Hajjar J J, Khuri R N, Bikhazi A B
Am J Physiol. 1975 Aug;229(2):518-23. doi: 10.1152/ajplegacy.1975.229.2.518.
The effect of bile salts on alanine absorption across four regional sites of rabbit intestine was examined using an in vivo single-pass perfusion technique. Na-deoxycholate at a concentration of 3 mM reduced alanine absorption across all levels of the intestine, and a higher concentration (10 mM) of Na-taurodeoxycholate (TDC) caused only a minimal reduction of alanine absorption in the jejunum. TDC, however, was more effective in in vitro experiments, causing an incrase in transmural serosal-to-mucosal flux of alanine and phenylalanine, particularly when present in both the mucosal and serosal media. It also reduced the mucosal-to-serosal alanine flux rate when present only in the mucosal medium. The influx of these amino acids across the mucosal brush border membrane was also decreased by TDC. These amino acid transport changes correlated fairly well with some observed histological changes of the intestinal epithelium. This suggests that bile salt inhibition of amino acid absorption is nonspecific in type and can be mainly explained as being the result of an injurious action of these surface-active agents on the rabbit intestine.
采用体内单通道灌注技术,研究了胆盐对兔肠道四个区域丙氨酸吸收的影响。浓度为3 mM的脱氧胆酸钠降低了肠道各部位的丙氨酸吸收,而较高浓度(10 mM)的牛磺脱氧胆酸钠(TDC)仅使空肠丙氨酸吸收略有减少。然而,TDC在体外实验中更有效,导致丙氨酸和苯丙氨酸的跨膜浆膜到粘膜通量增加,特别是当它同时存在于粘膜和浆膜介质中时。当仅存在于粘膜介质中时,它也降低了粘膜到浆膜的丙氨酸通量率。TDC还降低了这些氨基酸跨粘膜刷状缘膜的内流。这些氨基酸转运变化与观察到的肠道上皮组织学变化相当吻合。这表明胆盐对氨基酸吸收的抑制在类型上是非特异性的,主要可以解释为这些表面活性剂对兔肠道的损伤作用所致。