Miller M J, Zhang X J, Gu X, Tenore E, Clark D A
Dept. of Pediatrics, LSU School of Medicine, New Orleans 70112-2822.
Scand J Gastroenterol. 1991 Apr;26(4):379-84. doi: 10.3109/00365529108996498.
Loops of rabbit distal small intestine received luminal acetic acid (pH 4.0) alone or in combination with bovine casein, casein hydrolysate, or whey hydrolysate. Blood-to-lumen movement of 51Cr-labeled ethylenediaminetetraacetic acid (EDTA) (an index of epithelial permeability) and loop fluid histamine levels were quantified after 45 min. Luminal acetic acid caused a marked increase in 51Cr-EDTA accumulation which was not modified by the addition of bovine casein or hydrolysates by of casein or whey. However, acetic acid-induced histamine release was potentiated by casein and casein hydrolysate (six- and four-fold respectively) but was not altered by whey hydrolysate. Casein hydrolysate-dependent histamine release was evident in naloxone-pretreated rabbits, suggesting that beta-casomorphins were not solely responsible. We conclude that luminal casein or casein hydrolysate, but not whey hydrolysate. can activate intestinal mast cells under conditions of enhanced epithelial permeability. This effect appears to involve components other than beta-casomorphins.
将兔远端小肠肠袢单独给予腔内乙酸(pH 4.0),或与牛酪蛋白、酪蛋白水解物或乳清水解物联合给予。45分钟后,对51Cr标记的乙二胺四乙酸(EDTA)(上皮通透性指标)的血-腔转运以及肠袢液组胺水平进行定量分析。腔内乙酸导致51Cr-EDTA蓄积显著增加,添加牛酪蛋白或酪蛋白或乳清的水解物对此无影响。然而,酪蛋白和酪蛋白水解物(分别为6倍和4倍)增强了乙酸诱导的组胺释放,但乳清水解物未改变其释放。酪蛋白水解物依赖性组胺释放在纳洛酮预处理的兔子中明显,表明β-酪蛋白吗啡并非唯一原因。我们得出结论,腔内酪蛋白或酪蛋白水解物而非乳清水解物,可在上皮通透性增强的条件下激活肠道肥大细胞。这种作用似乎涉及β-酪蛋白吗啡以外的成分。