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1.
Food Funct ; 13(9): 5124-5134, 2022 May 10.
Artigo em Inglês | MEDLINE | ID: mdl-35416190

RESUMO

The objective of the present study was to examine the effects of hydroxy citric acid (HCA) extracts from Garcinia cambogia on metabolic, atherogenic and inflammatory biomarkers in obese women with non-alcoholic fatty liver disease (NAFLD). The present clinical trial was carried out on 40 overweight/obese women with NAFLD. The patients were randomly allocated into either the "HCA group" (receiving calorie-restricted diet (-700 kcal d-1) accompanied by HCA tablets) and the "control group" (receiving only calorie-restricted diet) for eight weeks. Weight, height, body mass index (BMI), and waist circumference (WC) were measured. Fasting blood sugar (FBS), lipid profile, liver enzymes, as well as inflammatory biomarkers were determined at baseline and after the intervention. Dietary intake was assessed at baseline and at the end of the trial and food intake data were analyzed by the Nutritionist IV software. Results showed a decrease in energy and macronutrient intake in both groups (p < 0.05). Weight, BMI, WC, and hip circumference as well as FBS, triglyceride (TG), low-density lipoprotein cholesterol (LDL-C) decreased and high-density lipoprotein cholesterol (HDL-C) increased significantly in the HCA group (p < 0.05). There were also significant reductions in WC, FBS, TG, total cholesterol, LDL-C in the control group while inter-group changes in FBS, TG, LDL-C and HDL-C were statistically significant. Although atherogenic indices reduced significantly in both groups, inter-group comparison revealed that the HCA group showed greater decrease in the TG/HDL-C ratio than the control group (p = 0.004). Other atherogenic indices including TC/HDL-C and non-HDL-C/HDL-C ratio showed greater reduction in the control versus HCA group (p < 0.01). Some inflammatory factors were reduced in the HCA group; however, no significant within- or between-group differences were revealed post-intervention. Our results indicated that HCA supplementation plus calorie-restricted diet could improve some metabolic factors without any significant effect on inflammation in patients with NAFLD.


Assuntos
Aterosclerose , Hepatopatia Gordurosa não Alcoólica , Aterosclerose/tratamento farmacológico , Biomarcadores , Restrição Calórica , Colesterol , HDL-Colesterol , LDL-Colesterol , Ácido Cítrico , Suplementos Nutricionais , Feminino , Humanos , Hidroxiácidos , Hepatopatia Gordurosa não Alcoólica/metabolismo , Obesidade/tratamento farmacológico , Triglicerídeos
2.
Food Funct ; 10(8): 4941-4952, 2019 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-31343010

RESUMO

Considering the importance of adipokines in the pathophysiology of non-alcoholic fatty liver disease (NAFLD), and due to the possible beneficial effects of α-lipoic acid (α-LA) on these adipose-derived hormones, this study aimed to investigate the effect of α-LA supplementation on adipokines and liver steatosis in obese patients with NAFLD. In a double-blind, placebo-controlled randomized clinical trial with two parallel groups, fifty patients with NAFLD were randomized to receive daily supplementation with either two capsules of α-LA (each capsule containing 600 mg α-LA) or two placebo capsules, daily for 12 weeks. At the baseline, all participants received consultation on how to implement a healthy diet into their daily lives. Anthropometric measures, dietary intakes, liver enzymes and adipokines were assessed at the baseline and after 12 weeks of intervention. A significant reduction was observed in the serum levels of insulin (P = 0.024) and leptin (P = 0.019) in the α-LA group compared to the placebo group, but changes in anthropometric and body composition measures, serum glucose (FSG), resistin, irisin and liver enzymes did not differ between the groups. α-LA supplementation resulted in a statistically significant elevation in the quantitative insulin sensitivity check index (QUICKI) (P = 0.033), serum levels of adiponectin (P = 0.008) and adiponectin-to-leptin ratio (P = 0.007) compared to the placebo. The liver steatosis intensity improved significantly. Nonetheless, no significant differences were observed between the study groups in the liver steatosis intensity, at the end of the study. According to the results, α-LA supplementation for 12 weeks improved insulin resistance, serum levels of insulin, adiponectin and leptin without changing anthropometric measures, serum liver enzymes, resistin and irisin.


Assuntos
Hepatopatia Gordurosa não Alcoólica/tratamento farmacológico , Ácido Tióctico/administração & dosagem , Adipocinas/sangue , Administração Oral , Adulto , Método Duplo-Cego , Feminino , Humanos , Insulina/sangue , Leptina/sangue , Fígado/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Masculino , Pessoa de Meia-Idade , Hepatopatia Gordurosa não Alcoólica/sangue , Hepatopatia Gordurosa não Alcoólica/patologia , Adulto Jovem
3.
Clin Endocrinol (Oxf) ; 90(1): 94-101, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30246883

RESUMO

BACKGROUND & AIMS: Low serum 25-hydroxyvitamin D (25OHD) is common in obese people. Obesity is associated with a state of low-grade inflammation (meta-inflammation). There is an increasing evidence indicating that vitamin D has anti-adipogenic activity and immunoregulatory effect. This study aimed to assess the effect of vitamin D supplementation on meta-inflammation and fat mass in obese subjects with vitamin D deficiency. MATERIALS AND METHODS: In this double-blind placebo-controlled randomized clinical trial, 44 obese subjects with vitamin D deficiency (25OHD < 50 nmol/L) were assigned into vitamin D (a weight reduction diet + bolus weekly dose of 50 000 IU vitamin D) or placebo group (weight reduction diet + edible paraffin weekly) for 12 weeks. Weight, fat mass and serum levels of 25OHD, calcium, parathyroid hormone (PTH), monocyte chemoattractant protein-1 (MCP-1), interleukin-1ß (IL-1ß) and Toll-like receptor 4 (TLR4) were assessed before and after the intervention. RESULTS: Vitamin D supplementation resulted in significant increase of serum 25OHD level (P < 0.001), and significant decrease in PTH (P < 0.001), MCP-1 (P < 0.05), IL-1ß (P < 0.05) and TLR-4 (P < 0.05); compared to the baseline values in vitamin D group. Weight, BMI and fat mass decreased in both groups (P < 0.05). Between the groups, there were significant decrease in weight, fat mass, serum MCP-1 and PTH concentrations and significant increase in serum 25OHD concentrations after intervention with vitamin D supplementation compared to placebo (P < 0.05). CONCLUSIONS: Improvement in vitamin D status in obese subjects with vitamin D deficiency in combination with weight loss diet resulted in weight, fat mass and MCP-1 decrease. Weight loss and vitamin D supplementation may act synergistically to reduce levels of meta-inflammation.


Assuntos
Distribuição da Gordura Corporal , Dieta Redutora , Suplementos Nutricionais , Inflamação/terapia , Obesidade/terapia , Deficiência de Vitamina D/tratamento farmacológico , Vitamina D/análogos & derivados , Tecido Adiposo/patologia , Adolescente , Adulto , Índice de Massa Corporal , Quimiocina CCL2/sangue , Feminino , Humanos , Irã (Geográfico) , Masculino , Pessoa de Meia-Idade , Obesidade/complicações , Obesidade/patologia , Vitamina D/farmacologia , Vitamina D/uso terapêutico , Adulto Jovem
4.
Women Health ; 55(7): 795-804, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26086066

RESUMO

Tomatoes and their products are the main source of lycopene, a powerful potent antioxidant. Tomato products improve antioxidant defenses and reduce the risk of oxidative stress, at least partly, due to the presence of lycopene. Lycopene, as an antioxidant, induces the upregulation of antioxidant enzymes and reinforces the total enzyme capacity of the human body. Obesity is a chronic condition in which destructive mechanisms increase the reactive oxygen species and attenuation of antioxidant status. We hypothesized that the consumption of a lycopene-rich food would improve the antioxidant defense of women who were overweight or obese. A total of seventy-five overweight or obese female students of the Tehran University of Medical Sciences were enrolled and randomly allocated to one of two groups, intervention (n = 40) or control (n = 35), consuming 330 ml/d of tomato juice or water, respectively, for a 20-day period. At baseline and day 20, total antioxidant capacity and antioxidant enzyme activity (superoxide dismutase, glutathione peroxidase, and catalase) were analyzed using ELISA kits and spectrophotometric methods and then compared between the two groups. Lycopene consumption had no effect on these aforementioned variables. Therefore, it seems that more research with longer duration and more sensitive indicators will be required.


Assuntos
Antioxidantes/farmacologia , Carotenoides/farmacologia , Obesidade/dietoterapia , Sobrepeso/dietoterapia , Estresse Oxidativo/efeitos dos fármacos , Solanum lycopersicum/química , Adulto , Antioxidantes/administração & dosagem , Bebidas , Carotenoides/administração & dosagem , Catalase/efeitos dos fármacos , Suplementos Nutricionais , Método Duplo-Cego , Feminino , Seguimentos , Glutationa Peroxidase/efeitos dos fármacos , Humanos , Irã (Geográfico) , Licopeno , Obesidade/sangue , Sobrepeso/sangue , Cooperação do Paciente , Superóxido Dismutase/efeitos dos fármacos , Resultado do Tratamento
5.
J Med Food ; 16(2): 147-54, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23342971

RESUMO

In this study, we investigated the effects of genistein, daidzein, and soy protein on paraoxonase and arylesterase activity, malondialdehyde (MDA) levels, and lipid profiles of arthritic rats in vivo and the results were compared with that of dexamethasone. Seventy-two female Sprague-Dawley rats were divided into six groups: healthy control, animals with collagen-induced arthritis (CIA), CIA-soy protein (7 g/kg)-treated rats, CIA-genistein (20 mg/kg)-treated animals, CIA-daidzein (20 mg/kg)-treated rats, and CIA-dexamethasone (1 mg/kg)-treated rats. Rheumatoid arthritis was induced using collagen type II and the treatments were carried out by daily gavages feedings for 50 days. The paraoxonase activity in serum was measured spectrophotometrically using paraoxon and phenylacetate as substrates. Serum MDA and lipids levels were determined using enzymatic colorimetric methods. Arthritis-induced decreases in paraoxonase and arylesterase activity was restored after treatment with soy protein and isoflavones (P<.05). MDA concentrations were lower after treatment with all tested compounds. However, only soy protein could partially improve the lipid profile.


Assuntos
Artrite Reumatoide/tratamento farmacológico , Artrite Reumatoide/enzimologia , Arildialquilfosfatase/sangue , Genisteína/administração & dosagem , Isoflavonas/administração & dosagem , Lipídeos/sangue , Extratos Vegetais/administração & dosagem , Proteínas de Soja/administração & dosagem , Animais , Artrite Reumatoide/metabolismo , Hidrolases de Éster Carboxílico/sangue , Modelos Animais de Doenças , Feminino , Humanos , Malondialdeído/sangue , Ratos , Ratos Sprague-Dawley , Glycine max/química
6.
Biochem Med (Zagreb) ; 21(3): 312-20, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22420246

RESUMO

INTRODUCTION: Recent epidemiological evidence suggests that alteration in calcium, phosphorous or magnesium metabolism may have direct cardiovascular consequences. However, it is unknown whether variations in serum values of these minerals are in relationship with lipid profile and adiposity as metabolic risk factors of cardiovascular events in premenopausal women independent of confounders. The aim of this study was to investigate the relationship between serum calcium, magnesium and phosphorous with lipid profile in healthy premenopausal women. MATERIALS AND METHODS: This study was performed on 82 reproductive age women aged 17-50 who were randomly selected from general population of Tabriz, Iran. They were assigned into obese and none-obese groups. Weight and height for BMI calculation were measured using a calibrated Seca scale and cotton ruler which was attached to the wall. Body composition was analyzed by bioelectrical impedance analysis (BIA). Serum magnesium, calcium and phosphorous were measured colorimetrically; fasting blood glucose (FBG) and serum lipids were assessed by enzymatic methods. RESULTS: Obese woman had significantly lower serum magnesium (P = 0.035) and significantly higher fasting blood glucose (P = 0.028), total cholesterol (P = 0.035), triglyceride (P = 0.019), low density lipoprotein (P =0.003) and parathyroid hormone concentrations (P = 0.031) compared to non obese women. In correlation coefficient analysis, serum calcium concentrations had a positive weak relationship with total cholesterol (r = 0.267, P = 0.013) and triglyceride (r = 0.301, P = 0.005) concentrations in all participants; whereas in separate analysis of subjects as obese and non obese groups, these relationships lost their significance. Serum phosphorous had a weak positive relationship with total cholesterol (r = 0.31, P = 0.002) and an inverse weak relationship with parathyroid hormone (r = -0.32, P = 0.002). After adjusting for confounding variables by multiple regression analysis, the positive relationship between serum calcium, triglyceride, high density lipoprotein and low density lipoprotein cholesterol were significant. CONCLUSION: Our results indicate that abnormality in serum calcium and phosphorous is significantly correlated with serum lipids. Further studies are warranted for interpretation of these associations and understanding the underlying mechanisms.


Assuntos
Cálcio/sangue , Lipídeos/sangue , Magnésio/sangue , Fósforo/sangue , Pré-Menopausa/sangue , Adolescente , Adulto , Cálcio/metabolismo , Estudos de Casos e Controles , Feminino , Saúde , Humanos , Irã (Geográfico)/epidemiologia , Metabolismo dos Lipídeos/fisiologia , Magnésio/metabolismo , Metaboloma , Pessoa de Meia-Idade , Obesidade/sangue , Obesidade/epidemiologia , Obesidade/metabolismo , Fósforo/metabolismo , Pré-Menopausa/metabolismo , Adulto Jovem
7.
Nutrition ; 26(11-12): 1117-21, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20080390

RESUMO

OBJECTIVE: The blood lipid-lowering effects of eicosapentaenoic acid (EPA) on hypertriglyceridemic subjects with different fatty acid-binding protein-2 (FABP2) genotypes have not, to our knowledge, been previously studied. METHODS: Twenty-three FABP2 Ala54 and 23 Thr54 carriers with hypertriglyceridemia (triacylglycerol level >200mg/dL) were enrolled in this study. Participants took 2g of pure EPA daily for 8 wk. Fasting blood lipid and lipoprotein profiles were determined and changes from baseline were measured. RESULTS: Blood lipids and lipoprotein responses of the FABP2 genotypes differed after EPA supplementation. Changes from baseline for triacylglycerol (19.2% decrease for Ala54 and 60.5% for Thr54, P<0.001), very low-density lipoprotein (20.0% decrease for Ala54 and 60.5% for Thr54, P<0.001), apolipoprotein CIII (22.8% decrease for Ala54 and 36.4% for Thr54, P<0.01), and high-density lipoprotein cholesterol (17.6% increase for Ala54 and 30.7% for Thr54, P<0.01) differed significantly between the two carrier groups. However, changes in total cholesterol, low-density lipoprotein cholesterol, and apolipoprotein B were not significant. EPA supplementation increased plasma EPA in Ala54 and Thr54 carriers. Although EPA supplementation increased the level of plasma EPA in both carrier groups, this effect was more pronounced in the Thr54 carriers. CONCLUSION: Therefore, EPA consumption has more favorable effects on blood lipids of hypertriglyceridemics with Thr54 genotype rather than those with Ala54. The level of plasma EPA increases after EPA supplementation. Because the FABP2 Thr54 polymorphism appears to be prevalent in hypertriglyceridemic subjects, increasing EPA intake in these subjects could be an effective strategy for reducing blood triacylglycerol concentration.


Assuntos
Ácido Eicosapentaenoico/uso terapêutico , Proteínas de Ligação a Ácido Graxo/genética , Hipertrigliceridemia/sangue , Hipertrigliceridemia/dietoterapia , Lipídeos/sangue , Lipoproteínas/sangue , Polimorfismo de Nucleotídeo Único , Adulto , Apolipoproteína C-III/sangue , HDL-Colesterol/sangue , Suplementos Nutricionais , Ácido Eicosapentaenoico/sangue , Feminino , Estudos de Associação Genética , Heterozigoto , Homozigoto , Humanos , Irã (Geográfico) , Lipoproteínas VLDL/sangue , Masculino , Pessoa de Meia-Idade , Triglicerídeos/sangue
8.
J Pak Med Assoc ; 59(4): 258-61, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19402296

RESUMO

OBJECTIVE: To determine the effect of vitamin D injection on Serum Magnesium concentration in obese and non obese women. METHOD: This Interventional study was performed on 82 women (17-50 years) which were randomly selected from general population of Tabriz city. They were assigned into two experimental groups. Obese group with stage 1 and 2 obesity and non obese group with normal weight. Weight was measured to the nearest 0.1 kg using a calibrated Seca scale. Height was measured using a cotton ruler which was pasted on the wall. Body mass index was calculated based on weight and height results. Biochemical parameters were measured before and after injection of 600000 IU doses of vitamin D. Serum Magnesium was measured calorimetrically and Serum 25 hydroxy vitamin D was estimated by Chemiluminescence Immune Assay method (CLIA). RESULTS: Baseline concentrations of serum Magnesium and 25 hydroxy vitamin D in obese individuals was lower than non obese individuals, the former being significant. Twenty seven percent of obese women versus 15% of non obese women were Magnesium deficient. Vitamin D injection caused a significant increase in serum Magnesium concentration in obese subjects but not in non obese subjects. There was also a significant increase of serum 25 hydroxy vitamin D in both groups. Mean elevation in serum Magnesium level among women who had Magnesium deficiency was higher than women with Magnesium adequacy (P < 0.05). CONCLUSION: Low serum Magnesium concentration in obese individuals can be modified by vitamin D injection.


Assuntos
Deficiência de Magnésio/etiologia , Magnésio/sangue , Obesidade/sangue , Obesidade/complicações , Vitamina D/análogos & derivados , Vitamina D/administração & dosagem , Adolescente , Adulto , Índice de Massa Corporal , Suplementos Nutricionais/efeitos adversos , Feminino , Humanos , Deficiência de Magnésio/sangue , Deficiência de Magnésio/tratamento farmacológico , Pessoa de Meia-Idade , Resultado do Tratamento , Vitamina D/sangue , Vitaminas/administração & dosagem , Vitaminas/efeitos adversos , Adulto Jovem
9.
Respirology ; 13(2): 294-8, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18339032

RESUMO

BACKGROUND AND OBJECTIVE: Increased production of reactive oxygen species secondary to phagocyte respiratory burst occurs in pulmonary tuberculosis (TB). The present study evaluated the efficacy of vitamin E-selenium supplementation on oxidative stress in newly diagnosed patients treated for pulmonary TB. METHODS: A double-blind, placebo-controlled trial including patients with newly diagnosed TB was conducted. The intervention group (n = 17) received vitamin E and selenium (vitamin E: 140 mg alpha-tocopherol and selenium: 200 microg) and the control group (n = 18) received placebo. Both groups received standard anti-TB treatment. Assessment of micronutrient levels, oxidative markers and total antioxidant capacity were carried out at baseline and 2 months after the intervention. RESULTS: Malondialdehyde levels were significantly reduced in the intervention group (P = 0.01), while there was minimal reduction in the control group. The mean plasma level of total antioxidants was increased significantly (P = 0.001) in both the intervention and the control groups. CONCLUSION: A 2-month intervention with vitamin E and selenium supplementation reduces oxidative stress and enhances total antioxidant status in patients with pulmonary TB treated with standard chemotherapy.


Assuntos
Antioxidantes/administração & dosagem , Suplementos Nutricionais , Estresse Oxidativo/fisiologia , Selênio/administração & dosagem , Tuberculose Pulmonar/metabolismo , Vitamina E/administração & dosagem , Adulto , Idoso , Antituberculosos/administração & dosagem , Método Duplo-Cego , Feminino , Humanos , Masculino , Malondialdeído/sangue , Pessoa de Meia-Idade , Tuberculose Pulmonar/tratamento farmacológico
10.
Nutrition ; 22(6): 638-44, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16635564

RESUMO

OBJECTIVE: Iron and vitamin A deficiencies are among the most prevalent nutritional problems. There are no data on iron bioavailability in Iran. In addition, interaction of vitamin A with iron bioavailability is not well documented, so we determined iron bioavailability from the most widely consumed food in Iran, lavash bread, and the effect of vitamin A on this bioavailability. METHODS: In vivo human studies for determining iron bioavailability are cumbersome, time consuming, and costly to perform, so we used an in vitro model in Caco-2 cells. Bread samples were digested with or without vitamin A (10 microg/1.0 g of dried bread). We used an iron solution containing vitamin C as a positive control. Iron absorption was measured using 59FeCl3. Bioavailability was defined as the percentage of radiolabeled iron taken up and transferred by Caco-2 cells after 1.5 h of incubation. Experiments were carried out two to four times. RESULTS: Mean +/- standard deviations for iron bioavailability in bread samples digested without or with additional vitamin A and in controls were 2.53 +/- 1.55%, 6.62 +/- 3.40%, and 20.80 +/- 2.30%, respectively (P < 0.001). Vitamin A caused a 2.62-fold increase in iron absorption from bread samples. CONCLUSIONS: Iranian lavash bread has low iron bioavailability, but this can be increased by vitamin A supplementation. Increasing vitamin A intake can be considered as a method for increasing iron bioavailability, thus combating iron and vitamin A deficiencies simultaneously.


Assuntos
Pão , Ferro da Dieta/farmacocinética , Vitamina A/farmacologia , Vitaminas/farmacologia , Disponibilidade Biológica , Células CACO-2 , Humanos , Técnicas In Vitro , Irã (Geográfico) , Deficiências de Ferro , Radioisótopos de Ferro , Deficiência de Vitamina A/prevenção & controle
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