Suppr超能文献

[肠道钙转运机制与调节的新发现]

[New findings on the mechanism and regulation of intestinal calcium transport].

作者信息

Karbach U

机构信息

Medizinische Klinik, Klinikum Innenstadt Ludwig Maximilians-Universität München.

出版信息

Z Gastroenterol. 1994 Sep;32(9):500-13.

PMID:7801657
Abstract

Only in the duodenum and in the colon calcium is absorbed by a cellular 1,25 alpha-Vitamin D3-dependent transport mechanism. Calcium absorption is highest in the proximal large intestine, about ten times higher than in the duodenum or in the descending colon. 1,25 alpha-Vitamin D3 stimulates calcium transport by genomic (slow effect: synthesis of cytosolic calcium binding protein CabP and basolateral Ca-ATPase) and non-genomic action (rapid effect: transcaltachyia, liponomic effect at the brush border membrane). CabP-dependent translocation across the cytosol is thought to be rate limiting step of cellular calcium transport. However, only about 50% of calcium absorption is cellular mediated but the same amount of calcium convectively is absorbed by transepithelial water flow across the paracellular pathway (solvent drag effect). 1,25 alpha-Vitamin D3 not only activates cellular calcium absorption but also increases paracellular permeability for calcium by an unknown mechanism. However, essential steps in the cascade from the interaction of 1,25 alpha-Vitamin D3 with the specific receptor over the regulation of the synthesis of calcium binding and transporting proteins to the induction of cellular calcium transport are not as yet clearly understood. The exact feedback mechanism of synchronized calcium transport across the distinct subcellular compartments seems also to be resolved. Cellular calcium transport is not found in the jejunum or in the ileum, what can be explained by the absence of specific 1,25 alpha-Vitamin D3-dependent carrier systems in these segments. On the other hand calcium is secreted across the jejunum and ileum by an anomalous solvent drag effect. Hence, intestinal calcium metabolism seems to underlie an eneteroenteral circuit: 1,25 alpha-Vitamin D3-controlled cellular calcium absorption across the duodenum is followed by paracellular calcium secretion across the jejunum and ileum. The carrier in the proximal colon which works at the optimal level already under normal nutritional condition could be of physiological importance for the reclamation of unabsorbed dietary calcium and for the reabsorption of calcium that is secreted across the distal small intestine. Under certain pathophysiological conditions, i.e. malabsorption in proximal segments or malnutrition, calcium in addition may be conserved by the 1,25 alpha-Vitamin D3-sensitive carrier in the descending colon.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

只有在十二指肠和结肠中,钙是通过一种细胞依赖1,25α-维生素D3的转运机制被吸收的。钙的吸收在近端大肠中最高,比在十二指肠或降结肠中高约十倍。1,25α-维生素D3通过基因组作用(缓慢效应:胞质钙结合蛋白CabP和基底外侧钙ATP酶的合成)和非基因组作用(快速效应:钙快速转运,刷状缘膜的脂质体效应)刺激钙转运。依赖CabP的跨细胞质转运被认为是细胞钙转运的限速步骤。然而,只有约50%的钙吸收是由细胞介导的,但相同量的钙通过跨细胞旁途径的上皮水流动(溶剂拖曳效应)以对流方式被吸收。1,25α-维生素D3不仅激活细胞钙吸收,还通过未知机制增加细胞旁对钙的通透性。然而,从1,25α-维生素D3与特异性受体相互作用,到钙结合和转运蛋白合成的调节,再到细胞钙转运的诱导这一过程中的关键步骤,目前尚未完全清楚。跨不同亚细胞区室同步钙转运的确切反馈机制似乎也有待解决。在空肠或回肠中未发现细胞钙转运,这可以用这些节段中缺乏特异性的1,25α-维生素D3依赖载体系统来解释。另一方面,钙通过异常的溶剂拖曳效应在空肠和回肠中分泌。因此,肠道钙代谢似乎构成了一个肠-肠循环:1,25α-维生素D3控制的钙通过十二指肠的细胞吸收,随后是钙通过空肠和回肠的细胞旁分泌。近端结肠中的载体在正常营养条件下就已处于最佳工作水平,这对于回收未吸收的膳食钙以及重吸收通过远端小肠分泌的钙可能具有生理重要性。在某些病理生理条件下,即近端节段吸收不良或营养不良时,降结肠中对1,25α-维生素D3敏感的载体还可以保存钙。(摘要截选至400字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验