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1.
Ann Hematol ; 97(4): 679-684, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29318368

RESUMO

The impaired biosynthesis of the ß-globin chain in ß-thalassemia leads to the accumulation of unpaired alpha globin chains, failure in hemoglobin formation, and iron overload due to frequent blood transfusion. Iron excess causes oxidative stress and massive tissue injuries. Advanced glycation end products (AGEs) are harmful agents, and their production accelerates in oxidative conditions. This study was conducted on 45 patients with major ß-thalassemia who received frequent blood transfusions and chelation therapy and were compared to 40 healthy subjects. Metabolic parameters including glycemic and iron indices, hepatic and renal functions tests, oxidative stress markers, and AGEs (carboxymethyl-lysine and pentosidine) levels were measured. All parameters were significantly increased in ß-thalassemia compared to the control except for glutathione levels. Blood glucose, iron, serum ferritin, non-transferrin-bound iron (NTBI), MDA, soluble form of low-density lipoprotein receptor, glutathione peroxidase, total reactive oxygen species (ROS), and AGE levels were significantly higher in the ß-thalassemia patients. Iron and ferritin showed a significant positive correlation with pentosidine (P < 0.01) but not with carboxymethyl-lysine. The NTBI was markedly increased in the ß-thalassemia patients, and its levels correlated significantly with both carboxymethyl-lysine and pentosidine (P < 0.05). Our findings confirm the oxidative status generated by the iron overload in ß-thalassemia major patients and highlight the enhanced formation of AGEs, which may play an important role in the pathogenesis of ß-thalassemia major.


Assuntos
Transfusão de Sangue , Produtos Finais de Glicação Avançada/sangue , Sobrecarga de Ferro/etiologia , Estresse Oxidativo , Reação Transfusional/fisiopatologia , Talassemia beta/sangue , Adolescente , Adulto , Biomarcadores/sangue , Terapia por Quelação/efeitos adversos , Terapia Combinada/efeitos adversos , Estudos Transversais , Deferiprona , Desferroxamina/uso terapêutico , Feminino , Humanos , Irã (Geográfico) , Sobrecarga de Ferro/prevenção & controle , Masculino , Piridonas/uso terapêutico , Receptores Depuradores Classe E/sangue , Adulto Jovem , Talassemia beta/terapia
2.
Indian J Pharmacol ; 48(4): 372-376, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27756946

RESUMO

OBJECTIVE: Carvedilol is a nonselective third generation ß-blocker that does not display the negative effects of traditional ß-blockers. Regarding the antioxidant, anti-inflammatory and distinct metabolic properties of carvedilol which are similar to that of high-density lipoprotein (HDL) and paraoxonase 1 (PON1), the present study intends to investigate the effects of carvedilol treatment on malondialdehyde (MDA) and soluble lectin-like ox-low-density lipoprotein (LDL) receptor (sLOX-1) as markers of oxidative stress in association to lipid profiles, apolipoproteins (apo), and PON1 activity in hypertensive patients. PATIENTS AND METHODS: This clinical trial study was performed on forty patients with mild to moderate essential hypertension. Subjects were studied before and after 2 months treatment with carvedilol, 25 mg daily. Lipids and lipoproteins were measured using a biochemistry analyzer. PON and arylesterase activity were assayed using paraoxon and phenyl acetate as substrates, respectively. MDA was quantified using a chemical colorimetric assay. ELISA was used to measure sLOX-1. RESULTS: Our results showed that carvedilol treatment decreased systolic and diastolic blood pressure as much as forty and 16 mmHg, respectively (P < 0.001). It also increased HDL, total cholesterol, and serum PON1 activity (P < 0.05), but the levels of triglyceride, LDL, apo A-I, and apo B did not significantly change. There was an inverse correlation between serum PON1 activity and serum MDA. CONCLUSION: This study confirmed the antihypertensive effect of the drug and its beneficial metabolic effects through augmenting HDL and PON1 activity. We propose that the antioxidant effects of carvedilol can be partially attributed to increased PON-1 activity.


Assuntos
Anti-Hipertensivos/uso terapêutico , Pressão Sanguínea/efeitos dos fármacos , Carbazóis/uso terapêutico , Hipertensão/tratamento farmacológico , Estresse Oxidativo/efeitos dos fármacos , Propanolaminas/uso terapêutico , Anti-Hipertensivos/administração & dosagem , Arildialquilfosfatase/metabolismo , Carbazóis/administração & dosagem , Carvedilol , HDL-Colesterol/sangue , Humanos , Hipertensão/sangue , Hipertensão/metabolismo , Propanolaminas/administração & dosagem , Estudos Prospectivos , Índice de Gravidade de Doença
3.
Jundishapur J Nat Pharm Prod ; 10(1): e22466, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25866724

RESUMO

BACKGROUND: Royal Jelly (RJ), a food item secreted by worker honeybees, is a mixture that contains protein, glucose, lipid, vitamins, and minerals; it is widely used as a commercial medical product. Previous studies have shown that RJ has a number of physiological effects, such as anti-inflammatory, antitumor, antiallergic and antioxidant activities. OBJECTIVES: In the present study, the anti-inflammatory properties of RJ were investigated in formalin-induced rat paw edema. MATERIALS AND METHODS: In this study, 30 male Wistar albino rats were divided into five equal groups (n = 6) as follows: test groups received different doses (25, 50 and 100 mg/kg, ip) of RJ and a negative control group received normal saline (5 mL/kg) and a positive control group received aspirin (300 mg/kg, i.p). Edema was induced on the right hind paw of the rat by a subplantar injection of 100 µL of formalin (2.5%) after 30 minutes. Paw edema was measured in the rats received the drugs, saline and aspirin before and after the formalin injection during 5 hours, using a plethysmometer. RESULTS: The results showed that RJ has a dose-dependent anti-inflammatory effect and the highest anti-inflammatory effect was observed in the doses of 50 and 100 mg/kg. CONCLUSIONS: Royal jelly has potent anti-inflammatory effects compared to aspirin and it could be used in the treatment of inflammation. However, further studies are required to determine the active components in RJ responsible for this effect and its mechanism of action.

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