Complicaciones en la anestesia general del perro : revisión de 265 casos

Un total de 265 perros fueron anestesiados por diferentes motivos diagnósticos y terapéuticos en los Servicios Clínicos de la Facultad de Veterinaria de Córdoba,siguiendo diversos protocolos anestésicos

Reversión de sedantes agonistas alfa-2-adrenérgicos en el perro

En el presente Artículo de Revisión se aporta una información amplia sobre los productos de LISO más frecuente en la reversión de los efectos sedantes de los agonistas alfa-2-adrenérgicos empleados en el perro: xilacina, medetomidina y romifidina. Se refieren los detalles farmacológicos, dosificación, efectos y aplicaciones de los siguientes productos: yohimbina, 4-aminopiridina, doxapram y atipamezol

Retrospective study of the prevalence of postanesthtic hypotermia in dogs

The anaesthetic records of 1525 dogs were examined to determine the prevalence of postanaesthetic hypothermia, its clinical predictors and consequences. Temperature was recorded throughout the anaesthesia. At the end of the procedure, details coded in were: hyperthermia (>39.50°C), normothermia (38.50°C–39.50°C), slight (38.49°C–36.50°C), moderate (36.49°C–34.00°C) and severe hypothermia (<34.00°C). Statistical analysis consisted of multiple regression to identify the factors that are associated with the temperature at the end of the procedure. Before premedication, the temperature was 38.7±0.6°C (mean±sd). At 60, 120 and 180 minutes from induction, the temperature was 36.7±1.3°C, 36.1±1.4°C and 35.8±1.5°C, respectively. The prevalence of hypothermia was: slight, 51.5 per cent (95 per cent CI 49.0 to 54.0 per cent); moderate, 29.3 per cent (27.1–31.7 per cent) and severe: 2.8% (2.0–3.7%). The variables that associated with a decrease in the temperature recorded at the end of the anaesthesia were: duration of the preanesthetic time, duration of the anaesthesia, physical condition (ASA III and ASA IV dogs showed lower temperatures than ASA I dogs), the reason for anaesthesia (anaesthesia for diagnostic procedures or thoracic surgery reduce the temperature when compared with minor procedures), and the recumbency during the procedure (sternal and dorsal recumbencies showed lower temperatures than lateral recumbency). The temperature before premedication and the body surface (BS) were associated with a higher temperature at the end of the anaesthesia, and would be considered as protective factors.Ciencias Experimentale

COLLECE 2.0: Un sistema para el aprendizaje colaborativo de la programación sobre Eclipse, con una metáfora multidimensional para la visualización de programas

La programación de ordenadores es una tarea compleja y un reto para los estudiantes principiantes. Son numerosas las dificultades para entender los conceptos de programación debido al alto nivel de abstracción que requiere su aprendizaje. Con el propósito de contribuir a paliar estas dificultades, hemos desarrollado el sistema COLLECE-2.0, un plug-in para la plataforma Eclipse, que proporciona un entorno colaborativo de programación, distribuido y en tiempo real. Su interfaz ha sido diseñada para potenciar los aspectos relacionados con el soporte al aprendizaje en grupo. Además, nuestra propuesta hace un especial énfasis en la visualización de los programas, incorporando un conjunto de representaciones gráficas multidimensionales basadas en una metáfora. Estas representaciones son aplicables a una variedad de escenarios que soportan diferentes mecanismos de interacción, dependiendo de la dimensionalidad de las representaciones gráficas y de los dispositivos empleados para su visualización. En este artículo se describen los detalles fundamentales del sistema COLLECE-2.0 y cómo pude emplearse en distintos escenarios, para visualizar e interactuar con aspectos estructurales de los programas y algoritmos.Computer programming is a complex task and a challenge for novice programmers. There are a wide range of difficulties in understanding programming concepts due to the high level of abstraction required to learn them. In order to address these difficulties, we have developed the COLLECE-2.0 system, a plug-in for the Eclipse platform, which provides a real-time, distributed, collaborative programming environment. Its interface has been designed to enhance aspects related to support for group learning. In addition, our proposal makes a special emphasis on the program visualization, incorporating a set of multidimensional graphic representations based on a metaphor. These representations are applicable to a variety of scenarios that support different interaction mechanisms, depending on the dimensionality of the graphic representations and the devices used for their visualization. This paper describes the main details of the COLLECE-2.0 system and how it can be used in different scenarios by visualizing and interacting with structural aspects of the programs and algorithms.Este trabajo ha sido financiado por el Ministerio de Economía, Industria y Competitividad y por el Fondo Europeo de Desarrollo Regional, con referencia TIN2015-66731-C2-2-R

Modification of the mechanical properties of core-shell liquid gallium nanoparticles by thermal oxidation at low temperature

Gallium nanoparticles (Ga NPs) are attracting increasing attention because of their appealing physical-chemical properties. In particular, their mechanical properties play a key role in the implementation of these core-shell structures on certain applications, such as soft and stretchable electronics. Thus, efforts are being addressed to modulate them mainly by chemical means. In contrast, this study investigates how the mechanical properties of the outer gallium thin oxide shell change when its thickness is increased through a thermal oxidation strategy. Specifically, as-deposited Ga NPs, as well as those subjected to thermal oxidation at 300 °C for three different times, are studied by performing single-particle indentations by atomic force microscopy over a wide range of NP radius. This analysis helps to confirm that the Reissner's thin-shell model for small deformations within the elastic regime is obeyed. From these data, the dependence of the shell stiffness and the Young's modulus of the gallium oxide on the thermal treatment is obtained. It is found that the shell stiffness increases with the annealing time, even by a factor of 50 under prolonged thermal oxidation, while the gallium oxide Young's modulus, close to 30 GPa, does not change significantlyThis research was supported by Spanish MINECO (Grants No. MAT2017-85089-C2-1R, CTQ2017-84309-C2-2-R, PID2019-106339GB-I00, PID2020-113142RB-C21) and the TRANSNANOAVANSENS program (Grant No.S2018/NMT-4349) from the Comunidad de Madrid and Junta de Andalucía (Research group INNANOMAT, ref. TEP-946). Co-funding from UE was also acknowledged. A.R.C. acknowledges Ramón y Cajal program (under Contract No. RYC-2015-18047). S.C.G and M.d.l.M. acknowledge Juan de la Cierva en Formación programmes (references FJC2019-041616-I and IJCI-2017-31507, respectively). F.J.P. was thankful for financial support by A.E. Consejo Superior de Investigaciones Científicas (under Grant No. CSIC-2019AEP150). TEM measurements were carried out at DME-SC-ICyT-UCA/ICTS-ELECM

Structural Determinants of the Dictyostatin Chemotype for Tubulin Binding Affinity and Antitumor Activity Against Taxane- and Epothilone-Resistant Cancer Cells

A combined biochemical, structural, and cell biology characterization of dictyostatin is described, which enables an improved understanding of the structural determinants responsible for the high-affinity binding of this anticancer agent to the taxane site in microtubules (MTs). The study reveals that this macrolide is highly optimized for MT binding and that only a few of the structural modifications featured in a library of synthetic analogues resulted in small gains in binding affinity. The high efficiency of the dictyostatin chemotype in overcoming various kinds of clinically relevant resistance mechanisms highlights its potential for therapeutic development for the treatment of drug-resistant tumors. A structural explanation is advanced to account for the synergy observed between dictyostatin and taxanes on the basis of their differential effects on the MT lattice. The X-ray crystal structure of a tubulin−dictyostatin complex and additional molecular modeling have allowed the rationalization of the structure−activity relationships for a set of synthetic dictyostatin analogues, including the highly active hybrid 12 with discodermolide. Altogether, the work reported here is anticipated to facilitate the improved design and synthesis of more efficacious dictyostatin analogues and hybrids with other MT-stabilizing agents.We thank Peter T. Northcote for peloruside A, W.-S. Fang for Flutax-2, K. H. Altmann for epothilone D, Dr. Paraskevi Giannakakou (Weill Cornell Medical Center, New York) for the 1A9, PTX10, PTX22, and A8 cell lines, and Prof. Richard Ludueñ a (University of Texas) for the HeLa βIII-transfected cells. We thank Matadero INCOVA (Segovia) for the calf brains for tubulin purification. This work was supported in part by grants BIO2013-42984-R (J.F.D.) and SAF2012-39760-C02-02 (F.G.) from Ministerio de Economia y Competitividad, grant S2010/ ́ BMD-2457 BIPEDD2 from Comunidad Autonoma de Madrid ́ (F.G. and J.F.D.), and the Swiss National Science Foundation grants 310030B_138659 and 31003A_166608 (M.O.S.). The authors acknowledge networking contribution by the COST Action CM1407 “Challenging organic syntheses inspired by naturefrom natural products chemistry to drug discovery” and the COST action CM1470. I.P. thanks the EPSRC and AstraZeneca for funding, Dr. John Leonard (AstraZeneca) for useful discussions, Dr. Stuart Mickel (Novartis) for the provision of chemicals, and the EPSRC UK National Mass Spectrometry Facility at Swansea University for mass spectra

Integrating magnetic capabilities to intracellular chips for cell trapping

Current microtechnologies have shown plenty of room inside a living cell for silicon chips. Microchips as barcodes, biochemical sensors, mechanical sensors and even electrical devices have been internalized into living cells without interfering their cell viability. However, these technologies lack from the ability to trap and preconcentrate cells in a specific region, which are prerequisites for cell separation, purification and posterior studies with enhanced sensitivity. Magnetic manipulation of microobjects, which allows a non-contacting method, has become an attractive and promising technique at small scales. Here, we show intracellular Ni-based chips with magnetic capabilities to allow cell enrichment. As a proof of concept of the potential to integrate multiple functionalities on a single device of this technique, we combine coding and magnetic manipulation capabilities in a single device. Devices were found to be internalized by HeLa cells without interfering in their viability. We demonstrated the tagging of a subpopulation of cells and their subsequent magnetic trapping with internalized barcodes subjected to a force up to 2.57 pN (for magnet-cells distance of 4.9 mm). The work opens the venue for future intracellular chips that integrate multiple functionalities with the magnetic manipulation of cells

Structural Determinants of the Dictyostatin Chemotype for Tubulin Binding Affinity and Antitumor Activity Against Taxane- and Epothilone-Resistant Cancer Cells

A combined biochemical, structural, and cell biology characterization of dictyostatin is described, which enables an improved understanding of the structural determinants responsible for the high-affinity binding of this anticancer agent to the taxane site in microtubules (MTs). The study reveals that this macrolide is highly optimized for MT binding and that only a few of the structural modifications featured in a library of synthetic analogues resulted in small gains in binding affinity. The high efficiency of the dictyostatin chemotype in overcoming various kinds of clinically relevant resistance mechanisms highlights its potential for therapeutic development for the treatment of drug-resistant tumors. A structural explanation is advanced to account for the synergy observed between dictyostatin and taxanes on the basis of their differential effects on the MT lattice. The X-ray crystal structure of a tubulin−dictyostatin complex and additional molecular modeling have allowed the rationalization of the structure−activity relationships for a set of synthetic dictyostatin analogues, including the highly active hybrid 12 with discodermolide. Altogether, the work reported here is anticipated to facilitate the improved design and synthesis of more efficacious dictyostatin analogues and hybrids with other MT-stabilizing agents.We thank Peter T. Northcote for peloruside A, W.-S. Fang for Flutax-2, K. H. Altmann for epothilone D, Dr. Paraskevi Giannakakou (Weill Cornell Medical Center, New York) for the 1A9, PTX10, PTX22, and A8 cell lines, and Prof. Richard Ludueñ a (University of Texas) for the HeLa βIII-transfected cells. We thank Matadero INCOVA (Segovia) for the calf brains for tubulin purification. This work was supported in part by grants BIO2013-42984-R (J.F.D.) and SAF2012-39760-C02-02 (F.G.) from Ministerio de Economia y Competitividad, grant S2010/ ́ BMD-2457 BIPEDD2 from Comunidad Autonoma de Madrid ́ (F.G. and J.F.D.), and the Swiss National Science Foundation grants 310030B_138659 and 31003A_166608 (M.O.S.). The authors acknowledge networking contribution by the COST Action CM1407 “Challenging organic syntheses inspired by naturefrom natural products chemistry to drug discovery” and the COST action CM1470. I.P. thanks the EPSRC and AstraZeneca for funding, Dr. John Leonard (AstraZeneca) for useful discussions, Dr. Stuart Mickel (Novartis) for the provision of chemicals, and the EPSRC UK National Mass Spectrometry Facility at Swansea University for mass spectra

Level of blood pressure control in a hypertensive population when measurements are performed outside the clinical setting

Background: To determine whether the number of optimally controlled hypertensive patients is higher using self-measurement of blood pressure at home and ambulatory monitoring, compared to using conventional blood pressure measurements at the doctor&#8217;s office. Method: An observational, cross-sectional, multicentre, descriptive study of a random sample of 237 primary health care patients, known to be hypertensive, from Badajoz (Spain). Blood pressure was measured at the doctor&#8217;s office and by self-measurement at home. Those patients showing good control by self-measurement were subjected to 24-hour ambulatory monitoring. Optimal control was understood as blood pressure < 140/90 mm Hg when measured at the doctor&#8217;s office, and < 135/85 mm Hg when self-measured at home and by daytime ambulatory monitoring. Results: Mean systolic/diastolic measurements at the doctor&#8217;s office and by self-measurement were 145.6/83.9 and 134.0/78.7 mm Hg, respectively (p < 0.000). In the population optimally controlled by self-measurement and who subsequently received ambulatory monitoring, the mean blood pressure was 121.8/73.4 and 125.6/76.2 mm Hg, respectively (p = 0.002; p < 0.000). When measured at the doctor&#8217;s office blood pressure was controlled in about 29.5% (95% CI 23.7-35.3%) of patients, in 38% when self-measured (95% CI 31.4-44.2%; p < 0.000), and in 24.5% when it was confirmed through ambulatory monitoring (95% CI 15.4-33.6%). Sensitivity and positive predictive values of the office measurements for the detection of patients who were well-controlled by self-measurement were 50% and 64.3%, respectively, and 53.4% and 73.8% as regards ambulatory monitoring. Conclusions: A higher level of control is achieved with self-measurement at home not confirmed by ambulatory monitoring. Therefore, the white coat effect does not seem to influence the percentage of well-controlled patients detected at the doctor&#8217;s office. Office blood pressure does not appear to be useful in distinguishing which individual patients are optimally controlled

Mesoscopic structure conditions the emergence of cooperation on social networks

We study the evolutionary Prisoner's Dilemma on two social networks obtained from actual relational data. We find very different cooperation levels on each of them that can not be easily understood in terms of global statistical properties of both networks. We claim that the result can be understood at the mesoscopic scale, by studying the community structure of the networks. We explain the dependence of the cooperation level on the temptation parameter in terms of the internal structure of the communities and their interconnections. We then test our results on community-structured, specifically designed artificial networks, finding perfect agreement with the observations in the real networks. Our results support the conclusion that studies of evolutionary games on model networks and their interpretation in terms of global properties may not be sufficient to study specific, real social systems. In addition, the community perspective may be helpful to interpret the origin and behavior of existing networks as well as to design structures that show resilient cooperative behavior.Comment: Largely improved version, includes an artificial network model that fully confirms the explanation of the results in terms of inter- and intra-community structur