{"title":"Effect of zinc on D-galactose and L-phenylalanine uptake in rat intestine in vitro.","authors":"A Lugea, A Barber, F Ponz","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effect of zinc on galactose and phenylalanine uptake was studied using rat everted jejunal rings. The rings were incubated for 2 min in oxygenated Krebs-Ringer-Tris (KRT) solution. Galactose and phenylalanine uptake was reduced by zinc in a dose-dependent manner, but not in a time-dependent way. One mM Zn2+ but not 0.5 mM Zn2+ inhibited galactose transport without modifying sugar diffusion. Na(+)-dependent phenylalanine transport was reduced by 0.5 mM and 1 mM Zn2+. However, the metal did not change phenylalanine diffusion obtained in the presence of 40 mM L-methionine or Na(2+)-independent phenylalanine transport. Therefore, zinc seems to interact only with the sodium-galactose or sodium-phenylalanine cotransporters. Zinc inhibited sugar and amino acid transport in a non-competitive way, without a significant change in the affinity of the transporters for their substrates and with a Vmax decrease. The inhibitory effect of Zn2+ on galactose and phenylalanine uptake was reversed by washing intestinal rings for 5 min with KRT solution. These results suggest that zinc might exert its inhibitory action by a weak binding to chemical groups related with sodium-substrate cotransporters and located in the luminal membrane of the enterocytes.</p>","PeriodicalId":21473,"journal":{"name":"Revista espanola de fisiologia","volume":"51 3","pages":"139-46"},"PeriodicalIF":0.0000,"publicationDate":"1995-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista espanola de fisiologia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The effect of zinc on galactose and phenylalanine uptake was studied using rat everted jejunal rings. The rings were incubated for 2 min in oxygenated Krebs-Ringer-Tris (KRT) solution. Galactose and phenylalanine uptake was reduced by zinc in a dose-dependent manner, but not in a time-dependent way. One mM Zn2+ but not 0.5 mM Zn2+ inhibited galactose transport without modifying sugar diffusion. Na(+)-dependent phenylalanine transport was reduced by 0.5 mM and 1 mM Zn2+. However, the metal did not change phenylalanine diffusion obtained in the presence of 40 mM L-methionine or Na(2+)-independent phenylalanine transport. Therefore, zinc seems to interact only with the sodium-galactose or sodium-phenylalanine cotransporters. Zinc inhibited sugar and amino acid transport in a non-competitive way, without a significant change in the affinity of the transporters for their substrates and with a Vmax decrease. The inhibitory effect of Zn2+ on galactose and phenylalanine uptake was reversed by washing intestinal rings for 5 min with KRT solution. These results suggest that zinc might exert its inhibitory action by a weak binding to chemical groups related with sodium-substrate cotransporters and located in the luminal membrane of the enterocytes.
采用大鼠外翻空肠环研究了锌对半乳糖和苯丙氨酸摄取的影响。将环在含氧KRT溶液中孵育2分钟。锌降低半乳糖和苯丙氨酸摄取呈剂量依赖性,但不呈时间依赖性。1 mM Zn2+而不是0.5 mM Zn2+抑制半乳糖转运,但不改变糖的扩散。Na(+)依赖性苯丙氨酸转运减少0.5 mM和1 mM Zn2+。然而,金属没有改变苯丙氨酸在40 mM l -蛋氨酸存在下的扩散或不依赖于Na(2+)的苯丙氨酸运输。因此,锌似乎只与半乳糖钠或苯丙氨酸钠共转运体相互作用。锌以非竞争性方式抑制糖和氨基酸的转运,转运体对底物的亲和力没有明显变化,但Vmax降低。用KRT溶液冲洗肠道环5min,逆转Zn2+对半乳糖和苯丙氨酸摄取的抑制作用。这些结果表明,锌可能通过与位于肠细胞腔膜上的钠-底物共转运体相关的化学基团弱结合来发挥其抑制作用。