979 resultados para TOXICIDAD POR INGESTION


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The plasma glucose excursion may influence the metabolic responses after oral glucose ingestion. Although previous studies addressed the effects of hyperglycemia in conditions of hyperinsulinemia, it has not been evaluated whether the route of glucose administration (oral vs. intravenous) plays a role. Our aim was to determine the effects of moderately controlled hyperglycemia on glucose metabolism before and after oral glucose ingestion. Eight normal men underwent two oral glucose clamps at 6 and 10 mmol/l plasma glucose. Glucose turnover and cycling rates were measured by infusion of [2H7]glucose. The oral glucose load was labeled by D-[6,6-2H2]glucose to monitor exogenous glucose appearance, and respiratory exchanges were measured by indirect calorimetry. Sixty percent of the oral glucose load appeared in the systemic circulation during both the 6 and 10 mmol/l plasma glucose tests, although less endogenous glucose appeared during the 10 mmol/l tests before glucose ingestion (P < 0.05). This inhibitory effect of hyperglycemia was not detectable after oral glucose ingestion, although glucose utilization was increased (+28%, P < 0.05) due to increased nonoxidative glucose disposal [10 vs. 6 mmol/l: +20%, not significant (NS) before oral glucose ingestion; +40%, P < 0.05 after oral glucose ingestion]. Glucose cycling rates were increased by hyperglycemia (+13% before oral glucose ingestion, P < 0.001; +31% after oral glucose ingestion, P < 0.05) and oral glucose ingestion during both the 6 (+10%, P < 0.05) and 10 mmol/l (+26%, P < 0.005) tests. A moderate hyperglycemia inhibits endogenous glucose production and contributes to glucose tolerance by enhancing nonoxidative glucose disposal. Hyperglycemia and oral glucose ingestion both stimulate glucose cycling.

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Se realizaron siete bioensayos estáticos con la Concha de Abanico (Argopecten purpuratus) con concentraciones de cobre que variaron de 0.007 a 0.74 ppm. El agua de mar de donde provinieron los individuos usados en el experimento tenía concentraciones de cobre entre 0.005-0.007 ppm. La bioacumulación inicial en los animales varó de 1.69 a 6.50 ppm. Como resultado preliminar se determinó que 0.13 ppm es la concentración letal media (LC 50) en 96 horas.

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A double-blinded, placebo controlled, cross-over design was used to investigate sodium citrate dihydrate (Na-CIT) supplementation improve 200m swimming performance. Ten well-trained, male swimmers (14.9 ± 0.4y; 63.5 ± 4kg) performed four 200m time trials: acute (ACU) supplementation (0.5g/kg), acute placebo (PLC-A), chronic (CHR) (0.1g/kg for 3 days and 0.3g/kg on the 4th day pre-trial), and chronic placebo (PLC-C). Na-CIT was administered 120min pre-trial in solution with 500mL of flavored water; placebo was flavored water. Blood lactate, base excess (BE), bicarbonate, pH, and PCO2 were analyzed at basal, 100min post-ingestion, and 3min post-trial via finger prick. Time, lactate, and rate of perceived exertion were not different between trials. BE and bicarbonate were significantly higher for the ACU and CHR trials compared to placebo. “Responders” improved by 1.03% (P=0.043) and attained significantly higher post-trial lactate concentrations in the ACU versus PLC-A trials and compared to non-responders in the ACU and CHR trials.

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Tesis (Maestría en Ciencias con Especialidad en Microbiología Industrial) UANL

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Tesis (Maestría en Ciencias con Especialidad en Microbiología Industrial) UANL

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Tesis (Maestría en Ciencias con Especialidad en Entomología Médica) UANL

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Tesis (Maestría en Ciencias con Especialidad en Biología Molecular e Ingeniería Genética) UANL

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Tesis (Maestría en Ciencias Odontológicas con orientación en Ortodoncia) UANL, 2014.

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Tesis (Doctorado en Ciencias, con Especialidad en Farmacología y Toxicología) UANL

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Tesis (Doctorado en Ciencias con Especialidad en Biología Molecular e Ingeniería Genética) UANL

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Tesis (Doctorado en Ciencias con Especialidad en Biotecnología) UANL

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Tesis (Doctorado en Medicina) UANL