Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Curr Top Med Chem ; 18(15): 1287-1303, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30277155

RESUMO

Giardia intestinalis infection causes enterocytes damage and loss of brush border of the epithelial cells of the intestine that leads to shortening of microvilli and altered epithelial barrier function. This pathology results in aqueous diarrhoea, steatorrhea, nausea, abdominal pain, vomiting and weight loss. However, most infections are asymptomatic. The main consequence of Giardia colonization is nutrients malabsorption. Several families of drugs with good efficacy are used for Giardia treatment, but sometime dosing regimens are suboptimal and emerging resistance begins to question their clinical value. Moreover, some of these drugs can cause side effects that result in patient discomfort and low adherence to the treatment. This paper reviews the drugs currently used for the treatment against Giardia: the mechanism of action, the efficacy, the normal dosing, side effects and in vitro and clinical studies. In addition, new therapies against Giardia such as those based on phytochemicals, Lactobacillus and nanotechnology are collected in this paper, trying to find the ideal treatment for this disease with maximum efficacy and minimum adverse effects.


Assuntos
Antiprotozoários/farmacologia , Giardia lamblia/efeitos dos fármacos , Giardíase/tratamento farmacológico , Antiprotozoários/química , Giardia lamblia/patogenicidade , Giardíase/microbiologia , Testes de Sensibilidade Parasitária
2.
Cell ; 103(7): 1033-45, 2000 Dec 22.
Artigo em Inglês | MEDLINE | ID: mdl-11163180

RESUMO

On each side of the midline of the Drosophila CNS, axons are organized into a series of parallel pathways. Here we show that the midline repellent Slit, previously identified as a short-range signal that regulates midline crossing, also functions at long range to pattern these longitudinal pathways. In this long-range function, Slit signals through the receptors Robo2 and Robo3. Axons expressing neither, one, or both of these receptors project in one of three discrete lateral zones, each successively further from the midline. Loss of robo2 or robo3 function repositions axons closer to the midline, while gain of robo2 or robo3 function shifts axons further from the midline. Local cues further refine the lateral position. Together, these long- and short-range guidance cues allow growth cones to select with precision a specific longitudinal pathway.


Assuntos
Axônios/fisiologia , Proteínas de Drosophila , Drosophila/embriologia , Regulação da Expressão Gênica no Desenvolvimento , Receptores Imunológicos/genética , Receptores Imunológicos/metabolismo , Animais , Axônios/química , Sistema Nervoso Central/citologia , Sistema Nervoso Central/embriologia , Drosophila/fisiologia , Dados de Sequência Molecular , Mutagênese/fisiologia , Proteínas do Tecido Nervoso/análise , Proteínas do Tecido Nervoso/genética , Proteínas do Tecido Nervoso/metabolismo , Neurônios/fisiologia , Neurônios/ultraestrutura , Receptores Imunológicos/análise , Proteínas Roundabout
3.
Neuron ; 28(3): 767-77, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11163265

RESUMO

In the Drosophila CNS, the midline repellent Slit acts at short range through its receptor Robo to control midline crossing. Longitudinal axons express high levels of Robo and avoid the midline; commissural axons that cross the midline express only low levels of Robo. Robo levels are in turn regulated by Comm. Here, we show that the Slit receptors Robo2 and Robo3 ensure the fidelity of this crossing decision: rare crossing errors occur in both robo2 and robo3 single mutants. In addition, low levels of either Robo or Robo2 are required to drive commissural axons through the midline: only in robo,robo2 double mutants do axons linger at the midline as they do in slit mutants. Robo2 and Robo3 levels are also tightly regulated, most likely by a mechanism similar to but distinct from the regulation of Robo by Comm.


Assuntos
Sistema Nervoso Central/embriologia , Sistema Nervoso Central/metabolismo , Proteínas de Drosophila , Receptores de Superfície Celular/metabolismo , Receptores Imunológicos/metabolismo , Animais , Axônios/metabolismo , Axônios/ultraestrutura , Sistema Nervoso Central/citologia , Regulação para Baixo/efeitos dos fármacos , Drosophila , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Cones de Crescimento/efeitos dos fármacos , Cones de Crescimento/metabolismo , Proteínas de Insetos/genética , Proteínas de Insetos/metabolismo , Proteínas de Membrana/metabolismo , Proteínas de Membrana/farmacologia , Mesoderma/patologia , Mutação , Proteínas do Tecido Nervoso/genética , Proteínas do Tecido Nervoso/metabolismo , Fenótipo , Receptores de Superfície Celular/genética , Receptores Imunológicos/genética , Proteínas Roundabout
4.
Dev Biol ; 191(1): 118-30, 1997 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-9356176

RESUMO

Glial cell differentiation in Drosophila melanogaster requires the activity of glide/gcm (glial cell deficient/glial cell missing). The role of this gene is to direct the cell fate switch between neurons and glial cells by activating the glial developmental program in multipotent precursor cells of the nervous system. In this paper, we show that glide/gcm is also expressed and required in the lineage of hemocytes/macrophages, scavenger cells that phagocytose cells undergoing programmed cell death. In addition, we show that, as for glial cells, glide/gcm plays an instructive role in hemocyte differentiation. Interestingly, it has been shown that in the development of the fly adult nervous system the role of scavenger cells is played by glial cells. These data and our findings on the dual role of glide/gcm indicate that glial cells and hemocytes/macrophages are functionally and molecularly related.


Assuntos
Drosophila melanogaster/embriologia , Neuroglia/citologia , Neuropeptídeos/biossíntese , Transativadores/biossíntese , Animais , Diferenciação Celular , Cruzamentos Genéticos , Proteínas de Ligação a DNA , Proteínas de Drosophila , Drosophila melanogaster/genética , Embrião não Mamífero/fisiologia , Feminino , Genes de Insetos , Genes Letais , Teste de Complementação Genética , Hemócitos/citologia , Hemócitos/fisiologia , Macrófagos/citologia , Macrófagos/fisiologia , Masculino , Mesoderma/citologia , Mesoderma/fisiologia , Morfogênese , Sistema Nervoso/embriologia , Neuroglia/fisiologia , Neuropeptídeos/genética , Proteínas Recombinantes de Fusão/biossíntese , Células-Tronco/citologia , Células-Tronco/fisiologia , Transativadores/genética , Fatores de Transcrição
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...