Caspary W F
Leber Magen Darm. 1977 Jun;7(3):150-9.
Starch is digested intraluminally by alpha-amylase to maltose, maltotriose, and alpha-limit dextrins. These products, as well as the disaccharides sucrose and lactose, undergo enzymatic hydrolysis to monosaccharides at the brush border surface. The monosaccharides enter the absorbing cell by specific transport mechanisms ("carriers"). Primary carbohydrate (CH) intolerance is characterized by the congenital or acquired absence of individual brush border enzymes or of monosaccharide "carriers" without morphologic abnormalities of the intestinal villus: lactose, sucrose and trehalose intolerance and glucose-galactose malabsorption (brush border diseases). Secondary CH intolerance arises when surface digestion and absorption are reduced due to structural changes of the intestinal mucosa: e.g., decrease or absence of villi with sprue and reduction of the absorbing surface with intestinal resection. Watery diarrhea is the lead symptom. Many drugs delay or interfere with CH absorption. This action may be viewed either as an unwanted side effect or as a welcome therapeutic principle.
淀粉在肠腔内被α-淀粉酶消化为麦芽糖、麦芽三糖和α-极限糊精。这些产物,以及二糖蔗糖和乳糖,在刷状缘表面进行酶促水解为单糖。单糖通过特定的转运机制(“载体”)进入吸收细胞。原发性碳水化合物(CH)不耐受的特征是先天性或后天性缺乏个体刷状缘酶或单糖“载体”,而肠绒毛无形态学异常:乳糖、蔗糖和海藻糖不耐受以及葡萄糖-半乳糖吸收不良(刷状缘疾病)。继发性CH不耐受是由于肠黏膜结构改变导致表面消化和吸收减少时出现的:例如,口炎性腹泻时绒毛减少或缺失,以及肠切除术后吸收表面减少。水样腹泻是主要症状。许多药物会延迟或干扰CH吸收。这种作用既可以被视为不良副作用,也可以被视为受欢迎的治疗原则。