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1.
Eur J Pediatr ; 2024 Oct 11.
Article in English | MEDLINE | ID: mdl-39390276

ABSTRACT

We aimed to compare the efficacy of Bifidobacterium longum KABP042 + Pediococcus pentosaceus KABP041 (BL + PP) vs. Limosilactobacillus reuteri DSM17938 (LR) in alleviating the symptoms of infant colic, as commercially available formulations. A randomized, multicenter, parallel, single-blind (investigator) trial was conducted in 112 colicky infants diagnosed as per Rome IV criteria and randomly allocated to receive BL + PP orally (109 colony-forming units [CFU]/day, n = 55) or LR (108 CFU/day, n = 57) for 21 days. Primary study outcomes were percentage of responders (≥ 50% reduction in crying and fussing time from baseline, as reported by parents in a structured diary) and daily crying and fussing time (minutes/day) on days 7, 14, and 21 after randomization. Study groups were comparable at baseline. Responder rate was significantly higher in BP + PP group vs. LR group at days 7 (61.1% vs. 37.5%, p = 0.013) and 14 (84.6% vs. 59.3%, p = 0.004). Crying and fussing time (median [IQR]) became significantly lower in BL + PP group vs. LR group on day 7 (119 [60-210] vs. 180 [110-270]; p = 0.028), day 14 (60.0 [30-105] vs. 120 [60-180]; p = 0.017), and day 21 (29 [0-85] vs. 67 [30-165]; p = 0.011). No significant differences were found in the number of adverse events between the groups. CONCLUSION: The specific formulation of B. longum KABP042 and P. pentosaceus KABP041 achieved a higher response rate and a larger reduction in crying and fussing time in colicky infants. Both probiotic interventions were well tolerated. TRIAL REGISTRATION: The study was retrospectively registered as NCT05271747 on February 28th, 2022. WHAT IS KNOWN: • L. reuteri DSM17938 (LR) is the most researched probiotic strain for infant colic against placebo in randomized, controlled clinical trials, and is recommended in various guidelines. A novel probiotic combining strains B. longum KABP042 and P. pentosaceus KABP041 (BL + PP) has also demonstrated efficacy in infant colic against placebo. WHAT IS NEW: • This randomized study provides the first direct comparison of two probiotics for infant colic. BL + PP seems to be superior to LR in reducing crying time.

2.
O.F.I.L ; 32(1): 83-86, enero 2022.
Article in Spanish | IBECS | ID: ibc-205737

ABSTRACT

Introducción: La infestación y mortalidad ocasionada por el coronavirus Sarv-Cov-2 (COVID-19) generó que los sistemas de salud desarrollaran acciones para promover nuevas investigaciones clínicas encaminadas a contar con esquemas de tratamientos efectivos, para un mejor manejo de esta enfermedad.En Cuba, con la existencia antes de la pandemia, de un plan de ensayos clínicos y la necesidad de promover nuevos, para hacer frente a la COVID-19; se propuso la elaboración de un sistema de acciones encaminadas a preservar la calidad de los mismos.Objetivo: Describir las principales acciones desarrolladas, por el Sistema Nacional de Salud cubano, para el desarrollo de las investigaciones clínicas durante la pandemia.Métodos: Se realizó una revisión bibliográfica en los principales sitios web regulatorios y vinculados con el tema de investigaciones clínicas en etapa de pandemia por la COVID-19. Los resultados alcanzados se tuvieron en cuenta para proponer un sistema de acciones propio, encaminado a respaldar los ensayos clínicos.Resultados: Se establecieron acciones en tres líneas de trabajo: el respaldo ético, los requerimientos regulatorios para las modificaciones a los estudios en curso y nuevos y para el control de los ensayos clínicos. El sistema de trabajo quedó conformado por 29 acciones encaminadas a que los ensayos clínicos tuvieran un respaldado ético, cumplieran con los requerimientos regulatorios en cuanto a los aspectos metodológicos, de diseño y de control para garantizar el cumplimiento de las Buenas Prácticas Clínicas. (AU)


Introduction: The infestation and mortality caused by the Sarv-Cov-2 (COVID-19) coronavirus led health systems to develop actions to promote new clinical research aimed at having effective treatment schemes for better management of this disease.In Cuba, with the existence before the pandemic, of a clinical trial plan and the need to promote new ones, to deal with COVID-19; it was proposed to develop a system of actions aimed at preserving their quality.Objective: Describe the main actions developed by the Cuban National Health System for the development of clinical research during the pandemic.Methods: A bibliographic review was carried out on the main regulatory websites and those related to the topic of clinical research in the pandemic stage of COVID-19. The results achieved were taken into account to propose an own action system, aimed at supporting clinical trials.Results: Actions were established in three lines of work: ethical support, regulatory requirements for modifications to ongoing and new studies, and the control of clinical trials. The work system was made up of 29 actions aimed at ensuring that clinical trials have ethical support, comply with regulatory requirements in terms of methodological, design aspects and their control to guarantee compliance with Good Clinical Practices. (AU)


Subject(s)
Humans , Health Systems , Coronavirus , Pandemics , Clinical Clerkship , Pathology
3.
J Mater Sci Mater Med ; 30(9): 99, 2019 Aug 27.
Article in English | MEDLINE | ID: mdl-31455977

ABSTRACT

Adipose-derived mesenchymal stem cells (ASCs) accelerate the osteointegration of bone grafts and improve the efficiency in the formation of uniform bone tissue, providing a practical and clinically attractive approach in bone tissue regeneration. In this work, the effect of nanofibrous biomimetic matrices composed of poly(ε-caprolactone) (PCL), nanometric hydroxyapatite (nHA) particles and 14-3-3 protein isoform epsilon on the initial stages of human ASCs (hASCs) osteogenic differentiation was investigated. The cells were characterized by flow cytometry and induction to differentiation to adipogenic and osteogenic lineages. The isolated hASCs were induced to differentiate to osteoblasts over all scaffolds, and adhesion and viability of the hASCs were found to be similar. However, the activity of alkaline phosphatase (ALP) as early osteogenic marker in the PCL-nHA/protein scaffold was four times higher than in PCL-nHA and more than five times than the measured in neat PCL.


Subject(s)
14-3-3 Proteins , Durapatite , Mesenchymal Stem Cells/drug effects , Osteogenesis/drug effects , Polyesters , Tissue Scaffolds/chemistry , 14-3-3 Proteins/chemistry , 14-3-3 Proteins/pharmacology , Cell Differentiation/drug effects , Cell Differentiation/physiology , Cells, Cultured , Durapatite/chemistry , Durapatite/pharmacology , Electroplating/methods , Humans , Materials Testing , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/physiology , Nanofibers/chemistry , Osteoblasts/drug effects , Osteoblasts/physiology , Osteogenesis/physiology , Polyesters/chemistry , Polyesters/pharmacology , Subcutaneous Fat, Abdominal/cytology , Surface Properties/drug effects , Tissue Engineering/methods
4.
Rev Gastroenterol Mex (Engl Ed) ; 84(3): 326-343, 2019.
Article in English, Spanish | MEDLINE | ID: mdl-31262552

ABSTRACT

Exercise in cirrhosis of the liver is an emerging topic in hepatology. Despite the known benefits of exercise in the general population, there are currently few studies addressing that issue in relation to cirrhosis and more evidence is still needed. Even though some studies have reported an acute, exercise-induced increase in the hepatic venous pressure gradient (HVPG), the opposite (a decrease in the HVPG) has been shown by recent data after an exercise program carried out for>14 weeks. In addition to that benefit, improvement has been described in the metabolic profile, quality of life, muscle mass, cardiopulmonary function, and nutritional status. Together, those features make exercise in cirrhosis a very attractive intervention. However, certain aspects must be taken into account before prescribing exercise in that population and they include cardiovascular risk, musculoskeletal disorders, and complications related to cirrhosis. After considering those factors, an individually tailored exercise program should be developed for each patient, according to the points stated above and the desired goal. Information about exercise-limiting factors, type of exercise prescribed, monitoring methods, and concomitant nutritional therapy is provided in the present review.


Subject(s)
Exercise Therapy/statistics & numerical data , Liver Cirrhosis/therapy , Prescriptions , Humans , Precision Medicine
5.
Mater Sci Eng C Mater Biol Appl ; 99: 1493-1501, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30889684

ABSTRACT

Tramadol is an analgesic usually prescribed for the management of pain, with a certain risk of addiction in chronic patients. The incorporation of tramadol in sustained-release systems results particularly attractive for the administration of accurate doses. In this work, emulsion electrospinning was used for the preparation of tramadol-loaded nanofibrous membranes based on poly(ε-caprolactone). Compositional and processing parameters were screened and evaluated in terms of the morphology of the resulting nanofibers, encapsulation efficiency and drug release in time. The polymer concentration, surfactant type and amount, and the homogenization rate used for the emulsions preparation were found to greatly affect the fluid stability and the resulting materials structure and functionality. The intrinsic features of the starting fluid studied in this work played a significant role for the modulation of tramadol release from nanofibrous matrices. The use of sodium dodecyl sulfate as surfactant with an optimal homogenization rate allowed the preparation of electrospun fibrous membranes with good encapsulation efficiency, a minimal burst release and a sustained delivery of tramadol in time.


Subject(s)
Emulsions/chemistry , Tissue Engineering/methods , Tramadol/pharmacology , Delayed-Action Preparations/pharmacology , Drug Liberation , Membranes, Artificial , Particle Size , Surface-Active Agents/chemistry , Thermogravimetry , X-Ray Diffraction
6.
J Med Case Rep ; 13(1): 28, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-30709425

ABSTRACT

BACKGROUND: Spontaneous remission in solid malignancies has been documented. However, spontaneous remission in aggressive diffuse large b cell lymphoma is exceedingly rare. Previous reports of lymphoma remission suggest that not yet fully characterized tumor-intrinsic and microenvironment mechanisms cooperate with spontaneous regression. CASE DESCRIPTION: Here, we report the case of an 88-year-old white woman with diffuse large b cell lymphoma (follicular lymphoma transformed) who achieved morphologic spontaneous remission 3 months after her diagnostic core biopsy. We examined 16 similar cases of diffuse large b cell lymphoma suggesting that spontaneous remission is preferentially observed in elderly patients soon after their biopsy microtrauma, especially if malignancies are Epstein-Barr virus driven and activated B-cell type. CONCLUSION: Our case and reported analysis highlight that anti-tumor adaptive T cell responses are potentially augmented in a subset of patients leading to lymphoma regression. In these patients, it is possible that "primed" innate anti-tumor T cell immunity is enhanced in immunogenic lymphoma subtypes after tissue biopsy. Our case and analysis not only reinforce the role of innate T cell anticancer immunity, but also originates potential proof of concept for investigation of unexplored pathways that could favorably impact T cell therapy.


Subject(s)
Immunity, Innate/physiology , Lymph Nodes/pathology , Lymphoma, Large B-Cell, Diffuse/pathology , T-Lymphocytes, Regulatory/immunology , Aged, 80 and over , Biopsy , Fatal Outcome , Female , Humans , Lymphoma, Large B-Cell, Diffuse/diagnostic imaging , Lymphoma, Large B-Cell, Diffuse/immunology , Remission, Spontaneous , Retrospective Studies , Tomography, X-Ray Computed
7.
Rev Gastroenterol Mex (Engl Ed) ; 83(4): 424-433, 2018.
Article in English, Spanish | MEDLINE | ID: mdl-30292583

ABSTRACT

One of the most important characteristics of malnutrition is the loss of muscle mass and the severe depletion of the protein reserve, secondarily affecting energy metabolism. That impacts nutritional status and the progression of disease-related complications. Nutritional treatment is one of the main factors in the comprehensive management of those patients. Achieving adequate energy intake that provides the macronutrients and micronutrients necessary to prevent or correct malnutrition is attempted through dietary measures. ESPEN, the European Society for Clinical Nutrition and Metabolism, recommends a caloric intake of 30-40kcal/kg/day, in which carbohydrates provide 45-60% of the daily energy intake and proteins supply 1.0-1.5g/kg/day. The remaining portion of the total energy expenditure should be covered by lipids. The administration of branched-chain amino acids has been shown to be beneficial not only in counteracting malnutrition, but also as a coadjuvant treatment in specific complications, thus playing a favorable role in outcome and quality of life. Therefore, branched-chain amino acids should be considered part of nutritional treatment in patients with advanced stages of cirrhosis of the liver, particularly in the presence of complications.


Subject(s)
Amino Acids, Branched-Chain/therapeutic use , Diet , Dietary Supplements , Liver Cirrhosis/diet therapy , Nutrition Therapy/methods , Humans , Nutritional Status
8.
Case Rep Hematol ; 2017: 1950724, 2017.
Article in English | MEDLINE | ID: mdl-28133556

ABSTRACT

Gelatinous marrow transformation (GMT) is a rare condition observed in severe illness or malnutrition, in which the bone marrow contains amorphous "gelatinous" extracellular material, and histopathology demonstrates varied degrees of fat cell atrophy and loss of hematopoietic elements. An association of GMT with imatinib use in chronic myeloid leukemia (CML) has been reported recently. The objective of this study is to describe a case of GMT associated with imatinib use and review the existing similar cases in the literature to identify epidemiological patterns and potential imatinib-induced mechanisms leading to gelatinous conversion.

10.
Psychopharmacology (Berl) ; 226(1): 177-88, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23093381

ABSTRACT

RATIONALE: Regulator of G-protein signaling (RGS) proteins, RGS4 and RGS10, may be involved in the pathophysiology of schizophrenia. RGS4 has attracted special interest since the reports of genetic association between SNPs in RGS4 and schizophrenia. However, there is no information about the subcellular distribution of RGS4 and RGS10 proteins in psychiatric disorders. OBJECTIVES: Plasma membrane RGS4 and cytosolic RGS10 protein immunoreactivity in prefrontal cortex from schizophrenic subjects (n = 25), non-diagnosed suicides (n = 13), and control subjects (n = 35), matched by age, gender, and postmortem delay, was analyzed by western blot. A second group of depressed subjects (n = 25) and control subjects (n = 25) was evaluated. The effect of the antipsychotic or antidepressant treatments was also assessed. RESULTS: No significant differences in plasma membrane RGS4 and cytosolic RGS10 protein expression were observed between schizophrenic subjects, non-diagnosed suicides, and control subjects. However, RGS4 immunoreactivity was significantly higher (Δ = 33 ± 10 %, p < 0.05) in the antipsychotic-treated subgroup (n = 12) than in the antipsychotic-free subgroup (n = 13). Immunodensities of plasma membrane RGS4 and cytosolic RGS10 proteins did not differ between depressed and matched control subjects. CONCLUSIONS: Expression of RGS4 and RGS10 proteins at their predominant subcellular location was studied in the postmortem brain of subjects with psychiatric disorders. The results suggest unaltered membrane RGS4 and cytosolic RGS10 proteins levels in schizophrenia and major depression. Antipsychotic treatment seems to increase membrane RGS4 immunoreactivity. Further studies are needed to elucidate RGS4 and RGS10 functional status.


Subject(s)
Antipsychotic Agents/therapeutic use , Depressive Disorder, Major/metabolism , Prefrontal Cortex/metabolism , RGS Proteins/biosynthesis , Schizophrenia/metabolism , Adult , Antipsychotic Agents/blood , Biopsy , Blotting, Western , Cell Membrane/metabolism , Cytosol/metabolism , Depressive Disorder, Major/drug therapy , Depressive Disorder, Major/pathology , Female , Humans , Male , Middle Aged , Postmortem Changes , Prefrontal Cortex/drug effects , Prefrontal Cortex/pathology , Schizophrenia/drug therapy , Schizophrenia/pathology , Suicide
11.
Bioelectromagnetics ; 33(7): 612-9, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22430866

ABSTRACT

Calculations of the induced currents created in the human body by external electromagnetic fields would be more accurate provided that more realistic experimental values of the electrical properties of the body were available. The purpose of this work is to experimentally obtain values for the conductivity of living organs in conditions close to the real situation. Two-electrode in vivo measurements of the bioimpedance of some porcine organs have been performed. From these measurements and taking into account geometrical considerations, the electrical conductivity for the kidney, liver, heart, and spinal cord has been obtained and were found to be higher than the values reported in the literature. Furthermore, a new experimental procedure is proposed where the conductivity is determined from the values of the electrical potential and currents that are induced by an external electromagnetic field created by a coil placed close to the organ under study.


Subject(s)
Electric Conductivity , Swine , Animals , Electrodes , Electromagnetic Fields , Humans , Organ Specificity
12.
Rev. chil. neuro-psiquiatr ; Rev. chil. neuro-psiquiatr;49(2): 149-156, 2011. ilus, tab
Article in Spanish | LILACS | ID: lil-597568

ABSTRACT

Children and teenagers with intellectual disability are a complex issue within the society and for the medical practice. Determining the more frequent forms of abuse, it's behaving in this particular population, and to evaluate the possible relationship between juvenile abuse and psychiatric co-morbidities were the main objectives in this investigation. 99 people with intellectual disability between 5 and 17 year old from three different communities (Felicia, Cocosol and Belen) located at Marianao municipality were selected by monoetapic conglomerate and studied firstly trough an analytic study with transversal cut seconded by a differentiated intervention according with the results. Taking into account the sociopsychiatric history, the psychiatric examination, using strictest observational techniques of the patient at home and the school, and applying the tools for diagnosis of infant abuse in this people, we concluded that juvenile abuse was a serious health problem in the studied population: negligence and carelessness the main types. The relationship between infant abuse and psychiatric co-morbities was demonstrated.


La condición de discapacidad intelectual convierte a niños y adolescentes en población de alta complejidad en la medicina. Determinar comportamiento y formas más frecuentes del maltrato en esta población, así como evaluar la relación entre maltrato infantil y comorbilidad psiquíatrica, fueron los objetivos fundamentales de esta investigación. Para ello se estudió una muestra de 99 pacientes discapacitados intelectuales en edades comprendidas entre 5 y 17 años de tres consejos populares (Felicia, Cocosol y Belén) del municipio Marianao, seleccionados por conglomerado monoetápico. Se realizó un estudio analítico de corte transversal en un primer momento, con intervención diferenciada según los resultados en un segundo momento. Mediante la historia socialpsiquíatrica, examen psiquiátrico, empleo de técnicas observacionales rigurosas del paciente en la casa y escuela y aplicación de instrumento para el diagnóstico de maltrato infantil en este tipo de población. Concluimos que el maltrato infantil fue un problema de salud en la muestra estudiada; el maltrato por negligencia o descuido fueron los más frecuentes. Se comprobó estrecha relación entre la existencia de maltrato infantil y comorbilidad psiquiátrica en los pacientes estudiados.


Subject(s)
Humans , Persons with Mental Disabilities , Child Abuse/diagnosis , Cross-Sectional Studies , Chile/epidemiology , Diagnosis, Dual (Psychiatry) , Surveys and Questionnaires
13.
Neuroscience ; 157(1): 105-19, 2008 Nov 11.
Article in English | MEDLINE | ID: mdl-18834930

ABSTRACT

Opiate addiction is a chronic medical disorder characterized by drug tolerance and dependence, behavioral sensitization, vulnerability to compulsive relapse, and high mortality. In laboratory animals, the potential effect of opiate drugs to induce cell death by apoptosis is a controversial topic. This postmortem human brain study examined the status of the extrinsic and intrinsic apoptotic pathways in the prefrontal cortex of a large group of well-characterized heroin or methadone abusers. In these subjects (n=36), the immunocontent of apoptosis-1 protein (Fas) death receptor did not differ from that in age-, gender-, and postmortem delay-matched controls. In contrast, Fas-associated protein with death domain (FADD), the mediator of the death signal, was significantly decreased in the same brain samples (all addicts: 30%, n=36; short-term abuse (ST): 31%, n=15; long-term abuse (LT): 29%, n=21). The initiator caspase-8 was not altered, but FLIP(L) (Fas-associated protein with death domain-like interleukin-1beta-converting enzyme-inhibitory protein), a dominant inhibitor of caspase-8, was increased in LT addicts (19%). In the intrinsic pathway, the pro-apoptotic mitochondrial proteins Bax (Bcl-2-associated X protein) and AIF (apoptosis-inducing factor) remained unchanged, but cytochrome c was decreased (all addicts: 25%; ST: 31%; LT: 20%) and anti-apoptotic B-cell leukemia 2 (Bcl-2) increased in LT addicts (24%). The content of executioner caspase-3 and the pattern of cleavage of the nuclear enzyme poly-(ADP-ribose)-polymerase-1 (PARP-1) were similar in opiate addicts and control subjects. Taken together, the data revealed that the extrinsic and intrinsic canonical apoptotic pathways are not abnormally activated in the prefrontal cortex of opiate abusers. Instead, the chronic modulation of some of their components (downregulation of FADD and cytochrome c; upregulation of FLIP(L) and Bcl-2) suggests the induction of non-apoptotic actions by opiate drugs related to phenomena of synaptic plasticity in the brain. These neurochemical adaptations could play a major role in the development of opiate tolerance, sensitization and relapse in human addicts.


Subject(s)
Apoptosis/physiology , Opioid-Related Disorders/pathology , Prefrontal Cortex/pathology , Signal Transduction/physiology , Acute Disease , Adult , Aging/metabolism , Apoptosis Regulatory Proteins/metabolism , Blotting, Western , Brain Chemistry , Chronic Disease , Female , Hair/chemistry , Humans , Male , Middle Aged , Narcotics/analysis , Narcotics/blood , Neuronal Plasticity/physiology , Opioid-Related Disorders/metabolism , Prefrontal Cortex/metabolism , Sex Characteristics , Synapses/physiology , Young Adult
14.
Phys Med Biol ; 53(6): 1701-13, 2008 Mar 21.
Article in English | MEDLINE | ID: mdl-18367798

ABSTRACT

The purpose of this work is to study the changes of the bioimpedance from its 'in vivo' value to the values measured in a few hours after the excision from the body. The evolution of electrical impedance with time after surgical extraction has been studied on two porcine organs: the liver and the kidney. Both in vivo and ex vivo measurements of electrical impedance, measuring its real and imaginary components, have been performed. The in vivo measurements have been carried out with the animal anaesthetized. The ex vivo measurements have been made more than 2 h after the extraction of the organ. The latter experiment has been carried out at two different stabilized temperatures: at normal body temperature and at the standard preservation temperature for transplant surgery. The measurements show a correlation between the biological evolution and the electrical bioimpedance of the organs, which increases from its in vivo value immediately after excision, multiplying its value by 2 in a few hours.


Subject(s)
Kidney/physiology , Liver/physiology , Swine , Animals , Body Temperature , Electric Impedance , Electrodes , Time Factors
15.
Int J Biochem Cell Biol ; 39(1): 133-45, 2007.
Article in English | MEDLINE | ID: mdl-16978906

ABSTRACT

While arginine-glycine-aspartic acid-based peptidomimetics have been employed for the treatment of cardiovascular disorders and cancer, their use in other contexts remains to be explored. Arginine-glycine-aspartic acid-serine induces Transforming growth factor-beta1 transcription in human mesangial cells, but the molecular mechanisms involved have not been studied extensively. We explored whether this effect could be due to Activator protein-1 activation and studied the potential pathways involved. Addition of arginine-glycine-aspartic acid-serine promoted Activator protein-1 binding to its cognate sequence within the Transforming growth factor-beta1 promoter as well as c-jun and c-fos protein abundance. Moreover, this effect was suppressed by curcumin, a c-Jun N terminal kinase inhibitor, and was absent when the Activator protein-1 cis-regulatory element was deleted. Activator protein-1 binding was dependent on the activity of integrin linked kinase, as transfection with a dominant negative mutant suppressed both Activator protein-1 binding and c-jun and c-fos protein increment. Integrin linked kinase was, in turn, dependent on Phosphoinositol-3 kinase activity. Arginine-glycine-aspartic acid-serine stimulated Phosphoinositol-3 kinase activity, and Transforming growth factor-beta1 promoter activation was abrogated by the use of Phosphoinositol-3 kinase specific inhibitors. In summary, we propose that arginine-glycine-aspartic acid-serine activates Integrin linked kinase via the Phosphoinositol-3 kinase pathway and this leads to activation of c-jun and c-fos and increased Activator protein-1 binding and Transforming growth factor-beta1 promoter activity. These data may contribute to understand the molecular mechanisms involved in the cellular actions of arginine-glycine-aspartic acid-related peptides and enhance their relevance as these products evolve into clinical therapeutic use.


Subject(s)
Mesangial Cells/metabolism , Peptides, Cyclic/pharmacology , Promoter Regions, Genetic , Signal Transduction/drug effects , Transcription Factor AP-1/metabolism , Transforming Growth Factor beta1/biosynthesis , Up-Regulation/drug effects , Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/metabolism , Cells, Cultured , Enzyme Activation/drug effects , Enzyme Activation/genetics , Humans , JNK Mitogen-Activated Protein Kinases/metabolism , Mutation , Neoplasms/drug therapy , Neoplasms/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Proto-Oncogene Proteins c-jun/metabolism , Signal Transduction/genetics , Transforming Growth Factor beta1/genetics
16.
Nefrologia ; 25 Suppl 2: 46-50, 2005.
Article in Spanish | MEDLINE | ID: mdl-16050402

ABSTRACT

Frequently underestimated, the deterioration of the renal function characteristic of the aging has very prominent clinical consequences. In the present article some aspects of the cellular and molecular biology of this process are analysed. The critical role of the oxidative stress and of TGFbeta are underlined. Determinant genetic factors are also mentioned. Such a knowledge can contribute to develop therapeutical strategies to prevent the decline of the.renal function that happens with the aging.


Subject(s)
Aging/physiology , Kidney/physiology , Age Factors , Aged , Aging/metabolism , Animals , Antioxidants/administration & dosage , Blotting, Northern , Extracellular Matrix/metabolism , Free Radicals , Glomerular Filtration Rate/physiology , Humans , Kidney/metabolism , Kidney Cortex/metabolism , Kidney Cortex/physiology , Oxidative Stress/physiology , RNA, Messenger/analysis , Rats , Superoxide Dismutase/metabolism , Transforming Growth Factor beta/genetics
17.
Nefrología (Madr.) ; 25(supl.2): 46-50, jun. 2005. graf
Article in Es | IBECS | ID: ibc-040024

ABSTRACT

Frecuentemente infraestimado, el deterioro de la función renal característico delenvejecimiento tiene consecuencias clínicas muy relevantes. En el presente artículose analizan algunos aspectos de la biología celular y molecular de este proceso,subrayándose el papel crítico del stress oxidativo y del TGF ��, así como tambiénprobablemente de condicionantes genéticos. Estos conocimientos pueden contribuira desarrollar estrategias terapéuticas útiles para prevenir el declinar de la funciónrenal que acontece con el envejecimiento


Frequently underestimated, the deterioration of the renal function characteristicof the aging has very prominent clinical consequences. In the present article someaspects of the cellular and molecular biology of this process are analysed. The criticalrole of the oxidative stress and of TGF �� are underlined. Determinant geneticfactors are also mentioned. Such a knowledge can contribute to develop therapeuticalstrategies to prevent the decline of the renal function that happens withthe aging


Subject(s)
Aged , Animals , Rats , Humans , Aging/metabolism , Aging/psychology , Kidney/metabolism , Kidney Cortex/metabolism , Kidney Cortex/physiology , Kidney/physiology , Age Factors , Antioxidants/administration & dosage , Blotting, Northern , Extracellular Matrix/metabolism , Free Radicals , Glomerular Filtration Rate/physiology , Oxidative Stress/physiology , RNA, Messenger/analysis
19.
J Mater Sci Mater Med ; 15(5): 559-65, 2004 May.
Article in English | MEDLINE | ID: mdl-15386963

ABSTRACT

PM2000 is a ferritic alloy obtained by powder metallurgy and is being investigated for potential applications as a biomaterial. This work aimed to assess the biological compatibility and to determine the influence of the processing route and further recrystallisation treatment on the magnetic behaviour. The magnetic behaviour has been analysed as a function of the hysteresis loop obtained by using an inductive method. The biocompatibility has been tested using human osteoblast-like cells seeded onto discs of PM2000. The ability of cells, on its surface, to attach, grow, and produce alkaline phosphatase (ALP) was determined. It is shown that PM2000 is a soft magnetic material irrespective of its material condition, its remanent magnetisation being very low (up to about 3% for the recrystallised swaged material). Fields close to 200 Oe are required to saturate the material. The saturation magnetisation is about 135 emu g(-1). In vitro tests indicate that cells are able to attach and grow onto its surface, and produce ALP, a specific marker of cells with bone-forming activity. In this respect, PM2000 holds promise as a suitable substrate for bone integration. These properties could make PM2000 a useful candidate for the preparation of medical devices where biocompatible and soft magnetic materials are sought. Applications for dental magnetic attachments could be envisaged.


Subject(s)
Aluminum/chemistry , Biocompatible Materials/chemistry , Chromium/chemistry , Crystallization/methods , Iron/chemistry , Magnetics , Osteoblasts/cytology , Osteoblasts/physiology , Titanium/chemistry , Cell Adhesion/physiology , Cell Line , Cell Proliferation , Cell Survival/physiology , Humans , Materials Testing , Microspheres , Osseointegration/physiology , Particle Size , Surface Properties
20.
Diagn Microbiol Infect Dis ; 47(2): 393-8, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14522512

ABSTRACT

Listeriosis (LT) is an important infection in immunocompromised patients, but no large series of LT in cancer patients have been recently described. We reviewed the records of 34 cancer patients with LT at our institution (1990-2001). Twenty patients (59%) had an underlying hematologic malignancy. In 11 patients, LT complicated bone marrow transplantation. Lymphocytopenia was observed in 62% of the patients. Twenty-six patients (76%) received prior corticosteroids. Bacteremia was the most common presentation of LT (74%) followed by meningoencephalitis (21%). The most common treatment of LT was ampicillin with or without gentamicin (68%). The median duration of treatment was 26 days (range, 8-74 days). The rate of response to antimicrobial therapy was 79%. No relapses were identified. LT contributed to death in 9 (75%) of the 12 patients who died. Meningoencephalitis had the worst prognosis (3 of 6 cases were fatal). Treatment of central nervous system LT continues to have a high failure rate.


Subject(s)
Listeria monocytogenes/isolation & purification , Listeriosis/epidemiology , Neoplasms/complications , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Bacteremia/epidemiology , Bacteremia/microbiology , Child, Preschool , Female , Hematologic Neoplasms/complications , Humans , Incidence , Listeria monocytogenes/drug effects , Listeriosis/drug therapy , Listeriosis/microbiology , Listeriosis/physiopathology , Male , Meningoencephalitis/epidemiology , Meningoencephalitis/microbiology , Microbial Sensitivity Tests , Middle Aged , Retrospective Studies
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