Abstract |
A new disaccharidase inhibitor, AO-128, showed 190-3900-fold more potent inhibition of purified rat small intestine sucrase- isomaltase (S-1) complex and 23-33-fold more potent inhibition of semipurified porcine small intestine disaccharidases than acarbose. AO-128 suppressed elevation of the blood glucose concentration after oral sucrose, maltose, and starch, but not after oral glucose, fructose, and lactose. The chronic addition of AO-128 to the diet produced antiobesity and antidiabetic actions in obese and/or diabetic animals. Undesirable side effects, such as diarrhea and soft feces, were observed only for the first 5-7 d and suppression of intestinal disaccharidase activities was observed even at the end of the experiment, suggesting that the suppressive or delaying effect of AO-128 on elevation of the postprandial blood glucose concentrations is involved in reduction in body weight gain and prevention and/or amelioration of the diabetic state. Thus, AO-128 is useful as an adjunct to the dietary management of obesity and diabetes.
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Authors | T Matsuo, H Odaka, H Ikeda |
Journal | The American journal of clinical nutrition
(Am J Clin Nutr)
Vol. 55
Issue 1 Suppl
Pg. 314S-317S
(01 1992)
ISSN: 0002-9165 [Print] United States |
PMID | 1728846
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Cyclohexanols
- Glycoside Hydrolase Inhibitors
- Trisaccharides
- AO 128
- Disaccharidases
- Oligo-1,6-Glucosidase
- Sucrase
- Acarbose
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Topics |
- Acarbose
- Animals
- Cyclohexanols
(pharmacology, therapeutic use)
- Diabetes Mellitus, Experimental
(drug therapy)
- Disaccharidases
(antagonists & inhibitors)
- Glycoside Hydrolase Inhibitors
- Intestines
(enzymology)
- Male
- Obesity
(drug therapy)
- Oligo-1,6-Glucosidase
(antagonists & inhibitors)
- Rats
- Rats, Inbred Strains
- Rats, Zucker
- Sucrase
(antagonists & inhibitors)
- Trisaccharides
(pharmacology)
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