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1.
J Microbiol Methods ; 83(2): 185-7, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20807554

RESUMO

hyplex®-MBL ID Multiplex PCR-ELISA, a novel method for identifying metallo-ß-lactamase genes directly in clinical specimens, was evaluated using a consecutive collection of 326 samples from three hospitals in Greece characterized by high prevalence of VIM producers. The method exhibited high sensitivity (98.0%) and specificity (98.6%) and was proven reliable in detecting bla(VIM) genes in blood, urine, pus, and sputum samples that, as confirmed by conventional methods, contained various VIM-producing species. Future multicenter studies should be considered for the thorough evaluation of this method and its potential diagnostic utility.


Assuntos
Proteínas de Bactérias/genética , Bactérias Gram-Negativas/enzimologia , Infecções por Bactérias Gram-Negativas/microbiologia , Reação em Cadeia da Polimerase/métodos , beta-Lactamases/genética , Proteínas de Bactérias/biossíntese , Ensaio de Imunoadsorção Enzimática/métodos , Bactérias Gram-Negativas/genética , Bactérias Gram-Negativas/isolamento & purificação , Grécia , Humanos , Testes de Sensibilidade Microbiana/métodos , Sensibilidade e Especificidade , beta-Lactamases/biossíntese
2.
J Psychopharmacol ; 23(8): 945-56, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18755816

RESUMO

Research in affective disorders is often performed without considering sex differences, although women are predominantly affected. Consequently, the potential sex-dependent action of antidepressants remains elusive. We investigated whether Flinders sensitive line (FSL) of rats, a model of depression, would present sex-differentiated responses to antidepressant treatment. FSL and Sprague-Dawley rats were treated with clomipramine 10 mg/kg/day for 14 days. Subsequently, they were subjected to either a single session of the forced swim test or an estimation of serotonergic function in the prefrontal cortex, hippocampus, amygdala and hypothalamus. Male FSL displayed increased immobility duration, decreased active behaviours, increased serotonin tissue levels and a reduced serotonin turnover rate in most brain areas studied. Female FSL showed a distinct profile, consisting of decreased immobility latency, increased climbing duration, limited serotonergic deviations and no difference in the serotonin turnover rate in comparison with controls. Interestingly, despite baseline differences, clomipramine treatment reversed all relevant behavioural responses and increased the serotonin turnover rate in both sexes. However, the latter effect was remarkably more pronounced in females. It is concluded that, in this animal model of depression, chronic clomipramine treatment attenuated baseline sex differences in the phenotype while maintaining or intensifying the sex differentiation in the serotonergic endophenotype.


Assuntos
Antidepressivos Tricíclicos/uso terapêutico , Clomipramina/uso terapêutico , Depressão/tratamento farmacológico , Animais , Depressão/psicologia , Modelos Animais de Doenças , Feminino , Ácido Hidroxi-Indolacético/análise , Masculino , Ratos , Ratos Sprague-Dawley , Serotonina/análise , Serotonina/metabolismo , Caracteres Sexuais , Natação
3.
Physiol Behav ; 93(3): 595-605, 2008 Feb 27.
Artigo em Inglês | MEDLINE | ID: mdl-18031771

RESUMO

Sex differences in behavioral and neurobiological responses to stress are considered to modulate the prevalence of some psychiatric disorders, including major depression. In the present study, we compared dopaminergic neurotransmission and behavior in response to two different stress paradigms, the Forced Swim Test (FST) and the Chronic Mild Stress (CMS). Male and female rats were subjected to one session of swim stress for two consecutive days (FST) or to a variety of mild stressors alternating for six weeks (CMS). Subsequently, the tissue levels of dopamine (DA) and its metabolites (HVA and DOPAC) in the hippocampus, the hypothalamus, the prefrontal cortex and the striatum were measured using high-performance liquid chromatography (HPLC). The ratios HVA/DA and DOPAC/DA were also calculated as indices of the dopaminergic activity. Results from the FST determined that males exhibited lower immobility, higher climbing duration and increased dopaminergic activity in the prefrontal cortex and the hippocampus compared to females. CMS induced alterations in sucrose intake in both sexes, while it only decreased dopaminergic activity in the prefrontal cortex of females. These findings show that FST and CMS have different effects on the dopaminergic activity of discrete brain regions depending on the sex of the animal. These data support the growing evidence that females display a differential response and adaptation to stress than males.


Assuntos
Química Encefálica/fisiologia , Dopamina/metabolismo , Caracteres Sexuais , Estresse Psicológico/metabolismo , Análise de Variância , Animais , Comportamento Animal , Encéfalo/metabolismo , Encéfalo/patologia , Feminino , Preferências Alimentares/fisiologia , Masculino , Ratos , Ratos Wistar , Estresse Psicológico/etiologia , Estresse Psicológico/patologia , Natação , Fatores de Tempo
4.
Eur Neuropsychopharmacol ; 10(5): 315-24, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10974601

RESUMO

The serotonergic activity in hippocampus was investigated following acute and chronic treatment with the antipsychotic drugs haloperidol and risperidone. Acute administration of risperidone, the serotonin(2) (5-HT(2)) receptor antagonist ketanserin, and the dopamine (DA)-D(2) receptor antagonist raclopride increased the 5-hydroxyindoleacetic acid/serotonin (5-HIAA/5-HT) ratio. In contrast, acute administration of haloperidol did not affect this ratio. Chronic administration of risperidone maintained the increased 5-HIAA/5-HT ratio; a challenge dose of risperidone after the chronic treatment and the subsequent washout period also maintained the increased ratio. Chronic administration of haloperidol as well as a challenge dose of haloperidol following chronic treatment did not affect the serotonergic activity in hippocampus. Administration of ketanserin or raclopride after chronic treatment and the washout period induced an additional increase in the 5-HIAA/5-HT ratio in risperidone-treated rats. Moreover, a challenge dose of ketanserin, but not raclopride, increased the 5-HIAA/5-HT ratio in haloperidol-treated rats. The present results indicate that acute and chronic treatment of haloperidol or risperidone modified serotonergic activity in the hippocampus in a different way. Moreover, the augmentation of serotonergic activity induced by risperidone did not seem to be solely related to dopaminergic or serotonergic properties and may be of particular relevance for the amelioration of schizophrenia symptoms.


Assuntos
Antipsicóticos/farmacologia , Haloperidol/farmacologia , Hipocampo/metabolismo , Ketanserina/farmacologia , Racloprida/farmacologia , Serotonina/metabolismo , Animais , Antagonistas dos Receptores de Dopamina D2 , Hipocampo/efeitos dos fármacos , Ácido Hidroxi-Indolacético/metabolismo , Masculino , Ratos , Ratos Wistar , Risperidona/farmacologia
5.
Psychoneuroendocrinology ; 25(3): 247-57, 2000 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10737696

RESUMO

This work was carried out to assess the effects of chronic mild stress (CMS) on thyroid function. The CMS model produced an anhedonic effect (reduced preference to sucrose) in Sprague-Dawley and Wistar rats and this effect was reversed by imipramine (IMI) treatment. The effects of CMS on thyroid function were assessed by measuring tT4 (total Thyroxine), tT3 (total Triiodothyronine), TSH (Thyroid Stimulating Hormone) and fT4 (free Thyroxine) serum levels with appropriate immunoassays. CMS increased tT4 and tT3 serum levels in Sprague-Dawley and Wistar rats, but not TSH and fT4 serum levels. Imipramine (IMI) treatment normalized tT4 values. Albumin which binds a fraction of peripheral tT4 and tT3 was also significantly increased in response to CMS, possibly contributing to tT4 and tT3 elevations. The above findings suggest an impact of CMS on thyroid function, especially in tT4 values the changes being reversed with IMI treatment.


Assuntos
Estresse Fisiológico/fisiopatologia , Glândula Tireoide/metabolismo , Animais , Antidepressivos Tricíclicos/farmacologia , Comportamento Animal/efeitos dos fármacos , Doença Crônica , Modelos Animais de Doenças , Ingestão de Alimentos/efeitos dos fármacos , Imipramina/farmacologia , Masculino , Ratos , Ratos Sprague-Dawley , Ratos Wistar , Albumina Sérica/metabolismo , Especificidade da Espécie , Estresse Fisiológico/sangue , Estresse Fisiológico/tratamento farmacológico , Testes de Função Tireóidea , Glândula Tireoide/efeitos dos fármacos , Tireotropina/sangue , Tiroxina/sangue , Tri-Iodotironina/sangue
6.
Proc Natl Acad Sci U S A ; 90(20): 9504-7, 1993 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-8415730

RESUMO

Radioimmunoassays specific for the N and C termini of human prothymosin alpha and the N terminus of human parathymosin alpha were employed for the measurement of the levels of alpha-thymosins in human thymus, spleen, and liver during normal growth and intestine and breast in malignant growth. A differential expression of the two alpha-thymosins was observed in thymus (prothymosin alpha-rich) and liver (parathymosin alpha-rich). A decline in the levels of both alpha-thymosins was found with age, with prothymosin alpha in thymus showing the sharpest change (15- to 30-fold). The levels of both alpha-thymosins were higher in malignant tissues as compared with healthy ones. In breast cancer, in particular, the mean increase for prothymosin alpha and parathymosin alpha was 17.9- and 11.5-fold, respectively. The major crossreactive material was characterized in all cases as intact prothymosin alpha and parathymosin alpha. These results suggest an in vivo relationship of the expression of alpha-thymosins with the human tissue cell proliferation activity.


Assuntos
Timosina/metabolismo , Adolescente , Adulto , Fatores Etários , Idoso , Divisão Celular , Criança , Pré-Escolar , Humanos , Lactente , Fígado/metabolismo , Pessoa de Meia-Idade , Neoplasias/metabolismo , Radioimunoensaio , Timosina/análogos & derivados , Timo/metabolismo
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