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甲状旁腺激素和氢氯噻嗪通过不同途径增加兔远端肾单位节段管腔膜的钙转运。

Parathyroid hormone and hydrochlorothiazide increase calcium transport by the luminal membrane of rabbit distal nephron segments through different pathways.

作者信息

Lajeunesse D, Bouhtiauy I, Brunette M G

机构信息

Research Center, Maisonneuve-Rosemont Hospital, Montréal, Québec, Canada.

出版信息

Endocrinology. 1994 Jan;134(1):35-41. doi: 10.1210/endo.134.1.7506210.

Abstract

The present study was designed to investigate the effect of PTH on calcium (Ca2+) transport through the luminal membrane of proximal and distal rabbit tubule segments. Proximal tubule and distal tubule segment suspensions were incubated with the hormone, and the luminal membranes were subsequently purified. Incubation with 10(-8) M human PTH(1-34) strongly increased initial Ca2+ uptake by the distal membranes. The effect of PTH was dose dependent, with an apparent ED50 of 8.2 +/- 1.0 nM. We recently reported the presence of two kinetics of Ca2+ uptake by the distal luminal membranes. PTH affected exclusively the high affinity component, increasing the maximum velocity from 0.31 +/- 0.02 to 0.76 +/- 0.07 pmol/micrograms.10 sec (P < 0.001), and leaving the Michaelis-Menten constant Ca2+ unchanged. The addition of 500 microM hydrochlorothiazide (HCTZ) to the luminal membranes of distal tubules incubated with PTH further enhanced Ca2+ uptake. The effect of HCTZ was on the low affinity system. HCTZ (100 microM) enhanced the maximum velocity from 2.5 +/- 0.3 to 3.7 +/- 0.6 pmol/micrograms protein.10 sec (P < 0.01) without affecting the Michaelis-Menten constant. Whereas 1 microM nitrendipine alone did not affect Ca2+ transport by the distal tubule luminal membranes, the Ca2+ channel inhibitor completely abolished the effect of PTH. Conversely, 1 microM Bay K 8644 increased Ca2+ uptake by membranes from PTH-treated distal tubules but was ineffective in membranes from control tubules. Neither PTH nor nitrendipine nor Bay K 8644 had any effect on the luminal membranes from proximal tubules. These results suggest that: 1) the high affinity, low velocity Ca2+ transport system in the luminal membrane from distal cortical segments is sensitive to PTH; 2) the effects of nitrendipine and Bay K 8644 on Ca2+ uptake were observed only in membranes from tubules incubated with PTH; 3) this uptake is distinct from the thiazide-sensitive Ca2+ transport system; and 4) PTH does not influence Ca2+ transport by the luminal membrane of proximal tubules.

摘要

本研究旨在探讨甲状旁腺激素(PTH)对兔近端和远端肾小管节段管腔膜钙(Ca2+)转运的影响。将近端肾小管和远端肾小管节段悬液与该激素一起孵育,随后纯化管腔膜。用10(-8)M人PTH(1 - 34)孵育可显著增加远端膜对Ca2+的初始摄取。PTH的作用呈剂量依赖性,表观半数有效剂量(ED50)为8.2±1.0 nM。我们最近报道远端管腔膜存在两种Ca2+摄取动力学。PTH仅影响高亲和力成分,将最大速度从0.31±0.02提高到0.76±0.07 pmol/μg·10秒(P<0.001),而米氏常数Ca2+不变。向与PTH孵育的远端肾小管管腔膜中添加500μM氢氯噻嗪(HCTZ)可进一步增强Ca2+摄取。HCTZ的作用于低亲和力系统。HCTZ(100μM)将最大速度从2.5±0.3提高到3.7±0.6 pmol/μg蛋白质·10秒(P<0.01),而不影响米氏常数。虽然单独使用1μM尼群地平不影响远端肾小管管腔膜的Ca2+转运,但该Ca2+通道抑制剂完全消除了PTH的作用。相反,1μM Bay K 8644增加了来自PTH处理的远端肾小管膜的Ca2+摄取,但对对照肾小管膜无效。PTH、尼群地平和Bay K 8644对近端肾小管的管腔膜均无任何影响。这些结果表明:(1)远端皮质节段管腔膜中的高亲和力、低速度Ca2+转运系统对PTH敏感;(2)仅在与PTH孵育的肾小管膜中观察到尼群地平和Bay K 8644对Ca2+摄取的影响;(3)这种摄取与噻嗪类敏感的Ca2+转运系统不同;(4)PTH不影响近端肾小管管腔膜的Ca2+转运。

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