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首页> 外文期刊>Zeitschrift fur Naturforschung, C. A Journal of Biosciences >Osmotic modulation of the ouabain-sensitive (Na++K+)ATPase from malpighian tubules of Rhodnius prolixus
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Osmotic modulation of the ouabain-sensitive (Na++K+)ATPase from malpighian tubules of Rhodnius prolixus

机译:罗氏罗非鱼马尔巴蒂管对哇巴因敏感的(Na ++ K +)ATPase的渗透调节

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摘要

The presence and regulation by hyperosmotic medium of the ouabain-sensitive (Na++K+)ATPase of the Malpighian tubule cells of Rhodnius prolixus was investigated. The ouabain-sensitive (Na++K+)ATPase activity was 5.4 +/- 0.5 nmol Pi x mg(-1) x min(-1). Vanadate 100 mu M completely abolished this ATPase activity. In hyperosmotic medium, obtained by addition of 180 mar mannitol, the (Na++K+)ATPase activity was inhibited by 60%. When the cell lysates were preincubated in hyperosmotic medium for 30 minutes and the ATPase activity was assayed in isosmotic medium, the (Na++K+)ATPase activity was not modified. Addition of 50 ng/ml sphingosine, a protein kinase C inhibitor, abolished the inhibition of (Na++K+)ATPase activity in hyperosmotic medium. Furthermore, phorbol ester (TPA), an activator of protein kinase C, mimicked the effect of hyperosmotic shock on (Na++K+)ATPase activity. The increase in Ca2+ concentration decreased the (Na++K+)ATPase activity by 60% in isosmotic medium, with maximal effect obtained in 10(-6) M Ca2+. No effect was observed in hyperosmotic medium. The inhibitory effect of Ca2+ on the (Na++K+)ATPase was not reversed by sphingosine. These results indicate that the ouabain-sensitive (Na++K+)ATPase activity of the Malpighlan tubule is regulated by both increasing Ca2+ concentration and by the osmolality of the medium by different and integrative ways. [References: 31]
机译:研究了高渗培养基对Rhodnius prolixus的Malpighian小管细胞的哇巴因敏感性(Na ++ K +)ATPase的存在和调控。哇巴因敏感性(Na ++ K +)ATPase活性为5.4 +/- 0.5 nmol Pi x mg(-1)x min(-1)。 100μM的钒酸盐完全消除了该ATP酶活性。在通过添加180 mar甘露醇获得的高渗培养基中,(Na ++ K +)ATPase活性被抑制60%。当将细胞裂解物在高渗培养基中预孵育30分钟,并在等渗培养基中测定ATPase活性时,(Na ++ K +)ATPase活性未改变。加入50 ng / ml的神经鞘氨醇鞘氨醇(一种蛋白激酶C抑制剂)取消了对高渗培养基中(Na ++ K +)ATPase活性的抑制作用。此外,佛波酯(TPA)是蛋白激酶C的激活剂,它模拟了高渗休克对(Na ++ K +)ATPase活性的影响。 Ca2 +浓度的增加在等渗培养基中使(Na ++ K +)ATPase活性降低60%,在10(-6)M Ca2 +中获得最大作用。在高渗培养基中未观察到效果。鞘氨醇不能逆转Ca2 +对(Na ++ K +)ATPase的抑制作用。这些结果表明,Malpighlan小管对哇巴因敏感的(Na ++ K +)ATPase活性通过增加Ca2 +浓度和通过介质的渗透压(渗透压)的不同方式进行调节。 [参考:31]

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