Literature DB >> 5552414

The metabolism of circulating maltose in man.

J M Young, E Weser.   

Abstract

The utilization of circulating maltose was compared to that of glucose in six normal fasting subjects after intravenous injection of 25 g of either sugar. Blood samples were obtained over a 2 hr period and were assayed for free fatty acids (FFA), insulin, glucose, and total reducing substances. Urine was collected for 2 hr after maltose administration and assayed enzymatically for glucose and maltose. Blood glucose concentrations did not increase after maltose infusion, although a significant rise in total reducing substances was noted, indicating the presence of this disaccharide in the blood. Less than 3% of the administered maltose was excreted in the urine either as maltose or glucose. Initially, there was a fourfold increase in serum insulin concentration after glucose and a threefold increase after maltose infusion. Therefore, serum insulin concentrations gradually declined in a similar manner for both sugars. The plasma FFA at 15 min decreased 371 uEq/liter after glucose and 338 uEq/liter after maltose infusion. In other studies, 10 g maltose containing 5 muCi maltose-U-(14)C were injected into five human subjects and expired CO(2) collected for 6 hr. Maximal (14)CO(2) specific activity was noted at 170 min and a mean of 61.1% of the injected radioactivity was recovered as (14)CO(2). Less than 8% of the injected (14)C was excreted in the urine. These results indicate that maltose administered intravenously has similar metabolic effects when compared to glucose, and may be efficiently utilized as a carbohydrate substrate. The oxidation of intravenously administered maltose-U(14)C to (14)CO(2) demonstrates that circulating maltose is readily metabolized. A solution of maltose could provide twice the mass of sugar (and of calories) per milliliter as an equimolar solution of glucose. Parenterally administered maltose may be of clinical value and should be further studied.

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Year:  1971        PMID: 5552414      PMCID: PMC292018          DOI: 10.1172/JCI106592

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  43 in total

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Journal:  J Bacteriol       Date:  1952-04       Impact factor: 3.490

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Journal:  Comp Biochem Physiol       Date:  1968-08

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Journal:  J Gen Microbiol       Date:  1969-08

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Journal:  Diabetes       Date:  1966-08       Impact factor: 9.461

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Journal:  J Appl Physiol       Date:  1967-11       Impact factor: 3.531

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  20 in total

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Authors:  H Förster; I Hoos; S Boecker
Journal:  Z Ernahrungswiss       Date:  1976-09

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3.  Targeting Pathogenic Lafora Bodies in Lafora Disease Using an Antibody-Enzyme Fusion.

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Journal:  Cell Metab       Date:  2019-07-25       Impact factor: 27.287

4.  Synthesis of [¹⁸F]-labelled maltose derivatives as PET tracers for imaging bacterial infection.

Authors:  Mohammad Namavari; Gayatri Gowrishankar; Aileen Hoehne; Erwan Jouannot; Sanjiv S Gambhir
Journal:  Mol Imaging Biol       Date:  2015-04       Impact factor: 3.488

5.  Non-enzymatic detection of serum glucose using a fluorescent nanopolymer probe.

Authors:  Juan Qiao; Qianrong Liu; Han Wu; Huiwu Cai; Li Qi
Journal:  Mikrochim Acta       Date:  2019-05-21       Impact factor: 5.833

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Journal:  Can Anaesth Soc J       Date:  1982-05

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Journal:  Z Ernahrungswiss       Date:  1976-09

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Journal:  Z Ernahrungswiss       Date:  1976-06

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Journal:  Eur J Intensive Care Med       Date:  1975-11

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Authors:  M Haslbeck; W Bachmann; H Mehnert
Journal:  Klin Wochenschr       Date:  1976-06-01
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