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2.
Mol Psychiatry ; 20(6): 685-94, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25980345

RESUMO

There is increasing clinical and molecular evidence for the role of hormones and specifically estrogen and its receptor in schizophrenia. A selective estrogen receptor modulator, raloxifene, stimulates estrogen-like activity in brain and can improve cognition in older adults. The present study tested the extent to which adjunctive raloxifene treatment improved cognition and reduced symptoms in young to middle-age men and women with schizophrenia. Ninety-eight patients with a diagnosis of schizophrenia or schizoaffective disorder were recruited into a dual-site, thirteen-week, randomized, double-blind, placebo-controlled, crossover trial of adjunctive raloxifene treatment in addition to their usual antipsychotic medications. Symptom severity and cognition in the domains of working memory, attention/processing speed, language and verbal memory were assessed at baseline, 6 and 13 weeks. Analyses of the initial 6-week phase of the study using a parallel groups design (with 39 patients receiving placebo and 40 receiving raloxifene) revealed that participants receiving adjunctive raloxifene treatment showed significant improvement relative to placebo in memory and attention/processing speed. There was no reduction in symptom severity with treatment compared with placebo. There were significant carryover effects, suggesting some cognitive benefits are sustained even after raloxifene withdrawal. Analysis of the 13-week crossover data revealed significant improvement with raloxifene only in attention/processing speed. This is the first study to show that daily, oral adjunctive raloxifene treatment at 120 mg per day has beneficial effects on attention/processing speed and memory for both men and women with schizophrenia. Thus, raloxifene may be useful as an adjunctive treatment for cognitive deficits associated with schizophrenia.


Assuntos
Transtorno do Deficit de Atenção com Hiperatividade/tratamento farmacológico , Antagonistas de Estrogênios/uso terapêutico , Transtornos da Memória/tratamento farmacológico , Cloridrato de Raloxifeno/uso terapêutico , Esquizofrenia/complicações , Caracteres Sexuais , Adolescente , Adulto , Transtorno do Deficit de Atenção com Hiperatividade/sangue , Transtorno do Deficit de Atenção com Hiperatividade/etiologia , Austrália , Estudos Cross-Over , Método Duplo-Cego , Feminino , Humanos , Estudos Longitudinais , Masculino , Transtornos da Memória/sangue , Transtornos da Memória/etiologia , Pessoa de Meia-Idade , Testes Neuropsicológicos , Cooperação do Paciente , Escalas de Graduação Psiquiátrica , Esquizofrenia/sangue , Esquizofrenia/tratamento farmacológico , Estatísticas não Paramétricas , Resultado do Tratamento , Adulto Jovem
3.
J Chem Phys ; 141(5): 054203, 2014 Aug 07.
Artigo em Inglês | MEDLINE | ID: mdl-25106580

RESUMO

Long-lived coherences (LLC's) are detectable magnetisation modes with favourable relaxation times that translate as sharp resonances upon Fourier transform. The frequency domain of LLC's was previously limited to the range of J-couplings within pairs of homonuclear spins. LLC evolution at high magnetic fields needs to be sustained by radio-frequency irradiation. We show that LLC-based spectral dispersion can be extended beyond the J-couplings domain using adapted carrier offsets and introduce a new reduced-power sustaining method to preserve LLC's within the required range of offsets. Spectral resolution is enhanced as the natively narrow lines of LLC's are further dispersed, making them potential probes for the study of biomolecules featuring strong resonance overlap and for media where NMR spectroscopy is commonly hindered by line broadening.


Assuntos
Algoritmos , Dipeptídeos/química , Dipeptídeos/efeitos da radiação , Espectroscopia de Prótons por Ressonância Magnética/métodos , Ubiquitina/química , Ubiquitina/efeitos da radiação , Fótons
4.
Psychol Med ; 44(13): 2729-38, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25065271

RESUMO

BACKGROUND: It has been previously demonstrated that a cognitive bias against disconfirmatory evidence (BADE) is associated with delusions. However, small samples of delusional patients, reliance on difference scores and choice of comparison groups may have hampered the reliability of these results. In the present study we aimed to improve on this methodology with a recent version of the BADE task, and compare larger groups of schizophrenia patients with/without delusions to obsessive-compulsive disorder (OCD) patients, a population with persistent and possibly bizarre beliefs without psychosis. METHOD: A component analysis was used to identify cognitive operations underlying the BADE task, and how they differ across four groups of participants: (1) high-delusional schizophrenia, (2) low-delusional schizophrenia, (3) OCD patients and (4) non-psychiatric controls. RESULTS: As in past studies, two components emerged and were labelled 'evidence integration' (the degree to which disambiguating information has been integrated) and 'conservatism' (reduced willingness to provide high plausibility ratings when justified), and only evidence integration differed between severely delusional patients and the other groups, reflecting delusional subjects giving higher ratings for disconfirmed interpretations and lower ratings for confirmed interpretations. CONCLUSIONS: These data support the finding that a reduced willingness to adjust beliefs when confronted with disconfirming evidence may be a cognitive underpinning of delusions specifically, rather than obsessive beliefs or other aspects of psychosis such as hallucinations, and illustrates a cognitive process that may underlie maintenance of delusions in the face of counter-evidence. This supports the possibility of the BADE operation being a useful target in cognitive-based therapies for delusions.


Assuntos
Delusões/fisiopatologia , Testes Neuropsicológicos , Transtorno Obsessivo-Compulsivo/fisiopatologia , Esquizofrenia/fisiopatologia , Pensamento/fisiologia , Adulto , Delusões/etiologia , Feminino , Humanos , Masculino , Esquizofrenia/complicações
5.
Phys Rev E Stat Nonlin Soft Matter Phys ; 83(3 Pt 1): 031310, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21517497

RESUMO

In this work we experimentally study the behavior of a freely rotating asymmetric probe immersed in a vibrated granular medium. For a wide variety of vibration conditions the probe exhibits a steady rotation whose direction is constant with respect to the asymmetry. By changing the vibration amplitude and by filtering the noise in different frequency bands we show that the velocity of rotation depends not only on the RMS acceleration Γ, but also on the amount of energy provided to two separate frequency bands, which are revealed to be important for the dynamics of the granular medium: The first band governs the transfer of energy from the grains to the probe, and the second affects the dynamics by altering the viscosity of the vibro-fluidized material.

6.
Biochem Biophys Res Commun ; 270(3): 1036-40, 2000 Apr 21.
Artigo em Inglês | MEDLINE | ID: mdl-10772946

RESUMO

Yeast cells exposed to adverse conditions employ a number of defense mechanisms in order to respond effectively to the stress and sustain a high proliferation rate. It has been shown that several glycolytic enzymes are induced upon heat treatment of yeast. In this work, we used a reporter plasmid construct to study the effects of oxidative stress, induced by the O(*-)(2)-generating compound paraquat (PQ), on the yeast 3-phosphoglycerate kinase gene (PGK) promoter. Our results show that (i) moderate, as opposed to excessive, doses of PQ induce increased stimulation of the PGK promoter, at midlogarithmic phase of growth; and (ii) the thiol antioxidant N-acetylcysteine cancels this stimulatory effect. These observations may represent one aspect of a more general role for glycolysis in maintaining the energy pools of yeast cells under stress.


Assuntos
Paraquat/farmacologia , Fosfoglicerato Quinase/genética , Regiões Promotoras Genéticas/efeitos dos fármacos , Saccharomyces cerevisiae/enzimologia , Acetilcisteína/farmacologia , Clonagem Molecular , Escherichia coli , Temperatura Alta , Cinética , Proteínas Recombinantes/biossíntese , Saccharomyces cerevisiae/efeitos dos fármacos , Saccharomyces cerevisiae/genética , Superóxidos , beta-Galactosidase/biossíntese , beta-Galactosidase/genética
7.
Biochem Biophys Res Commun ; 256(1): 63-7, 1999 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-10066423

RESUMO

Superoxide dismutase (SOD) is considered to be the first line of defense against oxygen toxicity. It exists as a family of three metalloproteins with copper,zinc (Cu,ZnSOD), manganese (MnSOD), and iron (FeSOD) forms. In this work, we have targeted Escherichia coli FeSOD to the mitochondrial intermembrane space (IMS) of yeast cells deficient in mitochondrial MnSOD. Our results show that FeSOD in the IMS increases the growth rate of the cells growing in minimal medium in air but does not protect the MnSOD-deficient yeast cells when exposed to induced oxidative stress. Cloned FeSOD must be targeted to the mitochondrial matrix to protect the cells from both physiological and induced oxidative stress. This confirms that the superoxide radical is mainly generated on the matrix side of the inner mitochondrial membrane of yeast cells, without excluding its potential appearance in the mitochondrial IMS where its elimination by SOD is beneficial to the cells.


Assuntos
Escherichia coli/enzimologia , Mitocôndrias/metabolismo , Estresse Oxidativo , Saccharomyces cerevisiae/metabolismo , Superóxido Dismutase/metabolismo , Western Blotting , Catalase/metabolismo , Divisão Celular/efeitos dos fármacos , Fracionamento Celular , Meios de Cultura , Citocromo-c Peroxidase/metabolismo , Escherichia coli/genética , Peróxido de Hidrogênio/metabolismo , Mitocôndrias/efeitos dos fármacos , Mitocôndrias/genética , Mutação , Estresse Oxidativo/efeitos dos fármacos , Oxigênio/metabolismo , Paraquat/farmacologia , Sinais Direcionadores de Proteínas/genética , Sinais Direcionadores de Proteínas/metabolismo , Proteínas Recombinantes de Fusão/metabolismo , Saccharomyces cerevisiae/citologia , Saccharomyces cerevisiae/efeitos dos fármacos , Saccharomyces cerevisiae/genética , Superóxido Dismutase/genética , Vitamina K/farmacologia
8.
Biochem Mol Biol Int ; 44(1): 41-9, 1998 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9503146

RESUMO

The iron superoxide dismutase (FeSOD) gene of Escherichia coli was cloned in Saccharomyces cerevisiae cells deficient in copper,zinc superoxide dismutase (Cu,ZnSOD). FeSOD replaced Cu,ZnSOD in protecting the yeast cells against oxidative stress. In the recombinant strains the FeSOD gene, which was under the transcriptional control of the yeast phosphoglycerate kinase gene promoter, was functionally expressed at two different levels on episomal and centromeric plasmids. Despite suppression of methionine and lysine auxotrophy, the higher level of FeSOD activity was more beneficial to growth of the mutant yeast cells only when these were exposed to higher levels of oxidative stress induced by paraquat or 100% oxygen. In the presence of paraquat, there was a novel stimulation of FeSOD activity. This was associated with a marked increase in catalase activity, and a decrease in glutathione reductase activity.


Assuntos
Citosol/enzimologia , Escherichia coli/enzimologia , Saccharomyces cerevisiae/enzimologia , Superóxido Dismutase/metabolismo , Antioxidantes/metabolismo , Clonagem Molecular , Ativação Enzimática/efeitos dos fármacos , Escherichia coli/genética , Expressão Gênica , Glutationa Peroxidase/metabolismo , Lisina/efeitos dos fármacos , Metionina/efeitos dos fármacos , Estresse Oxidativo/genética , Oxigênio/toxicidade , Paraquat/toxicidade , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/crescimento & desenvolvimento , Superóxido Dismutase/biossíntese , Superóxido Dismutase/deficiência , Superóxido Dismutase/genética
9.
Proc Natl Acad Sci U S A ; 92(10): 4219-23, 1995 May 09.
Artigo em Inglês | MEDLINE | ID: mdl-7753785

RESUMO

A gene encoding a fusion protein consisting of Escherichia coli iron superoxide dismutase (FeSOD) with the mitochondrial targeting presequence of yeast manganese superoxide dismutase (MnSOD) was cloned and expressed in E. coli and in Saccharomyces cerevisiae DL1Mn- yeast cells deficient in MnSOD. In the yeast cells the fusion protein was imported into the mitochondrial matrix. However, the presequence was not cleaved. In a control set of experiments, the E. coli FeSOD gene without the yeast MnSOD leader sequence was also cloned and expressed in S. cerevisiae DL1Mn- cells. In this case the FeSOD was located in the cytosol and was not imported into the mitochondrial matrix. E. coli FeSOD, with and without the yeast MnSOD presequence, proved to be active in yeast, but, whereas the FeSOD targeted to the mitochondria of yeast cells deficient in MnSOD protected the cells from the toxic effects of oxidative stress, FeSOD without the yeast MnSOD presequence did not protect the yeast cells deficient in MnSOD against oxidative stress.


Assuntos
Escherichia coli/enzimologia , Mitocôndrias/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Paraquat/toxicidade , Saccharomyces cerevisiae/metabolismo , Superóxido Dismutase/metabolismo , Sequência de Aminoácidos , Sequência de Bases , Clonagem Molecular , Vetores Genéticos , Isoenzimas/biossíntese , Isoenzimas/metabolismo , Cinética , Mitocôndrias/efeitos dos fármacos , Dados de Sequência Molecular , Oxigênio , Plasmídeos , Sinais Direcionadores de Proteínas/biossíntese , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/metabolismo , Mapeamento por Restrição , Saccharomyces cerevisiae/efeitos dos fármacos , Saccharomyces cerevisiae/crescimento & desenvolvimento , Superóxido Dismutase/biossíntese
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