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在T3诱导的心肌肥大的发生和消退过程中,离体大鼠心脏对钙激活的能量代谢反应。

Energy metabolism response to calcium activation in isolated rat hearts during development and regression of T3-induced hypertrophy.

作者信息

Lortet S, Heckmann M, Ray A, Rossi A, Aussedat J, Grably S, Zimmer H G

机构信息

Laboratory of Cardiac Cellular Physiology, J. Fourier University, Grenoble, France.

出版信息

Mol Cell Biochem. 1995 Oct 18;151(2):99-106. doi: 10.1007/BF01322331.

Abstract

The effect of calcium activation on energy production was investigated in isolated perfused hearts from rats treated with triiodothyronine (T3) during 15 days (0.2 mg/kg/day) and in hearts of rats allowed to recover after T3-treatment during 15 days. Changes in phosphorylated compound concentrations were followed in the isolated hearts perfused with a glucose-pyruvate medium by 31P-NMR spectroscopy, when the external calcium concentration was increased from 0.5-1, 1.5 and 2 mM. As expected, T3-treatment resulted in the hypertrophy of the heart (50% increase in HW/BW) that was nearly reversible 15 days after discontinuation of the treatment. When compared to controls, creatine, phosphocreatine (PCr) and glycogen contents were lower (58, 24 and 17% decrease respectively) in the hypertrophied hearts and higher (10, 14 and 18% respectively) after regression of hypertrophy. Intracellular pH, ATP, inorganic phosphate concentrations and the phosphorylation potential were not altered under T3-treatment and after regression of hypertrophy, while calculated free ADP concentration was lower in hypertrophied hearts (control: 40 +/- 2 microM, T3-treatment: 21 +/- 1 microM, regression: 37 +/- 1 microM). Increasing the calcium concentration induced a similar increase in left ventricular developed pressure in the three groups of hearts, with inorganic phosphate concentration increasing with cardiac work. The PCr concentration slightly decreased while the ATP concentration did not change. In spite of different initial PCr concentrations, the evolutions of PCr and Pi concentrations for each stepwise increase in external calcium were similar in the three groups. It is concluded that, in spite of the well-known decrease in efficiency induced by the drug, the mechanisms of PCr (ATP) production remain able to respond to an acute moderate increase in energy demand provoked by a physiological stimulus. This adaptation also persists after the treatment when the energy metabolism balance is apparently improved.

摘要

研究了钙激活对能量产生的影响,实验对象为连续15天接受三碘甲状腺原氨酸(T3)治疗(0.2毫克/千克/天)的大鼠的离体灌注心脏,以及T3治疗15天后恢复的大鼠心脏。当外部钙浓度从0.5毫摩尔/升增加到1毫摩尔/升、1.5毫摩尔/升和2毫摩尔/升时,通过31P-核磁共振波谱法跟踪在葡萄糖-丙酮酸培养基中灌注的离体心脏中磷酸化化合物浓度的变化。正如预期的那样,T3治疗导致心脏肥大(心脏重量/体重增加50%),在停药15天后几乎可逆。与对照组相比,肥大心脏中的肌酸、磷酸肌酸(PCr)和糖原含量较低(分别降低58%、24%和17%),肥大消退后则较高(分别升高10%、14%和18%)。在T3治疗期间和肥大消退后,细胞内pH值、ATP、无机磷酸盐浓度和磷酸化电位没有改变,而肥大心脏中计算出的游离ADP浓度较低(对照组:40±2微摩尔,T3治疗组:21±1微摩尔,消退组:37±1微摩尔)。钙浓度增加导致三组心脏的左心室舒张末压出现类似增加,无机磷酸盐浓度随心脏工作而增加。PCr浓度略有下降,而ATP浓度没有变化。尽管初始PCr浓度不同,但三组中随着外部钙的逐步增加,PCr和Pi浓度的变化相似。结论是,尽管该药物会导致效率降低这一点众所周知,但PCr(ATP)产生的机制仍能够对生理刺激引起的能量需求的急性适度增加做出反应。在治疗后,当能量代谢平衡明显改善时,这种适应性仍然存在。

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