Contribution of Villous Atrophy to Reduced Intestinal Maltase in Infants With Malnutrition

• Published in: Journal of pediatric gastroenterology and nutrition Vol. 30; no. 5; pp. 494 - 502
• Main Authors: Nichols, Buford L, Nichols, Veda N, Putman, Margaret, Avery, Stephen E, Fraley, J Kennard, Quaroni, Andrea, Shiner, Margot, Sterchi, Erwin E, Carrazza, Francisco R
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins, Inc 01-05-2000; Lippincott
• Subjects: Actins - genetics; alpha-Glucosidases - genetics; alpha-Glucosidases - metabolism; Atrophy; Biological and medical sciences; Biopsy; Carrier Proteins - genetics; Child, Preschool; Female; Gastroenterology. Liver. Pancreas. Abdomen; Humans; Infant; Intestinal Mucosa - enzymology; Intestinal Mucosa - pathology; Intestines - enzymology; Intestines - pathology; Male; Medical sciences; Membrane Glycoproteins - genetics; Microfilament Proteins - genetics; Monosaccharide Transport Proteins - genetics; Nutrition Disorders - enzymology; Nutrition Disorders - pathology; Nutritional Status; Other diseases. Semiology; RNA, Messenger - metabolism; Sodium-Glucose Transporter 1; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Human; Enzyme; Pathogenesis; Nutrition disorder; Atrophy; Enzymatic activity; α-Glucosidase; Glycosidases; Digestive diseases; Hydrolases; Intestinal disease; Intestinal villi; Malnutrition; O-Glycosidases; Child
• ISSN: 0277-2116; 1536-4801
• DOI: 10.1097/00005176-200005000-00007

BACKGROUNDIt has been known for many years that small intestinal maltase activities are reduced in malnourished infants and in other patients with villous atrophy. The recent availability of human maltase-glucoamylase cDNA provides the opportunity to test the hypothesis that villous atrophy accounts for the reduced maltase enzyme activity in malnourished infants.
METHODSMucosal biopsy specimens obtained for clinical evaluation of malnourished infants with poor responses to refeeding were examined by quantitative methods for enzyme activity and mRNA levels.
RESULTSMaltase activity and maltase-glucoamylase mRNA were reduced (approximately 45% of normal). When maltase-glucoamylase message was normalized to villin message, a structural protein expressed only in enterocytes, a preservation of maltase messages in surviving enterocytes was documented. The luminal glucose transporter–villin message was also preserved.
CONCLUSIONSThe loss of maltase-glucoamylase message paralleled the reduction in villin message and degree of villous atrophy. The reduced maltase-glucoamylase message also paralleled sucrase-isomaltase message, previously found to be decreased in proportion to villous atrophy of malnourished infants. The data directly demonstrate, for the first time, that the terminal steps of starch 1-4 starch digestion and sucrase-isomaltase 1-6 starch digestion are decreased in malnourished infants, secondary to villous atrophy. These data in prior and present reports suggest that mechanisms underlying the chronic villous atrophy of malnutrition should be a priority for investigations in malnourished infants with slower than expected weight gain during refeeding.