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[钙的肠道吸收及其调节。组织、膜和分子层面的事件]

[Intestinal absorption of calcium and its regulation. Tissue, membrane and molecular events].

作者信息

Pansu D, Bellaton C, Roche C

出版信息

Diabete Metab. 1984 May;10(2):106-20.

PMID:6378683
Abstract

The intestinal absorption of calcium involves an active transport against an electrochemical gradient, a saturable and a nonsaturable transfer following the gradient. The active and the saturable components are transcellular, the nonsaturable component is partly paracellular. Calcium transfer through the intestinal cell includes three steps: 1) the "down-hill" crossing of the brush-border implies binding to specific sites, carrier-mediated transport using channels or carrier proteins specific to Ca and dependent upon composition phosphorylations alkaline phosphatases; the phospholipid composition of the brush-border also plays a role; 2) the intracellular transfer is characterized by an uptake by such organelles as mitochondria, lysosomes and Golgi vesicles and by a transfer on a specific calcium-binding protein; 3) the "up-hill" transfer across the baso-lateral membrane requires energy and energy is mediated by an ATP-activated Ca2+ pump and a Na+/Ca2+ antiport. 1.25 dihydroxycholecalciferol, steroid hormone synthetized from vitamin D3 is the major direct regulator of Ca absorption: in the vitamin D-deprived animal, it increases the selective permeability for Ca of the brush-border, induces the synthesis of proteins after genomic transcription, activates the Ca-ATPases, and acts as a trophic hormone. The other hormones principally act by modulation of the renal biosynthesis of 1.25 dihydroxycholecalciferol. The efficiency of Ca absorption depends on site, with duodenum greater than jejunum greater than caecum greater than ileum. Dietary constituents such as carbohydrates and amino acids increase Ca absorption whereas phytic acid and excess of phosphorus decrease it. They act by modifying Ca bioavailability and perhaps brush-border permeability. Adaptation to increased demand occurs during growth, pregnancy and lactation in normal states but disappears during vitamin D deficiency. In man, lowered efficiency with increasing age is often aggravated by a low calcium diet.

摘要

钙的肠道吸收涉及逆电化学梯度的主动转运、顺梯度的可饱和转运和不饱和转运。主动和可饱和成分是跨细胞的,不饱和成分部分是细胞旁的。钙通过肠细胞的转运包括三个步骤:1)刷状缘的“下坡”穿越意味着与特定位点结合,通过特定于钙的通道或载体蛋白介导的载体转运,并依赖于组成磷酸化碱性磷酸酶;刷状缘的磷脂组成也起作用;2)细胞内转运的特征是被线粒体、溶酶体和高尔基体小泡等细胞器摄取,并转移到特定的钙结合蛋白上;3)跨基底外侧膜的“上坡”转运需要能量,能量由ATP激活的Ca2+泵和Na+/Ca2+反向转运体介导。1,25-二羟胆钙化醇是一种由维生素D3合成的类固醇激素,是钙吸收的主要直接调节剂:在维生素D缺乏的动物中,它增加了刷状缘对钙的选择性通透性,诱导基因组转录后蛋白质的合成,激活Ca-ATP酶,并作为一种营养激素起作用。其他激素主要通过调节1,25-二羟胆钙化醇的肾脏生物合成起作用。钙吸收的效率取决于部位,十二指肠大于空肠大于盲肠大于回肠。碳水化合物和氨基酸等膳食成分增加钙的吸收,而植酸和过量的磷则降低钙的吸收。它们通过改变钙的生物利用度和可能的刷状缘通透性起作用。在正常状态下,生长、怀孕和哺乳期间会出现对需求增加的适应性,但在维生素D缺乏时会消失。在人类中,随着年龄的增长,效率降低往往因低钙饮食而加剧。

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