Glucose-galactose malabsorption: demonstration of specific jejunal brush border membrane defect.
نویسندگان
چکیده
Jejunal brush border glucose transport was studied in a patient with glucose-galactose malabsorption and in controls, using jejunal brush border membrane vesicles (BBMV) prepared from conventional jejunal biopsies. Whereas BBMV from controls showed a seven-fold enhancement of D-glucose uptake in the presence of an inwardly directed sodium gradient compared with its absence, no such enhancement was seen in the patient's vesicles. In BBMV from the patient, initial D-glucose uptake under sodium gradient conditions was only 10% of the mean control value. In contrast, sodium/proton exchange in BBMV from the patient was intact. These data provide the first unequivocal evidence that the jejunal brush border membrane is the site of a specific defect in sodium dependent glucose transport in glucose-galactose malabsorption. Measurement of glucose uptake by BBMV may well be the optimal diagnostic technique in this disorder.
منابع مشابه
Genetic Disorders of Membrane Transport I. Glucose Galactose Malabsorption
Wright, Ernest M. Genetic Disorders of Membrane Transport. I. Glucose Galactose Malabsorption. Am. J. Physiol. 275 (Gastrointest. Liver Physiol. 38): G879–G882, 1998.—Glucose Galactose Malabsorption is a genetic disorder caused by a defect in glucose and galactose transport across the intestinal brush border. Normally, lactose in milk is broken down into glucose and galactose by lactase, an ect...
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عنوان ژورنال:
- Gut
دوره 29 12 شماره
صفحات -
تاریخ انتشار 1988