Speed of sound measurements in deuterium oxide (D 2 O) at temperatures between (276.97 and 363.15) K and at pressures up to 210 MPa

partially_open3embargoed_20211119Lago Simona, Giuliano Albo Paolo Alberto, Cavuoto GiuseppeLago, Simona; GIULIANO ALBO, PAOLO ALBERTO; Cavuoto, Giusepp

Speed of sound measurements in deuterium oxide (D2O) at temperatures between (276.97 and 363.15) K and at pressures up to 210 MPa

This paper presents speed of sound measurements in heavy water (deuterium oxide, ) along six isotherms between 276.97 K and 363.15 K for pressures up to 210 MPa using a double pulse-echo method. The experimental apparatus was validated measuring the speed of sound in ordinary water at ambient pressure and at temperatures between 295.5 K and 363.15 K with results found in agreement with values calculated from the reference equation of state for water by Wagner and Pruß within 0.005%. The relative combined expanded uncertainty of our speed of sound measurements, at a confidence level of 95%, is estimated to be less than 0.03% for pressures up to 10 MPa and in the order of 0.05% for pressures up to 210 MPa in the whole investigated temperature range. The speed of sound results have been compared with values calculated from the reference equation for heavy water the IAPS84 Formulation by Hill et al. (1982), and with the prediction of the newly developed equation of state for heavy water by Herrig et al. (2018). The relative deviations of these comparison were found to be consistent with the reference equations within their combined uncertainty. The results presented here were also compared with the most recent data by Wegge et al. and found to be in agreement within 0.05%

The late MIS 5 Mediterranean tephra markers: A reappraisal from peninsular Italy terrestrial records

We present new tephrostratigraphic records from the late MIS 5 (ca 110e80 ka) terrestrial sediments from southern and central Italy. On the one hand, the central Italy record consists of an outcropping lacustrine sequence from the Sulmona intermountain basin that contains four trachyticephonolitic tephra layers (POP3, POP2a, POP2b, POP1), all of which show a K-alkaline affinity that is typical for the Roman co-magmatic Province. The POP3 and POP1 layers were dated by 40Ar/39Ar method at 106.2 1.3 ka (2s) and 92.4 4.6 ka (2s), respectively. The sequence in southern Italy, on the other hand, is represented by post-Tyrrhenian coastal deposits of the Cilento area, Campania, which contain two trachytic layers (CIL2, CIL1) that show the same K-alkaline affinity. Based on their chemical compositions and radiometric ages, POP3 and POP1 are firmly correlated with the marine tephra layers X-5 (105 2 ka) and C-22 (ca 90 ka), which, in turn, match tephras TM-25 and TM-23-11, respectively, in the lacustrine sequence of Lago Grande di Monticchio (southern Italy). Of note, the POP1 layer also matches the Adriatic Sea tephra PRAD 2517 that was previously correlated with the older X-5 layer. The tephra couplet POP2a and POP2b (ca 103 and 103.5 ka, extrapolated ages) are compatible with the TM- 24b and TM-24-3 tephras in Monticchio, which match both the stratigraphic positions and the chemical compositions. In the Cilento area, as well as the already described X-6 layer (ca 108 ka) (CIL2), we recognise a new stratigraphic superimposed layer (CIL1) that matches the POP3/TM-25/C-27/X-5 Mediterranean marker(s). In summary, the data presented here provide new chemical and 40Ar/39Ar chronological constraints towards a robust late MIS 5 tephrostratigraphy of the central Mediterranean, although at the same time, they also reveal how the tephrostratigraphy itself might be flawed when dealing with tephra markers that are not adequately constrained and characterised.Published31-451V. Storia eruttivaJCR Journa

Effects of Cannabinoids on Caffeine Contractures in Slow and Fast Skeletal Muscle Fibers of the Frog

The effect of cannabinoids on caffeine contractures was investigated in slow and fast skeletal muscle fibers using isometric tension recording. In slow muscle fibers, WIN 55,212-2 (10 and 5 μM) caused a decrease in tension. These doses reduced maximum tension to 67.43 ± 8.07% (P = 0.02, n = 5) and 79.4 ± 14.11% (P = 0.007, n = 5) compared to control, respectively. Tension-time integral was reduced to 58.37 ± 7.17% and 75.10 ± 3.60% (P = 0.002, n = 5), respectively. Using the CB1 cannabinoid receptor agonist ACPA (1 μM) reduced the maximum tension of caffeine contractures by 68.70 ± 11.63% (P = 0.01, n = 5); tension-time integral was reduced by 66.82 ± 6.89% (P = 0.02, n = 5) compared to controls. When the CB1 receptor antagonist AM281 was coapplied with ACPA, it reversed the effect of ACPA on caffeine-evoked tension. In slow and fast muscle fibers incubated with the pertussis toxin, ACPA had no effect on tension evoked by caffeine. In fast muscle fibers, ACPA (1 μM) also decreased tension; the maximum tension was reduced by 56.48 ± 3.4% (P = 0.001, n = 4), and tension-time integral was reduced by 57.81 ± 2.6% (P = 0.006, n = 4). This ACPA effect was not statistically significant with respect to the reduction in tension in slow muscle fibers. Moreover, we detected the presence of mRNA for the cannabinoid CB1 receptor on fast and slow skeletal muscle fibers, which was significantly higher in fast compared to slow muscle fiber expression. In conclusion, our results suggest that in the slow and fast muscle fibers of the frog cannabinoids diminish caffeine-evoked tension through a receptor-mediated mechanism

A global characterization of the translational and transcriptional programs induced by methionine restriction through ribosome profiling and RNA-seq

Background: Among twenty amino acids, methionine has a special role as it is coded by the translation initiation codon and methionyl-tRNAi (Met-tRNAi) is required for the assembly of the translation initiation complex. Thus methionine may play a special role in global gene regulation. Methionine has also been known to play important roles in cell growth, development, cancer, and aging. In this work, we characterize the translational and transcriptional programs induced by methionine restriction (MetR) and investigate the potential mechanisms through which methionine regulates gene expression, using the budding yeast S. cerevisiae as the model organism. Results: Using ribosomal profiling and RNA-seq, we observed a broad spectrum of gene expression changes in response to MetR and identified hundreds of genes whose transcript level and/or translational efficiency changed significantly. These genes show clear functional themes, suggesting that cell slows down its growth and cell cycle progression and increases its stress resistance and maintenance in response to MetR. Interestingly, under MetR cell also decreases glycolysis and increases respiration, and increased respiration was linked to lifespan extension caused by caloric restriction. Analysis of genes whose translational efficiency changed significantly under MetR revealed different modes of translational regulation: 1) Ribosome loading patterns in the 5'UTR and coding regions of genes with increased translational efficiency suggested mechanisms both similar and different from that for the translational regulation of Gcn4 under general amino acid starvation condition; 2) Genes with decreased translational efficiency showed strong enrichment of lysine, glutamine, and glutamate codons, supporting the model that methionine can regulate translation by controlling tRNA thiolation. Conclusions: MetR induced a broad spectrum of gene expression changes at both the transcriptional and translational levels, with clear functional themes indicative of the physiological state of the cell under MetR. Different modes of translational regulation were induced by MetR, including the regulation of the ribosome loading at 5'UTR and regulation by tRNA thiolation. Since MetR extends the lifespan of many species, the list of genes we identified in this study can be good candidates for studying the mechanisms of lifespan extension.National Institutes of Health [AG043080]SCI(E)ARTICLE1

Alterations to Melanocortinergic, GABAergic and Cannabinoid Neurotransmission Associated with Olanzapine-Induced Weight Gain

Background/Aim: Second generation antipsychotics (SGAs) are used to treat schizophrenia but can cause serious metabolic side-effects, such as obesity and diabetes. This study examined the effects of low to high doses of olanzapine on appetite/ metabolic regulatory signals in the hypothalamus and brainstem to elucidate the mechanisms underlying olanzapineinduced obesity. Methodology/Results: Levels of pro-opiomelanocortin (POMC), neuropeptide Y (NPY) and glutamic acid decarboxylase (GAD65, enzyme for GABA synthesis) mRNA expression, and cannabinoid CB1 receptor (CB1R) binding density (using [ 3 H]SR-141716A) were examined in the arcuate nucleus (Arc) and dorsal vagal complex (DVC) of female Sprague Dawley rats following 0.25, 0.5, 1.0 or 2.0 mg/kg olanzapine or vehicle (36/day, 14-days). Consistent with its weight gain liability, olanzapine significantly decreased anorexigenic POMC and increased orexigenic NPY mRNA expression in a dose-sensitive manner in the Arc. GAD65 mRNA expression increased and CB1R binding density decreased in the Arc and DVC. Alterations to neurotransmission signals in the brain significantly correlated with body weight and adiposity. The minimum dosage threshold required to induce weight gain in the rat was 0.5 mg/kg olanzapine. Conclusions: Olanzapine-induced weight gain is associated with reduced appetite-inhibiting POMC and increased NPY. This study also supports a role for the CB1R and GABA in the mechanisms underlying weight gain side-effects, possibly b