Genistein Attenuates Postischemic Depressed Myocardial Function by Increasing Myofilament Ca 2+ Sensitivity in Rat Myocardium 1

The present study investigated whether genistein, a broad-spectrum tyrosine kinase inhibitor, could increase the myofilament Ca 2+ sensitivity and partially reverse postischemic depressed myocardial function. Left ventricular papillary muscles were isolated from adult Wistar rats and loaded with the...

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Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 2002-09, Vol.227 (8), p.632-638
Hauptverfasser: Min, Jiang-Yong, Liao, Haisun, Wang, Ju-Feng, Sullivan, Matthew F., Ito, Toshiro, Morgan, James P.
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container_title Experimental biology and medicine (Maywood, N.J.)
container_volume 227
creator Min, Jiang-Yong
Liao, Haisun
Wang, Ju-Feng
Sullivan, Matthew F.
Ito, Toshiro
Morgan, James P.
description The present study investigated whether genistein, a broad-spectrum tyrosine kinase inhibitor, could increase the myofilament Ca 2+ sensitivity and partially reverse postischemic depressed myocardial function. Left ventricular papillary muscles were isolated from adult Wistar rats and loaded with the Ca 2+ indicator, aequorin. The use of fluorocarbon immersion with hypoxia simulated a model of ischemia. Myofilament responsiveness to Ca 2+ was evaluated from force-[Ca 2+ ], relationship recorded during tetani in papillary muscles. Protein levels of troponin I (Tnl) were measured in postischemic papillary muscles with the Western blot technique. Isometric contraction was depressed during the period of ischemia and remained low after 60 min of reoxygenation without a corresponding significant change of peak [Ca 2+ ], in the control group (n = 7). In contrast, the depression of isometric contraction was ameliorated during ischemia in muscle preparations in the presence of genistein (2 μM; n = 8), and postischemic depressed myocardial contractility partially recovered after a 60-min reperfusion. The myofilament Ca 2+ responsiveness was significantly increased in papillary muscles in the presence of genistein. Protein levels of Tnl were reduced in postischemic papillary muscles, whereas genistein partially restored decreased protein levels of Tnl. Our results reveal that genistein produces an effective attenuation of postischemic depressed myocardial function and improves myofibrillar Ca 2+ responsiveness in rat myocardium.
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Left ventricular papillary muscles were isolated from adult Wistar rats and loaded with the Ca 2+ indicator, aequorin. The use of fluorocarbon immersion with hypoxia simulated a model of ischemia. Myofilament responsiveness to Ca 2+ was evaluated from force-[Ca 2+ ], relationship recorded during tetani in papillary muscles. Protein levels of troponin I (Tnl) were measured in postischemic papillary muscles with the Western blot technique. Isometric contraction was depressed during the period of ischemia and remained low after 60 min of reoxygenation without a corresponding significant change of peak [Ca 2+ ], in the control group (n = 7). In contrast, the depression of isometric contraction was ameliorated during ischemia in muscle preparations in the presence of genistein (2 μM; n = 8), and postischemic depressed myocardial contractility partially recovered after a 60-min reperfusion. The myofilament Ca 2+ responsiveness was significantly increased in papillary muscles in the presence of genistein. Protein levels of Tnl were reduced in postischemic papillary muscles, whereas genistein partially restored decreased protein levels of Tnl. 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