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1.
Intensive Care Med ; 17(3): 141-8, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1712801

RESUMO

Intentional normovolemic hemodilution was chosen as the model to compare a 6% low molecular weight hydroxyethyl starch (LMW HES) to 4% albumin. The study ran over the plasma exchange period for 24 h. Nine patients, scheduled for abdominal aortic surgery, were included in each group. After basal measurements, blood was withdrawn and simultaneously replaced by either 4% albumin (Group 1) or 6% LMW HES (Group 2) to achieve a final hematocrit of approximately 30%. Hemodynamic blood oxygen gas and hormonal plasma levels were determined before hemodilution then at 30 min, 1, 2, 3, and 24 h after the end of hemodilution. Basal value for total blood volume was 4377 +/- 162 ml in group 1 and 4138 +/- 315 ml in group 2. As in both groups the decrease in blood cell volume was exactly compensated by the increase in plasma volume, no significant change in total blood volume (respectively 4432 +/- 159 and 4305 +/- 267 ml) was observed. Throughout the study, in both groups, no significant change in mean arterial and right atrial pressures was observed. In group 2 (LMW HES), a significant increase of pulmonary capillary wedge pressure was noted 120 min after hemodilution. After hemodilution, despite a significant decrease in arterial oxygen O2 content, systemic oxygen transport did not significantly vary until 24 h in relation to the increased cardiac index. An increase in O2 extraction was observed after the exchange but no further increase was observed until the 24 h. No significant changes either in global O2 consumption or in lactate concentration were detected.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Albuminas/uso terapêutico , Hemodiluição/métodos , Derivados de Hidroxietil Amido/uso terapêutico , Idoso , Albuminas/farmacologia , Gasometria , Volume Sanguíneo/efeitos dos fármacos , Hematócrito , Hemodiluição/normas , Hemodinâmica/efeitos dos fármacos , Hormônios/sangue , Humanos , Derivados de Hidroxietil Amido/farmacologia , Pessoa de Meia-Idade , Consumo de Oxigênio/efeitos dos fármacos , Cuidados Pré-Operatórios
5.
J Clin Pathol ; 31(2): 175-8, 1978 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-204665

RESUMO

Electron microscopy, immune electron microscopy and complement fixation as methods of detecting rotavirus in the stools of young children with gastroenteritis were compared in a blind study during the winter of 1975-6. Complement fixation was the simplest to perform, was as sensitive as the other two, and allowed a quantitative measurement of viral excretion. Absorption of faecal extracts with fetal calf serum usually removed the anticomplementary activity of faecal extracts.


Assuntos
Fezes/microbiologia , Vírus de RNA/isolamento & purificação , Rotavirus/isolamento & purificação , Viroses/diagnóstico , Criança , Testes de Fixação de Complemento , Diarreia/etiologia , Humanos , Rotavirus/ultraestrutura
7.
J Bacteriol ; 127(3): 1389-99, 1976 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-783144

RESUMO

Mutants of Escherichia coli defective in the regulation of the fatty acids beta oxidation pathway show an ultrastructural deficiency in septum formation at high growth rate. Several independent pairs of parent and mutant strains have been analyzed biochemically. Each parent strain displays a well-defined pattern of cellular phospholipids, which varies with the growth conditions. High ratios of phosphatidylglycerol to cardiolipin characterize fast-growth conditions. None of the mutant strains, although they grow in mass nearly as rapidly as their respective parents, can reach these high ratios. The beta oxidation pathway regulatory mutation leads to an increased turnover of the glycerol moieties of these phospholipids in the inner as well as in the outer cell membrane.


Assuntos
Escherichia coli/crescimento & desenvolvimento , Ácidos Graxos/metabolismo , Genes , Fosfolipídeos/metabolismo , Acetatos/metabolismo , Cardiolipinas/metabolismo , Escherichia coli/metabolismo , Escherichia coli/ultraestrutura , Glicerol/metabolismo , Glicerofosfatos/metabolismo , Mutação , Fosfatidilgliceróis/metabolismo
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