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降钙素抑制钠离子梯度依赖性磷酸盐通过肾刷状缘膜的摄取。

Calcitonin inhibits Na+ gradient-dependent phosphate uptake across renal brush-border membranes.

作者信息

Yusufi A N, Berndt T J, Murayama N, Knox F G, Dousa T P

出版信息

Am J Physiol. 1987 Apr;252(4 Pt 2):F598-604. doi: 10.1152/ajprenal.1987.252.4.F598.

Abstract

This study was undertaken to determine whether calcitonin inhibits Na+-(Pi) cotransport across luminal brush-border membrane (BBM) of proximal tubules. Further, we determined the relative inhibitions of inorganic phosphate (Pi) transport in BBM vesicles (BBMV) derived from superficial cortical tissue (BBMV-SC) and juxtamedullary tissue (BBMV-JM). The effects of maximally phosphaturic doses of calcitonin were compared with those of parathyroid hormone (PTH). Experiments were performed in acutely thyroparathyroidectomized (TPTX) rats fed either normal (NPD, 0.7%) or low (LPD, 0.07%) Pi diets. After measurement of the fractional excretion of phosphate (FEPi) by clearance, the BBMV-SC and BBMV-JM were prepared from kidneys of the same animals and uptakes of 32Pi were determined. Both calcitonin and PTH inhibited BBMV transport of Pi to a greater degree in BBMV-JM than in BBMV-SC, in rats fed NPD or LPD. Kinetic analysis shows that administration of calcitonin resulted in marked decrease of apparent Vmax for Pi without any changes in apparent Km for Pi. However, in spite of a decreased capacity for Na+ gradient-dependent 32Pi uptake in BBMV-JM and much lesser in BBMV-SC in response to administration of calcitonin and PTH in Pi-deprived rats, these phosphaturic peptides did not increase FEPi. We conclude that calcitonin administration decreases the capacity for Na+-Pi cotransport across BBM in proximal tubules of the acutely TPTX rat.

摘要

本研究旨在确定降钙素是否抑制近端小管管腔刷状缘膜(BBM)对Na⁺-(Pi)的协同转运。此外,我们还测定了来自浅表皮质组织(BBMV-SC)和近髓组织(BBMV-JM)的BBM囊泡(BBMV)中无机磷酸盐(Pi)转运的相对抑制情况。将最大排磷剂量的降钙素的作用与甲状旁腺激素(PTH)的作用进行了比较。实验在急性甲状腺甲状旁腺切除(TPTX)的大鼠中进行,这些大鼠分别喂食正常(NPD,0.7%)或低(LPD,0.07%)磷饮食。通过清除率测定磷酸盐的排泄分数(FEPi)后,从同一只动物的肾脏中制备BBMV-SC和BBMV-JM,并测定³²Pi的摄取量。在喂食NPD或LPD的大鼠中,降钙素和PTH对BBMV-JM中Pi转运的抑制程度均大于对BBMV-SC中Pi转运的抑制程度。动力学分析表明,给予降钙素导致Pi的表观Vmax显著降低,而Pi的表观Km没有任何变化。然而,尽管在缺磷大鼠中给予降钙素和PTH后,BBMV-JM中依赖Na⁺梯度的³²Pi摄取能力下降,BBMV-SC中下降程度较小,但这些排磷肽并未增加FEPi。我们得出结论,给予降钙素会降低急性TPTX大鼠近端小管BBM上Na⁺-Pi协同转运的能力。

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