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DOI 10.1139/y10-076

Медицинская библиотека · Canadian journal of physiology and pharmacology · 2010

Restricted feeding improves postischemic recovery of Langendorff-perfused rat hearts.

Jaitovich María M, Varela Alicia, Sbarbati Cintia, Hermann Romina, Torresín María E, Savino Enrique A, Marina Prendes María G

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Jaitovich María M, Varela Alicia, Sbarbati Cintia, Hermann Romina, Torresín María E, Savino Enrique A, Marina Prendes María G. Restricted feeding improves postischemic recovery of Langendorff-perfused rat hearts.. Canadian journal of physiology and pharmacology. 2010. DOI: 10.1139/y10-076.

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