RESUMEN
Ba0.6K0.4Fe2Se3 (BKFS) single crystals were investigated by means of measurements of powder x-ray diffraction, temperature-dependent resistivity, anisotropic dc magnetization, ac magnetic susceptibility and specific heat. The powder x-ray diffraction indicates staggered iron displacements along the ladders with short and long Fe-Fe bond lengths (2.64(2) and 2.91(2) Å) variation. The resistivity of BKFS exhibits variable range hopping behavior with ln(ρ) ~ T(-1/2) at low temperature. The magnetic susceptibility χ(T) exhibits a sharp cusp at around 20 K in a zero-field-cooled process. The frequency-dependent ac magnetic susceptibility reveals that the cusp feature is attributable to spin glass behavior. The anisotropic ac magnetic susceptibility indicates that BKFS is probably an anisotropic Heisenberg-like spin glass with its easy magnetization plane perpendicular to the chain direction. The specific heat also supports an insulating and spin glass ground state. Extended Curie-Weiss behavior above 40 K was observed with a reduced effective moment (µ(eff) = 1.66 µ(B)/Fe for H is perpendicular to b and µ(eff) = 1.82 µB/Fe for H is parallel to b) in BKFS, which is close to the spin-only magnetism with S=1/2.
RESUMEN
We have synthesized a new oxypnictide, Ba2Ti2Fe2As4O, via a solid-state reaction under a vacuum. The compound crystallizes in a body-centered tetragonal lattice, which can be viewed as an intergrowth of BaFe2As2 and BaTi2As2O, thus containing Fe2As2 layers and Ti2O sheets. Bulk superconductivity at 21 K is observed after annealing the as-prepared sample at 773 K for 40 h. In addition, an anomaly in resistivity and magnetic susceptibility around 125 K is revealed, suggesting a charge- or spin-density wave transition in the Ti sublattice.
RESUMEN
Obesity is one major cardiovascular risk factor. We tested effects of endurance exercise on cannabinoid receptor type 1 (CB1) and peroxisome proliferator-activated receptor-delta (PPAR-delta)-dependent pathways in adipose tissue. Male Wistar rats were randomly assigned to standard laboratory chow or a high-fat diet without and with regular endurance exercise. Exercise in rats on high-fat diet significantly reduced visceral fat mass, blood pressure, and adipocyte size (each p<0.05). Adipocyte hypertrophy induced by high-fat diet was accompanied by increased CB1 expression in adipose tissue, whereas exercise significantly reduced CB1 expression (each p<0.05). CB1 receptor expression and adipocyte differentiation were directly regulated by PPAR-delta. Adipocyte hypertrophy induced by high-fat diet was accompanied by reduced PPAR-delta. Furthermore, selective silencing of PPAR-delta by RNA interference in 3T3-L1-preadipocyte cells significantly increased CB1 expression from 1.00+/-0.06 (n=3) to 1.91+/-0.06 (n=3; p<0.01) and increased adipocyte differentiation, whereas adenovirus-mediated overexpression of PPAR-delta significantly reduced CB1 expression to 0.39+/-0.03 (n=3; p<0.01) and reduced adipocyte differentiation. In the presence of the CB1 antagonist rimonabant adipocyte differentiation in stimulated 3T3 L1 preadipocyte cells was significantly reduced. The study indicates that high-fat diet-induced hypertrophy of adipocytes is associated with increased CB1 receptor expression which is directly regulated by PPAR-delta. Both CB1 and PPAR-delta are intimately involved in therapeutic interventions against a most important cardiovascular risk factor.