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1.
Biomarkers ; 28(2): 238-248, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36576409

ABSTRACT

Objective: In this study, we aimed to determine the role of Psidium cattleianum extract (PCE) and compare its effects with those of metformin (Met) in an animal model with type 2 diabetes mellitus (T2DM).Methods: T2DM was induced in rats using a high-fat diet (HFD), followed by a single dose of streptozotocin (STZ). Met and PCE were administered intragastrically once a day throughout the experiment, and their effects on biochemical, inflammatory, oxidative, and histological parameters were evaluated.Results: Met and PCE prevented the increase in serum levels of glucose, total cholesterol (TC), triacylglycerol (TG), very low-density lipoprotein (VLDL) and interleukin-6 (IL-6) induced by T2DM, and restored redox homeostasis in the liver and brain. Met increased the serum levels of anti-inflammatory cytokine and interleukin-10 (IL-10). Furthermore, both treatments restored the liver and pancreas from marked cellular disorganisation, vacuolisation, and necrosis, with PCE being more effective than Met in recovering histological changes.Conclusion: PCE is a promising agent for the prevention of T2DM complications.


Subject(s)
Diabetes Mellitus, Experimental , Diabetes Mellitus, Type 2 , Metformin , Psidium , Animals , Rats , Blood Glucose , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Experimental/pathology , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/pathology , Fruit , Hypoglycemic Agents/pharmacology , Metformin/pharmacology , Metformin/therapeutic use , Models, Animal
2.
Int J Epidemiol ; 50(1): 256-265, 2021 03 03.
Article in English | MEDLINE | ID: mdl-32888008

ABSTRACT

BACKGROUND: Ultra-processed food consumption and obesity have been highlighted as an important relationship to public health. We aimed to evaluate the association between ultra-processed food consumption and body fat from 6 to 11 years of age. METHODS: We assessed the association between ultra-processed food consumption (from food frequency questionnaires) and body fat (measured by air displacement plethysmography) between 6 and 11 years of age among participants of the Pelotas-Brazil 2004 Birth Cohort. The NOVA classification was used to classify foods according to the processing degree. Body fat was evaluated relative to the height using fat mass index (FMI). Generalized estimating equations were used to answer the main research question and mediation analyses were run to assess the direct and indirect effect of ultra-processed food in body fat. RESULTS: At fully adjusted analysis, an increase of 100 g in contribution from ultra-processed food to daily food intake at between 6 and 11 years of age was associated with a gain of 0.14 kg/m² in FMI in the same period; 58% of the total effect of ultra-processed food intake at 6 years (in grams) over the change in FMI from 6 to 11 years was mediated by its calorie content. CONCLUSIONS: Ultra-processed food consumption was associated with an increase in body fat from childhood to early adolescence, and this association was not just due to the effect of ultra-processed food on calorie content.


Subject(s)
Energy Intake , Fast Foods , Adolescent , Brazil , Child , Cohort Studies , Diet , Humans , Obesity
3.
J Food Biochem ; : e13442, 2020 Aug 17.
Article in English | MEDLINE | ID: mdl-32803896

ABSTRACT

The aim of the current study was to evaluate the effect of chronic administration of Eugenia uniflora fruit extract on behavioral parameters, oxidative stress markers, and acetylcholinesterase activity in an animal model of depression, which was induced by chronic unpredictable stress (CUS). Mice were divided into six groups as follows: control/vehicle (water), control/fluoxetine (20 mg/kg), control/extract (200 mg/kg), CUS/vehicle, CUS/fluoxetine (20 mg/kg), and CUS/extract (200 mg/kg). Animals of the CUS group were exposed to a series of stressors for a period of 21 days. Vehicle, fluoxetine, and hydroalcoholic extract were administered daily by gavage. Results showed that E. uniflora treatment: (a) prevented the depressant-like effect induced by CUS; (b) regulated the activity of acetylcholinesterase; (c) reduced oxidative damage to lipids and reactive oxygen species production, in the prefrontal cortex and hippocampus; and (d) prevented the reduction of glutathione peroxidase in the hippocampus of animals subjected to CUS protocol. Taken together, our findings suggested that E. uniflora extract exerts a neuroprotective effect by preventing oxidative damage and decreasing CUS-induced acetylcholinesterase activity, thus, ameliorating depressive-type behavior. PRACTICAL APPLICATIONS: E. uniflora fruit extract revealed an antidepressant-like effect and prevented the oxidative damage as well as cholinergic alterations caused by chronic stress in mice. Therefore, we believe that the results obtained in this study can be used to develop an alternative therapy for the management of depressive disorders.

4.
Biomarkers ; 25(5): 417-424, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32519899

ABSTRACT

Aim: This study investigated the effects of polar Butia odorata fruit extract on metabolic, inflammatory, and oxidative stress parameters in rats submitted to a hyperlipidaemia condition induced by tyloxapol.Methods: Animals were divided into 3 groups: saline, saline plus tyloxapol, and B. odorata extract plus tyloxapol. Animals were treated for 15 days with a saline solution or B. odorata fruit extract and after hyperlipidaemia was induced by tyloxapol.Results: Treatment with B. odorata extract reduced serum triglyceride, total cholesterol, C-reactive protein, and adenosine deaminase and butyrylcholinesterase activities when compared to the tyloxapol group. HDL-cholesterol and paraoxonase 1 activity were higher in B. odorata extract treated animals when compared to tyloxapol-treated animals. No differences were observed in hepatic oxidative stress parameters. Phenolic compounds present in B. odorata fruit extract were identified and quantified by LC-MS/MS.Conclusion: These findings indicated that phenolic rich B. odorata extract has hypolipidemic and anti-inflammatory effects in hyperlipidemic rats.


Subject(s)
Arecaceae/chemistry , Aryldialkylphosphatase/genetics , Liver/drug effects , Oxidative Stress/drug effects , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , C-Reactive Protein/metabolism , Cholesterol, HDL/blood , Chromatography, Liquid , Fruit/chemistry , Humans , Hypolipidemic Agents/chemistry , Hypolipidemic Agents/pharmacology , Male , Phenols/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacology , Rats , Tandem Mass Spectrometry , Triglycerides/blood
5.
Biomed Pharmacother ; 92: 935-941, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28618655

ABSTRACT

The aim of this study was to investigate the effect of Eugenia uniflora fruit (red type) extract on metabolic status, as well as on neurochemical and behavioral parameters in an animal model of metabolic syndrome induced by a highly palatable diet (HPD). Rats were treated for 150days and divided into 4 experimental groups: standard chow (SC) and water orally, SC and E. uniflora extract (200mg/kg daily, p.o), HPD and water orally, HPD and extract. Our data showed that HPD caused glucose intolerance, increased visceral fat, weight gain, as well as serum glucose, triacylglycerol, total cholesterol and LDL cholesterol; however, E. uniflora prevented these alterations. The extract decreased lipid peroxidation and prevented the reduction of superoxide dismutase and catalase activities in the prefrontal cortex, hippocampus and striatum of animals submitted to HPD. We observed a HPD-induced reduction of thiol content in these cerebral structures. The extract prevented increased acetylcholinesterase activity in the prefrontal cortex caused by HPD and the increase in immobility time observed in the forced swim test. Regarding chemical composition, LC/MS analysis showed the presence of nine anthocyanins as the major compounds. In conclusion, E. uniflora extract showed benefits against metabolic alterations caused by HPD, as well as exhibited antioxidant and antidepressant-like effects.


Subject(s)
Antidepressive Agents/pharmacology , Antioxidants/pharmacology , Brain/drug effects , Depression/prevention & control , Eugenia/chemistry , Fruit/chemistry , Metabolic Syndrome/prevention & control , Plant Extracts/pharmacology , Acetylcholinesterase/metabolism , Adiposity/drug effects , Animals , Antidepressive Agents/isolation & purification , Antidepressive Agents/standards , Antioxidants/isolation & purification , Antioxidants/standards , Behavior, Animal/drug effects , Biomarkers/blood , Blood Glucose/drug effects , Blood Glucose/metabolism , Brain/metabolism , Brain/physiopathology , Catalase/metabolism , Depression/blood , Depression/physiopathology , Depression/psychology , Diet, High-Fat , Dietary Sucrose , Disease Models, Animal , Dyslipidemias/blood , Dyslipidemias/chemically induced , Dyslipidemias/prevention & control , GPI-Linked Proteins/metabolism , Glucose Intolerance/blood , Glucose Intolerance/chemically induced , Glucose Intolerance/prevention & control , Lipid Peroxidation/drug effects , Lipids/blood , Male , Metabolic Syndrome/blood , Metabolic Syndrome/physiopathology , Motor Activity/drug effects , Obesity/blood , Obesity/chemically induced , Obesity/prevention & control , Phytotherapy , Plant Extracts/isolation & purification , Plant Extracts/standards , Plants, Medicinal , Rats, Wistar , Superoxide Dismutase/metabolism , Time Factors , Weight Gain/drug effects
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