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Influence of potassium sodium perfusion pressure and isoprenaline on renin release induced by acute calcium deprivation

机译:钾钠灌注压和异丙肾上腺素对急性钙缺乏引起的肾素释放的影响

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摘要

1. These studies were conducted in isolated perfused rat kidneys to determine the influence of perfusion pressure, isoprenaline, K, and Na on renin release stimulated by acute Ca deprivation.2. Removing Ca from the perfusion medium for 10 min stimulated renin release and reintroducing Ca returned it toward control values.3. Lowering concentration of Ca in the perfusion medium from 5 to 0 mM increased the effectiveness of low perfusion pressure (50 mmHg) and isoprenaline (2·43 μM) in stimulating renin release.4. At higher perfusion pressure (150 mmHg), renin release was inhibited in perfusion medium containing 2·5 mM-Ca but not in medium containing no Ca. In fact, high perfusion pressure stimulated renin release when the perfusion medium was without Ca.5. Raising concentration of K in the perfusion medium partially inhibited the renin release induced by Ca deprivation. Adding 5 mM-EGTA to Ca-deprived medium stimulated a greater rate of renin release than that of Ca-deprived medium alone. This greater renin release was also partially inhibited by raising K concentration in the perfusion medium.6. Lowering concentration of Na in the perfusion medium from 145 to 25 mM partially inhibited the renin release induced by Ca deprivation in the presence of low perfusion pressure or isoprenaline.7. These findings support the hypothesis that a decreased concentration of Ca in the cytoplasm of the juxtaglomerular cell stimulates renin release and increased Ca inhibits renin release. The sequence of events which leads to changes in cytoplasmic Ca might depend on the concentration of Ca in the perfusion medium, the renal perfusion pressure, the membrane potential of the juxtaglomerular cells, and Ca—Na exchange mechanisms.
机译:1.这些研究是在离体灌流的大鼠肾脏中进行的,以确定灌流压力,异丙肾上腺素,钾和钠对急性钙剥夺刺激的肾素释放的影响。从灌注介质中去除钙10分钟可刺激肾素释放,然后再注入钙使其恢复至控制值。3。将灌注介质中的Ca浓度从5 mM降低至0 mM,可提高低灌注压力(50 mmHg)和异戊二烯(2·43μM)刺激肾素释放的有效性。4。在较高的灌注压力(150 mmHg)下,在含有2·5 mM-Ca的灌注培养基中抑制了肾素释放,但在不含Ca的培养基中没有抑制。实际上,当灌注培养基不含Ca.5时,高灌注压力会刺激肾素释放。灌注介质中钾浓度的升高部分抑制了钙缺乏引起的肾素释放。与不含钙的培养基相比,向不含钙的培养基中添加5 mM-EGTA刺激的肾素释放速率更高。增加灌注介质中的钾浓度也部分抑制了这种更大的肾素释放。6。在低灌注压或异丙肾上腺素存在的情况下,将灌注培养基中的Na浓度从145降低至25 mM可以部分抑制钙缺乏引起的肾素释放。7。这些发现支持这样的假说,即在近肾小球细胞的细胞质中降低的Ca浓度会刺激肾素释放,而增加的Ca会抑制肾素释放。导致细胞质Ca改变的事件的顺序可能取决于灌注介质中Ca的浓度,肾脏灌注压力,近肾小管细胞的膜电位以及Ca-Na交换机制。

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