DaDoEval @ EVALITA 2020: Same-genre and cross-genre dating of historical documents

In this paper we introduce the DaDoEval shared task at EVALITA 2020, aimed at automatically assigning temporal information to documents written in Italian. The evaluation exercise comprises three levels of temporal granularity, from coarse-grained to year-based, and includes two types of test sets, either having the same genre of the training set, or a different one. More specifically, DaDoEval deals with the corpus of Alcide De Gasperi's documents, providing both public documents and letters as test sets. Two systems participated in the competition, achieving results always above the baseline in all subtasks. As expected, coarse-grained classification into five periods is rather easy to perform automatically, while the year-based one is still an unsolved problem also due to the lack of enough training data for some years. Results showed also that, although De Gasperi's letters in our test set were written in standard Italian and in a style which was not too colloquial, cross-genre classification yields remarkably lower results than the same-genre setting

Electrocardiographic Observations Regarding Transfusions in Geriatrics

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Pre-torsors and Galois comodules over mixed distributive laws

We study comodule functors for comonads arising from mixed distributive laws. Their Galois property is reformulated in terms of a (so-called) regular arrow in Street's bicategory of comonads. Between categories possessing equalizers, we introduce the notion of a regular adjunction. An equivalence is proven between the category of pre-torsors over two regular adjunctions $(N_A,R_A)$ and $(N_B,R_B)$ on one hand, and the category of regular comonad arrows $(R_A,\xi)$ from some equalizer preserving comonad ${\mathbb C}$ to $N_BR_B$ on the other. This generalizes a known relationship between pre-torsors over equal commutative rings and Galois objects of coalgebras.Developing a bi-Galois theory of comonads, we show that a pre-torsor over regular adjunctions determines also a second (equalizer preserving) comonad ${\mathbb D}$ and a co-regular comonad arrow from ${\mathbb D}$ to $N_A R_A$, such that the comodule categories of ${\mathbb C}$ and ${\mathbb D}$ are equivalent.Comment: 34 pages LaTeX file. v2: a few typos correcte

Calcium-activated chloride currents in olfactory sensory neurons from mice lacking bestrophin-2

none8noOlfactory sensory neurons use a chloride-based signal amplification mechanism to detect odorants. The binding of odorants to receptors in the cilia of olfactory sensory neurons activates a transduction cascade that involves the opening of cyclic nucleotide-gated channels and the entry of Ca2+ into the cilia. Ca2+ activates a Cl- current that produces an efflux of Cl- ions and amplifies the depolarization. The molecular identity of Ca2+-activated Cl- channels is still elusive, although some bestrophins have been shown to function as Ca2+ -activated Cl- channels when expressed in heterologous systems. In the olfactory epithelium, bestrophin-2 (Best2) has been indicated as a candidate for being a molecular component of the olfactory Ca2+-activated Cl- channel. In this study, we have analysed mice lacking Best2. We compared the electrophysiological responses of the olfactory epithelium to odorant stimulation, as well as the properties of Ca2+-activated Cl- currents in wild-type (WT) and knockout (KO) mice for Best2. Our results confirm that Best2 is expressed in the cilia of olfactory sensory neurons, while odorant responses and Ca2+ -activated Cl- currents were not significantly different between WT and KO mice. Thus, Best2 does not appear to be the main molecular component of the olfactory channel. Further studies are required to determine the function of Best2 in the cilia of olfactory sensory neurons. © 2009 The Authors. Journal compilation © 2009 The Physiological Society.openPifferi S.; Dibattista M.; Sagheddu C.; Boccaccio A.; Al Qteishat A.; Ghirardi F.; Tirindelli R.; Menini A.Pifferi, S.; Dibattista, M.; Sagheddu, C.; Boccaccio, A.; Al Qteishat, A.; Ghirardi, F.; Tirindelli, R.; Menini, A

Increased tumor necrosis factor alpha-converting enzyme activity induces insulin resistance and hepatosteatosis in mice

Tumor necrosis factor alpha-converting enzyme (TACE, also known as ADAM17) was recently involved in the pathogenesis of insulin resistance. We observed that TACE activity was significantly higher in livers of mice fed a high-fat diet (HFD) for 1 month, and this activity was increased in liver > white adipose tissue > muscle after 5 months compared with chow control. In mouse hepatocytes, C(2)C(12) myocytes, and 3T3F442A adipocytes, TACE activity was triggered by palmitic acid, lipolysaccharide, high glucose, and high insulin. TACE overexpression significantly impaired insulin-dependent phosphorylation of AKT, GSK3, and FoxO1 in mouse hepatocytes. To test the role of TACE activation in vivo, we used tissue inhibitor of metalloproteinase 3 (Timp3) null mice, because Timp3 is the specific inhibitor of TACE and Timp3(-/-) mice have higher TACE activity compared with wild-type (WT) mice. Timp3(-/-) mice fed a HFD for 5 months are glucose-intolerant and insulin-resistant; they showed macrovesicular steatosis and ballooning degeneration compared with WT mice, which presented only microvesicular steatosis. Shotgun proteomics analysis revealed that Timp3(-/-) liver showed a significant differential expression of 38 proteins, including lower levels of adenosine kinase, methionine adenosysltransferase I/III, and glycine N-methyltransferase and higher levels of liver fatty acid-binding protein 1. These changes in protein levels were also observed in hepatocytes infected with adenovirus encoding TACE. All these proteins play a role in fatty acid uptake, triglyceride synthesis, and methionine metabolism, providing a molecular explanation for the increased hepatosteatosis observed in Timp3(-/-) compared with WT mice. Conclusion: We have identified novel mechanisms, governed by the TACE-Timp3 interaction, involved in the determination of insulin resistance and liver steatosis during overfeeding in mice

TMEM16A calcium-activated chloride currents in supporting cells of the mouse olfactory epithelium

Glial-like supporting (or sustentacular) cells are important constituents of the olfactory epithelium that are involved in several physiological processes such as production of endocannabinoids, insulin, and ATP and regulation of the ionic composition of the mucus layer that covers the apical surface of the olfactory epithelium. Supporting cells express metabotropic P2Y purinergic receptors that generate ATP-induced Ca2+ signaling through the activation of a PLC-mediated cascade. Recently, we reported that a subpopulation of supporting cells expresses also the Ca2+-activated Cl- channel TMEM16A. Here, we sought to extend our understanding of a possible physiological role of this channel in the olfactory system by asking whether Ca2+ can activate Cl- currents mediated by TMEM16A. We use whole-cell patch-clamp analysis in slices of the olfactory epithelium to measure dose-response relations in the presence of various intracellular Ca2+ concentrations, ion selectivity, and blockage. We find that knockout of TMEM16A abolishes Ca2+-activated Cl- currents, demonstrating that TMEM16A is essential for these currents in supporting cells. Also, by using extracellular ATP as physiological stimuli, we found that the stimulation of purinergic receptors activates a large TMEM16A-dependent Cl- current, indicating a possible role of TMEM16A in ATP-mediated signaling. Altogether, our results establish that TMEM16A-mediated currents are functional in olfactory supporting cells and provide a foundation for future work investigating the precise physiological role of TMEM16A in the olfactory system

TMEM16A and TMEM16B modulate pheromone-evoked action potential firing in mouse vomeronasal sensory neurons

The mouse vomeronasal system controls several social behaviors. Pheromones and other social cues are detected by sensory neurons in the vomeronasal organ (VNO). Stimuli activate a transduction cascade that leads to membrane potential depolarization, increase in cytosolic Ca2+ level, and increased firing. The Ca2+-activated chloride channels TMEM16A and TMEM16B are co-expressed within microvilli of vomeronasal neurons, but their physiological role remains elusive. Here, we investigate the contribution of each of these channels to vomeronasal neuron firing activity by comparing wild-type (WT) and knock-out (KO) mice. Performing loosepatch recordings from neurons in acute VNO slices, we show that spontaneous activity is modified by Tmem16a KO, indicating that TMEM16A, but not TMEM16B, is active under basal conditions. Upon exposure to diluted urine, a rich source of mouse pheromones, we observe significant changes in activity. Vomeronasal sensory neurons (VSNs) from Tmem16a cKO and Tmem16b KO mice show shorter interspike intervals (ISIs) compared with WT mice, indicating that both TMEM16A and TMEM16B modulate the firing pattern of pheromone-evoked activity in VSNs

A Role for STOML3 in Olfactory Sensory Transduction

Stomatin-like protein-3 (STOML3) is an integral membrane protein expressed in the cilia of olfactory sensory neurons, but its functional role in this cell type has never been addressed. STOML3 is also expressed in dorsal root ganglia neurons, where it has been shown to be required for normal touch sensation. Here, we extended previous results indicating that STOML3 is mainly expressed in the knob and proximal cilia of olfactory sensory neurons. We additionally showed that mice lacking STOML3 have a morphologically normal olfactory epithelium. Due to its presence in the cilia, together with known olfactory transduction components, we hypothesized that STOML3 could be involved in modulating odorant responses in olfactory sensory neurons. To investigate the functional role of STOML3, we performed loose patch recordings from wild type and Stoml3 KO olfactory sensory neurons. We found that spontaneous mean firing activity was lower with additional shift in interspike intervals distributions in Stoml3 KOs compared to wild type neurons. Moreover, the firing activity in response to stimuli was reduced both in spike number and duration in neurons lacking STOML3 compared to wildtype neurons. Control experiments suggested that the primary deficit in neurons lacking STOML3 was at the level of transduction and not at the level of action potential generation. We conclude that STOML3 has a physiological role in olfaction, being required for normal sensory encoding by olfactory sensory neurons.Significance Statement Olfactory transduction comprises a series of well-characterized molecular steps that take place in the cilia of olfactory sensory neurons (OSNs) terminating in action potential firing. Here, we introduce a possible new player: stomatin-like protein 3 (STOML3). Indeed, STOML3 is localized in olfactory cilia, and we show that STOML3 plays a role in OSN physiology. First, it allows OSNs to broaden the possible frequency range of their spontaneous activity. Second, STOML3 modulates odorant-evoked action potential firing by regulating both the number of spikes and response duration. These new findings call for a reconsideration of the patterns of the peripheral coding of sensory stimuli

CARACTERIZAÇÃO QUÍMICA DE ÓLEOS ESSENCIAIS DE PLANTAS MEDICINAIS

Os óleos essenciais são substâncias naturais de grande importância econômica, sendo utilizados como medicamentos, perfumarias, alimentos e cosméticos. São obtidos por diferentes métodos de extração e encontrados em diferentes partes das plantas. Desta forma o trabalho teve como objetivo a coleta, preparação e a extração do óleo essencial de várias espécies realizada através de hidrodestilação durante 4 horas utilizando o aparelho Clevenger. Foi avaliado o rendimento de extração do óleo essencial e a sua composição química por cromatografia a gás com detectores FID e Espectrometria de Massas. A identificação dos constituintes dos óleos essênciais foi realizada através de comparação com dados da biblioteca do equipamento de Espectrometria de Massas e os cálculos do Índice de Kovats. Os teores em % (massa/massa) dos óleo essenciais foram: alecrim 1,13%, levante 0,58%, manjericão 0,24%, hortelã 0,25% e hortelã pimenta 0,75%. Foram identificados vários compostos majoritários tais como:alfa-pineno, o-cimene, germacreno-D, Linalol, Acetato de linalila e cariofileno