20 research outputs found
DN interaction from meson exchange
A model of the DN interaction is presented which is developed in close
analogy to the meson-exchange KbarN potential of the Juelich group utilizing
SU(4) symmetry constraints. The main ingredients of the interaction are
provided by vector meson (rho, omega) exchange and higher-order box diagrams
involving D*N, D\Delta, and D*\Delta intermediate states. The coupling of DN to
the pi-Lambda_c and pi-Sigma_c channels is taken into account. The interaction
model generates the Lambda_c(2595) resonance dynamically as a DN quasi-bound
state. Results for DN total and differential cross sections are presented and
compared with predictions of an interaction model that is based on the
leading-order Weinberg-Tomozawa term. Some features of the Lambda_c(2595)
resonance are discussed and the role of the near-by pi-Sigma_c threshold is
emphasized. Selected predictions of the orginal KbarN model are reported too.
Specifically, it is pointed out that the model generates two poles in the
partial wave corresponding to the Lambda(1405) resonance.Comment: 14 pages, 8 figure
Angiotensin-converting-enzyme gene insertion/deletion polymorphism and response to physical training
Background
The function of local renin-angiotensin systems in skeletal muscle and adipose tissue remains largely unknown. A polymorphism of the human angiotensin converting enzyme (ACE) gene has been identified in which the insertion (I) rather than deletion (D) allele is associated with lower ACE activity in body tissues and increased response to some aspects of physical training. We studied the association between the ACE gene insertion or deletion polymorphism and changes in body composition related to an intensive exercise programme, to investigate the metabolic effects of local human renin-angiotensin systems.
Methods
We used three independent methods (bioimpedance, multiple skinfold-thickness assessment of whole-body composition, magnetic resonance imaging of the mid-thigh) to study changes in body composition in young male army recruits over 10 weeks of intensive physical training.
Findings
Participants with the II genotype had a greater anabolic response than those with one or more D alleles for fat mass (0·55 vs −0·20 kg, p=0·04 by bioimpedance) and non-fat mass (1·31 vs −0·15 kg, p=0·01 by bioimpedance). Changes in body morphology with training measured by the other methods were also dependent on genotype.
Interpretation
II genotype, as a marker of low ACE activity in body tissues, may conserve a positive energy balance during rigorous training, which suggests enhanced metabolic efficiency. This finding may explain some of the survival and functional benefits of therapy with ACE inhibitors