Said H M, Redha R, Tipton W, Nylander W
Department of Pediatric Gastroenterology, Vanderbilt University School of Medicine, Nashville, TN.
Am J Clin Nutr. 1988 Jan;47(1):75-9. doi: 10.1093/ajcn/47.1.75.
Uptake of folic acid (PteGlu) was examined in remnant ileum of rats after resection of 65% of the small intestine with the brush border-membrane vesicle technique. The results were compared to that of sham-operated rats. In both rat groups transport of PteGlu was linear for approximately 40 s of incubation and was similar in the presence of a Na+ and a K+ gradient (out greater than in). In resected rats transport of PteGlu was inhibited by the structural analogues 5-methyltetrahydrofolate (5-CH3H4PteGlu) and methotrexate (MTX), by sulfasalazine, and by 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS) and was saturable as a function of concentration (apparent Kt = 18.3 microM). In the ileum of sham-operated rats, on the other hand, transport of PteGlu was not affected by 5-CH3H4PteGlu, MTX, sulfasalazine, or DIDS and was linear with concentration. These results suggest that the PteGlu transport system is induced in remnant ileum of the rat after extensive intestinal resection.
采用刷状缘膜囊泡技术,对小肠65%切除术后大鼠的残余回肠叶酸(蝶酰谷氨酸)摄取情况进行了检测。并将结果与假手术大鼠进行比较。在两个大鼠组中,蝶酰谷氨酸的转运在孵育约40秒时呈线性,且在存在Na⁺和K⁺梯度(外向内)时相似。在切除大鼠中,蝶酰谷氨酸的转运受到结构类似物5-甲基四氢叶酸(5-CH₃H₄PteGlu)和甲氨蝶呤(MTX)、柳氮磺胺吡啶以及4,4'-二异硫氰酸根合芪-2,2'-二磺酸(DIDS)的抑制,并且作为浓度的函数是可饱和的(表观Kt = 18.3微摩尔)。另一方面,在假手术大鼠的回肠中,蝶酰谷氨酸的转运不受5-CH₃H₄PteGlu、MTX、柳氮磺胺吡啶或DIDS的影响,且与浓度呈线性关系。这些结果表明,大鼠广泛肠道切除术后,其残余回肠中的蝶酰谷氨酸转运系统被诱导。