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1.
Artigo em Inglês | MEDLINE | ID: mdl-7584847

RESUMO

The activity and some kinetic parameters of the key enzymes of the glycolysis, the gluconeogenesis and the amino acid catabolism from the liver of male and female mink have been determined and compared to the corresponding activities from rat and cat. The activities of glucose-6-phosphatase and pyruvate kinase are dependent on sex, both being higher in females. Except for pyruvate carboxylase the glycolytic and the gluconeogenic enzyme activities of the mink are higher than those of rat and cat; especially the activities of phosphoenolpyruvate carboxykinase and glucose-6-phosphatase are markedly higher. The activities of glutamate dehydrogenase and glutamate oxaloacetate transaminase are smaller than the corresponding activities of rat but higher than those of cat. The results suggest that mink has a high capacity for gluconeogenesis compared to rat.


Assuntos
Aminoácidos/metabolismo , Metabolismo dos Carboidratos , Gluconeogênese/fisiologia , Glicólise/fisiologia , Fígado/enzimologia , Vison/metabolismo , Animais , Gatos , Dieta , Feminino , Concentração de Íons de Hidrogênio , Cinética , Masculino , Ratos , Especificidade da Espécie
2.
Antonie Van Leeuwenhoek ; 65(2): 133-42, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-7979318

RESUMO

Glyceraldehyde 3-phosphate dehydrogenase (EC 1.2.1.13) was purified 386 fold to apparent homogeneity from the thermophilic cyanobacterium Synechococcus sp. grown at optimum light intensities in batch cultures. The molecular mass of the tetrameric form of the enzyme was 160 kDa as determined by gel filtration and sucrose gradient centrifugation in a phosphate buffer containing DTT. The pH optimum for the oxidation of NADPH was broad (6-8) and the enzyme had a pI of 4.5. The turnover number was 36,000 min-1 at 40 degrees C. The activation energy was 12.4 Kcal for t > 29 degrees C and 20.6 Kcal for t < 29 degrees C. The specific absorption coefficient, A 1% 1cm 280 mm of the pure enzyme in phosphate buffer at pH 6.8 was 15.2. By SDS gel electrophoresis molecular masses of 78 kDa and 39 kDa were found, indicating that the purified enzyme is a tetramer, probably a homotetramer. When Tris was used as buffer in the homogenization and phosphate and DTT were omitted, a high molecular form with a molecular mass above 500 kDa was found. This form was less active than the purified tetrameric form. Acetone and other organic solvents stimulated the native enzyme several fold.


Assuntos
Cianobactérias/enzimologia , Gliceraldeído-3-Fosfato Desidrogenases/isolamento & purificação , Gliceraldeído-3-Fosfato Desidrogenases/química , Gliceraldeído-3-Fosfato Desidrogenases/metabolismo , Concentração de Íons de Hidrogênio , Ponto Isoelétrico , Peso Molecular , Conformação Proteica , Termodinâmica
3.
Comp Biochem Physiol B ; 74(3): 459-66, 1983.
Artigo em Inglês | MEDLINE | ID: mdl-6839715

RESUMO

1. Repeated treatment of male flounder with 5 and 100 microgram doses of estradiol-17 beta increases the level of phospholipid, triglyceride, free fatty acids and total lipid in serum as a function of time and dose, during a period of 17 days. 2. The glucose level in serum is increased and decreased respectively by doses of 5 and 100 micrograms. 3. Five and 100 microgram doses decrease the level of glycogen in liver. 4. Five microgram doses do not affect the activity of the measured enzymes considerably, with the exception of phosphorylase a. 5. One hundred microgram doses increase the activity of glucose-6-phosphate dehydrogenase after 11 days. 6. One hundred microgram doses increase the activity of pyruvate kinase continuously during the experimental period and decrease phosphorylase a and glucose-6-phosphatase activity.


Assuntos
Metabolismo dos Carboidratos , Estradiol/farmacologia , Peixes/metabolismo , Fígado/metabolismo , Animais , Glicemia/metabolismo , Ácidos Graxos não Esterificados/sangue , Feminino , Lipídeos/sangue , Glicogênio Hepático/metabolismo , Masculino , Fosfolipídeos/sangue , Fatores de Tempo , Triglicerídeos/sangue
4.
Pharmacopsychiatria ; 15(6): 183-6, 1982 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-6218507

RESUMO

Paroxetine, a new, potent and selective serotonin (5-HT) uptake inhibitor has been evaluated in an open study for its clinical effect as well as its effect on the 5-HT concentration in whole blood in 19 patients with depressive illness. Paroxetine was administered in daily doses of 20 to 60 mg. The global evaluation after six to eight weeks showed a marked improvement in 11 patients, a moderate improvement in four and no change in four patients. Assessment with the Hamilton Rating Scale for Depression in ten patients showed a reduction from a mean score of 22.7 to 6.6 in six weeks. Maximal reduction was, however, first seen in three of the patients after 8 to 12 weeks. No correlation between the antidepressant effect and plasma concentrations of paroxetine was found. The only side effects noted with paroxetine were that two patients complained of dry mouth in the beginning of the treatment and a further patient experienced a burning sensation together with periodical light headache. Generally laboratory examinations did not show any trend towards pathological values except in one patient, where a moderate leucopenia was observed. Crista puncture/biopsy showed, however, no specific bone marrow reaction. The 5-HT concentration in whole blood was reduced to about 0.02 micrograms/ml indicating a total depletion of 5-HT from the thrombocytes. The present study indicates that paroxetine possesses a good antidepressive effect in combination with a very low frequency of side effects.


Assuntos
Transtorno Depressivo/tratamento farmacológico , Piperidinas/uso terapêutico , Adulto , Idoso , Avaliação de Medicamentos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Paroxetina , Piperidinas/administração & dosagem , Piperidinas/efeitos adversos , Serotonina/sangue
5.
Psychopharmacology (Berl) ; 63(3): 241-3, 1979 Jun 21.
Artigo em Inglês | MEDLINE | ID: mdl-113809

RESUMO

Femoxetine, a phenylpiperidine derivative with potent serotonin (5-HT)-uptake inhibitory properties, was investigated in 12 depressive patients for its clinical effect as well as its effect on 5-HT concentration in whole blood. The global evaluation after 6 weeks showed a good effect in six patients. The 5-HT concentration was found to be reduced from a mean value of 0.21 to about 0.05 micrograms/ml, indicating a total depletion of 5-HT from the thrombocytes. The steady-state concentrations of femoxetine resulted in reduction of 5-HT to the same level in all patients. No correlation between degree of 5-HT reduction and therapeutic effect was found.


Assuntos
Anisóis/farmacologia , Depressão/sangue , Piperidinas/farmacologia , Antagonistas da Serotonina/farmacologia , Serotonina/sangue , Depressão/tratamento farmacológico , Depressão Química , Feminino , Humanos , Escalas de Graduação Psiquiátrica , Antagonistas da Serotonina/efeitos adversos , Antagonistas da Serotonina/uso terapêutico , Fatores de Tempo
6.
Comp Biochem Physiol B ; 58(2): 167-71, 1977.
Artigo em Inglês | MEDLINE | ID: mdl-318264

RESUMO

1. During vitellogenesis in nature the concentration of phospholipid in serum of female flounders is correlated to the concentration of vitellogenin. 2. High levels of glucose and total lipid in blood occur before the onset of vitellogenesis. During early vitellogenesis the values decrease. At spawning they reach maximum levels. After spawning they decrease to low levels. 3. The concentration of glycogen in the liver oscillates during the period August to May. The phosphorylase activity shows peak activities with high concentrations of glycogen in the liver. There is no simple correlation between glycogen concentration in the liver and glucose concentration in the blood.


Assuntos
Glicemia/metabolismo , Linguados/metabolismo , Linguado/metabolismo , Lipídeos/sangue , Glicogênio Hepático/análise , Fosforilase a/metabolismo , Fosforilases/metabolismo , Vitelogênese , Animais , Fígado/enzimologia , Fígado/metabolismo
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