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尿毒症时钙二醇的肝脏合成减少。

Reduced hepatic synthesis of calcidiol in uremia.

机构信息

Service de Néphrologie et Centre de Recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Québec, Canada.

出版信息

J Am Soc Nephrol. 2010 Sep;21(9):1488-97. doi: 10.1681/ASN.2009080815. Epub 2010 Jul 1.

Abstract

Calcidiol insufficiency is highly prevalent in chronic kidney disease (CKD), but the reasons for this are incompletely understood. CKD associates with a decrease in liver cytochrome P450 (CYP450) enzymes, and specific CYP450 isoforms mediate vitamin D(3) C-25-hydroxylation, which forms calcidiol. Abnormal levels of parathyroid hormone (PTH), which also modulates liver CYP450, could also contribute to the decrease in liver CYP450 associated with CKD. Here, we evaluated the effects of PTH and uremia on liver CYP450 isoforms involved in calcidiol synthesis in rats. Uremic rats had 52% lower concentrations of serum calcidiol than control rats (P < 0.002). Compared with controls, uremic rats produced 71% less calcidiol and 48% less calcitriol after the administration of vitamin D(3) or 1alpha-hydroxyvitamin D(3), respectively, suggesting impaired C-25-hydroxylation of vitamin D(3). Furthermore, uremia associated with a reduction of liver CYP2C11, 2J3, 3A2, and 27A1. Parathyroidectomy prevented the uremia-associated decreases in calcidiol and liver CYP450 isoforms. In conclusion, these data suggest that uremia decreases calcidiol synthesis secondary to a PTH-mediated reduction in liver CYP450 isoforms.

摘要

活性维生素 D 缺乏在慢性肾脏病(CKD)中非常普遍,但原因尚不完全清楚。CKD 与肝脏细胞色素 P450(CYP450)酶减少有关,而特定的 CYP450 同工酶介导维生素 D(3) C-25 羟化,形成活性维生素 D。甲状旁腺激素(PTH)水平异常,也调节肝脏 CYP450,也可能导致与 CKD 相关的肝脏 CYP450 减少。在这里,我们评估了 PTH 和尿毒症对参与大鼠活性维生素 D 合成的肝脏 CYP450 同工酶的影响。尿毒症大鼠的血清活性维生素 D 浓度比对照组低 52%(P < 0.002)。与对照组相比,尿毒症大鼠在给予维生素 D(3) 或 1alpha-羟基维生素 D(3) 后,分别产生 71%和 48%较少的活性维生素 D 和 1,25-二羟维生素 D,提示维生素 D(3) 的 C-25 羟化受损。此外,尿毒症与肝脏 CYP2C11、2J3、3A2 和 27A1 减少有关。甲状旁腺切除术可预防尿毒症相关的活性维生素 D 和肝脏 CYP450 同工酶减少。总之,这些数据表明尿毒症通过 PTH 介导的肝脏 CYP450 同工酶减少导致活性维生素 D 合成减少。

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