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1.
Biol Trace Elem Res ; 199(12): 4516-4524, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33462793

RESUMO

Fibroblast growth factor 23 (FGF23) gene is found to be responsible for autosomal dominant hypophosphatemic rickets, and is highly expressed in chronic kidney disease (CKD) and end-stage renal disease patients with iron deficiency anemia (IDA). We evaluated the efficacy of different iron treatments on FGF23 levels in dialysis-dependent and non-dialysis-dependent CKD patients with IDA. We performed a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing different types of iron treatment versus placebo in CKD patients up to May 2020. We investigated the efficacy of iron treatment on the levels of FGF23 and C-terminal FGF23 (cFGF23) in CKD patients. We estimated weighted mean differences (WMDs) and 95% confidence intervals (CIs) using the random-effects model. Nine studies with 11 arms were included in the meta-analysis. Overall, iron treatment showed a significant reduction in FGF23 levels compared to control group (WMD: - 60.56 pg/ml, 95% CI: - 92.17, - 28.95). Compared to placebo, subgroup analysis showed that oral iron therapy (WMD: - 6.98 pg/ml, 95% CI: - 10.66, - 3.31) was more effective than intravenous (IV) iron therapy (WMD: 4.90 pg/ml, 95% CI: - 12.03, 21.83) on FGF23 levels. There was no significant change in cFGF23 levels between iron treatment and control group (WMD: - 64.72 Ru/ml, 95% CI: - 147.69, 18.25). Subgroup analysis showed that oral iron therapy resulted in a significant reduction in cFGF23 levels compared to control group (WMD: - 150.48 RU/ml, 95% CI: - 151.31, - 149.65). In conclusion, iron treatment was associated with a significant decrease in FGF23 levels in CKD patients.


Assuntos
Ferro , Insuficiência Renal Crônica , Suplementos Nutricionais , Fator de Crescimento de Fibroblastos 23 , Fatores de Crescimento de Fibroblastos , Humanos , Insuficiência Renal Crônica/tratamento farmacológico
2.
Pharm Biol ; 54(8): 1326-33, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26439719

RESUMO

CONTEXT: Zygophyllum album L. (Zygophyllaceae), commonly known as Bougriba, is widely used to treat diabetes, digestive tract spasm, and hypertension in folk medicine, in Tunisia. OBJECTIVE: This study investigates the antidiabetic, antidiarrheal, and antihypertensive activities of the leaves of the essential oil from Zygophyllum album (OZA) in alloxan-induced diabetic rats. MATERIALS AND METHODS: The oil was obtained by hydrodistillation and analyzed by GC-MS. Males rats were divided into four groups: control, diabetic-untreated group, diabetic-treated group with acarbose (10 mg/kg), and diabetic-treated rats with OZA (200 mg/kg) for 30 d. RESULTS: At the end of the experimental period, the OZA significantly decreased the activity of α-amylase in pancreas and serum of the diabetic rats by 43% and 38%, respectively, which led to reduce the serum glucose level by 60% and lower of glycated hemoglobin (HbA1c) rate by 17% as compared with untreated diabetic animals. Moreover, the OZA treatment attenuated symptoms of diarrhea, improved lipid disorders, and hypertension through inhibiting the pancreatic lipase and angiotensin-converting enzyme (ACE) activities by 47% and 25%, respectively, in serum of diabetic rats. CONCLUSION: OZA showed a good effect in the management of diabetes mellitus and exerted preventive action from related hypertension.


Assuntos
Aloxano , Antidiarreicos/farmacologia , Anti-Hipertensivos/farmacologia , Complicações do Diabetes/prevenção & controle , Diabetes Mellitus Experimental/tratamento farmacológico , Inibidores Enzimáticos/farmacologia , Hipoglicemiantes/farmacologia , Óleos Voláteis/farmacologia , Óleos de Plantas/farmacologia , Inibidores da Enzima Conversora de Angiotensina/farmacologia , Animais , Antidiarreicos/isolamento & purificação , Anti-Hipertensivos/isolamento & purificação , Glicemia/efeitos dos fármacos , Glicemia/metabolismo , Pressão Sanguínea/efeitos dos fármacos , Cromatografia Líquida , Complicações do Diabetes/sangue , Complicações do Diabetes/enzimologia , Diabetes Mellitus Experimental/sangue , Diabetes Mellitus Experimental/induzido quimicamente , Diabetes Mellitus Experimental/enzimologia , Digestão/efeitos dos fármacos , Inibidores Enzimáticos/isolamento & purificação , Cromatografia Gasosa-Espectrometria de Massas , Hemoglobinas Glicadas/metabolismo , Hipoglicemiantes/isolamento & purificação , Masculino , Óleos Voláteis/isolamento & purificação , Pâncreas/efeitos dos fármacos , Pâncreas/enzimologia , Fitoterapia , Folhas de Planta , Óleos de Plantas/isolamento & purificação , Plantas Medicinais , Ratos Wistar , Fatores de Tempo , Zygophyllum/química , alfa-Amilases/antagonistas & inibidores , alfa-Amilases/sangue
3.
J. physiol. biochem ; 71(2): 281-288, jun. 2015.
Artigo em Inglês | IBECS | ID: ibc-140535

RESUMO

The present study was designed to evaluate the cardioprotective effect of Tunisian flaxseed oil (Linum usitatissimum) against isoproterenol-induced myocardial infarction in rats by studying hypertensive and cardiac damage markers especially electrocardiographic changes and troponin T serum level. In vitro, the extracted oil showed an important inhibition of angiotensin converting enzyme (ACE) with an IC50 = 85.96 μg/ml. According to chemical analysis, this extract is composed essentially of alpha linolenic acid (ALA), an n-3 polyunsaturated fatty acid (58.59 %). Male rats were randomly divided into three groups, namely control (C), isoproterenol (ISO), and isoproterenol-treated group with flaxseed oil (FO + ISO). Isoproterenol injection showed changes in ECG pattern, including ST-segment elevation (diagnostic of myocardial infarction), increase in the serum levels ofTroponin T and cardiac injury markers (creatine kinase-MB (CK-MB), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), aspartate transaminase (AST), and alanine transaminase (ALT)). However, Linum oil pre-co-treatment prevented almost all the parameters isoproterenol-induced myocardial infarction in rats. Results of the present study proved that flaxseed oil has a significant effect by heart protection against isoproterenol-induced myocardial infarction through beneficial effect of the important fraction of ALA


Assuntos
Animais , Ratos , Infarto do Miocárdio/fisiopatologia , Cardiotônicos/farmacocinética , Óleo de Semente do Linho/farmacocinética , Isoproterenol/efeitos adversos , Substâncias Protetoras/farmacocinética , Eletrocardiografia , Troponina/farmacocinética , Modelos Animais de Doenças
4.
J Physiol Biochem ; 71(2): 281-8, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25910460

RESUMO

The present study was designed to evaluate the cardioprotective effect of Tunisian flaxseed oil (Linum usitatissimum) against isoproterenol-induced myocardial infarction in rats by studying hypertensive and cardiac damage markers especially electrocardiographic changes and troponin T serum level. In vitro, the extracted oil showed an important inhibition of angiotensin converting enzyme (ACE) with an IC50 = 85.96 µg/ml. According to chemical analysis, this extract is composed essentially of alpha linolenic acid (ALA), an n-3 polyunsaturated fatty acid (58.59 %). Male rats were randomly divided into three groups, namely control (C), isoproterenol (ISO), and isoproterenol-treated group with flaxseed oil (FO + ISO). Isoproterenol injection showed changes in ECG pattern, including ST-segment elevation (diagnostic of myocardial infarction), increase in the serum levels of Troponin T and cardiac injury markers (creatine kinase-MB (CK-MB), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), aspartate transaminase (AST), and alanine transaminase (ALT)). However, Linum oil pre-co-treatment prevented almost all the parameters isoproterenol-induced myocardial infarction in rats. Results of the present study proved that flaxseed oil has a significant effect by heart protection against isoproterenol-induced myocardial infarction through beneficial effect of the important fraction of ALA.


Assuntos
Cardiotônicos/farmacologia , Isoproterenol/efeitos adversos , Óleo de Semente do Linho/química , Óleo de Semente do Linho/farmacologia , Infarto do Miocárdio/prevenção & controle , Animais , Peso Corporal/efeitos dos fármacos , Eletrocardiografia , Enzimas/sangue , Ácidos Graxos/análise , Linho/química , Masculino , Infarto do Miocárdio/induzido quimicamente , Infarto do Miocárdio/metabolismo , Tamanho do Órgão/efeitos dos fármacos , Peptidil Dipeptidase A/metabolismo , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Ratos Wistar , Troponina T/metabolismo
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