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1.
Can J Physiol Pharmacol ; 88(10): 1002-9, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20962900

RESUMO

The goal of the present study was to assess the effects of a restricted feeding schedule (RFS) on postischemic contractile recovery in relation to triacylglycerol (TAG), glycogen, and ATP content. Glucose-6-phosphate dehydrogenase (G6PDH) activity, reduced/oxidized glutathione ratio (GSH/GSSG), and thiobarbituric acid reactive substances (TBARS) levels were also determined. Isolated rat hearts entrained to daily RFS (2 h food access starting at 1200) or fed ad libitum (FED) for 3 weeks were Langendorff-perfused (25 min ischemia, 30 min reperfusion) with Krebs-Ringer bicarbonate solution (10 mmol/L glucose). RFS improved the recovery of contractility and reduced creatine kinase (CK) release upon reperfusion. Further, at the end of reperfusion, RFS hearts exhibited increased G6PDH activity and repletion of tissue glycogen, TAG, and ATP that was not observed in the FED hearts. GSH/GSSG at the end of reperfusion fell to the same value in both nutritional states, and TBARS levels were higher in the RFS hearts. In conclusion, RFS improved postischemic functional recovery, which was accompanied by a reduction in CK release and a striking energy recovery. Although enhanced G6PDH activity was displayed, RFS was unable to reduce lipid peroxidation, supporting a clear dissociation between protection against mechanical dysfunction and CK release on the one hand and oxidative damage on the other.


Assuntos
Restrição Calórica , Isquemia Miocárdica/prevenção & controle , Trifosfato de Adenosina/metabolismo , Animais , Creatina Quinase/metabolismo , Modelos Animais de Doenças , Feminino , Glucosefosfato Desidrogenase/metabolismo , Glutationa/metabolismo , Glicogênio/metabolismo , Testes de Função Cardíaca , Ventrículos do Coração/metabolismo , Ventrículos do Coração/fisiopatologia , Peroxidação de Lipídeos/fisiologia , Contração Miocárdica/fisiologia , Isquemia Miocárdica/fisiopatologia , Perfusão , Ratos , Ratos Wistar , Triglicerídeos/metabolismo , Função Ventricular Esquerda/fisiologia
2.
Clin Exp Pharmacol Physiol ; 36(7): 637-42, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19076169

RESUMO

1. Fasting, which increases the catabolism of fatty acids, gives functional protection to the ischaemic-reperfused heart. To obtain further knowledge of this cardioprotective effect, changes in mitochondrial permeability transition (MPT) were measured by the entrapment of 2-deoxy-[(3)H]-glucose (2-DG). We also assessed whether MPT is associated with changes in glutathione status, the activity of glucose-6-phosphate-dehydrogenase (G6PDH) and tissue oxidative damage, estimated by the measurement of Thiobarbituric acid-reactive substances (TBARS). 2. Spontaneously beating hearts of fed and 24 h fasted rats were Langendorff perfused with Krebs'-Ringer bicarbonate solution (10 mmol/L glucose) and exposed to 25 min global ischaemia, followed by 30 min reperfusion. 3. Ischaemia-reperfusion resulted in a fourfold increase in mitochondrial entrapment of 2-DG in the fed group. This response was 29% lower in the fasted group, but there were no concomitant changes in total retention of 2-DG in the heart. Fasting increased the activity of G6PDH by a factor of 1.4 and caused a 2.8-fold increase in the ratio of reduced glutathione to oxidized glutathione (GSH:GSSG) at the end of the pre-ischaemic period. Ischaemia-reperfusion did not affect G6PDH activity, but reduced the GSH:GSSG ratio in both the fed and fasted groups by 50%. Therefore, the GSH:GSSG ratio remained higher in the fasted group. Fasting also decreased cellular levels of TBARS by approximately 25%. Lipolysis of endogenous triacylglycerol was increased during the pre-ischaemic period in the fasted group. 4. These data suggest that the enhancement of fatty acid catabolism that occurs in fasting activates mechanisms that tend to reduce oxidative damage and limit MPT.


Assuntos
Jejum/metabolismo , Glutationa/metabolismo , Mitocôndrias Cardíacas/metabolismo , Proteínas de Transporte da Membrana Mitocondrial/metabolismo , Traumatismo por Reperfusão Miocárdica/metabolismo , Estresse Oxidativo/fisiologia , Via de Pentose Fosfato/fisiologia , Animais , Feminino , Potencial da Membrana Mitocondrial/fisiologia , Poro de Transição de Permeabilidade Mitocondrial , Traumatismo por Reperfusão Miocárdica/prevenção & controle , Permeabilidade , Ratos , Ratos Wistar
3.
Artigo em Inglês | BINACIS | ID: bin-14776

RESUMO

Diabetic nephropathy is associated with increased urinary albumin and reduce kallikrein excretion. Increased activity of the renal kallikrein-kinin system has been suggested as one of the possible mechanisms underlying diabetic hyperfiltration. The present study shown that kallikrein-kinin system is progressively increased in the diabetic-pregnant rats at 7, 14, 21 days; 48 and 7 days after pregnancy (P<0.05 vs Control). However, this increase during diabetic pregnancy did not reached the levels of control pregnancy. On the other hand albumin excretion shown a significant and progressive renal damage in the diabetic state. These findings suggest that the diabetic pregnancy could impair the renal hemodynamic, but, on the other side could modulate the vasodilatador system at pregnancy in the attempt protect the fetus. (AU)


Assuntos
Feminino , Humanos , Animais , RESEARCH SUPPORT, NON-U.S. GOVT , Gravidez , Calicreínas/urina , Gravidez em Diabéticas/patologia , Diabetes Mellitus Experimental/patologia , Nefropatias Diabéticas/patologia , Ratos Wistar , Pressão Sanguínea , Gravidez em Diabéticas/fisiopatologia , Diabetes Mellitus Experimental/fisiopatologia , Nefropatias Diabéticas/fisiopatologia
4.
Artigo em Inglês | LILACS | ID: lil-245920

RESUMO

Diabetic nephropathy is associated with increased urinary albumin and reduce kallikrein excretion. Increased activity of the renal kallikrein-kinin system has been suggested as one of the possible mechanisms underlying diabetic hyperfiltration. The present study shown that kallikrein-kinin system is progressively increased in the diabetic-pregnant rats at 7, 14, 21 days; 48 and 7 days after pregnancy (P<0.05 vs Control). However, this increase during diabetic pregnancy did not reached the levels of control pregnancy. On the other hand albumin excretion shown a significant and progressive renal damage in the diabetic state. These findings suggest that the diabetic pregnancy could impair the renal hemodynamic, but, on the other side could modulate the vasodilatador system at pregnancy in the attempt protect the fetus.


Assuntos
Feminino , Humanos , Animais , Gravidez , Diabetes Mellitus Experimental/patologia , Nefropatias Diabéticas/patologia , Calicreínas/urina , Gravidez em Diabéticas/patologia , Pressão Sanguínea , Diabetes Mellitus Experimental/fisiopatologia , Nefropatias Diabéticas/fisiopatologia , Gravidez em Diabéticas/fisiopatologia , Ratos Wistar
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