A new species of Cololejeunea (Lejeuneaceae: Cololejeuneoideae) from Panama

A new species of Cololejeunea section Protocolea, is described from Cerro Fábrega in Panama. The diagnostic characteristics of C. tixierii are lobes ovate-lanceolate, lobules never inflate but explanate or folded without forming a keel, reaching about half of the lobe length and perianth only faintly keeled at maturity

The role of three-nucleon potentials within the shell model: past and present

We survey the impact of nuclear three-body forces on structure properties of nuclei within the shell model. It has long been acknowledged, since the seminal works of Zuker and coworkers, that three-body forces play a fundamental role in making the monopole component of shell-model Hamiltonians, derived from realistic nucleon-nucleon potentials, able to reproduce the observed evolution of the shell structure. In the vast majority of calculations, however, their effects have been taken into account by shell-model practitioners by introducing ad hoc modifications of the monopole matrix elements. During last twenty years, a new theoretical approach, framed within the chiral perturbation theory, has progressed in developing nuclear potentials, where two- and many-body components are naturally and consistently built in. This new class of nuclear forces allows to carry out nuclear structure studies that are improving our ability to understand nuclear phenomena in a microscopic approach. We provide in this work an update on the status of the nuclear shell model based on realistic Hamiltonians that are derived from two- and three-nucleon chiral potentials, focusing on the role of the three-body component to provide the observed shell evolution and closure properties, as well as the location of driplines. To this end, we present the results of shell-model calculations and their comparison with recent experimental measurements, which enlighten the relevance of the inclusion of three-nucleon forces to master our knowledge of the physics of atomic nuclei.Comment: Accepted for publication in Progress in Particle and Nuclear Physic

Experimental increase in baseline corticosterone level reduces oxidative damage and enhances innate immune response

Glucocorticoid (GC) hormones are significant regulators of homeostasis. The physiological effects of GCs critically depend on the time of exposure (short vs. long) as well as on their circulating levels (baseline vs. stress-induced). Previous experiments, in which chronic and high elevation of GC levels was induced, indicate that GCs impair both the activity of the immune system and the oxidative balance. Nonetheless, our knowledge on how mildly elevated GC levels, a situation much more common in nature, might influence homeostasis is limited. Therefore, we studied whether an increase in GC level within the baseline range suppresses or enhances condition (body mass, hematocrit and coccidian infestation) and physiological state (humoral innate immune system activity and oxidative balance). We implanted captive house sparrows Passer domesticus with either 60 days release corticosterone (CORT) or control pellets. CORT-treated birds had elevated baseline CORT levels one week after the implantation, but following this CORT returned to its pre-treatment level and the experimental groups had similar CORT levels one and two months following the implantation. The mass of tail feathers grown during the initial phase of treatment was smaller in treated than in control birds. CORT implantation had a transient negative effect on body mass and hematocrit, but both of these traits resumed the pre-treatment values by one month post-treatment. CORT treatment lowered oxidative damage to lipids (malondialdehyde) and enhanced constitutive innate immunity at one week and one month post-implantation. Our findings suggest that a relatively short-term (i.e. few days) elevation of baseline CORT might have a positive and stimulatory effect on animal physiology

Tailored carrier/bacteria technology for rehabilitation of areas with pesticide-containing pollution – AQUAREHAB WP2

Postprint (published version

ACTIVIDAD DE ANTISEPTICOS EN Malassezia pachydermatys AISLADA DE OIDO EXTERNO EN PERROS Y GATOS

Se estudiaron en agar Sabouraud dextrosado, muestras obtenidas del conducto auditivo externo de 80 perros y 22 gatos aparentemente sanos. El examen micológico directo y las características morfofisiológicas y bioquímicas, permitieron determinar la presencia de Malassezia pachydermatis en el 61,3% de las muestras provenientes de perros y en el 13,6% de los gatos. La susceptibilidad de esta levadura se determinó en medios sólidos, por el método de dilución in vitro frente a soluciones de yodo, timerosal y violeta de genciana. Todas las cepas fueron inhibidas en las siguientes concentraciones: Yodo 1.0 g/l; Timerosal 0,0125 g/l y Violeta de genciana a 0,0078 g/l, lo que representa su dilución comercial diluida 641 veces

Bradykinin Release Avoids High Molecular Weight Kininogen Endocytosis

Human H-kininogen (120 kDa) plays a role in many pathophysiological processes and interacts with the cell surface through protein receptors and proteoglycans, which mediate H-kininogen endocytosis. in the present work we demonstrate that H-kininogen containing bradykinin domain is internalized and different endogenous kininogenases are present in CHO-K1 cells. We used CHO-K1 (wild type) and CHO-745 (mutant deficient in proteoglycans biosynthesis) cell lines. H-kininogen endocytosis was studied using confocal microscopy, and its hydrolysis by cell lysate fraction was determined by immunoblotting. Bradykinin release was also measured by radioimmunoassay. H-kininogen interaction with the cell surface of CHO-745 cells resulted in bradykinin release by serine proteases. in CHO-K1 cells, which produce heparan and chondroitin sulfate proteoglycans, internalization of H-kininogen through its bradykinin domain can occur on lipid raft domains/caveolae. Nevertheless bradykinin-free H-kininogen was not internalized by CHO-K1 cells. the H-kininogen present in acidic endosomal vesicles in CHO-K1 was approximately 10-fold higher than the levels in CHO-745. CHO-K1 lysate fractions were assayed at pH 5.5 and intact H-kininogen was totally hydrolyzed into a 62 kDa fragment. By contrast, at an assay pH 7.4, the remained fragments were 115 kDa, 83 kDa, 62 kDa and 48 kDa in size. the anti-pain-Sepharose chromatography separated endogenous kininogenases from CHO-K1 lysate fraction. No difference was detected in the assays at pH 5.5 or 7.4, but the proteins in the fraction bound to the resin released bradykinin from H-kininogen. However, the proteins in the unbound fraction cleaved intact H-kininogen at other sites but did not release bradykinin. H-kininogen can interact with extravascular cells, and is internalized dependent on its bradykinin domain and cell surface proteoglycans. After internalization, H-kininogen is proteolytically processed by intracellular kininogenases. the present data also demonstrates that serine or cysteine proteases in lipid raft domains/caveolae on the CHO cell can hydrolyze H-kininogen, thus releasing kinins.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundacao de Apoio a Universidade Federal de São Paulo-FAP/UNIFESPUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Bioquim, São Paulo, SP, BrazilUniv Anhanguera São Paulo UNIAN SP, Programa Biomat, São Paulo, SP, BrazilUniv Anhanguera São Paulo UNIAN SP, Programa Biotecnol, São Paulo, SP, BrazilUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Biofis, São Paulo, SP, BrazilUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Bioquim, São Paulo, SP, BrazilUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Biofis, São Paulo, SP, BrazilCNPq: CNPq 472403/2007-9FAPESP: FAPESP 13/05822-9FAPESP: FAPESP 2012/50219-6Web of Scienc

Nutrient Stress Activates Inflammation and Reduces Glucose Metabolism by Suppressing AMP-Activated Protein Kinase in the Heart

OBJECTIVE: Heart failure is a major cause of mortality in diabetes and may be causally associated with altered metabolism. Recent reports indicate a role of inflammation in peripheral insulin resistance, but the impact of inflammation on cardiac metabolism is unknown. We investigated the effects of diet-induced obesity on cardiac inflammation and glucose metabolism in mice. RESEARCH DESIGN AND METHODS: Male C57BL/6 mice were fed a high-fat diet (HFD) for 6 weeks, and heart samples were taken to measure insulin sensitivity, glucose metabolism, and inflammation. Heart samples were also examined following acute interleukin (IL)-6 or lipid infusion in C57BL/6 mice and in IL-6 knockout mice following an HFD. RESULTS: Diet-induced obesity reduced cardiac glucose metabolism, GLUT, and AMP-activated protein kinase (AMPK) levels, and this was associated with increased levels of macrophages, toll-like receptor 4, suppressor of cytokine signaling 3 (SOCS3), and cytokines in heart. Acute physiological elevation of IL-6 suppressed glucose metabolism and caused insulin resistance by increasing SOCS3 and via SOCS3-mediated inhibition of insulin receptor substrate (IRS)-1 and possibly AMPK in heart. Diet-induced inflammation and defects in glucose metabolism were attenuated in IL-6 knockout mice, implicating the role of IL-6 in obesity-associated cardiac inflammation. Acute lipid infusion caused inflammation and raised local levels of macrophages, C-C motif chemokine receptor 2, SOCS3, and cytokines in heart. Lipid-induced cardiac inflammation suppressed AMPK, suggesting the role of lipid as a nutrient stress triggering inflammation. CONCLUSIONS: Our findings that nutrient stress activates cardiac inflammation and that IL-6 suppresses myocardial glucose metabolism via inhibition of AMPK and IRS-1 underscore the important role of inflammation in the pathogenesis of diabetic heart

Molecular relaxations in polyfluorene based cast films

This article reports a study of the thermal relaxation in cast films of two polyfluorene based polymers, poly{9,9-dioctylfluorenyl-2,7-diyl} (BE329) and poly{(9,9-dioctyl-2,7-divinylene-fluorenylene)-alt-co-[2-methoxy-5-(2-ethyl-hexyloxy)-1,4-phenylene]} (GE108). The relaxation processes were identified by Dynamical Mechanical Thermal Analysis (DMTA), which revealed three processes in both samples: process at lower temperatures and two relaxations at higher temperatures (named as ˛A and ˛B). The\ud relaxations mechanics were elucidated by Solid-State Nuclear Magnetic Resonance (NMR) methods. The results revealed that the relaxation is related to molecular motions in the side-groups, while the second and third relaxations can be attributed to local rotations in the backbone and to a glass transition. The molecular relaxations were also identified by the temperature dependence of the fluorescence spectra, which were also associated with their molecular nature.FAPESPCNPqMCT/PADCT/IMM