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细胞外钠对乳头集合管细胞胞质钙、前列腺素E2和环磷酸腺苷的影响。

Effects of extracellular sodium on cytosolic calcium, PGE2 and cAMP in papillary collecting tubule cells.

作者信息

Craven P A, DeRubertis F R

机构信息

Department of Medicine, University of Pittsburgh, Pennsylvania.

出版信息

Kidney Int. 1991 Apr;39(4):591-7. doi: 10.1038/ki.1991.69.

Abstract

An increase in cytosolic calcium (Cai2+), induced by an increase in extracellular calcium concentration or addition of the calcium ionophore A23187, has been shown to suppress basal and AVP responsive cAMP and inhibit water flow in the collecting tubule. In the present study, the relationships between extracellular Na+ concentration, Cai2+, PGE2 and AVP-responsive cAMP production were examined in cultured rat papillary collecting tubule (RPCT) cells. Reducing extracellular Na+ concentration from 144 to 24 mM increased Cai2+ and PGE2 production approximately below 144 mM on Cai2+ or PGE2 was not due to a change in media osmolality or chloride concentration, since these parameters were maintained at constant levels by addition of tetramethylammonium chloride (TMA) or choline chloride. Exposure of RPCT cells to media containing 24 mM Na+ significantly suppressed basal and AVP responsive cAMP compared to that observed at 144 mM Na+. This suppression was mimicked by the calcium ionophore A23187 which also increased Cai2+ and PGE2. The increase in Cai2+ and PGE2 and the suppression of basal and AVP responsive cAMP, which were observed at 24 versus 144 mM Na+, were abolished in calcium free media and were likely due to influx of extracellular calcium. Indomethacin did not prevent the suppressive effects of reducing extracellular Na+ concentration below 144 mM on basal or AVP responsive cAMP, suggesting that the enhanced production of PGE2 did not mediate the reduction in AVP responsiveness. In contrast to cAMP, reductions in extracellular Na+ concentration from 144 to 24 mM did not influence basal cGMP or the cGMP responses to atrial natriuretic peptide or nitroprusside.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

细胞外钙浓度升高或添加钙离子载体A23187诱导的胞质钙(Cai2+)增加,已被证明可抑制基础和抗利尿激素(AVP)反应性环磷酸腺苷(cAMP),并抑制集合管中的水流。在本研究中,在培养的大鼠乳头集合管(RPCT)细胞中研究了细胞外钠离子(Na+)浓度、Cai2+、前列腺素E2(PGE2)与AVP反应性cAMP产生之间的关系。将细胞外Na+浓度从144 mM降至24 mM会增加Cai2+和PGE2的产生,在144 mM以下,Cai2+或PGE2的增加并非由于培养基渗透压或氯离子浓度的变化,因为通过添加四甲基氯化铵(TMA)或氯化胆碱将这些参数维持在恒定水平。与在144 mM Na+时观察到的相比,将RPCT细胞暴露于含24 mM Na+的培养基中可显著抑制基础和AVP反应性cAMP。钙离子载体A23187模拟了这种抑制作用,它也增加了Cai2+和PGE2。在无钙培养基中,24 mM与144 mM Na+时观察到的Cai2+和PGE2增加以及基础和AVP反应性cAMP的抑制作用被消除,这可能是由于细胞外钙的内流。吲哚美辛不能阻止将细胞外Na+浓度降至144 mM以下对基础或AVP反应性cAMP的抑制作用,这表明PGE2产生的增加并未介导AVP反应性的降低。与cAMP相反,细胞外Na+浓度从144 mM降至24 mM并不影响基础环磷酸鸟苷(cGMP)或对心房利钠肽或硝普钠的cGMP反应。(摘要截短于250字)

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