with weakly bound nuclei.Comment: 7 pages, 7 figures, submitted to Phys. Rev.