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成年猫中牛磺酸高亲和力载体介导的肠道转运的消退

Regression of high-affinity carrier-mediated intestinal transport of taurine in adult cats.

作者信息

Wolffram S, Hagemann C, Scharrer E

机构信息

Institute of Veterinary Physiology, University of Zurich, Switzerland.

出版信息

Am J Physiol. 1991 Nov;261(5 Pt 2):R1089-95. doi: 10.1152/ajpregu.1991.261.5.R1089.

DOI:10.1152/ajpregu.1991.261.5.R1089
PMID:1659232
Abstract

The sulfur-containing beta-amino acid taurine is an essential nutrient for cats. Owing to some metabolic peculiarities, cats are more dependent on dietary sources of taurine than other mammals. We therefore studied taurine uptake by intestinal brush-border membrane vesicles (BBMV) isolated from cat small intestine. Taurine uptake by feline BBMV was not influenced by a transmembrane Na+ gradient compared with Na(+)-free conditions. Kinetic analysis of initial taurine uptake yielded no evidence for a carrier-mediated transport process. These findings cannot be attributed to an overall inability of cumulative substrate uptake in our vesicle preparations because D-glucose uptake was strongly Na+ dependent, showing the overshoot phenomenon typically associated with active transport in vesicle experiments. Furthermore, L-leucine transport was mediated by a single Na(+)-dependent carrier mechanism (maximal transport velocity 1.2 nmol.mg protein-1.s-1, Km = 2.1 mM). In contrast to taurine uptake by feline BBMV, transport of taurine by pig intestinal BBMV was markedly enhanced by an inwardly directed Na+ gradient. Thus, differing from other mammalian species, taurine uptake across the intestinal brush-border membrane of the adult cat seems not to be mediated by a specific transport mechanism. Therefore taurine absorption from the gastrointestinal tract will possibly become a limiting factor for maintenance of taurine homeostasis in the cat under conditions of decreased dietary taurine intake.

摘要

含硫β-氨基酸牛磺酸是猫必需的营养物质。由于一些代谢特性,猫比其他哺乳动物更依赖膳食中的牛磺酸来源。因此,我们研究了从猫小肠分离的肠刷状缘膜囊泡(BBMV)对牛磺酸的摄取。与无钠条件相比,猫BBMV对牛磺酸的摄取不受跨膜钠梯度的影响。对初始牛磺酸摄取的动力学分析没有发现载体介导的转运过程的证据。这些发现不能归因于我们的囊泡制剂中底物累积摄取的总体无能,因为D-葡萄糖摄取强烈依赖于钠,显示出在囊泡实验中通常与主动转运相关的过冲现象。此外,L-亮氨酸转运由单一的钠依赖性载体机制介导(最大转运速度1.2 nmol·mg蛋白-1·s-1,Km = 2.1 mM)。与猫BBMV对牛磺酸的摄取不同,猪肠BBMV对牛磺酸的转运通过内向的钠梯度显著增强。因此,与其他哺乳动物不同,成年猫肠刷状缘膜对牛磺酸的摄取似乎不是由特定的转运机制介导的。因此,在膳食牛磺酸摄入量减少的情况下,胃肠道对牛磺酸的吸收可能会成为维持猫体内牛磺酸稳态的限制因素。

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