Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 17 de 17
Filtrar
1.
Rev Sci Instrum ; 93(3): 034102, 2022 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-35364973

RESUMEN

This paper describes the development of a novel medical x-ray imaging system adapted to the needs and constraints of low- and middle-income countries. The developed system is based on an indirect conversion chain: a scintillator plate produces visible light when excited by the x rays, and then, a calibrated multi-camera architecture converts the visible light from the scintillator into a set of digital images. The partial images are then unwarped, enhanced, and stitched through parallel field programmable gate array processing units and specialized software. All the detector components were carefully selected focusing on optimizing the system's image quality, robustness, cost-effectiveness, and capability to work in harsh tropical environments. With this aim, different customized and commercial components were characterized. The resulting detector can generate high quality medical diagnostic images with detective quantum efficiency levels up to 60% (@2.34 µGy), even under harsh environments, i.e., 60 °C and 98% humidity.


Asunto(s)
Países en Desarrollo , Programas Informáticos , Luz , Radiografía , Rayos X
2.
J Pediatr Gastroenterol Nutr ; 70(6): 820-824, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32443041

RESUMEN

OBJECTIVES: Dumping syndrome (DS) is mostly described as a complication of antireflux surgery in oesophageal atresia (OA) but we previously reported 2 cases of DS before any other surgery in infants operated at birth for OA. The objectives of the present study were to assess the prevalence of abnormal oral glucose tolerance test (OGTT) at 3 months of age in infants operated at birth with type C OA, to describe symptoms and clinical features, and to assess risk factors in infants presenting with abnormal OGTT suggestive of DS. METHODS: A prospective case series study including infants with type C OA without fundoplication, born between 2013 and 2016 in 8 centres was conducted. An OGTT was performed between 2.5 and 3.5 months. Abnormal OGTT was defined as early hyperglycaemia (>1.8 g/L until 30 minutes; >1.7 g/L between 30 minutes and 2 hours; and >1.4 g/L between 2 and 3 hours) and/or late hypoglycaemia (<0.6 g/L after 2 hours). RESULTS: Eleven of the 38 OGTT (29%) showed abnormalities. None of the patients' demographics (birth weight, sex, prematurity, associated malformation, use of enteral nutrition) or conditions of the surgery tested was associated with abnormal OGTT. No clinical sign was specific for it. CONCLUSIONS: DS should be considered in every infant operated at birth for OA presenting with digestive symptoms. No risk factor was predictive for abnormal OGTT. An OGTT to screen for potential DS around 3 months of age should be considered in infants born with EA. CLINICAL TRIAL NAME AND REGISTRATION NUMBER: DUMPING NCT02525705.


Asunto(s)
Atresia Esofágica , Síndrome de Vaciamiento Rápido/diagnóstico , Síndrome de Vaciamiento Rápido/epidemiología , Síndrome de Vaciamiento Rápido/etiología , Atresia Esofágica/cirugía , Fundoplicación , Prueba de Tolerancia a la Glucosa , Humanos , Lactante , Recién Nacido , Estudios Prospectivos
3.
J Pediatr ; 211: 120-125.e1, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31072651

RESUMEN

OBJECTIVE: To identify predictors of and factors associated with the performance of antireflux surgery during the first year of life in children born with esophageal atresia. STUDY DESIGN: All patients were included in a French registry for esophageal atresia. All 38 multidisciplinary French centers completed questionnaires about perinatal characteristics and one-year outcome for children born with esophageal atresia. RESULTS: Of 835 infants with esophageal atresia born in France from 2010 to 2014, 682 patients, excluding those with long-gap esophageal atresia, were included. Three patients had type I, 669 had type III, and 10 had type IV esophageal atresia. Fifty-three children (7.8%) received fundoplication during the first year of life. The median age at the time of the end-to-end esophageal anastomosis was 1.1 day (range 0-15). Multivariate analysis identified three perioperative factors that predicted the need for early antireflux surgery: anastomotic tension (P = .004), associated malformations (P = .019), and low birth weight (P = .018). Six other factors, measured during the first year of life, were associated with the need for antireflux surgery: gastroesophageal reflux (P < .001), anastomotic stricture (P < .001), gastrostomy (P < .001), acute life-threatening event (P = .002), respiratory complications (P = .045), and poor nutritional status (P < .001). CONCLUSIONS: Gastroesophageal reflux disease, low birth weight, poor nutrition, and surgical anastomosis difficulties predicted the performance of antireflux surgery in the first year of life in infants with esophageal atresia.


Asunto(s)
Atresia Esofágica/cirugía , Fundoplicación , Anastomosis Quirúrgica/efectos adversos , Constricción Patológica , Atresia Esofágica/clasificación , Femenino , Francia , Reflujo Gastroesofágico/cirugía , Gastrostomía , Humanos , Lactante , Recién Nacido de Bajo Peso , Recién Nacido , Masculino , Análisis Multivariante , Estado Nutricional , Sistema de Registros
4.
Bioorg Med Chem ; 26(18): 5169-5180, 2018 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-30253886

RESUMEN

Free fatty acid-2 (FFA2) receptor is a G-protein coupled receptor of interest in the development of therapeutics in metabolic and inflammatory disease areas. The discovery and optimization of an N-thiazolylamide carboxylic acid FFA2 agonist scaffold is described. Dual key objectives were to i) evaluate the potential of this scaffold for lead optimization in particular with respect to safety de-risking physicochemical properties, i.e. lipophilicity and aromatic content, and ii) to demonstrate the utility of selected lead analogues from this scaffold in a pertinent in vivo model such as oral glucose tolerance test (OGTT). As such, a concomitant improvement in bioactivity together with lipophilic ligand efficiency (LLE) and fraction sp3 content (Fsp3) parameters guided these efforts. Compound 10 was advanced into studies in mice on the basis of its optimized profile vs initial lead 1 (ΔLLE = 0.3, ΔFsp3 = 0.24). Although active in OGTT, 10 also displayed similar activity in the FFA2-knockout mice. Given this off-target OGTT effect, we discontinued development of this FFA2 agonist scaffold.


Asunto(s)
Diabetes Mellitus Experimental/tratamiento farmacológico , Modelos Animales de Enfermedad , Descubrimiento de Drogas , Receptores de Superficie Celular/agonistas , Tiazoles/farmacología , Animales , Relación Dosis-Respuesta a Droga , Humanos , Ratones , Ratones Noqueados , Estructura Molecular , Ratas , Receptores de Superficie Celular/deficiencia , Receptores de Superficie Celular/metabolismo , Relación Estructura-Actividad , Tiazoles/química
5.
Eur Urol ; 74(2): 167-176, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-29472143

RESUMEN

BACKGROUND: Laparoscopic mesh sacropexy (LS) or transvaginal mesh repair (TVM) are surgical techniques used to treat cystoceles. Health authorities have highlighted the need for comparative studies to evaluate the safety of surgeries with meshes. OBJECTIVE: To compare the rate of complications, and functional and anatomical outcomes between LS and TVM. DESIGN, SETTING, AND PARTICIPANTS: Multicenter randomized controlled trial from October 2012 to April 2014 in 11 French public hospitals. Women with cystocele stage ≥2 (pelvic organ prolapse quantification), aged 45-75 yr, without previous prolapse surgery. INTERVENTION: Synthetic nonabsorbable mesh placed in the vesicovaginal space, sutured to the promontory (LS) or maintained by arms through pelvic ligaments (TVM). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Rate of surgical complications ≥grade II according to the modified Clavien-Dindo classification at 1 yr. Secondary outcomes were reintervention rate, and functional and anatomical results. RESULTS AND LIMITATIONS: A total of 130 women were randomized in LS and 132 in TVM; five women withdrew before intervention, leaving 129 in LS and 128 in TVM. The rate of complications ≥grade II was lower after LS than after TVM, but did not meet statistical significance (17% vs 26%, treatment difference 8.6% [95% confidence interval, CI -1.5 to 18]; p=0.088). The rate of complications of grade III or higher was nonetheless significantly lower after LS (LS=0.8%, TVM=9.4%, treatment difference 8.6% [95% CI 3.4%; 15%]; p=0.001). LS was converted to TVM in 6.3%. The total reoperation rate was lower after LS but did not meet statistical significance (LS=4.7%, TVM=10.9%, treatment difference 6.3% [95% CI -0.4 to 13.3]; p=0.060). There was no difference in symptoms, quality of life, improvement, composite definition of success, anatomical results rates between groups except for the vaginal apex and length, and dyspareunia (in favor of LS). CONCLUSIONS: LS is a valuable option for primary repair of cystocele in sexually active patients. LS is safer than TVM, but may not be feasible in all cases. Both techniques offer same functional outcomes, success rates, and anatomical outcomes, but sexual function is better preserved by LS. PATIENT SUMMARY: Our study demonstrates that laparoscopic sacropexy (LS) is a valuable option for primary repair of cystocele. LS offers equivalent success rates to vaginal mesh procedures, but is safer with a lower rate of complications and reoperations, and sexual function is better preserved.


Asunto(s)
Cistocele/cirugía , Diafragma Pélvico/cirugía , Mallas Quirúrgicas , Procedimientos Quirúrgicos Urológicos/instrumentación , Procedimientos Quirúrgicos Urológicos/métodos , Anciano , Cistocele/diagnóstico , Cistocele/fisiopatología , Femenino , Francia , Humanos , Laparoscopía/efectos adversos , Persona de Mediana Edad , Diafragma Pélvico/fisiopatología , Complicaciones Posoperatorias/etiología , Calidad de Vida , Recuperación de la Función , Factores de Riesgo , Técnicas de Sutura , Factores de Tiempo , Resultado del Tratamiento , Procedimientos Quirúrgicos Urológicos/efectos adversos
6.
J Pediatr ; 193: 204-210, 2018 02.
Artículo en Inglés | MEDLINE | ID: mdl-29212620

RESUMEN

OBJECTIVE: To evaluate the status of congenital diaphragmatic hernia (CDH) management in France and to assess predictors of adverse outcomes. STUDY DESIGN: We reviewed the first-year outcome of all cases of CDH reported to the French National Register in 2011. RESULTS: A total of 158 cases were included. Of these, 83% (131) were prenatally diagnosed, with a mortality rate of 39% (44 of 112) for live born infants with a known outcome at hospital discharge. Mortality increased to 47% (60 of 128) including those with termination of pregnancy and fetal loss. This contrasts with the 7% (2 of 27) mortality rate of the patients diagnosed postnatally (P = .002). Mortality worsened with 1 prenatal marker of CDH severity (OR 3.38 [1.30-8.83] P = .013) and worsened further with 2 markers (OR 20.64 [5.29-80.62] P < .001). Classic postnatal risk factors of mortality such as side of hernia (nonleft P = .001), prematurity (P < .001), low birth weight (P = .002), and size of the defect (P < .001) were confirmed. Of the 141 live births (114 prenatal and 27 postnatal diagnosis) with known outcomes, 93 (67%) survived to hospital discharge, 68 (60%) with a prenatal diagnosis and 25 (93%) with a postnatal diagnosis. The median time to hospital discharge was 34 days (IQR, 19.25-62). Of these survivors, 71 (76%) were followed up for 1 year. CONCLUSIONS: Despite advances in management of CDH, mortality was high and associated with prenatal risk factors. Postnatally, severe persistent pulmonary hypertension was difficult to predict and presented persistent challenges in management.


Asunto(s)
Hernias Diafragmáticas Congénitas/mortalidad , Femenino , Francia , Hernias Diafragmáticas Congénitas/terapia , Humanos , Lactante , Mortalidad Infantil , Recién Nacido , Masculino , Embarazo , Atención Prenatal , Diagnóstico Prenatal , Estudios Prospectivos , Sistema de Registros , Factores de Riesgo , Tasa de Supervivencia , Resultado del Tratamiento
7.
Clin Case Rep ; 4(7): 692-5, 2016 07.
Artículo en Inglés | MEDLINE | ID: mdl-27386131

RESUMEN

Kasabach-Merritt phenomenon can be encountered in the perinatal period. No consensus exists regarding prenatal management. We report one prenatal case leading to therapeutic abortion and one neonatal case, successfully treated by a multimodal therapy. Prenatal counseling should include the possibility of neonatal multimodal treatment that can lead to favorable outcomes.

8.
J Med Chem ; 58(7): 3060-82, 2015 Apr 09.
Artículo en Inglés | MEDLINE | ID: mdl-25738882

RESUMEN

Neurokinin-3 receptor (NK3R) has recently emerged as important in modulating the tonic pulsatile gonadotropin-releasing hormone (GnRH) release. We therefore decided to explore NK3R antagonists as therapeutics for sex-hormone disorders that can potentially benefit from lowering GnRH pulsatility with consequent diminished levels of plasma luteinizing hormone (LH) and correspondingly attenuated levels of circulating androgens and estrogens. The discovery and lead optimization of a novel N-acyl-triazolopiperazine NK3R antagonist chemotype achieved through bioisosteric lead change from the high-throughput screening (HTS) hit is described. A concomitant improvement in the antagonist bioactivity and ligand lipophilic efficiency (LLE) parameter were the principal guidelines in the lead optimization efforts. Examples of advanced lead analogues to demonstrate the amenability of this chemotype to achieving a suitable pharmacokinetic (PK) profile are provided as well as pharmacokinetic-pharmacodynamic (PKPD) correlations to analyze the trends observed for LH inhibition in castrated rats and monkeys that served as preliminary in vivo efficacy models.


Asunto(s)
Ensayos Analíticos de Alto Rendimiento/métodos , Receptores de Neuroquinina-3/antagonistas & inhibidores , Relación Estructura-Actividad , Andrógenos/sangre , Animales , Encéfalo/efectos de los fármacos , Encéfalo/metabolismo , Células CHO/efectos de los fármacos , Células CACO-2/efectos de los fármacos , Técnicas de Química Sintética , Cricetulus , Cristalografía por Rayos X , Descubrimiento de Drogas , Canal de Potasio ERG1 , Enfermedades del Sistema Endocrino/sangre , Enfermedades del Sistema Endocrino/tratamiento farmacológico , Canales de Potasio Éter-A-Go-Go/química , Canales de Potasio Éter-A-Go-Go/metabolismo , Humanos , Ligandos , Hormona Luteinizante/sangre , Masculino , Ratas Sprague-Dawley , Receptores de Neuroquinina-3/genética
9.
Orphanet J Rare Dis ; 9: 206, 2014 Dec 11.
Artículo en Inglés | MEDLINE | ID: mdl-25496976

RESUMEN

BACKGROUND: The aim of the present national prospective population-based study was to assess the early morbidity of esophageal atresia (EA). METHODS: All 38 multidisciplinary French centers that care for patients with EA returned a specific questionnaire about the 1-year outcome for each patient. This information was centralized, checked, and entered into a database. RESULTS: From the total population of 307 EA patients born in 2008 and 2009, data about the 1-year outcome were obtained from 301 (98%) patients, of whom 4% were lost to follow-up and 5% died. Medical complications occurred in 34% of the patients: anastomotic leaks (8%), recurrent tracheoesophageal fistula (4%), and anastomotic stenosis (22%); all of the latter group needed dilation (median, 2 dilations/patient). A new hospitalization was required for 59% of patients (2.5 hospitalizations/patient) for digestive (52%) or respiratory (48%) reasons. Twelve percent of patients required antireflux surgery at a median age of 164 days (range, 33-398 days), and 1% underwent an aortopexy for severe tracheomalacia. The weight/age Z-score was -0.8 (range, -5.5 to 3.7 months) at 12 months. Fifteen percent of patients were undernourished at 12 months of age, whereas 37% presented with respiratory symptoms and 15% had dysphagia at the last follow-up. Significant independent factors associated with medical complications were anastomotic esophageal tension (p = .0009) and presence of a gastrostomy (p = .0002); exclusive oral feeding at discharge was associated with a decreased risk of complications (p = .007). CONCLUSIONS: Digestive and respiratory morbidities remain frequent during the first year of life and are associated with difficult anastomosis and lack of full oral feeding.


Asunto(s)
Atresia Esofágica/diagnóstico , Atresia Esofágica/epidemiología , Vigilancia de la Población , Sistema de Registros , Atresia Esofágica/terapia , Femenino , Estudios de Seguimiento , Francia/epidemiología , Hospitalización/tendencias , Humanos , Lactante , Recién Nacido , Masculino , Vigilancia de la Población/métodos , Factores de Tiempo , Resultado del Tratamiento
10.
Pediatrics ; 134(3): e790-7, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25092937

RESUMEN

OBJECTIVES: High-fidelity simulation is an effective tool in teaching neonatal resuscitation skills to professionals. We aimed to determine whether in situ simulation training (for ∼80% of the delivery room staff) improved neonatal resuscitation performed by the staff at maternities. METHODS: A baseline evaluation of 12 maternities was performed: a random sample of 10 professionals in each unit was presented with 2 standardized scenarios played on a neonatal high-fidelity simulator. The medical procedures were video recorded for later assessments. The 12 maternities were then randomly assigned to receive the intervention (a 4-hour simulation training session delivered in situ for multidisciplinary groups of 6 professionals) or not receive it. All maternities were evaluated again at 3 months after the intervention. The videos were assessed by 2 neonatologists blinded to the pre-/postintervention as well as to the intervention/control groups. The performance was assessed using a technical score and a team score. RESULTS: After intervention, the median technical score was significantly higher for scenarios 1 and 2 for the intervention group compared with the control group (P = .01 and 0.004, respectively), the median team score was significantly higher (P < .001) for both scenarios. In the intervention group, the frequency of achieving a heart rate >90 per minute at 3 minutes improved significantly (P = .003), and the number of hazardous events decreased significantly (P < .001). CONCLUSIONS: In situ simulation training with multidisciplinary teams can effectively improve technical skills and teamwork in neonatal resuscitation.


Asunto(s)
Competencia Clínica , Maniquíes , Partería/educación , Médicos , Resucitación/educación , Resucitación/métodos , Competencia Clínica/normas , Humanos , Recién Nacido , Partería/normas , Médicos/normas , Resucitación/normas
11.
Bioorg Med Chem Lett ; 23(1): 47-54, 2013 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-23218716

RESUMEN

Tsitsikammamines are marine alkaloids whose structure is based on the pyrroloiminoquinone scaffold. These and related compounds have attracted attention due to various interesting biological properties, including cytotoxicity, topoisomerase inhibition, antimicrobial, antifungal and antimalarial activity. Indoleamine 2,3-dioxygenase (IDO1) is a well-established therapeutic target as an important factor in the tumor immune evasion mechanism. In this preliminary communication, we report the inhibitory activity of tsitsikammamine derivatives against IDO1. Tsitsikammamine A analogue 11b displays submicromolar potency in an enzymatic assay. A number of derivatives are also active in a cellular assay while showing little or no activity towards tryptophan 2,3-dioxygenase (TDO), a functionally related enzyme. This IDO1 inhibitory activity is rationalized by molecular modeling studies. An interest is thus established in this class of compounds as a potential source of lead compounds for the development of new pharmaceutically useful IDO1 inhibitors.


Asunto(s)
Indolamina-Pirrol 2,3,-Dioxigenasa/antagonistas & inhibidores , Pirroles/química , Quinolinas/química , Alcaloides/síntesis química , Alcaloides/química , Alcaloides/toxicidad , Sitios de Unión , Línea Celular , Supervivencia Celular/efectos de los fármacos , Humanos , Indolamina-Pirrol 2,3,-Dioxigenasa/metabolismo , Simulación del Acoplamiento Molecular , Estructura Terciaria de Proteína , Pirroles/síntesis química , Pirroles/toxicidad , Quinolinas/síntesis química , Quinolinas/toxicidad , Relación Estructura-Actividad
12.
Bioorg Med Chem Lett ; 21(7): 1991-6, 2011 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-21376585

RESUMEN

A series of 3-aryl-5-acylpiperazinyl-pyrazoles (e.g., 3a-b) initially identified through a high-throughput screening campaign using the aequorin Ca(2+) bioluminescence assay as novel, potent small molecule antagonists of the G protein-coupled human tachykinin NK(3) receptor (hNK3-R) is described. Preliminary profiling revealed poor plasma and metabolic stability for these structures in rodents. Further optimization efforts resulted in analogs with improved potency, stability, and pharmacokinetic properties as well as good brain permeability, for example, compounds 26 and 42. Unexpected cytotoxicity was observed in such N-Me pyrazole structures as compounds 41-42.


Asunto(s)
Pirazoles/química , Pirazoles/farmacología , Receptores de Neuroquinina-3/antagonistas & inhibidores , Animales , Línea Celular Tumoral , Descubrimiento de Drogas , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Concentración 50 Inhibidora , Pirazoles/farmacocinética , Ratas , Relación Estructura-Actividad
13.
Eur J Med Chem ; 46(7): 3058-65, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21419531

RESUMEN

Indoleamine 2,3-dioxygenase (IDO) is an important new therapeutic target for the treatment of cancer. With the aim of discovering novel IDO inhibitors, a virtual screen was undertaken and led to the discovery of the keto-indole derivative 1a endowed with an inhibitory potency in the micromolar range. Detailed kinetics were performed and revealed an uncompetitive inhibition profile. Preliminary SARs were drawn in this series and corroborated the putative binding orientation as suggested by docking.


Asunto(s)
Antineoplásicos/química , Inhibidores Enzimáticos/química , Indolamina-Pirrol 2,3,-Dioxigenasa/antagonistas & inhibidores , Indoles/química , Simulación del Acoplamiento Molecular , Proteínas de Neoplasias/antagonistas & inhibidores , Animales , Línea Celular Tumoral , Bases de Datos de Compuestos Químicos , Descubrimiento de Drogas , Pruebas de Enzimas , Escherichia coli/genética , Expresión Génica , Ensayos Analíticos de Alto Rendimiento , Humanos , Indolamina-Pirrol 2,3,-Dioxigenasa/química , Indolamina-Pirrol 2,3,-Dioxigenasa/genética , Ratones , Proteínas de Neoplasias/química , Proteínas de Neoplasias/genética , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Relación Estructura-Actividad , Triptófano/química
14.
Bioorg Med Chem ; 19(4): 1550-61, 2011 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-21269836

RESUMEN

Indoleamine 2,3-dioxygenase (IDO) is a heme dioxygenase which has been shown to be involved in the pathological immune escape of diseases such as cancer. The synthesis and structure-activity relationships (SAR) of a novel series of IDO inhibitors based on the indol-2-yl ethanone scaffold is described. In vitro and in vivo biological activities have been evaluated, leading to compounds with IC(50) values in the micromolar range in both tests. Introduction of small substituents in the 5- and 6-positions of the indole ring, indole N-methylation and variations of the aromatic side chain are all well tolerated. An iron coordinating group on the linker is a prerequisite for biological activity, thus corroborating the virtual screening results.


Asunto(s)
Etano/química , Indolamina-Pirrol 2,3,-Dioxigenasa/antagonistas & inhibidores , Indoles/química , Indoles/farmacología , Dominio Catalítico , Línea Celular , Humanos , Indolamina-Pirrol 2,3,-Dioxigenasa/química , Modelos Moleculares , Dominios y Motivos de Interacción de Proteínas , Relación Estructura-Actividad
15.
J Med Chem ; 53(15): 5576-86, 2010 Aug 12.
Artículo en Inglés | MEDLINE | ID: mdl-20684600

RESUMEN

Success in discovering bioactive peptide mimetics is often limited by the difficulties in correctly transposing known binding elements of the active peptide onto a small and metabolically more stable scaffold while maintaining bioactivity. Here we describe a scanning approach using a library of pyranose-based peptidomimetics that is structurally diverse in a systematic manner, designed to cover all possible conformations of tripeptide motifs containing two aromatic groups and one positive charge. Structural diversity was achieved by efficient selection of various chemoforms, characterized by a choice of pyranose scaffold of defined chirality and substitution pattern. A systematic scanning library of 490 compounds was thus designed, produced, and screened in vitro for activity at the somatostatin (sst(1-5)) and melanin-concentrating hormone (MCH(1)) receptors. Bioactive compounds were found for each target, with specific chemoform preferences identified in each case, which can be used to guide follow-on drug discovery projects without the need for scaffold hopping.


Asunto(s)
Monosacáridos/química , Oligopéptidos/química , Aminoácidos/química , Animales , Unión Competitiva , Células CHO , Cricetinae , Cricetulus , Bases de Datos Factuales , Humanos , Modelos Moleculares , Conformación Molecular , Imitación Molecular , Monosacáridos/farmacología , Oligopéptidos/farmacología , Ensayo de Unión Radioligante , Receptores de Somatostatina/antagonistas & inhibidores , Estereoisomerismo , Relación Estructura-Actividad
16.
Anal Chem ; 78(1): 35-43, 2006 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-16383308

RESUMEN

G protein-coupled receptors (GPCRs) constitute important targets for drug discovery against a wide range of ailments including cancer, inflammatory, and cardiovascular diseases. Efforts are underway to screen selective modulators of GPCRs and also to deorphanize GPCRs with unidentified natural ligands. Most GPCR-based cellular screens depend on labeling or recombinant expression of receptor or reporter proteins, which may not capture the true physiology or pharmacology of the GPCRs. In this paper, we describe a noninvasive and label-free assay for GPCRs that can be used with both engineered and nonengineered cell lines. The assay is based on using cell-electrode impedance to measure minute changes in cellular morphology as a result of ligand-dependent GPCR activation. We have used this technology to assay the functional activation of GPCRs coupled to different signaling pathways and have compared it to standard assays. We have used pharmacological modulators of GPCR signaling pathways to demonstrate the specificity of impedance-based measurements. Our data indicate that cell-electrode impedance measurements offer a convenient, sensitive, and quantitative method for assessing GPCR function. Moreover, the noninvasive nature of the readout offers the added advantage of performing multiple treatments in the same well to study events such as desensitization and receptor cross-talk.


Asunto(s)
Electrónica , Receptores Acoplados a Proteínas G/metabolismo , Transducción de Señal , Animales , Western Blotting , Células CHO/metabolismo , Células CHO/ultraestructura , Cricetinae , Cricetulus , AMP Cíclico/metabolismo , Dopamina/metabolismo , Impedancia Eléctrica , Células HeLa/metabolismo , Células HeLa/ultraestructura , Histamina/metabolismo , Humanos , Inmunoprecipitación , Fosfatos de Inositol/metabolismo , Cinética , Ligandos , Microscopía Fluorescente , Receptores Dopaminérgicos/genética , Receptores Dopaminérgicos/metabolismo , Receptores Histamínicos/genética , Receptores Histamínicos/metabolismo , Receptores de Vasopresinas/genética , Receptores de Vasopresinas/metabolismo , Análisis Espectral , Vasopresinas/metabolismo
17.
J Cutan Pathol ; 32(7): 506-11, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16008696

RESUMEN

Fucosidosis is a rare lysosomal storage disease due to alpha-L-fucosidase deficiency. It presents clinically with neurological, skeletal, and cutaneous findings, including mainly angiokeratoma corporis diffusum. Electronmicroscopic examination reveals characteristic electron-lucent cytoplasmic vacuolization present in several cell types of the skin and other tissues. We present here a new patient suffering from fucosidosis with angiokeratoma, whose normal and diseased skin was studied by lightmicroscopy and electronmicroscopy. The salient clinicopathological features of this disease are briefly reviewed.


Asunto(s)
Enfermedad de Fabry/patología , Fucosidosis/patología , Piel/patología , Adolescente , Biomarcadores/metabolismo , Enfermedad de Fabry/complicaciones , Enfermedad de Fabry/enzimología , Femenino , Fucosidosis/complicaciones , Fucosidosis/enzimología , Humanos , Inmunohistoquímica , Microscopía Electrónica de Transmisión , Piel/enzimología , Telangiectasia/patología , Vacuolas/ultraestructura , alfa-L-Fucosidasa/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...