The jejunal absorption of glucose oligomers in the absence of pancreatic enzymes
- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:

ABSTRACT Summary: We compared the absorption of carbohydrate from solutions of glucose oligomers and glucose in jejunal Thiry-Vella fistulae, a preparation deprived of pancreatic secretions.
The studies were performed with two concentrations (90 and 360 mg/dl) of both glucose and the glucose oligomers. Carbohydrate absorption from glucose solutions (33.1 × 2.8, 115.9 × 8.9
μg/cm/min) was significantly greater (_P_ < 0.025; _P_ < 0.005) than that from oligomer solutions (26.6 × 2.1 and 92.4 × 9.0 μg/cm/min). Thin-layer analyses of the perfusates
demonstrate digestion of oligomers with a chain length up to eleven and suggest digestion of oligomers of even greater chain length. Atrophy of the jejunal mucosa occurred over the course of
the study as evidenced by a decrease in the ratio of villous height to crypt depth from 3.8 to 0.3, and by a 80% decrease in the activity of maltase, sucrase, and lactase. Atrophy was
accompanied by a significant decline in the absorption of both glucose oligomers (_P_ < 0.005) and glucose (_P_ < 0.01) from the more concentrated solutions but the decrement in
absorption of both carbohydrates was similar, glucose oligomers, 79.3 × 19.4 μg/cm/min; and glucose, 69.8 × 14 μg/cm/min (_P_ > 0.20). Water absorption was enhanced by both carbohydrates,
but there was no demonstrable difference between solutions of glucose and glucose oligomers. The osmolality of the solutions clearly influenced water absorption (_P_ < 0.025) but failed
to effect the absorption of carbohydrates. Speculation: In patients with pancreatic insufficiency, solutions of glucose oligomers with low osmolality may provide an adequate source of
calories. Although glucose is better absorbed than glucose oligomers from a short segment of jejunum, the length of the small intestine should be adequate to compensate for this
difference.~h~ absorption of the glucose oligomers may be a function of polymer length and therefore studies with subfractions separated according to chain length will demonstrate which
oligomers are most efficiently absorbed. such information may provide the theoretical hasis for the construction of an ideal carbohydrate supplement for patients with pancreatic
insufficiency. SIMILAR CONTENT BEING VIEWED BY OTHERS NEOKESTOSE SUPPRESSES THE INCREASE IN PLASMA GLUCOSE CAUSED BY ORAL ADMINISTRATION OF SUCROSE IN A STREPTOZOTOCIN‑INDUCED DIABETIC RAT
Article Open access 19 July 2024 REGULATORY MECHANISMS OF GLUCOSE ABSORPTION IN THE MOUSE PROXIMAL SMALL INTESTINE DURING FASTING AND FEEDING Article Open access 05 July 2023 EFFECTS OF
INTRAGASTRIC ADMINISTRATION OF L-TRYPTOPHAN ON THE GLYCAEMIC RESPONSE TO A NUTRIENT DRINK IN MEN WITH TYPE 2 DIABETES — IMPACTS ON GASTRIC EMPTYING, GLUCOREGULATORY HORMONES AND GLUCOSE
ABSORPTION Article Open access 05 January 2021 ARTICLE PDF AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Pediatrics, Ohio State University, Children's Hospital, 700
Children's Drive, Columbus, Ohio, USA Benny Kerzner, Howard R Sloan, Gerald Haase, H Juhling Mcclung & Anton H Ailabouni Authors * Benny Kerzner View author publications You can
also search for this author inPubMed Google Scholar * Howard R Sloan View author publications You can also search for this author inPubMed Google Scholar * Gerald Haase View author
publications You can also search for this author inPubMed Google Scholar * H Juhling Mcclung View author publications You can also search for this author inPubMed Google Scholar * Anton H
Ailabouni View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Kerzner,
B., Sloan, H., Haase, G. _et al._ The Jejunal Absorption of Glucose Oligomers in the Absence of Pancreatic Enzymes. _Pediatr Res_ 15, 250–253 (1981).
https://doi.org/10.1203/00006450-198103000-00010 Download citation * Issue Date: 01 March 1981 * DOI: https://doi.org/10.1203/00006450-198103000-00010 SHARE THIS ARTICLE Anyone you share the
following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer
Nature SharedIt content-sharing initiative KEYWORDS * glucose * glucose oligomers * intestine * pancreatic enzymes