Spin-Vacancy-Induced Long-Range Order in a New Haldane-Gap Antiferromagnet

Magnetic susceptibility, high-field magnetization and inelastic neutron scattering experiments are used to study the magnetic properties of a new S=1 quasi-1-dimensional antiferromagnet PbNi2V2O8. Inter-chain interactions are shown to be almost, but not quite, strong enough to destroy the nonmagnetic singlet ground state and the energy gap in the magnetic excitation spectrum. Substituting nonmagnetic Mg$^{2+}$ (S=0) ions for Ni$^{2+}$ (S=1) induces a magnetically ordered state at low temperatures. To our knowledge this is the first observation of doping-induced long-range order in a Haldane-gap system.Comment: 5 pages including 4 figure

Tuning the spin Hamiltonian of NENP by external pressure: a neutron scattering study

We report an inelastic neutron scattering study of antiferromagnetic spin dynamics in the Haldane chain compound Ni(C2H8N2)2NO2ClO4 (NENP) under external hydrostatic pressure P = 2.5 GPa. At ambient pressure, the magnetic excitations in NENP are dominated by a long-lived triplet mode with a gap which is split by orthorhombic crystalline anisotropy into a lower doublet centered at $\Delta_\perp\approx$ 1.2meV and a singlet at $\Delta_\parallel\approx$ 2.5meV. With pressure we observe appreciable shifts in these levels, which move to $\Delta_\perp{(2.5GPa)}\approx$ 1.45 meV and $\Delta_\parallel(2.5GPa)\approx$ 2.2meV. The dispersion of these modes in the crystalline c-direction perpendicular to the chain was measured here for the first time, and can be accounted for by an interchain exchange J'_c approximately 3e-4*J which changes only slightly with pressure. Since the average gap value $\Delta_H\approx$ 1.64 meV remains almost unchanged with P, we conclude that in NENP the application of external pressure does not affect the intrachain coupling J appreciably, but does produce a significant decrease of the single-ion anisotropy constant from D/J = 0.16(2) at ambient pressure to D/J = 0.09(7) at P = 2.5 GPa.Comment: LaTeX file nenp_p.tex, 10 pages, 1 table, 5 figures. Submitted to Phys. Rev.

Zazie@60: some linguistic considerations

This article considers the colloquial language used in Zazie dans le métro from a sociolinguistic viewpoint. To the extent that a fictional work can be said to provide evidence of linguistic variation, Zazie offers glimpses into the pronunciation, grammar and vocabulary of French at the time it was written, as well as confirmation of other sources regarding social variation, notably working-class speech and the style dimension, partly in relation to regional variation, or rather its absence. For this reason, the novel remains a valuable point of reference for contemporary linguists. The novel, in conjunction with other works by Queneau, prompts further questions to do with the level of cognition at work when linguistic variation takes place

Renal ischemic preconditioning improves recovery of kidney function and decreases alpha-smooth muscle actin expression in a rat model

PURPOSE: We determined the role of ischemic preconditioning on renal function and histology in a rat model. MATERIALS AND METHODS: A total of 34 Sprague-Dawley rats (Janvier Laboratories, Le Genet-St-Isle, France) were divided into 6 groups, including sham operation, ischemic preconditioning alone (5 minutes of bilateral ischemia followed by 5 minutes of reperfusion for 3 cycles), ischemia alone (60 minutes of bilateral renal pedicle clamping), ischemic preconditioning before bilateral ischemia, ischemic preconditioning before ischemia in left nephrectomized rats and ischemic preconditioning of the left kidney alone before 60 minutes of bilateral warm ischemia to assess the effect of left kidney preconditioning on the contralateral kidney. Serum creatinine and malondialdehyde levels were recorded at days 0, 1, 3, 11 and 15. Kidneys were harvested at day 15 for histological study and alpha-smooth muscle actin typing. RESULTS: At days 1 and 3 serum creatinine and malondialdehyde levels were significantly lower in the ischemic preconditioning group compared to levels in the ischemia alone group. At days 11 and 15 creatinine and malondialdehyde levels were similar in all groups and comparable to levels at day 0. At day 15 ischemic preconditioning kidneys showed significantly decreased fibrosis and alpha-smooth muscle actin expression than ischemia alone kidneys. CONCLUSIONS: Ischemic preconditioning improves the ability of rat kidney to tolerate subsequent ischemic injury in the first 3 days after reperfusion. Moreover, fibrosis and alpha-smooth muscle actin expression are decreased in ischemic preconditioning kidneys 15 days after reperfusion, suggesting a potential interest of ischemic preconditioning in surgical situations that expose kidneys to prolonged warm ischemia

Genetic and Pharmacologic Inhibition of mTORC1 Promotes EMT by a TGF-β-independent mechanism

International audienceEpithelial-to-mesenchymal transition (EMT) is a transdifferentiation process that converts epithelial cells into highly motile mesenchymal cells. This physiologic process occurs largely during embryonic development but is aberrantly reactivated in different pathologic situations, including fibrosis and cancer. We conducted a siRNA screening targeted to the human kinome with the aim of discovering new EMT effectors. With this approach, we have identified mTOR complex 1 (mTORC1), a nutrient sensor that controls protein and lipid synthesis, as a key regulator of epithelial integrity. Using a combination of RNAi and pharmacologic approaches, we report here that inhibition of either mTOR or RPTOR triggers EMT in mammary epithelial cells. This EMT was characterized by the induction of the mesenchymal markers such as fibronectin, vimentin, and PAI-1, together with the repression of epithelial markers such as E-cadherin and ZO-3. In addition, mTORC1 blockade enhanced in vivo migratory properties of mammary cells and induced EMT independent of the TGF-β pathway. Finally, among the transcription factors known to activate EMT, both ZEB1 and ZEB2 were upregulated following mTOR repression. Their increased expression correlated with a marked reduction in miR-200b and miR-200c mRNA levels, two microRNAs known to downregulate ZEB1 and ZEB2 expression. Taken together, our findings unravel a novel function for mTORC1 in maintaining the epithelial phenotype and further indicate that this effect is mediated through the opposite regulation of ZEB1/ZEB2 and miR-200b and miR-200c. Furthermore, these results suggest a plausible etiologic explanation for the progressive pulmonary fibrosis, a frequent adverse condition associated with the therapeutic use of mTOR inhibitors