122 research outputs found
Threading Through Macrocycles Enhances the Performance of Carbon Nanotubes as Polymer Fillers
In this work we study the reinforcement of polymers by mechanically
interlocked derivatives of single-walled carbon nanotubes (SWNTs). We compare
the mechanical properties of fibers made of polymers and of composites with
pristine single-walled carbon nanotubes (SWNTs), mechanically interlocked
derivatives of SWNTs (MINTs) and the corresponding supramolecular models.
Improvements of both Young's modulus and tensile strength of up to 200 % were
observed for the polystyrene-MINTs samples with an optimized loading of just
0.01 wt.%, while the supramolecular models with identical chemical composition
and loading showed negligible or even detrimental influence. This behavior is
found for three different types of SWNTs and two types of macrocycles.
Molecular dynamics simulations show that the polymer adopts an elongated
conformation parallel to the SWNT when interacting with MINT fillers,
irrespective of the macrocycle chemical nature, whereas a more globular
structure is taken upon facing with either pristine SWNTs or supramolecular
models. The MINT composite architecture thus leads to a more efficient
exploitation of the axial properties of the SWNTs and of the polymer chain at
the interface, in agreement with experimental results. Our findings demonstrate
that the mechanical bond imparts distinctive advantageous properties to SWNT
derivatives as polymer fillers.Comment: 39 pages, 19 figure
Epigenetic and post-transcriptional regulation of somatostatin receptor subtype 5 (SST5) in pituitary and pancreatic neuroendocrine tumors
Somatostatin receptor subtype 5 (SST5) is an emerging biomarker and actionable target in pituitary (PitNETs) and pancreatic (PanNETs) neuroendocrine tumors. Transcriptional and epigenetic regulation of SSTR5 gene expression and mRNA biogenesis is poorly understood. Recently, an overlapping natural antisense transcript, SSTR5-AS1, potentially regulating SSTR5 expression, was identified. We aimed to elucidate whether epigenetic processes contribute to the regulation of SSTR5 expression in PitNETs (somatotropinomas) and PanNETs. We analyzed the SSTR5/SSTR5-AS1 human locus in silico to identify CpG islands. SSTR5 and SSTR5-AS1 expression was assessed by quantitative real-time PCR (qPCR) in 27 somatotropinomas, 11 normal pituitaries (NPs), and 15 PanNETs/paired adjacent (control) samples. We evaluated methylation grade in four CpG islands in the SSTR5/SSTR5-AS1 genes. Results revealed that SSTR5 and SSTR5-AS1 were directly correlated in NP, somatotropinoma, and PanNET samples. Interestingly, selected CpG islands were differentially methylated in somatotropinomas compared with NPs. In PanNETs cell lines, SSTR5-AS1 silencing downregulated SSTR5 expression, altered aggressiveness features, and influenced pasireotide response. These results provide evidence that SSTR5 expression in PitNETs and PanNETs can be epigenetically regulated by the SSTR5-AS1 antisense transcript and, indirectly, by DNA methylation, which may thereby impact tumor behavior and treatment response.Junta de AndalucíaMinisterio de EconomíaMinisterio de Ciencia e Innovació
Synthesis, structure, and photophysical properties of platinum(II) (N, C, N) pincer complexes derived from purine nucleobases
The synthesis of a series of Pt{κ3-N,C,N′-[L]}X (X = Cl, RC≡C) pincer complexes derived from purine and purine nucleosides is reported. In these complexes, the 6-phenylpurine skeleton provides the N,C-cyclometalated fragment, whereas an amine, imine, or pyridine substituent of the phenyl ring supplies the additional N′-coordination point to the pincer complex. The purine N,C-fragment has two coordination positions with the metal (N1 and N7), but the formation of the platinum complexes is totally regioselective. Coordination through the N7 position leads to the thermodynamically favored [6.5]-Pt{κ3-N7,C,N′-[L]}X complexes. However, the coordination through the N1 position is preferred by the amino derivatives, leading to the isomeric kinetic [5.5]-Pt{κ3-N1,C,N′-[L]}X complexes. Extension of the reported methodology to complexes having both pincer and acetylide ligands derived from nucleosides allows the preparation of novel heteroleptic bis-nucleoside compounds that could be regarded as organometallic models of Pt-induced interstrand cross-link. Complexes having amine or pyridine arms are green phosphorescence emitters upon photoexcitation at low concentrations in CH2Cl2 solution and in poly(methyl methacrylate) (PMMA) films. They undergo self-quenching at high concentrations due to molecular aggregation. The presence of intermolecular π–π stacking and weak Pt···Pt interactions was also observed in the solid state by X-ray diffraction analysis
Epigenetic and post-transcriptional regulation of somatostatin receptor subtype 5 (SST5 ) in pituitary and pancreatic neuroendocrine tumors.
Somatostatin receptor subtype 5 (SST5 ) is an emerging biomarker and actionable target in pituitary (PitNETs) and pancreatic (PanNETs) neuroendocrine tumors. Transcriptional and epigenetic regulation of SSTR5 gene expression and mRNA biogenesis is poorly understood. Recently, an overlapping natural antisense transcript, SSTR5-AS1, potentially regulating SSTR5 expression, was identified. We aimed to elucidate whether epigenetic processes contribute to the regulation of SSTR5 expression in PitNETs (somatotropinomas) and PanNETs. We analyzed the SSTR5/SSTR5-AS1 human locus in silico to identify CpG islands. SSTR5 and SSTR5-AS1 expression was assessed by quantitative real-time PCR (qPCR) in 27 somatotropinomas, 11 normal pituitaries (NPs), and 15 PanNETs/paired adjacent (control) samples. We evaluated methylation grade in four CpG islands in the SSTR5/SSTR5-AS1 genes. Results revealed that SSTR5 and SSTR5-AS1 were directly correlated in NP, somatotropinoma and PanNET samples. Interestingly, selected CpG islands were differentially methylated in somatotropinomas compared with NPs. In PanNETs cell lines, SSTR5-AS1 silencing downregulated SSTR5 expression, altered aggressiveness features, and influenced pasireotide response. These results provide evidence that SSTR5 expression in PitNETs and PanNETs can be epigenetically regulated by the SSTR5-AS1 antisense transcript and, indirectly, by DNA methylation, which may thereby impact tumor behavior and treatment response
CareCloud: Plataforma de soporte y asistencia a cuidadores
El aumento de las personas con discapacidad está demandando la aparición de nuevos modelos de cuidado en los que el cuidador informal desarrolle un papel fundamental como fuente de provisión de cuidados. La falta de preparación del cuidador junto con los frecuentes episodios de estrés y depresión que sufren ante la elevada carga psicológica y laboral, tienen un impacto muy negativo tanto en la condición del cuidador como en las tareas de cuidado. Con el objetivo de mejorar los cuidados provistos y la calidad de vida de los cuidadores informales surge la plataforma CareCloud. Esta plataforma proporciona al cuidador informal servicios destinados a la provisión de contenidos personalizados de formación sobre los distintos cuidados que prestan a sus familiares. Además, permite la gestión de los cuidados a través de servicios de coordinación entre distintos cuidadores, así como procedimientos de evaluación del cuidado que permitan detectar problemas ocurridos en la asistencia prestada
Manejo Anestésico en la enfermedad de Steinert. A propósito de 2 Casos
La enfermedad de Steinert o distrofia miotónica tipo I es el síndrome miotónico más frecuente de la edad adulta. Tiene una incidencia de 3-5/100.000 y una herencia autosómica dominante, en la mayoría de los casos la transmisión es por parte de la madre. El gen para este desorden está localizado en el brazo largo del cromosoma 19. El comienzo de esta enfermedad se sitúa entre las segunda y tercera década de la vida, aunque en algunas familias se produce el fenómeno del acortamiento cromosómico adelantándose la presentación en las siguientes generaciones. Es una enfermedad del músculo, no del sistema nervioso periférico ni de la unión neuromuscular producida por un defecto de la función de los canales de sodio y cloro, que determinan una inestabilidad eléctrica de la membrana muscular y un automantenimiento de la depolarización. La sintomatología que caracteriza a esta enfermedad se produce por la miotonía, la atrofia muscular y las manifestaciones de las patologías asociadas. Las causas más frecuentes de morbi-mortalidad en estos enfermos son las debidas a problemas cardíacos o respiratorios.
El manejo anestésico de estos enfermos es un reto para el anestesiólogo por la gran variedad de complicaciones que se pueden presentar tanto en el intraoperatorio como en el postoperatorio, tanto por la evolución de la enfermedad como por la susceptibilidad a la gran mayoría de los agentes anestésicos
Predicting the onset and persistence of episodes of depression in primary health care. The predictD-Spain study: Methodology
Background:
The effects of putative risk factors on the onset and/or persistence of depression remain unclear. We aim to develop comprehensive models to predict the onset and persistence of episodes of depression in primary care. Here we explain the general methodology of the predictD-Spain study and evaluate the reliability of the questionnaires used.
Methods:
This is a prospective cohort study. A systematic random sample of general practice attendees aged 18 to 75 has been recruited in seven Spanish provinces. Depression is being measured with the CIDI at baseline, and at 6, 12, 24 and 36 months. A set of individual, environmental, genetic, professional and organizational risk factors are to be assessed at each follow-up point. In a separate reliability study, a proportional random sample of 401 participants completed the test-retest (251 researcher-administered and 150 self-administered) between October 2005 and February 2006. We have also checked 118,398 items for data entry from a random sample of 480 patients stratified by province.
Results:
All items and questionnaires had good test-retest reliability for both methods of administration, except for the use of recreational drugs over the previous six months. Cronbach's alphas were good and their factorial analyses coherent for the three scales evaluated (social support from family and friends, dissatisfaction with paid work, and dissatisfaction with unpaid work). There were 191 (0.16%) data entry errors.
Conclusion:
The items and questionnaires were reliable and data quality control was excellent. When we eventually obtain our risk index for the onset and persistence of depression, we will be able to determine the individual risk of each patient evaluated in primary health car
Multicentric standardization of protocols for the diagnosis of human mitochondrial respiratory chain defects
The quantification of mitochondrial respiratory chain (MRC) enzymatic activities is essential for diagnosis of a wide range of mitochondrial diseases, ranging from inherited defects to secondary dysfunctions. MRC lesion is frequently linked to extended cell damage through the generation of proton leak or oxidative stress, threatening organ viability and patient health. However, the intrinsic challenge of a methodological setup and the high variability in measuring MRC enzymatic activities represents a major obstacle for comparative analysis amongst institutions. To improve experimental and statistical robustness, seven Spanish centers with extensive experience in mitochondrial research and diagnosis joined to standardize common protocols for spectrophotometric MRC enzymatic measurements using minimum amounts of sample. Herein, we present the detailed protocols, reference ranges, tips and troubleshooting methods for experimental and analytical setups in different sample preparations and tissues that will allow an international standardization of common protocols for the diagnosis of MRC defects. Methodological standardization is a crucial step to obtain comparable reference ranges and international standards for laboratory assays to set the path for further diagnosis and research in the field of mitochondrial diseases. © 2022 by the authors. Licensee MDPI, Basel, Switzerland
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