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Mol Biol Rep ; 51(1): 11, 2023 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-38085359

RESUMO

BACKGROUND: Diabetes is a life-threatening health condition that requires expensive treatment and places a significant financial burden on society. Consequently, this study aimed to explore the potential of low and high concentrations of ginger extract, ZnO-NPs, and a combination of both to help manage diabetes and reduce high levels of lipids in diabetic rats. METHODS AND RESULTS: The research focused on agglomerated nanoparticles under 100 nm, specifically ZnO nanoparticles. The size of the nanoparticles was determined using X-ray diffraction analysis and scanning electron microscopy analysis, with a monodisperse particle size distribution of 20 to 48 nm and an average size of 38 nm, as shown by dynamic light scattering. Fourier transform infrared spectroscopy revealed the presence of typical peaks of ginger extract and ZnO-NPs in the nanocomposite structure. The pancreatic tissue histopathological study indicated that a concentration of 10 mg/kg of the composite had the most significant antidiabetic effect compared to other treatments. Lower concentrations could significantly reduce and balance fasting blood sugar and triglycerides levels while also increasing the high-density lipoproteins levels. However, all treatments induced a significant decrease in total cholesterol and low-density lipoproteins levels. Only metformin and ZnO-NPs in lower concentrations could decrease very low-density lipoproteins levels. The molecular technique showed that a low concentration of the composite led to the most significant decrease in Tnf-α gene expression compared to the diabetic group. The expression of the glutathione peroxidase 1 (Gpx1) gene in treated groups had no significant difference with the level of Gpx1 expression in the control rats. CONCLUSIONS: In general, this study demonstrated that lower concentrations of the treatments, especially composite, were more effective for treating diabetic rats due to reduced pancreatic tissue damage.


Assuntos
Diabetes Mellitus Experimental , Nanopartículas Metálicas , Nanopartículas , Óxido de Zinco , Ratos , Animais , Óxido de Zinco/farmacologia , Óxido de Zinco/química , Fator de Necrose Tumoral alfa/genética , Glucose , Diabetes Mellitus Experimental/tratamento farmacológico , Diabetes Mellitus Experimental/genética , Diabetes Mellitus Experimental/metabolismo , Glutationa Peroxidase GPX1 , Extratos Vegetais/farmacologia , Extratos Vegetais/química , Nanopartículas/química , Lipoproteínas LDL , Lipídeos , Nanopartículas Metálicas/química , Antibacterianos/farmacologia , Espectroscopia de Infravermelho com Transformada de Fourier , Difração de Raios X
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