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1.
Neuropsychiatr ; 23(3): 174-83, 2009.
Artículo en Alemán | MEDLINE | ID: mdl-19703383

RESUMEN

OBJECTIVE: The aim of this study was to evaluate the effectiveness of a psycho-educational, coping-oriented therapy programme for patients with schizophrenia or schizo-affective disorder. METHOD: Controlled, prospective study design. In the experimental group the Therapy Manual for Psycho-education and Coping with Illness (PKB) was used, providing targeted information on the illness, medical treatment, prodromal symptoms, and health behaviour. Controls participated in supportive dialogues or in an occupational rehabilitation programme. Psychopathology, re-hospitalisations, knowledge, functional outcome and coping strategies were assessed before, directly after and 12 months post therapy. RESULTS: 82 patients participated. In both groups (experimental, control) a significant improvement in psychopathology and general functioning level were observed. Specific advantages for patients of the experimental group were limited to a few aspects, including rehospitalizations in the first year and certain coping strategies. CONCLUSION: In the treatment of schizophrenia different forms of psycho-social intervention (experimental, control) can be effective. Identification of subgroups profiting specially from certain types of intervention should be subject of future research.


Asunto(s)
Adaptación Psicológica , Educación del Paciente como Asunto , Psicoterapia de Grupo , Trastornos Psicóticos/terapia , Esquizofrenia/terapia , Psicología del Esquizofrénico , Adulto , Estudios de Casos y Controles , Femenino , Humanos , Estudios Longitudinales , Masculino , Readmisión del Paciente , Estudios Prospectivos , Escalas de Valoración Psiquiátrica , Resultado del Tratamiento , Adulto Joven
2.
J Comp Neurol ; 501(5): 716-30, 2007 Apr 10.
Artículo en Inglés | MEDLINE | ID: mdl-17299753

RESUMEN

Huntington disease (HD) is a progressive neurodegenerative disorder characterized by emotional, cognitive, and motor dysfunctions. Aggregation of huntingtin is a hallmark of HD and, therefore, a crucial parameter for the evaluation of HD animal models. We investigated here the regional, cellular, and subcellular distribution of N-terminal huntingtin aggregates and associated neuropathological changes in the forebrain of a rat transgenic for HD (tgHD). The tgHD rat brain showed enormously enlarged lateral ventricles and a similar atrophy of cortical and subcortical areas as known in HD patients. Huntingtin aggregates of varying size and forms were regionally identified in neuronal nuclei, cytoplasm, dendrites, dendritic spines, axons, and synaptic terminals, closely resembling the results described earlier for human HD brains and in established HD mouse models. Huntingtin aggregates in mitochondria support mitochondrial dysfunction as contributing to the disease pathogenesis. Dark cell degeneration was reminiscent of results in HD individuals and HD mouse models. Interestingly, huntingtin aggregates were especially well accumulated in two interacting limbic forebrain systems, the ventral striatopallidum and the extended amygdala, which may contribute to the early onset of emotional changes observed in the tgHD rat. In conclusion, the tgHD rat model reflects to a remarkable extent the cellular and subcellular neuropathological key features as observed in human HD and HD mouse brains and hints of changes in limbic forebrain systems, which may elucidate the emotional dysfunction in the tgHD rat and affective disturbances in HD patients.


Asunto(s)
Encéfalo/patología , Enfermedad de Huntington/patología , Cuerpos de Inclusión/patología , Proteínas del Tejido Nervioso/metabolismo , Neuronas/patología , Proteínas Nucleares/metabolismo , Amígdala del Cerebelo/metabolismo , Amígdala del Cerebelo/patología , Animales , Animales Modificados Genéticamente , Ganglios Basales/metabolismo , Ganglios Basales/patología , Encéfalo/metabolismo , Núcleo Celular/metabolismo , Núcleo Celular/patología , Citoplasma/metabolismo , Citoplasma/patología , Dendritas/metabolismo , Dendritas/patología , Modelos Animales de Enfermedad , Humanos , Proteína Huntingtina , Enfermedad de Huntington/genética , Enfermedad de Huntington/metabolismo , Cuerpos de Inclusión/metabolismo , Ratones , Microscopía Electrónica de Transmisión , Mitocondrias/metabolismo , Mitocondrias/patología , Degeneración Nerviosa/metabolismo , Degeneración Nerviosa/patología , Proteínas del Tejido Nervioso/genética , Neuronas/metabolismo , Proteínas Nucleares/genética , Terminales Presinápticos/metabolismo , Terminales Presinápticos/patología , Ratas , Ratas Sprague-Dawley
3.
Eur Psychiatry ; 18(4): 149-54, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12814846

RESUMEN

Although there is now strong evidence confirming the efficacy of psychological therapies in schizophrenia, the therapeutic processes which they activate remain widely unknown. In order to effectively implement them in clinical practice, identification of these processes is essential. In a controlled study, the efficacy of a coping-oriented therapy approach for schizophrenia patients was tested. Furthermore, the study aimed at establishing preliminary hypotheses on the therapeutically relevant factors. Treatment effects were found in the prominence of psychopathology, the extent of cognizance of the disorder, and the level of social functioning. Moreover, a better psychopathological and social outcome as measured 12 and 18 months after completion of therapy was best predicted by the patients' mastery of active, problem-focused coping strategies immediately after completion of therapy. The findings underscore the clinical relevance of specific coping styles and corroborate the appropriateness of focusing on aspects of coping behavior in psychological interventions for schizophrenia patients.


Asunto(s)
Terapia Cognitivo-Conductual/métodos , Psicoterapia de Grupo/métodos , Esquizofrenia/terapia , Psicología del Esquizofrénico , Actividades Cotidianas/psicología , Adulto , Terapia Combinada , Terapia Familiar/métodos , Femenino , Estudios de Seguimiento , Conductas Relacionadas con la Salud , Humanos , Masculino , Solución de Problemas , Ajuste Social , Apoyo Social
4.
J Comp Neurol ; 458(1): 78-97, 2003 Mar 24.
Artículo en Inglés | MEDLINE | ID: mdl-12577324

RESUMEN

The lateral habenular complex is part of the habenular nuclei, a distinct structure in the dorsal diencephalon of all vertebrates. In contrast to the bewildering diversity of behaviors, in which the lateral habenular complex is thought to be involved, there is an astonishing lack of information concerning its cellular organization, its neuronal circuits, and the neurophysiological mechanisms, which may provide the physiological and molecular basis for its diverse biological functions. This problem may be due to an unexpected heterogeneity of the lateral habenular complex. Recently, a detailed subnuclear organization has been described (Andres et al. [1999] J Comp Neurol 407:130-150), which provides the base for a subsequent physiological and behavioral analysis of this area. Available criteria, however, can be applied to semithin sections only. To facilitate further investigations, the present work aimed to elaborate novel morphologic and immunocytochemical criteria that can be applied to conventional cryostat or Vibratome sections to allow identification and delineation of subnuclei of the lateral habenular complex. Consequently, the regional, cellular, and subcellular localization of approximately 30 different neuroactive molecules was investigated. Of these candidate molecules, gamma-aminobutyric acid-B receptor protein, Kir3.2 potassium channel protein, tyrosine hydroxylase, and neurofilament heavy chain proved to be suitable markers. Our observation suggests that the habenular subnuclei express distinct immunocytochemical characteristics. These features may be used to identify and delineate the subnuclei on conventional cryostat or Vibratome sections. From our results, it is expected that the further functional analysis of the lateral habenular complex will be facilitated considerably.


Asunto(s)
Habénula/anatomía & histología , Habénula/química , Proteínas del Tejido Nervioso/análisis , Proteínas de Neurofilamentos/análisis , Canales de Potasio de Rectificación Interna/análisis , Receptores de GABA-B/análisis , Tirosina 3-Monooxigenasa/análisis , Acetilcolinesterasa/análisis , Animales , Biomarcadores/análisis , Crioultramicrotomía , Habénula/enzimología , Inmunohistoquímica , Masculino , Ratas , Ratas Wistar
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