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Métodos Terapéuticos y Terapias MTCI
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1.
Pharm Biol ; 56(1): 138-144, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29409377

RESUMEN

CONTEXT: Polyphenols and flavonoids in artichoke leaf tincture (ALT) protect cells against oxidative damage. OBJECTIVES: We examined ALT effects on deoxyribonucleic acid (DNA) damage and lipid profiles in rat plasma and gene expression in rat aorta [haemeoxygenase-1 (HO1), haemeoxygenase-2 (HO2), NADPH oxidase 4 (NOX-4), monocyte chemoattractant protein-1 (MCP-1) and nuclear factor (erythroid-derived 2)-like 2 (Nrf2)]. MATERIALS AND METHODS: Eighteen male Wistar albino rats were divided into three groups (n = 6/group): The control group (CG) was fed with standard pellet chow for 11 weeks; the AD group was fed for a similar period of time with pellet chow supplemented with 2% cholesterol, 3% sunflower oil and 1% sodium cholate. The ADA group was fed with pellet chow (for 1 week), the atherogenic diet (see above) for the following 4 weeks and then with ALT (0.1 mL/kg body weight) and atherogenic diet for 6 weeks. According to HPLC analysis, the isolated main compounds in ALT were chlorogenic acid, caffeic acid, isoquercitrin and rutin. RESULTS: Normalized HO-1 [0.11 (0.04-0.24)] and MCP-1 [0.29 (0.21-0.47)] mRNA levels and DNA scores [12.50 (4.50-36.50)] were significantly lower in the ADA group than in the AD group [0.84 (0.35-2.51)], p = 0.021 for HO-1 [0.85 (0.61-3.45)], p = 0.047 for MCP-1 and [176.5 (66.50-221.25)], p = 0.020 for DNA scores. HO-1 mRNA was lower in the ADA group than in the CG group [0.30 (0.21-0.71), p = 0.049]. CONCLUSIONS: Supplementation with ALT limited the effects of the atherogenic diet through reduced MCP-1 expression, thereby preventing oxidative damage.


Asunto(s)
Aterosclerosis/dietoterapia , Cynara scolymus , Daño del ADN/efectos de los fármacos , Dieta Aterogénica/efectos adversos , Extractos Vegetales/uso terapéutico , Hojas de la Planta , Animales , Aterosclerosis/sangre , Aterosclerosis/etiología , Daño del ADN/fisiología , Masculino , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Ratas , Ratas Wistar
2.
Vojnosanit Pregl ; 73(2): 178-87, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27071286

RESUMEN

UNLABELLED: BACKGROUNG/AIM: Since combining conventional drugs with herbal medicinal products is in current research focus and possible of great interest as therapy improvement way, the aim of this study was to determine the effects of well-established antiatherosclerotic drug atorvastatin (CAS number 134523-00-5) and commercially available artichoke leaf tincture (ALTINC), used as combined therapy, as well as to compare effects of these two treatments separately. METHODS: Experimental animals were divided into five groups: the group I (the control group of rats fed with standard diet during 11 weeks), and the remaining 4 groups of rats (II, III, IV and V) fed with standard diet during the first week and then with hypercholesterolemic diet during the next 10 weeks. The group II of rats were left without treatment, while in the groups III, IV and V were rats treated per os with atorvastatin (1.15 mg/kg body weight--b.w.), ALTINC (0.1 mL/kg b.w.) and their combination in same doses, respectively, for the last six weeks. RESULTS: The cholesterol rich diet led to pronounced hyperlipidemia which could not be overcame with the therapy. However, the therapy showed positive effects on abdominal aorta wall thickness and parameters of oxidative stress (malondialdehyde--MDA, proxidative-antioxidative balance--PAB) and antioxidative protection (reduced glutathione--GSH, paraoxanase 1--PON1, superoxide dismutase--SODA SH groups), especially ALTINC was successful in oxidative status improvement. CONCLUSION: Separate treatments comparison showed that artichoke leaf tincture is very potent antioxidant with beneficial effects in early stages of atherosclerosis. Since atorvastatin and constituents of ALTINC probably have different mechanisms of action, simultaneous use of both therapies could be beneficial but should be further investigated since our results showed that ALTINC is less effective when used in combination with atorvastatin.


Asunto(s)
Atorvastatina/farmacología , Cynara scolymus , Hipercolesterolemia/tratamiento farmacológico , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/farmacología , Animales , Anticolesterolemiantes/farmacología , Antioxidantes/farmacología , Modelos Animales de Enfermedad , Monitoreo de Drogas , Sinergismo Farmacológico , Interacciones de Hierba-Droga , Hipercolesterolemia/metabolismo , Fitoterapia/métodos , Hojas de la Planta , Ratas , Resultado del Tratamiento
3.
Adv Clin Exp Med ; 23(4): 575-83, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25166442

RESUMEN

BACKGROUND: As a physiological condition closely linked with increased susceptibility to oxidative stress, pregnancy can be further compromised by cigarette smoking. Inadequate nutrition and reduced intake of antioxidants can also disrupt the prooxidant/antioxidant relationship and contribute to oxidative stress. Increased oxidative stress during pregnancy may be involved in several complications of pregnancy, such as preterm labor, fetal growth restriction, preeclampsia and miscarriage. OBJECTIVES: The aim of this study was to investigate the influence of maternal smoking habits before pregnancy on the parameters of oxidative stress and the antioxidative defense system, lipid profile parameters and paraoxonase-1 (PON1) activity during the third trimester of uncomplicated pregnancies. MATERIAL AND METHODS: Healthy pregnant women (n = 86) were divided into non-smoking and smoking groups, and into groups taking vitamin supplements and not taking them. Oxidative damage was measured through the levels of thiobarbituric acid-reacting substances (TBARS) and plasma antioxidant status was evaluated by measuring total antioxidant capacity (TAC). RESULTS: TBARS concetration was significantly higher (p < 0.05) and PON1 activity was significantly lower (p < 0.05) in the smokers' group. No significant differences were found in the investigated parameters in relation to vitamin supplement intake. CONCLUSIONS: Habitual smoking before pregnancy is associated with increased oxidative stress. Vitamin supplementation has no effect on the oxidative stress status of healthy pregnant women.


Asunto(s)
Antioxidantes/administración & dosificación , Estrés Oxidativo , Embarazo/metabolismo , Fumar/efectos adversos , Adulto , Antioxidantes/metabolismo , Arildialquilfosfatasa/metabolismo , Suplementos Dietéticos , Femenino , Humanos , Sustancias Reactivas al Ácido Tiobarbitúrico/análisis , Vitaminas/administración & dosificación
4.
Phytother Res ; 27(10): 1536-42, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23192897

RESUMEN

The purpose of the study was to examine the effects of astaxanthin (Asx) on paraoxonase (PON1) activities and oxidative stress status in soccer players. Forty soccer players were randomly assigned in a double-blind fashion to Asx and placebo (P) group. Blood samples were obtained before, 45 and 90 days after supplementation. PON1 activity was assessed by using two substrates: paraoxon and diazoxon. The oxidative stress biomarkers were also examined: total sulphydryl group content (-SH groups), thiobarbituric acid-reactive substances (TBARS), advanced oxidation protein products and redox balance. The significant interaction effect of supplementation and training (p < 0.05) on PON1 activity toward paraoxon was observed. The PON1 activity toward diazoxon increased in Asx group after 90 days (p < 0.01), while there was no significant difference in P group. SH groups content rose from pre- to post-supplementation period only in Asx group (supplementation and training, p < 0.05; training, p < 0.01). TBARS levels decreased after 45 days and increased after 90 days of regular soccer training in both groups (training, p < 0.001). Redox balance decreased significantly in response to the regular training, regardless of treatment group (training, p < 0.001). Asx supplementation might increase total SH groups content and improve PON1 activity through protection of free thiol groups against oxidative modification.


Asunto(s)
Antioxidantes/farmacología , Arildialquilfosfatasa/metabolismo , Atletas , Estrés Oxidativo/efectos de los fármacos , Adolescente , Antioxidantes/administración & dosificación , Arildialquilfosfatasa/genética , Biomarcadores/sangre , Biomarcadores/metabolismo , Composición Corporal , Suplementos Dietéticos , Método Doble Ciego , Humanos , Lípidos/sangre , Masculino , Compuestos Organofosforados/sangre , Oxidación-Reducción , Consumo de Oxígeno , Paraoxon/sangre , Polimorfismo Genético , Estudios Prospectivos , Fútbol , Sustancias Reactivas al Ácido Tiobarbitúrico/análisis , Xantófilas/administración & dosificación , Xantófilas/farmacología
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