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1.
Expert Rev Neurother ; 20(11): 1143-1156, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-32842799

RESUMO

INTRODUCTION: Non-pharmacological interventions that promote quality of life in people with dementia are urgently needed. To accelerate development, evidence-based psychotherapies used in other populations can be considered. Mindfulness-based interventions with standardized protocols, namely mindfulness-based cognitive therapy (MBCT) and mindfulness-based stress reduction (MBSR), may be effective in people with dementia, although tailoring for cognitive impairment may be needed. Evidence from other cognitive disorders can inform research. AREAS COVERED: The authors reviewed 12 studies of MBCT/MBSR conducted in people with cognitive impairments, including 10 in stroke, traumatic brain injury, and mild cognitive impairment; and two in dementia. Protocol modifications, outcomes, and evidence quality were analyzed. Common themes to address cognitive difficulties included: shortened session duration, use of memory aids, increase in repetition, simplified language, and omitted retreat sessions. EXPERT OPINION: MBCT and MBSR can be applied without drastic modifications in people with cognitive impairment. Their effectiveness in people with dementia remains unknown: empirical studies using/adapting evidence-based MBCT/MBSR protocols in this population is seriously lacking. Studies used a diverse range of outcome measures, which made direct comparison difficult. Further research with high methodological quality, sufficient power, and longer follow-up is urgently needed. Development of manuals would enhance the replicability of future studies.


Assuntos
Disfunção Cognitiva/reabilitação , Demência/reabilitação , Atenção Plena , Avaliação de Resultados em Cuidados de Saúde , Humanos , Atenção Plena/métodos
2.
J Investig Dermatol Symp Proc ; 18(2): S81-S84, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28941500

RESUMO

Elevated levels of prostaglandin D2 (PGD2) have been shown to be present in the bald scalp of androgenic alopecia (AGA) patients and to functionally inhibit hair growth. However, its precise mechanism in AGA has yet to be clearly defined. Although testosterone plays a critical role in the initiation and progression of AGA, the existence of a possible link between PGD2 and testosterone in skin has not been investigated. Here we show that human keratinocytes treated with PGD2 show enhanced capacity to convert the weak androgen, androstenedione, to testosterone. At the same time, treatment with PGD2 induced reactive oxygen species as indicated by generation of the lipid peroxidation product, 4-hydroxynonenal. To determine whether these two events are linked, we used the reactive oxygen species scavenger N-acetyl-cysteine, which blocked the enhanced testosterone production from PGD2-treated keratinocytes. Our study suggests the existence of a possible crosstalk between the PGD2-reactive oxygen species axis and testosterone metabolism in keratinocytes. Thus, we propose that AGA patients might benefit from the use of N-acetyl-cysteine or other antioxidants as a supplement to currently available or emerging AGA therapies such as finasteride, minoxidil, and PGD2 receptor blockers.


Assuntos
Androstenodiona/metabolismo , Queratinócitos/metabolismo , Prostaglandina D2/farmacologia , Espécies Reativas de Oxigênio/metabolismo , Testosterona/biossíntese , Acetilcisteína/farmacologia , Aldeídos/metabolismo , Alopecia , Células Cultivadas , Sequestradores de Radicais Livres/farmacologia , Humanos , Transdução de Sinais
3.
Behav Modif ; 41(6): 764-787, 2017 11.
Artigo em Inglês | MEDLINE | ID: mdl-28689469

RESUMO

This article describes a 10-session group-based Mindfulness Program for people with mild to moderate dementia. It aims to equip people with dementia with skills to manage psychological distress, with support from carers. The Mindfulness Program was developed through reviews of existing literature, consultation with experts, and a focus group with people with dementia. In a randomized controlled feasibility and pilot trial with people with mild to moderate dementia in care homes, it was found to significantly increase quality of life. The manual presented here is designed to be administered flexibly to promote participants' personhood. The protocol is designed for use by therapists with experience in practicing mindfulness meditation.


Assuntos
Demência/reabilitação , Manuais como Assunto , Atenção Plena/métodos , Desenvolvimento de Programas/métodos , Psicoterapia de Grupo/métodos , Estresse Psicológico/terapia , Humanos
5.
Cancer Cell ; 1(3): 257-67, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12086862

RESUMO

Striking homology between signaling molecules in zebrafish and humans suggests that compounds known to inhibit human kinases may enable a chemical genetic approach to dissect signaling pathways in the zebrafish embryo. We tested this hypothesis using a vascular endothelial growth factor receptor inhibitor, PTK787/ZK222584. Zebrafish embryos treated with this compound lacked all major blood vessels. Overexpression of AKT/PKB, a putative effector of vascular endothelial growth factor signaling, allowed blood vessels to form in the presence of drug. Endothelial cell apoptosis induced by the drug is prevented by increasing AKT/PKB activity, thus establishing the physiological relevance of AKT/PKB in the angiogenic process. This approach allowed us to examine the effects of blood flow and the role of endothelial signals in organogenesis.


Assuntos
Embrião não Mamífero/irrigação sanguínea , Neovascularização Fisiológica/fisiologia , Proteínas Serina-Treonina Quinases , Piridinas , Transdução de Sinais/fisiologia , Peixe-Zebra/embriologia , Sequência de Aminoácidos , Inibidores da Angiogênese/farmacologia , Animais , DNA Complementar , Endotélio Vascular/citologia , Inibidores Enzimáticos/farmacologia , Hibridização In Situ , Marcação In Situ das Extremidades Cortadas , Dados de Sequência Molecular , Ftalazinas/farmacologia , Proteínas Proto-Oncogênicas/metabolismo , Proteínas Proto-Oncogênicas c-akt , RNA/metabolismo , Receptores Proteína Tirosina Quinases/antagonistas & inibidores , Receptores Proteína Tirosina Quinases/metabolismo , Receptores de Fatores de Crescimento/antagonistas & inibidores , Receptores de Fatores de Crescimento/metabolismo , Receptores de Fatores de Crescimento do Endotélio Vascular , Homologia de Sequência de Aminoácidos , Regulação para Cima
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