Room temperature saturation magnetization (M(S)) of Fe(89-x-y)Co(

Room temperature saturation magnetization (M(S)) of Fe(89-x-y)Co(y)B(x)Zr(11) alloys not only increases from 93 to 127 emu/g in the amorphous state upon Co substitution, but also enhances to 173 emu/g with MFA. Coercivity (H(C)) increases significantly when annealed up to 673 K and decreases slightly beyond 673 K. All samples annealed at 923 K showed large H(C) (> 100 Oe) due to the formation of Fe(Co)-Zr compounds. Large M(S) (173 emu/g) and low H(C) (0.4 Oe) were obtained for an Fe(69)Co(10)B(10)Zr(11) alloy annealed at 823 K. Lorentz microscopy results reveal that the average size of the domains decreases with increasing Co content and magnetic ripple structures are observed in samples

annealed above 823 K. The observed enhancement in magnetic softness is correlated with the microstructure and magnetic domain structure. www.selleckchem.com/ALK.html (C) 2011 American Institute of Physics. [doi: 10.1063/1.3533256]“
“Epidemiological evidence links exposure to stressful life events with increased risk for mental illness. However, there is significant individual variability in vulnerability to environmental risk factors, and genetic variation is thought to play a major role in determining who will become ill. Several studies have shown, for example, that individuals carrying the S (short) allele of the serotonin transporter (5-HTT) gene-linked polymorphic region (5-HTTLPR) have selleckchem an increased

risk for major depression following exposure to stress in adulthood. Identifying the molecular mechanisms underlying this gene-by-environment risk factor could help our understanding of the individual differences in resilience to stress. Here, we present a mouse model of the 5-HTT-by-stress risk factor. Wild-type and heterozygous 5-HTT knockout male mice were subjected to three weeks of chronic psychosocial stress. The 5-HTT genotype did not affect the physiological consequences of stress as measured by changes in body temperature, body weight gain and plasma corticosterone. However, when compared with wild-type littermates, heterozygous

5-HTT knockout mice experiencing high levels of stressful life events showed significantly depressed locomotor LY2228820 supplier activity and increased social avoidance toward an unfamiliar male in a novel environment. Heterozygous 5-HTT knockout mice exposed to high stress also showed significantly lower levels of serotonin turnover than wild-type littermates, selectively in the frontal cortex, which is a structure that is known to control fear and avoidance responses, and that is implicated in susceptibility to depression. These data may serve as a useful animal model for better understanding the increased vulnerability to stress reported in individuals carrying the 5-HTTLPR S allele, and suggest that social avoidance represents a behavioral endophenotype of the interaction between 5-HTT and stress.

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