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ATP耗竭对成年大鼠离体心脏细胞钙内流的抑制作用。

Inhibition of calcium influx in isolated adult rat heart cells by ATP depletion.

作者信息

Haworth R A, Goknur A B, Hunter D R, Hegge J O, Berkoff H A

出版信息

Circ Res. 1987 Apr;60(4):586-94. doi: 10.1161/01.res.60.4.586.

Abstract

Using 45Ca, indo1, and quin2, calcium uptake was measured in isolated quiescent adult rat heart cells under different metabolic conditions. Exposure of cells in a medium containing 1 mM CaCl2 to rotenone and uncoupler resulted in adenosine triphosphate (ATP) depletion from 17.08 +/- 2.26 to 0.63 +/- 0.11 nmol/mg within 8 minutes, and the cells went into contracture. In this time, the cells lost 1.65 +/- 0.1 nmol Ca/mg of total rapidly exchangeable cellular calcium, and the level of free cytosolic calcium as measured by indo1 rose from 47.4 +/- 16.3 nM to 79.8 +/- 27.6 nM. The subsequent rate of rise of intracellular free calcium concentration was just 4 nM/min for at least 40 minutes. Therefore, we investigated the effect of ATP depletion on the rate of calcium entry. In cells loaded with sodium by ouabain treatment without calcium, the initial rate of calcium influx on calcium addition was inhibited by 82-84% when cellular ATP was depleted, as measured by 45Ca or indo1. Quin2 also showed a strong inhibition of calcium influx by ATP depletion, but itself also caused a strong inhibition of calcium influx. The rate of calcium influx declined even further in ATP-depleted cells after the initial influx: Between 1 and 12 minutes after calcium addition, the residual 45Ca uptake rate of the first minute was inhibited by an additional 90%. We conclude that ATP depletion per se does not quickly elevate cytoplasmic free calcium and that such an elevation is prevented by a very strong inhibition of the rate of calcium entry.

摘要

利用45Ca、indo1和quin2,在不同代谢条件下对分离的成年大鼠静止心肌细胞的钙摄取进行了测量。将含有1 mM氯化钙的培养基中的细胞暴露于鱼藤酮和解偶联剂中,导致三磷酸腺苷(ATP)在8分钟内从17.08±2.26 nmol/mg消耗至0.63±0.11 nmol/mg,细胞进入挛缩状态。在此期间,细胞每毫克可快速交换的细胞总钙损失1.65±0.1 nmol钙,通过indo1测量的游离胞质钙水平从47.4±16.3 nM升至79.8±27.6 nM。随后至少40分钟内细胞内游离钙浓度的上升速率仅为4 nM/分钟。因此,我们研究了ATP耗竭对钙内流速率的影响。在用哇巴因处理使细胞加载钠但无钙的情况下,当细胞ATP耗竭时,通过45Ca或indo1测量,添加钙时钙内流的初始速率被抑制了82 - 84%。Quin2也显示出ATP耗竭对钙内流有强烈抑制作用,但其本身也对钙内流有强烈抑制作用。在初始内流后,ATP耗竭的细胞中钙内流速率进一步下降:在添加钙后1至12分钟之间,第一分钟的残余45Ca摄取速率又被额外抑制了90%。我们得出结论,ATP耗竭本身不会迅速升高细胞质游离钙,并且这种升高被钙内流速率的非常强烈的抑制所阻止。

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