88 research outputs found
La congiunzione âeâ nei processi di riconciliazione. Riflessioni alla luce della filosofia di Franz Rosenzweig
Reconciliation presents three dimensions in which the conjunction âandâ â as Rosenzweig conceives it â constitutes a fundamental category: on one hand, it has a temporal dimension, as it is a process in which the old and the new are combined, and where the âandâ expresses the present that unites; on the other hand, it has a dimension of otherness as a relationship between an âIâ and an âotherâ, a relationship where the âandâ is the language. Finally, there is in reconciliation a dimension of reparation (tikkun olam) or return to the alliance with the Good, that is expressed in a peace (shalom) that is the fulfilling of the divine promise: that of the peace between the man âandâ the world. God is the âandâ that fulfils the aspiration to mundane happiness âandâ human fullness. These three dimensions, analysed in the light of Rosenzweigâs thought, introduce new keys to the reconciliation process that today constitute an urgent task
I Congreso internacional de la Red española de FilosofĂa Los retos de la filosofĂa en el siglo XXI
Reseña del I Congreso internacional de la Red española de FilosofĂa Los retos de la filosofĂa en el siglo XXI, p. 361
A propĂłsito de Butler: una fenomenologĂa del cuerpo vivido, narrado y representado
In this paper we take Judith Butlerâs thinking as a basis from which to consider the ideas of three authors. In our view, these authors complement Butlerâs project of helping excluded people to fight for a dignified life, a âliveable lifeâ; and specifically to the idea of using performative resignifications of discourses and practices. On one hand, we present the writings of Sarah Ahmed and Lanei Rodemeyer; they consider the spatiality and temporality of the lived body (Ahmed) and the relationship between the lived body and discourse (Rodemeyer). In both cases, âpure phenomenologyâ (and not hermeneutics) is applied to the question of sexual diversity. On the other hand, we delve into the works of Louise Bourgeois, for whom artistic creation is a way of exorcising pain and becoming free of socially constructed prisons. Starting from the paths opened by these authors, we believe that a phenomenology is possible in which there is place for what does not fit into the norm. this phenomenology would make it possible, on one side, to rend visibility to those who do not fit into the established norms and categories and, on another side, to contribute to a reformulation of discourse, such a transformation that allows the excluded to inhabit them. âPureâ phenomenology, that aims at going to âthe things themselvesâ do not naturalise oppressions, but it is rather an ally to recognise, denounce and provide a reparation for them.En este artĂculo partimos del pensamiento de Butler para adentrarnos en las propuestas de tres autoras que consideramos que complementan su proyecto de ayudar a las personas excluidas en su lucha por una vida mĂĄs digna, una vida âvivibleâ, asĂ como la estrategia de lograrlo mediante resignificaciones performativas de discursos y prĂĄcticas. Por un lado, presentamos los trabajos de Sarah Ahmed y Lanei Rodemeyer, para atender a la espacialidad y temporalidad del cuerpo vivido (Ahmed), y a la relaciĂłn entre el cuerpo y el discurso (Rodemeyer). En ambos casos se aplica la fenomenologĂa pura, no hermenĂ©utica, a la cuestiĂłn de la diversidad sexual. Por otro lado, nos adentramos en las obras de Luise Bourgeois, para quien la creaciĂłn artĂstica es un modo de exorcizar el dolor y de liberarse de las cĂĄrceles socialmente construidas. Partiendo de la lĂnea que recorren y abren estas autoras, creemos que se puede elaborar una fenomenologĂa en la que quepa lo que se suele quedar en los mĂĄrgenes. Esta fenomenologĂa permitirĂa, por un lado, visibilizar a quienes no encajan en los conceptos y categorĂas establecidas, y por otro, contribuir a una reformulaciĂłn de los discursos que les permita habitar en ellos. La fenomenologĂa de las cosas mismas no naturaliza las opresiones, como podrĂa sospecharse, creemos que mĂĄs bien es una aliada para reconocerlas, denunciarlas y repararlas
Vida precaria y sexualidad. Elementos para una Ă©tica sexual
In this paper we explore the possibilities of a sexual ethics that responds to our times of precariousness. We sustain that the task of a reconsidered sexual ethics can contribute to a more livable life for persons rendered fragile beyond our constitutive embodied fragility. Thus, we connect Judith Butler with 20th century dialogical philosophies as well as with some analysis on sexuality and ethics in authors like Thomas Nagel and Margaret Farley. In all this a key category will be that of justice.En este trabajo exploramos las posibilidades de una Ă©tica sexual que responda a tiempos de precariedad. Defendemos que la tarea de una Ă©tica sexual repensada puede contribuir a una vida mĂĄs vivible para personas fragilizadas mĂĄs allĂĄ de nuestra vulnerabilidad constitutiva por tener cuerpo. Ponemos en interlocuciĂłn a Judith Butler con la filosofĂa dialĂłgica del siglo XX y los anĂĄlisis sobre sexualidad y Ă©tica de Thomas Nagel y Margaret Farley. En todo ello, una categorĂa clave serĂĄ la justicia
Premature Birth Infants Present Elevated Inflammatory Markers in the Meconium
Introduction: Prematurity, a well-established risk factor for various intestinal diseases
in newborns, results in increased morbidity and mortality. However, the intestinal
inflammatory status of preterm (PT) infants has been poorly characterized. Here we have
broadly described the intestinal and systemic inflammatory status of PT children.
Materials and Methods: Meconium and plasma from 39 PT and 32 full term (T)
newborns were studied. Fecal calprotectin, polymorphonuclear leukocyte elastase
(PMN-E), TNF, IL-17A, IL-8, IP-10, MCP-1, MIP-1, IL-1ÎČ, IL-1α, and E-selectin and
the enzymatic activities of myeloperoxidase (MPO) and alkaline phosphatase (AP) in
meconium were measured. Plasma levels of AP, hepatocyte growth factor, nerve growth
factor (NGF), proinflammatory cytokines, leptin, adiponectin, PAI-1, and resistin were also
determined. Correlations with gestational age (GA) and birth weight (BW) were studied.
Results: Neutrophil derived PMN-E, MPO and calprotectin were increased in the
meconium of PT compared to T newborns, while AP was decreased. No significant
differences were found in other inflammatory parameters. Considering data from all
children, GA and BW showed inverse correlation with neutrophil markers, while AP
directly correlated with BW. Plasma levels of IL-1ÎČ and NGF were enhanced in PT infants,
and were also negatively correlated with BW. PT children additionally showed neutropenia
and decreased adiponectin, leptin, haematocrit, and haemoglobin. These parameters
(neutrophils, adiponectin, and so forth) were positively correlated with GA and BW, while
IL-8, MCP-1, PAI-1, and plasma AP were negatively correlated. PT children showing
postnatal morbidity exhibited increased meconium MPO and MIP-1α.
Conclusion: PT neonates present a significant elevation of intestinal inflammatory
parameters, characterized by the presence of neutrophil markers, associated with mild
systemic inflammation.Ministry of Economy and CompetitivityEuropean Commission
SAF2017-88457-R
AGL2017-85270-R
BFU2014-57736-P
AGL2014-58883-RJunta de Andalucia
CTS235
CTS164University of Granada (Contrato Puente Program-Plan Propio)Ministry of Education [Spain]Instituto de Salud Carlos III
European Commissio
Clinical outcomes after CPX-351 in patients with high-risk acute myeloid leukemia: A comparison with a matched cohort from the Spanish PETHEMA registry
Acute myeloid leukemia; Clinical observations; Intensive chemotherapyLeucemia mieloide aguda; Observaciones clĂnicas; Quimioterapia intensivaLeucĂšmia mieloide aguda; Observacions clĂniques; QuimioterĂ pia intensivaBackground
CPX-351 is approved for the treatment of therapy related acute myeloid leukemia (t-AML) and AML with myelodysplastic related changes (MRC-AML). The benefits of this treatment over standard chemotherapy has not been addressed in well matched cohorts of real-life patients.
Methods
Retrospective analysis of AML patients treated with CPX-351 as per routine practice. A propensity score matching (PSM) was used to compare their main outcomes with those observed in a matched cohort among 765 historical patients receiving intensive chemotherapy (IC), all of them reported to the PETHEMA epidemiologic registry.
Results
Median age of 79 patients treated with CPX-351 was 67âyears old (interquartile range 62â71), 53 were MRC-AML. The complete remission (CR) rate or CR without recovery (CRi) after 1 or 2âcycles of CPX-351 was 52%, 60-days mortality 18%, measurable residual disease <0.1% in 54% (12 out of 22) of them. Stem cell transplant (SCT) was performed in 27 patients (34%), median OS was 10.3âmonths, and 3-year relapse incidence was 50%. Using PSM, we obtained two comparable cohorts treated with CPX-351 (nâ=â52) or IC (nâ=â99), without significant differences in CR/CRi (60% vs. 54%) and median OS (10.3âmonths vs. 9.1âmonths), although more patients were bridged to SCT in the CPX-351 group (35% vs. 12%). The results were confirmed when only 3â+â7 patients were included in the historical cohort. In multivariable analyses, SCT was associated with better OS (HR 0.33 95% CI: 0.18â0.59), pâ<â0.001.
Conclusion
Larger post-authorization studies may provide evidence of the clinical benefits of CPX-351 for AML in the real-life setting.This study was funded in part by a research grant from the Jazz Pharmaceuticals
Leptin-resistant Zucker rats with trinitrobenzene sulfonic acid colitis present a reduced inflammatory response but enhanced epithelial damage
The study was funded the following grants of the Ministerio de EconomĂa y Competitividad and the Fondo Europeo de Desarrollo Regional FEDER (SAF2011-22922, SAF2011-22812, BFU2014- 57736-P, and AGL2014-58883-R) and Junta de AndalucĂa (CTS164, CTS235, and CTS6736). B. Rivero-Guti errez, R. GĂĄmez-Belmonte, and M. Arredondo-Amador were supported by fellowships from the Ministerio de EducaciĂłn.The role of leptin in the development of intestinal inflammation remains controversial, since proinflammatory and anti-inflammatory
effects have been described. This study describes the effect of the absence of leptin signaling in intestinal inflammation.
Experimental colitis was induced by intrarectal administration of trinitrobenzene sulfonic acid (TNBS) to lean and obese Zucker
rats (n = 10). Effects on inflammation and mucosal barrier were studied. Bacterial translocation and LPS concentration were evaluated
together with colonic permeability to 4-kDa FITC-dextran. Obese Zucker rats showed a lower intestinal myeloperoxidase
and alkaline phosphatase activity, reduced alkaline phosphatase sensitivity to levamisole, and diminished colonic expression of
Nos2, Tnf, and Il6, indicating attenuated intestinal inflammation, associated with attenuated STAT3, AKT, and ERK signaling in
the colonic tissue. S100a8 and Cxcl1 mRNA levels were maintained, suggesting that in the absence of leptin signaling neutrophil
activation rather than infiltration is hampered. Despite the lower inflammatory response, leptin resistance enhanced intestinal
permeability, reflecting an increased epithelial damage. This was shown by augmented LPS presence in the portal vein of colitic
obese Zucker rats, associated with induction of tissue nonspecific alkaline phosphatase, LPS-binding protein, and CD14 hepatic
expression (involved in LPS handling). This was linked to decreased ZO-1 immunoreactivity in tight junctions and lower occludin
expression. Our results indicate that obese Zucker rats present an attenuated inflammatory response to TNBS, but increased intestinal epithelial damage allowing the passage of bacterial antigens.Ministerio de EconomĂa y Competitividad and the Fondo Europeo de Desarrollo Regional FEDER (SAF2011-22922, SAF2011-22812, BFU2014- 57736-P, and AGL2014-58883-R)Junta de AndalucĂa (CTS164, CTS235, and CTS6736)Ministerio de EducaciĂł
Green Alga Ulva spp. Hydrolysates and Their Peptide Fractions Regulate Cytokine Production in Splenic Macrophages and Lymphocytes Involving the TLR4-NFkB/MAPK Pathways
Hydrolysates of food protein sources have immunomodulatory effects, which are of interest
for use as functional foods. In this study, we have characterized the immune regulatory effect
on rat splenocytes, macrophages and T lymphocytes of Ulva spp. hydrolysates and their peptide
fractions with or without in vitro gastrointestinal digestion and/or ultrafiltration. IL-10 was induced
in almost all conditions and cell types obtained from wild type animals. The induction was in
general increased by ultrafiltration and in vitro gastrointestinal digestion. TNF was also induced in
basal conditions. In turn, TNF and IFN-
production was attenuated by the hydrolysate products
in lipopolysaccharide or concanavalin A immune stimulated cells. Inhibitors for the activation
of NF B, MAPK p38 and JNK inhibited IL-10 induction in rat splenocytes. The response was
dramatically attenuated in TLR4-/- cells, and only modestly in TLR2-/- cells. Food peptides
from Ulva spp. genus exert anti-inflammatory effects in immune cells mediated by TLR4 and NF B.
Similarity with the immunomodulatory profile of protein hydrolysates from other sources suggests a
common mechanism.This work was supported by funds from the Ministry of Economy and Competitivity, partly with
Fondo Europeo de Desarrollo Regional FEDER funds [SAF2017-88457-R, AGL2017-85270-R, BFU2014-57736-P,
AGL2014-58883-R] and by Junta de AndalucĂa [CTS235, CTS164]. C.H.-C. and R.G.-B. were supported by
the University of Granada (Contrato Puente ProgramâPlan Propio) and the Ministry of Education [Spain],
respectively. CIBERehd is funded by Instituto de Salud Carlos III
Deficiency in Tissue Non-Specific Alkaline Phosphatase Leads to Steatohepatitis in Mice Fed a High Fat Diet Similar to That Produced by a Methionine and Choline Deficient Diet
Funding: This research was funded by the Ministry of Economy and Competitivity of Spain, partly
with Fondo Europeo de Desarrollo Regional FEDER funds [BFU2014-57736-P, AGL2014-58883-R,
SAF2017-88457-R, AGL2017-85270-R] and by Junta de AndalucĂa [CTS235, CTS164]. MTG, RGB
and CHC were supported by fellowships from the Ministry of Education. CIBERehd is funded by
Instituto de Salud Carlos III.
Institutional Review Board Statement: The study was conducted according to the guidelines of the
Guide for the Care and Use of Laboratory Animals, and approved by the Animal Welfare Committee
of the University of Granada (registry number: CEEA 01/03/2017â029).
Informed Consent Statement: Not applicable for studies not involving humans.
Acknowledgments: We gratefully acknowledge the assistance of Mercedes GonzĂĄlez and the rest of
the group.The liver expresses tissue-nonspecific alkaline phosphatase (TNAP), which may participate in the defense against bacterial components, in cell regulation as part of the purinome or in bile secretion, among other roles. We aimed to study the role of TNAP in the development of hepatosteatosis. TNAP+/â haplodeficient and wild type (WT) mice were fed a control diet (containing 10% fat w/w) or the same diet deficient in methionine and choline (MCD diet). The MCD diet induced substantial weight loss together with hepatic steatosis and increased alanine aminotransferase (ALT) plasma levels, but no differences in IL-6, TNF, insulin or resistin. There were no substantial differences between TNAP+/â and WT mice fed the MCD diet. In turn, TNAP+/â mice receiving the control diet presented hepatic steatosis with alterations in metabolic parameters very similar to those induced by the MCD diet. Nevertheless, no weight loss, increased ALT plasma levels or hypoglycemia were observed. These mice also presented increased levels of liver TNF and systemic resistin and glucagon compared to WT mice. The phenotype of TNAP+/â mice fed a standard diet was normal. In conclusion, TNAP haplodeficiency induces steatosis comparable to that produced by a MCD diet when fed a control diet.Ministry of Economy and Competitivity of SpainEuropean Commission
BFU2014-57736-P
AGL2014-58883-R
SAF2017-88457-R
AGL2017-85270-RJunta de Andalucia
CTS235
CTS164Ministry of EducationInstituto de Salud Carlos III
European Commissio
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