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雏鸡离体肾小管中25-羟基维生素D-1α-羟化酶的调节:前列腺素E2、速尿和乙酰水杨酸的作用

Regulation of 25-hydroxy-vitamin D-1 alpha-hydroxylase in chick isolated renal tubules: effects of prostaglandin E2, frusemide and acetylsalicylic acid.

作者信息

Wark J D, Larkins R G, Eisman J A, Wilson K R

出版信息

Clin Sci (Lond). 1981 Jul;61(1):53-9. doi: 10.1042/cs0610053.

Abstract
  1. Isolated renal tubules were prepared from vitamin D-deficient chicks. The effects of added prostaglandin E2 (PGE2) and agents which modify prostaglandin metabolism on the metabolism of 25-hydroxy-vitamin D3 were studied. 2. Frusemide (0.1 mmol/l) raised the prostaglandin E (PGE) content of the tubule incubation medium; it significantly increased 1,25-dihydroxy-vitamin D3 [1,25-(OH)2D3] production from 25-hydroxy-vitamin D3 [25-(OH)D3] and significantly inhibited the net production of 24,25-dihydroxy-vitamin D3 [24,25-(OH)2D3]. 3. Acetylsalicylic acid (aspirin; 0.1 mmol/l) decreased the PGE content of the tubule incubation medium and significantly inhibited 1,25-(OH)2D3 production. 4. In the presence of 1,25-(OH)2D3, 4 h exposure of tubules from vitamin D-deficient chicks to concentrations of PGE2 between 2.8 X 10(-6) and 2.8 X 10(-8) mol/l significantly enhanced 1,25-(OH)2D3 production. 5. It is concluded that, in view of the effects of modulation of endogenous prostaglandin levels by frusemide in aspirin, and the stimulatory effect of exogenous PGE2, prostaglandins should be considered potential regulators of the renal 25-hydroxy-vitamin D-1 alpha-hydroxylase [25-(OH)D-1 alpha-hydroxylase] enzyme.
摘要
  1. 从维生素D缺乏的雏鸡中制备分离的肾小管。研究了添加前列腺素E2(PGE2)以及改变前列腺素代谢的药物对25-羟基维生素D3代谢的影响。

  2. 速尿(0.1 mmol/l)提高了肾小管孵育培养基中前列腺素E(PGE)的含量;它显著增加了25-羟基维生素D3[25-(OH)D3]生成1,25-二羟基维生素D3[1,25-(OH)2D3]的量,并显著抑制了24,25-二羟基维生素D3[24,25-(OH)2D3]的净生成量。

  3. 乙酰水杨酸(阿司匹林;0.1 mmol/l)降低了肾小管孵育培养基中PGE的含量,并显著抑制了1,25-(OH)2D3的生成。

  4. 在1,25-(OH)2D3存在的情况下,将维生素D缺乏的雏鸡的肾小管暴露于浓度为2.8×10(-6)至2.8×10(-8)mol/l的PGE2中4小时,可显著增强1,25-(OH)2D3的生成。

  5. 得出结论,鉴于速尿和阿司匹林对内源性前列腺素水平的调节作用以及外源性PGE2的刺激作用,前列腺素应被视为肾25-羟基维生素D-1α-羟化酶[25-(OH)D-1α-羟化酶]的潜在调节因子。

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