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1.
PLoS One ; 11(6): e0157640, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27322070

RESUMEN

OBJECTIVES: Assessment of the clinical severity of Fabry disease (FD), an X-linked, rare, progressive disorder based on a genetic defect in alpha-galactosidase is challenging, especially regarding cardiac involvement. The aim of the study was to evaluate the diagnostic value of cardiac troponin I (cTnI) in discriminating FD patients with cardiac involvement in a large FD patient cohort. METHODS: cTnI levels were measured with a contemporary sensitive assay in plasma samples taken routinely from FD patients. The assay was calibrated to measure cTnI levels ≥0.01 ng/ml. Elevated cTnI values (cut-off ≥0.04 ng/ml) were correlated with clinical data. RESULTS: cTnI was assessed in 62 FD patients (median age: 47 years, males: 36%). Elevated cTnI levels were detected in 23 (37%) patients. Patients with a cTnI elevation were older (median 55 years versus 36 years, p<0.001). Elevated cTnI levels were associated with the presence of a LVH (16/23 versus 1/39; OR 65.81, CI: 6.747-641.859; p<0.001). In almost all patients with a left ventricular hypertrophy (LVH) elevated cTnI levels were detected (16/17, 94%). Absolute cTnI levels in patients with LVH were higher than in those without (median 0.23 ng/ml versus 0.02 ng/ml; p<0.001). A cTnI level <0.04ng/ml had a high negative predictive value regarding the presence of a LVH (38/39, 97%). In a control group of non-FD patients (n = 17) with LVH (due to hypertension) none showed cTnI levels ≥0.01 ng/ml. CONCLUSIONS: Elevated cTnI levels are common in FD patients, reflecting cardiac involvement. FD patients might benefit from a continuous cTnI monitoring.


Asunto(s)
Enfermedad de Fabry/sangre , Miocardio/patología , Troponina I/sangre , Factores de Edad , Biomarcadores/sangre , Femenino , Humanos , Hipertrofia Ventricular Izquierda/sangre , Modelos Logísticos , Masculino , Persona de Mediana Edad , Caracteres Sexuales
2.
Biol Chem ; 389(12): 1505-12, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18844452

RESUMEN

The calpain inhibitor A-705253 and the Na(+)/H(+)-exchange inhibitor Cariporide were studied in isolated perfused rabbit hearts subjected to 60 min occlusion of the ramus interventricularis of the left coronary artery (below the origin of the first diagonal branch), followed by 120 min of reperfusion. The inhibitors were added to the perfusion fluid solely or in combination at the beginning of reperfusion. Hemodynamic monitoring and biochemical analysis of perfusion fluid from the coronary outflow were performed. Myocardial infarct size and area at risk (transiently not perfused myocardium) were determined from left ventricular slices after a special staining procedure with Evans blue and 2,3,5-triphenyltetrazolium chloride. The infarcted area (dead myocardium) was 72.7+/-4.0% of the area at risk in untreated controls, but was significantly smaller in the presence of the inhibitors. The largest effect was seen with 10(-6) m A-705253, which reduced the infarcted area to 49.2+/-4.1% of the area at risk, corresponding to a reduction of 33.6%. Cariporide at 10(-6) m reduced the infarct size to the same extent. The combination of both inhibitors, however, did not further improve cardioprotection. No statistical difference was observed between the experimental groups in coronary perfusion, left ventricular pressure, heart rate, and in the release of lactate dehydrogenase and creatin kinase from heart muscle.


Asunto(s)
Antiarrítmicos/uso terapéutico , Benzamidas/uso terapéutico , Calpaína/antagonistas & inhibidores , Guanidinas/uso terapéutico , Corazón/efectos de los fármacos , Infarto del Miocardio/prevención & control , Intercambiadores de Sodio-Hidrógeno/antagonistas & inhibidores , Sulfonas/uso terapéutico , Animales , Presión Sanguínea/efectos de los fármacos , Circulación Coronaria/fisiología , Femenino , Frecuencia Cardíaca/efectos de los fármacos , Técnicas In Vitro , Masculino , Infarto del Miocardio/patología , Miocardio/patología , Potasio/metabolismo , Conejos , Función Ventricular Izquierda/efectos de los fármacos
3.
Br J Nutr ; 98(6): 1170-7, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17640415

RESUMEN

We have recently shown that a polyphenol-rich insoluble dietary fibre preparation from carob pulp (Ceratonia siliqua L; carob fibre) decreased postprandial acylated ghrelin, TAG and NEFA during an acute liquid meal challenge test. However, delayed effects of carob fibre consumption are unknown. Therefore, a randomized controlled crossover study in nineteen healthy volunteers consuming foods with or without 50 g carob fibre was conducted. On the subsequent day (day 2), glucose, TAG, total and acylated ghrelin as well as insulin, NEFA and leptin were assessed at baseline and at timed intervals for 300 min after ingestion of standardized bread. Consumption of carob fibre-enriched foods did not affect fasting concentrations of glucose, TAG, total ghrelin, NEFA, insulin and leptin. Fasting acylated ghrelin was increased on the day subsequent to carob fibre consumption compared with control (P = 0.046). After consumption of the standard bread on day 2, glucose response (P = 0.029) was increased, and TAG (P = 0.033) and NEFA (P < 0.001) responses were decreased compared with control. Postprandial responses of total and acylated ghrelin, insulin and leptin on day 2 were unaffected by carob fibre consumption the previous day. In conclusion, an increase in total and acylated plasma ghrelin accompanied by enhanced lipid metabolism after carob fibre consumption suggests higher lipid utilization and suppressed lipolysis on the day subsequent to carob fibre consumption. However, elevated glucose levels after carob fibre consumption need to be addressed in future studies.


Asunto(s)
Fibras de la Dieta/administración & dosificación , Flavonoides/administración & dosificación , Galactanos , Ghrelina/sangre , Lípidos/sangre , Mananos , Fenoles/administración & dosificación , Gomas de Plantas , Acilación , Adulto , Consumo de Bebidas Alcohólicas , Análisis de Varianza , Glucemia/análisis , Composición Corporal , Colon/metabolismo , Estudios Cruzados , Ácidos Grasos no Esterificados/sangre , Femenino , Humanos , Insulina/sangre , Masculino , Persona de Mediana Edad , Polifenoles , Triglicéridos/análisis
4.
J Nutr ; 136(6): 1533-8, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16702317

RESUMEN

Ghrelin is an orexigenic hormone that may affect substrate utilization in humans. Ghrelin is influenced by macronutrients, but the effects of insoluble dietary fiber and polyphenols are unknown. We investigated the effects of a polyphenol-rich insoluble dietary fiber preparation from carob pulp (carob fiber) on postprandial ghrelin responses and substrate utilization. Dose-dependent effects of the consumption of carob fiber were investigated in a randomized, single-blind, crossover study in 20 healthy subjects, aged 22-62 y. Plasma total and acylated ghrelin, triglycerides, and serum insulin and nonesterified fatty acids (NEFA) levels were repeatedly assessed before and after ingestion of an isocaloric standardized liquid meal with 0, 5, 10, or 20 g of carob fiber over a 300-min period. The respiratory quotient (RQ) was determined after consumption of 0 or 20 g of carob fiber. Carob fiber intake lowered acylated ghrelin to 49.1%, triglycerides to 97.2%, and NEFA to 67.2% compared with the control meal (P < 0.001). Total ghrelin and insulin concentrations were not affected by consumption of a carob fiber-enriched liquid meal. Postprandial energy expenditure was increased by 42.3% and RQ was reduced by 99.9% after a liquid meal with carob fiber compared with a control meal (P < 0.001). We showed that the consumption of a carob pulp preparation, an insoluble dietary fiber rich in polyphenols, decreases postprandial responses of acylated ghrelin, triglycerides, and NEFA and alters RQ, suggesting a change toward increased fatty acid oxidation. These results indicate that carob fiber might exert beneficial effects in energy intake and body weight.


Asunto(s)
Antidiarreicos/farmacología , Fibras de la Dieta/farmacología , Flavonoides/farmacología , Galactanos/farmacología , Mananos/farmacología , Hormonas Peptídicas/sangre , Fenoles/farmacología , Adulto , Antidiarreicos/administración & dosificación , Calorimetría Indirecta , Estudios Cruzados , Ácidos Grasos no Esterificados/sangre , Femenino , Galactanos/administración & dosificación , Ghrelina , Humanos , Peroxidación de Lípido/efectos de los fármacos , Masculino , Mananos/administración & dosificación , Persona de Mediana Edad , Gomas de Plantas , Polifenoles , Periodo Posprandial , Triglicéridos/sangre
5.
Biol Chem ; 385(11): 1077-82, 2004 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-15576328

RESUMEN

Two novel calpain inhibitors (A-705239 and A-705253) were studied in isolated perfused rabbit hearts subjected to 60-min occlusion of the ramus interventricularis of the left coronary artery (below the origin of the first diagonal branch), followed by 120 min of reperfusion. The inhibitors were added to the perfusion fluid in various final concentrations from the beginning of the experiments before the coronary artery was blocked. Hemodynamic monitoring and biochemical analysis of perfusion fluid from the coronary outflow were carried out. Myocardial infarct size and the area at risk (transiently non-perfused myocardium) were determined from left ventricular slices after a special staining procedure with Evans blue and 2,3,5-triphenyltetrazolium chloride. The infarcted area (dead myocardium) was 77.9+/-2.3% of the area at risk in untreated controls ( n =12). The infarct size was significantly reduced in the presence of both calpain inhibitors. The best effect was achieved with 10 -8 M A-705253 ( n =8), which reduced ( p <0.001) the infarcted area to 49.3+/-3.9% of the area at risk, corresponding to an infarct reduction of 61.8%. No statistical difference was observed between the experimental groups in coronary perfusion, left ventricular pressure, and in the release of lactate dehydrogenase and creatine kinase from heart muscle.


Asunto(s)
Benzamidas/farmacología , Calpaína/antagonistas & inhibidores , Inhibidores Enzimáticos/farmacología , Corazón/efectos de los fármacos , Infarto del Miocardio/prevención & control , Animales , Femenino , Técnicas In Vitro , Masculino , Potasio/metabolismo , Conejos
6.
Biol Chem ; 384(12): 1597-603, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14719802

RESUMEN

The effects of the novel calpain inhibitor A-705239 were studied in isolated perfused rabbit hearts subjected to 45 min of global ischemia, followed by 60 min of reperfusion. During 15 min of perfusion the inhibitor accumulated in myocardial tissue up to 16 times the concentration in the perfusate. Almost complete recovery and survival of heart function (90%) was seen with an inhibitor concentration of 10(-8) M in the perfusion fluid when the compound was administered prior to ischemia. Left ventricular pressure amplitude and coronary flow showed significantly higher values during reperfusion in the presence of the inhibitor. A-705239 significantly reduced the release of creatine kinase, from 166+/-49 U/l in untreated hearts to 44+/-10 U/l, and diminished the release of lactate dehydrogenase from 118+/-20 U/l in untreated hearts to 63+/-4 U/l. Mitochondrial dysfunction following ischemia and reperfusion was markedly attenuated by the inhibitor. Thus, the state 3 respiration rate only decreased to 4.2 in contrast to 2.6 nmol O2/(min x mg s.w.) in untreated hearts, reflecting a reduced damage of oxidative phosphorylation. Furthermore, in the presence of the inhibitor the inner mitochondrial membranes became less permeable as indicated by a smaller leak respiration. The excellent properties of A-705239 should make this compound a valuable tool for further pharmacological studies.


Asunto(s)
Benzamidas/farmacología , Calpaína/antagonistas & inhibidores , Corazón/efectos de los fármacos , Mitocondrias Cardíacas/efectos de los fármacos , Daño por Reperfusión Miocárdica/tratamiento farmacológico , Miocardio/enzimología , Adenosina Difosfato/farmacología , Animales , Antimicina A/farmacología , Atractilósido/farmacología , Benzamidas/análisis , Circulación Coronaria/efectos de los fármacos , Creatina Quinasa/metabolismo , Citocromos c/farmacología , Relación Dosis-Respuesta a Droga , Femenino , Corazón/fisiopatología , Frecuencia Cardíaca/efectos de los fármacos , Técnicas In Vitro , L-Lactato Deshidrogenasa/metabolismo , Masculino , Mitocondrias Cardíacas/metabolismo , Contracción Miocárdica/efectos de los fármacos , Daño por Reperfusión Miocárdica/metabolismo , Daño por Reperfusión Miocárdica/fisiopatología , Miocardio/metabolismo , Consumo de Oxígeno/efectos de los fármacos , Conejos , Función Ventricular Izquierda/efectos de los fármacos , Presión Ventricular/efectos de los fármacos
7.
Clin Biochem ; 35(5): 355-62, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12270764

RESUMEN

OBJECTIVES: Heparin is thought to play a crucial role in the clinical monitoring of patients with acute coronary syndrome as well as after coronary bypass surgery in that it interferes with different commercial immunoassay test systems for cardiac troponin T (cTnT) and troponin I (cTnI). The mechanism, however, by which heparin apparently affects the cTnT and cTnI levels in plasma is not yet resolved. DESIGN AND METHODS: We analyzed the effect of heparin by simultaneously collecting serum and heparin plasma samples from 32 patients after coronary bypass surgery. The cTnT and cTnI levels were determined using the Roche/Elecsys, the Dade-Behring/Opus and the Bayer/ACS:Centaur immunoassay systems in the absence or in the presence of either heparinase or protamine. Association between the cardiac troponins and the anticoagulant has been demonstrated by affinity chromatography using heparin as the ligand. RESULTS: The data obtained indicate that heparin produces an apparent decrease in cTnT as well as of cTnI levels, analyzed either by the Elecsys, the Opus or the ACS:Centaur immunoassay systems. Individual patients show a wide variation in the discrepancies between serum and heparin plasma troponin especially in the cTnT immunoassay. Pretreatment of the heparin plasma samples either with heparinase or protamine cannot completely reverse the heparin-induced decrease in cTnT and cTnI levels and therefore addition of these reagents to the commercial test systems could not significantly improve the performance of the assay. When serum is supplemented with increasing concentrations of heparin, and cardiac troponin levels were reanalysed, significantly lower recoveries for the cTnT than for the cTnI immunoassays were detectable. Affinity chromatography with heparin Sepharose demonstrates that cTnT and cTnI interact differentially with the negatively charged ligand. Whereas cTnI shows minor affinity to the immobilized heparin and is eluted at near physiological conditions, cTnT is bound and can be quantitatively recovered only by solutions of high ionic strength. CONCLUSIONS: We conclude, therefore, that the apparent decrease in cTnT values by addition of heparin is a result of direct molecular interaction between the negatively charged glycosaminoglycan and clusters of basic residues within the sequence of the cardiac protein. In contrast, the effect of heparin on the cTnI immunoassay systems, is primarily indirect, most possibly induced by changes within the sample matrix itself.


Asunto(s)
Recolección de Muestras de Sangre/métodos , Puente de Arteria Coronaria , Heparina/metabolismo , Troponina I/sangre , Troponina I/metabolismo , Troponina T/sangre , Troponina T/metabolismo , Anciano , Secuencia de Aminoácidos , Anticoagulantes/sangre , Anticoagulantes/química , Anticoagulantes/metabolismo , Artefactos , Cromatografía de Afinidad , Heparina/sangre , Heparina/química , Liasa de Heparina/metabolismo , Humanos , Inmunoensayo , Ligandos , Datos de Secuencia Molecular , Periodo Posoperatorio , Unión Proteica , Sefarosa , Troponina I/química , Troponina T/química
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