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本文引用的文献

1
THE EFFECTS OF SALINE INFUSION ON SODIUM REABSORPTION BY THE PROXIMAL TUBULE OF THE DOG.盐水输注对犬近端小管钠重吸收的影响。
J Clin Invest. 1965 Jul;44(7):1160-70. doi: 10.1172/JCI105223.
2
THE MECHANISM OF SODIUM DURESIS AFTER SALINE INFUSION IN THE DOG.狗静脉输注生理盐水后钠利尿的机制
J Clin Invest. 1963 Aug;42(8):1261-76. doi: 10.1172/JCI104811.
3
Correlation of ultrastructure with function in the rat kidney.大鼠肾脏超微结构与功能的相关性
Am J Pathol. 1962 Feb;40(2):199-218.
4
Effects of parathyroid hormone and calcitonin on electrolyte excretion in the rabbit.甲状旁腺激素和降钙素对家兔电解质排泄的影响。
Kidney Int. 1980 Apr;17(4):473-8. doi: 10.1038/ki.1980.55.
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Hydrostatic pressure changes related to paracellular shunt ultrastructure in proximal tubule.与近端小管旁细胞旁路超微结构相关的流体静压变化
Kidney Int. 1980 Jun;17(6):732-48. doi: 10.1038/ki.1980.86.
6
Sodium transport inhibitor in proximal tubular urine during acute volume expansion.急性容量扩张时近端肾小管尿液中的钠转运抑制剂。
Pflugers Arch. 1983 Feb;396(2):110-4. doi: 10.1007/BF00615514.
7
Direct effect of metolazone on sodium-dependent transport across the renal brush border membrane.
J Lab Clin Med. 1983 Feb;101(2):308-16.
8
Prostaglandin E2 and parathyroid hormone: comparisons of their actions on the rabbit proximal tubule.前列腺素E2与甲状旁腺激素:它们对兔近端小管作用的比较
Kidney Int. 1984 Oct;26(4):404-10. doi: 10.1038/ki.1984.189.
9
Inhibition of renal brush border phosphate transport and stimulation of renal gluconeogenesis by cyclic amp and parathyroid hormone.环磷酸腺苷和甲状旁腺激素对肾刷状缘磷酸盐转运的抑制及对肾糖异生的刺激作用。
Biochem Pharmacol. 1983 May 1;32(9):1533-7. doi: 10.1016/0006-2952(83)90478-1.
10
Preparation and study of fragments of single rabbit nephrons.单个兔肾单位片段的制备与研究
Am J Physiol. 1966 Jun;210(6):1293-8. doi: 10.1152/ajplegacy.1966.210.6.1293.

体内进行的容量扩张对体外灌注的离体兔近端小管转运的抑制作用。

Inhibitory effects of volume expansion performed in vivo on transport in the isolated rabbit proximal tubule perfused in vitro.

作者信息

Pitts T O, McGowan J A, Chen T C, Silverman M, Rose M E, Puschett J B

机构信息

Department of Medicine, Presbyterian-University, Pittsburgh, Pennsylvania.

出版信息

J Clin Invest. 1988 Apr;81(4):997-1003. doi: 10.1172/JCI113454.

DOI:10.1172/JCI113454
PMID:3350975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC329623/
Abstract

To examine the renal tubular sites and mechanisms involved in the effects of hypooncotic volume expansion (VE) on renal electrolyte excretion, we performed clearance and isolated tubular perfusion studies using intact and thyroparathyroidectomized (TPTX) rabbits. We also examined the effect of VE on luminal brush border transport. In the microperfusion studies, proximal convoluted (PCT) and straight (PST) tubules were taken from rabbits without prior VE or after 30 min of 6% (body wt) VE. Acute VE increased the percentage excretion of Na, Ca, and P in TPTX animals and the percentage and absolute excretions of these ions in intact rabbits. In PST from VE animals, fluid flux (Jv) was depressed compared with Jv in PST from nonVE rabbits: Jv = 0.18 +/- 0.03, (VE) vs. 0.31 +/- 0.03 nl/mm.min, (nonVE) P less than 0.02. Phosphate transport (Jp) in the PST from VE animals was also depressed: JP = 1.58 +/- 0.10 (VE) vs. 2.62 +/- 0.47 pmol/mm.min, (nonVE) P less than 0.05. Similar results were obtained with TPTX animals. In the PCT from VE animals, Jv was decreased (0.49 +/- 0.10 (VE) vs. 0.97 +/- 0.14 nl/mm.min, (nonVE) P less than 0.02), but JP was not affected significantly. Transport inhibition was stable over approximately 90 min of perfusion. In the brush border vesicle studies, sodium-dependent phosphate transport was inhibited compared with that in control animals, at the 9-, 30-, and 60-s time points. These findings indicate that the inhibition of renal ionic transport by VE occurs in both PCT and PST and is, in part, the result of a direct effect of VE on tubular transport mechanisms.

摘要

为研究低渗性容量扩张(VE)对肾脏电解质排泄影响所涉及的肾小管部位及机制,我们使用完整的和甲状腺甲状旁腺切除(TPTX)的兔子进行了清除率和离体肾小管灌注研究。我们还研究了VE对管腔刷状缘转运的影响。在微灌注研究中,从未经预先VE处理或经6%(体重)VE处理30分钟后的兔子获取近端曲管(PCT)和直小管(PST)。急性VE增加了TPTX动物中Na、Ca和P的排泄百分比以及完整兔子中这些离子的排泄百分比和绝对排泄量。在来自VE动物的PST中,与来自非VE兔子的PST相比,液体通量(Jv)降低:Jv = 0.18 ± 0.03(VE)对0.31 ± 0.03 nl/mm.min(非VE),P < 0.02。来自VE动物的PST中的磷酸盐转运(Jp)也降低:Jp = 1.58 ± 0.10(VE)对2.62 ± 0.47 pmol/mm.min(非VE),P < 0.05。TPTX动物也得到了类似结果。在来自VE动物的PCT中,Jv降低(0.49 ± 0.10(VE)对0.97 ± 0.14 nl/mm.min(非VE),P < 0.02),但Jp未受到显著影响。在大约90分钟的灌注过程中,转运抑制作用稳定。在刷状缘小泡研究中,与对照动物相比,在9秒、30秒和60秒时间点钠依赖性磷酸盐转运受到抑制。这些发现表明,VE对肾脏离子转运的抑制作用发生在PCT和PST中,并且部分是VE对肾小管转运机制直接作用的结果。