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运动训练减弱了ZDF大鼠心肌中蛋白激酶B(PKB)和糖原合成酶激酶-3(GSK-3)的去磷酸化作用。

Exercise training attenuated the PKB and GSK-3 dephosphorylation in the myocardium of ZDF rats.

作者信息

Lajoie Claude, Calderone Angelino, Trudeau François, Lavoie Nathalie, Massicotte Guy, Gagnon Sylvain, Béliveau Louise

机构信息

Department of Kinesiology, University of Montreal, Montreal, Québec H3C 3J7, Canada.

出版信息

J Appl Physiol (1985). 2004 May;96(5):1606-12. doi: 10.1152/japplphysiol.00853.2003. Epub 2003 Dec 29.

Abstract

Cardiac dysfunction is a severe secondary effect of Type 2 diabetes. Recruitment of the protein kinase B/glycogen synthase kinase-3 pathway represents an integral event in glucose homeostasis, albeit its regulation in the diabetic heart remains undefined. Thus the following study tested the hypothesis that the regulation of protein kinase B/glycogen synthase kinase-3 was altered in the myocardium of the Zucker diabetic fatty rat. Second, exercise has been shown to improve glucose homeostasis, and, in this regard, the effect of swimming training on the regulation of protein kinase B/glycogen synthase kinase-3 in the diabetic rat heart was examined. In the sedentary Zucker diabetic fatty rats, glucose levels were elevated, and cardiac glycogen content increased, compared with wild type. A 13-wk swimming regimen significantly reduced plasma glucose levels and cardiac glycogen content and partially normalized protein kinase B-serine473, protein kinase B-threonine308, and glycogen synthase kinase-3alpha phosphorylation in Zucker diabetic fatty rats. In conclusion, hyperglycemia and increased cardiac glycogen content in the Zucker diabetic fatty rats were associated with dysregulation of protein kinase B/glycogen synthase kinase-3 phosphorylation. These anomalies in the Zucker diabetic fatty rat were partially normalized with swimming. These data support the premise that exercise training may protect the heart against the deleterious consequences of diabetes.

摘要

心脏功能障碍是2型糖尿病的一种严重继发效应。蛋白激酶B/糖原合酶激酶-3信号通路的激活是葡萄糖稳态中的一个重要事件,尽管其在糖尿病心脏中的调节机制仍不明确。因此,以下研究检验了一个假设,即Zucker糖尿病肥胖大鼠心肌中蛋白激酶B/糖原合酶激酶-3的调节发生了改变。其次,运动已被证明可改善葡萄糖稳态,在这方面,研究了游泳训练对糖尿病大鼠心脏中蛋白激酶B/糖原合酶激酶-3调节的影响。与野生型相比,久坐不动的Zucker糖尿病肥胖大鼠血糖水平升高,心脏糖原含量增加。13周的游泳训练方案显著降低了Zucker糖尿病肥胖大鼠的血糖水平和心脏糖原含量,并使蛋白激酶B-丝氨酸473、蛋白激酶B-苏氨酸308和糖原合酶激酶-3α的磷酸化部分恢复正常。总之,Zucker糖尿病肥胖大鼠的高血糖和心脏糖原含量增加与蛋白激酶B/糖原合酶激酶-3磷酸化的失调有关。Zucker糖尿病肥胖大鼠的这些异常通过游泳部分恢复正常。这些数据支持了运动训练可能保护心脏免受糖尿病有害后果影响的前提。

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