Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Chin Med Assoc ; 87(7): 664-669, 2024 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-38810093

RESUMO

BACKGROUND: This study aimed to evaluate the effects of rosuvastatin and pravastatin on glucose homeostasis and other biomarkers in individuals at high risk of developing diabetes. METHODS: This prospective, randomized, open-labeled, and controlled trial included prediabetic individuals with impaired fasting glucose and impaired glucose tolerance. The participants were randomized into three groups: rosuvastatin (10 mg), pravastatin (40 mg), or control. Biomarkers of diabetes and glucose and insulin responses to oral glucose tolerance tests were assessed at baseline and after 6 months of treatment. The primary outcomes were comparisons of glucose homeostasis and biomarkers of diabetes among groups at baseline and after 6 months of treatment. RESULTS: A total of 141 subjects with impaired fasting glucose (IFG) were screened and 41 participants were recruited. Twenty-two subjects were randomized to either the rosuvastatin or pravastatin group and 19 subjects were assigned to the control group. After 6 months of treatment, all groups had similar cholesterol and triglyceride levels. Likewise, HbA1c levels, glucose, and insulin excursions during oral glucose tolerance test, were similar among the three groups. However, compared to the other groups, the rosuvastatin group had higher homeostasis model assessment for insulin resistance (HOMA-IR) (insulin resistance) and a lower Matsuda index (insulin sensitivity). CONCLUSION: Among prediabetic individuals with IFG, rosuvastatin treatment was associated with increased insulin resistance and decreased insulin sensitivity compared to pravastatin and control groups. Further research is needed to elucidate the underlying mechanisms and clinical implications of these findings.


Assuntos
Glicemia , Homeostase , Inibidores de Hidroximetilglutaril-CoA Redutases , Pravastatina , Estado Pré-Diabético , Rosuvastatina Cálcica , Humanos , Estado Pré-Diabético/tratamento farmacológico , Estado Pré-Diabético/sangue , Rosuvastatina Cálcica/uso terapêutico , Masculino , Inibidores de Hidroximetilglutaril-CoA Redutases/uso terapêutico , Feminino , Pessoa de Meia-Idade , Estudos Prospectivos , Homeostase/efeitos dos fármacos , Pravastatina/uso terapêutico , Pravastatina/farmacologia , Glicemia/análise , Glicemia/efeitos dos fármacos , Adulto , Resistência à Insulina , Teste de Tolerância a Glucose , Idoso
2.
Ther Apher Dial ; 26(4): 854-855, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-34898003
3.
Nat Commun ; 4: 1544, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23443572

RESUMO

Organic fluorescent nanoparticles, excitation-dependent photoluminescence, hydrogen-bonded clusters and lysobisphosphatidic acid are four interesting individual topics in materials and biological sciences. They have attracted much attention not only because of their unique properties and important applications, but also because the nature of their intriguing phenomena remained unclear. Here we report a new type of organic fluorescent nanoparticles with intense blue and excitation-dependent visible fluorescence in the range of 410-620 nm. The nanoparticles are composed of ten bis(monoacylglycerol)bisphenol-A molecules and the self-assembly occurs only in elevated concentrations of 2-monoacylglycerol via radical-catalysed 3,2-acyl migration from 3-monoacylglycerol in neat conditions. The excitation-dependent fluorescence behaviour is caused by chromophores composed of hydrogen-bonded monoacylglycerol clusters, which are linked by an extensive hydrogen-bonding network between the ester carbonyl groups and the protons of the alcohols with collective proton motion and HO···C=O (n→π) interactions.


Assuntos
Corantes Fluorescentes/química , Lisofosfolipídeos/química , Monoglicerídeos/química , Nanopartículas/química , Compostos Benzidrílicos/química , Análise por Conglomerados , Ligação de Hidrogênio , Lisofosfolipídeos/síntese química , Modelos Moleculares , Conformação Molecular , Monoglicerídeos/síntese química , Nanopartículas/ultraestrutura , Fenóis/química , Polímeros/química , Teoria Quântica , Espectrometria de Fluorescência , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...