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1.
Br J Haematol ; 192(5): 922-931, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33476407

RESUMO

Sickle cell anaemia (SCA) is a debilitating genetic haemoglobinopathy predominantly affecting the disenfranchised strata of society in Africa and the Americas. The most common pharmacological treatment for this disease is the administration of hydroxycarbamide (HC) for which questions remain regarding its mechanism of action, efficacy and long-term toxicity specifically in paediatric individuals. A multiplatform metabolomics approach was used to assess the metabolome of plasma samples from a population of children and adolescents with SCA with and without HC treatment along with non-SCA individuals. Fifty-three metabolites were identified by ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS) and 1 H nuclear magnetic resonance (NMR) with a predominance of membrane lipids, amino acids and organic acids. The partial least-squares discriminant analysis (PLS-DA) analysis allowed a clear discrimination between the different studied groups, revealing clear effects of the HC treatment in the patients' metabolome including rescue of specific metabolites to control levels. Increased creatine/creatinine levels under HC treatment suggests a possible increase in the arginine pool and increased NO synthesis, supporting existing models for HC action in SCA. The metabolomics results extend the current knowledge on the models for SCA pathophysiology including impairment of Lands' cycle and increased synthesis of sphingosine 1-phosphate. Putative novel biomarkers are suggested.


Assuntos
Anemia Falciforme/sangue , Antidrepanocíticos/uso terapêutico , Hidroxiureia/uso terapêutico , Metabolômica , Ácidos/sangue , Síndrome Torácica Aguda/etiologia , Adolescente , Aminoácidos/sangue , Anemia Falciforme/complicações , Anemia Falciforme/tratamento farmacológico , Antidrepanocíticos/farmacologia , Arteriopatias Oclusivas/etiologia , Biomarcadores , Butiratos/sangue , Criança , Cromatografia Líquida de Alta Pressão , Creatina/sangue , Creatinina/sangue , Feminino , Humanos , Hidroxiureia/farmacologia , Lisofosfolipídeos/sangue , Masculino , Espectrometria de Massas , Lipídeos de Membrana/sangue , Modelos Biológicos , Ressonância Magnética Nuclear Biomolecular , Esfingosina/análogos & derivados , Esfingosina/sangue
2.
Braz J Psychiatry ; 38(3): 243-6, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27304256

RESUMO

Autism spectrum disorders (ASDs) are characterized by deficits in the individual's ability to socialize, communicate, and use the imagination, in addition to stereotyped behaviors. These disorders have a heterogenous phenotype, both in relation to symptoms and regarding severity. Organic problems related to the gastrointestinal tract are often associated with ASD, including dysbiosis, inflammatory bowel disease, exocrine pancreatic insufficiency, celiac disease, indigestion, malabsorption, food intolerance, and food allergies, leading to vitamin deficiencies and malnutrition. In an attempt to explain the pathophysiology involved in autism, a theory founded on opioid excess has been the focus of various investigations, since it partially explains the symptomatology of the disorder. Another hypothesis has been put forward whereby the probable triggers of ASDs would be related to the presence of bacteria in the bowel, oxidative stress, and intestinal permeability. The present update reviews these hypotheses.


Assuntos
Transtorno do Espectro Autista/etiologia , Transtorno do Espectro Autista/metabolismo , Gastroenteropatias/metabolismo , Peptídeos Opioides/efeitos adversos , Peptídeos Opioides/metabolismo , Transtorno do Espectro Autista/fisiopatologia , Gastroenteropatias/fisiopatologia , Microbioma Gastrointestinal , Trato Gastrointestinal/metabolismo , Trato Gastrointestinal/microbiologia , Trato Gastrointestinal/fisiopatologia , Humanos , Peptídeos Opioides/análise , Estresse Oxidativo , Compostos de Sulfidrila/metabolismo
3.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 38(3): 243-246, July-Sept. 2016.
Artigo em Inglês | LILACS | ID: lil-792749

RESUMO

Autism spectrum disorders (ASDs) are characterized by deficits in the individual’s ability to socialize, communicate, and use the imagination, in addition to stereotyped behaviors. These disorders have a heterogenous phenotype, both in relation to symptoms and regarding severity. Organic problems related to the gastrointestinal tract are often associated with ASD, including dysbiosis, inflammatory bowel disease, exocrine pancreatic insufficiency, celiac disease, indigestion, malabsorption, food intolerance, and food allergies, leading to vitamin deficiencies and malnutrition. In an attempt to explain the pathophysiology involved in autism, a theory founded on opioid excess has been the focus of various investigations, since it partially explains the symptomatology of the disorder. Another hypothesis has been put forward whereby the probable triggers of ASDs would be related to the presence of bacteria in the bowel, oxidative stress, and intestinal permeability. The present update reviews these hypotheses.


Assuntos
Humanos , Peptídeos Opioides/efeitos adversos , Peptídeos Opioides/metabolismo , Transtorno do Espectro Autista/etiologia , Transtorno do Espectro Autista/metabolismo , Gastroenteropatias/metabolismo , Compostos de Sulfidrila/metabolismo , Estresse Oxidativo , Peptídeos Opioides/análise , Trato Gastrointestinal/fisiopatologia , Trato Gastrointestinal/metabolismo , Trato Gastrointestinal/microbiologia , Transtorno do Espectro Autista/fisiopatologia , Microbioma Gastrointestinal , Gastroenteropatias/fisiopatologia
4.
Ciênc. cult. (Säo Paulo) ; 43(4): 310-2, July-Aug. 1991. tab
Artigo em Inglês | LILACS | ID: lil-113795

RESUMO

Diante das importantes funçöes celulares como a endocitose, a digestäo e a desintoxicaçäo, exercidas pelos diferentes componentes do compartimento lisossômico, decidimos estudar os efeitos in vivo do esteviosídeo sobre a atividade lisossômica. Näo foram observadas mudanças estatisticamente significantes na estabilidade das membranas lisossômicas do rim e do fígado, em camundongos tratados com 50mg/Kg peso corporal/dia. Na dose de 100mg/Kg/dia foi observado um pequeno efeito labilizador nos lisossomos hepáticos, mas näo sobre os renais


Assuntos
Animais , Masculino , Feminino , Camundongos , Ratos , Glucosídeos/farmacologia , Lisossomos/efeitos dos fármacos , Terpenos/farmacologia , Fígado/citologia , Fígado , Rim/citologia , Rim/efeitos dos fármacos , Distribuição Aleatória
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