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1α-羟基维生素D3在雏鸡体内的代谢

Metabolism of 1alpha-hydroxyvitamin D3 in the chick.

作者信息

Holick S A, Holick M F, Tavela T E, Schnoes H K, DeLuca H F

出版信息

J Biol Chem. 1976 Feb 25;251(4):1025-8.

PMID:1249065
Abstract

Chicks convert both orally and intravenously administered 1alpha-hydroxy[6-3H]vitamin D3 rapidly to 1alpha,25-dihydroxy[6-3H]vitamin D3. The maximal accumulation of 1alpha,25-dihydroxy[6-3H]vitamin D3 in intestine precedes the intestinal absorption response to 1alpha-hydroxyvitamin D3 by at least 2 hours. Oral administration results in the highest concentrations of 1alpha,25-dihydroxy[6-3H]vitamin D3 in intestine, giving a level about 1.5 times that achieved with an intravenous dose. On the other hand, an oral dose of 1alpha-hydroxy[6-3H]vitaminD3 gives much lower amounts of both 1alpha-hydroxy[6-3H]vitamin D3 and 1alpha,25-dihydroxy[6-3H]vitamin D3 in bone and blood than an intravenous dose, which suggests that the 1alpha-hydroxy[6-3H]vitamin D3 may not be utilized as well by the oral route as by an intravenous route. Liver homogenates from both rat and chick convert 1alpha-hydroxy[6-3H]vitamin D3 to 1alpha,25-dihydroxy[6-3H]vitamin D3. However, intestinal homogenates from chick, but not rat, can also cary out this conversion, which may account for the higher concentration of 1alpha,25-dihydroxy[6-3H]vitamin D3 found in the intestine of chicks given an oral dose of 1alpha-hydroxy[6-3H]vitamin D3.

摘要

雏鸡能迅速将经口和静脉注射给予的1α-羟基[6-³H]维生素D3转化为1α,25-二羟基[6-³H]维生素D3。1α,25-二羟基[6-³H]维生素D3在肠道中的最大蓄积比肠道对1α-羟基维生素D3的吸收反应至少提前2小时。经口给药后,肠道中1α,25-二羟基[6-³H]维生素D3的浓度最高,约为静脉注射剂量所达到浓度的1.5倍。另一方面,经口给予1α-羟基[6-³H]维生素D3时,骨骼和血液中1α-羟基[6-³H]维生素D3和1α,25-二羟基[6-³H]维生素D3的含量均远低于静脉注射剂量,这表明1α-羟基[6-³H]维生素D3经口给药时的利用率可能不如静脉给药。大鼠和雏鸡的肝脏匀浆均可将1α-羟基[6-³H]维生素D3转化为1α,25-二羟基[6-³H]维生素D3。然而,雏鸡而非大鼠的肠道匀浆也能进行这种转化,这可能是经口给予1α-羟基[6-³H]维生素D3的雏鸡肠道中1α,25-二羟基[6-³H]维生素D3浓度较高的原因。

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