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1.
Bull Exp Biol Med ; 147(1): 36-8, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19526125

RESUMO

We showed that sphingomyelinase activity in the liver increased only during the acute phase of toxic hepatitis. Peroxidative modification of hepatocyte membrane bilayer prevailed during the acute phase, while after transformation of the process to the chronic phase phospholipase pathway predominated.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/enzimologia , Bicamadas Lipídicas , Peroxidação de Lipídeos , Fígado/enzimologia , Fosfolipase D/metabolismo , Fosfolipases A2/metabolismo , Esfingomielina Fosfodiesterase/metabolismo , Doença Aguda , Animais , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Doença Crônica , Fígado/metabolismo , Ratos , Ratos Wistar
2.
Bull Exp Biol Med ; 146(6): 726-9, 2008 Dec.
Artigo em Inglês, Russo | MEDLINE | ID: mdl-19513367

RESUMO

Activities of sphingomyelinase and ceramidase decreased in the liver in chronic toxic hepatitis and the balance between the levels of proapoptotic ceramide and antiapoptotic sphyngosine-1-phosphate shifts towards the latter substance. Pronounced changes in the qualitative and quantitative composition of fatty acids in the sphingomyelin cycle effector molecules were revealed.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Hepatite Crônica/metabolismo , Fígado/metabolismo , Esfingomielinas/metabolismo , Animais , Ceramidases/metabolismo , Ceramidas/metabolismo , Fígado/enzimologia , Fígado/patologia , Lisofosfolipídeos/metabolismo , Masculino , Ratos , Esfingomielina Fosfodiesterase/metabolismo , Esfingosina/análogos & derivados , Esfingosina/metabolismo
3.
Artigo em Inglês | MEDLINE | ID: mdl-7671883

RESUMO

The purpose of this study was to compare oxygen uptake (VO2) values collected with a new portable indirect calorimeter (AeroSport TEEM 100 Metabolic Analysis System) against a more traditional large calorimeter system that has been reported to be valid and reliable (SensorMedics 2900 Metabolic Measurement Cart). Minute ventilations ranging from rest up to heavy exercise were compared with simultaneous measurements from a 120-1 Tissot gasometer. Each of the three TEEM 100 pneumotachs were tested. Three hundred and sixty-one separate ventilation tests were performed using the low-flow, medium-flow, and high-flow heads of the portable calorimeter. For each of the pneumotachs, the correlation between the portable calorimeter values and the gasometer values exceeded r = 0.94. The standard error of estimate for the low-medium- and high-flow pneumotach were 5.96, 4.89 and 9.0%, respectively, expressed relative to the mean gasometer value. Simultaneous measurements of VO2 using the portable calorimeter and the SensorMedics 2900 unit were compared during rest and at work rates starting at zero watts, increasing by 25 W to 150 W. Each work rate was of 4 min duration. The average of data from minutes 3 and 4 were used in all analyses. There was very close agreement between the two metabolic measurement systems. Except at the 100-W work rate, where the VO2 difference was small (3.9%), yet statistically significant, all of the other differences in VO2 were small and non-significant. The scatter plot of VO2 for the SensorMedics versus the portable Aero-Sport calorimeter revealed close agreement; the correlation was r = 0.96, (SEE = 3.95%).(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Calorimetria Indireta/instrumentação , Adulto , Estudos de Avaliação como Assunto , Exercício Físico/fisiologia , Feminino , Humanos , Masculino , Consumo de Oxigênio/fisiologia , Testes de Função Respiratória/instrumentação
4.
Adv Neuroimmunol ; 5(2): 171-88, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7496611

RESUMO

The central thesis of this essay is that the cytokine network in brain is a key element in the humoral regulation of sleep responses to infection and in the physiological regulation of sleep. We hypothesize that many cytokines, their cellular receptors, soluble receptors, and endogenous antagonists are involved in physiological sleep regulation. The expressions of some cytokines are greatly amplified by microbial challenge. This excess cytokine production during infection induces sleep responses. The excessive sleep and wakefulness that occur at different times during the course of the infectious process results from dynamic changes in various cytokines that occur during the host's response to infectious challenge. Removal of any one somnogenic cytokine inhibits normal sleep, alters the cytokine network by changing the cytokine mix, but does not completely disrupt sleep due to the redundant nature of the cytokine network. The cytokine network operates in a paracrine/autocrine fashion and is responsive to neuronal use. Finally, cytokines elicit their somnogenic actions via endocrine and neurotransmitter systems as well as having direct effects neurons and glia. Evidence in support of these postulates is reviewed in this essay.


Assuntos
Citocinas/fisiologia , Sono/fisiologia , Reação de Fase Aguda , Sequência de Aminoácidos , Infecções Bacterianas/complicações , Infecções Bacterianas/fisiopatologia , Parede Celular/química , Hormônio Liberador de Hormônio do Crescimento/fisiologia , Dados de Sequência Molecular , Ácidos Murâmicos/farmacologia , Neuroimunomodulação/fisiologia , Neurônios/fisiologia , RNA de Cadeia Dupla/farmacologia , RNA Viral/farmacologia , Sono/efeitos dos fármacos , Transtornos do Sono-Vigília/etiologia , Transtornos do Sono-Vigília/fisiopatologia , Viroses/complicações , Viroses/fisiopatologia
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