Improved tolerance to sequential glucose loading (Staub-Traugott effect): size and mechanisms (Articolo in rivista)

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  • Improved tolerance to sequential glucose loading (Staub-Traugott effect): size and mechanisms (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1152/ajpendo.00127.2009 (literal)
Alternative label
  • Bonuccelli, S. Muscelli, E. Gastaldelli, A. Barsotti, E. Astiarriaga, B. D. Holst, J. J. Mari, A. Ferrannini, E. (2009)
    Improved tolerance to sequential glucose loading (Staub-Traugott effect): size and mechanisms
    in American journal of physiology: endocrinology and metabolism; American Physiological Society, Bethesda (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Bonuccelli, S. Muscelli, E. Gastaldelli, A. Barsotti, E. Astiarriaga, B. D. Holst, J. J. Mari, A. Ferrannini, E. (literal)
Pagina inizio
  • E532 (literal)
Pagina fine
  • e537 (literal)
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  • http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19531643 (literal)
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  • http://www.ncbi.nlm.nih.gov/pubmed/19531643 (literal)
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  • 297 (literal)
Rivista
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  • 6 (literal)
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  • 2 (literal)
Note
  • ISI Web of Science (WOS) (literal)
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  • [ 1,2,4,5,8 ] Univ Pisa, Dept Internal Med, Sch Med, I-56126 Pisa, Italy [ 3 ] CNR, Inst Clin Physiol, Consiglio Nazl Ric, I-56100 Pisa, Italy [ 6 ] Univ Copenhagen, Panum Inst, Dept Biomed Sci, DK-2200 Copenhagen, Denmark [ 7 ] Inst Biomed Engn, Consiglio Nazl Ric, Padua, Italy (literal)
Titolo
  • Improved tolerance to sequential glucose loading (Staub-Traugott effect): size and mechanisms (literal)
Abstract
  • Improved glucose tolerance to sequential glucose loading (Staub-Traugott effect) is an important determinant of day-to-day glycemic exposure. Its mechanisms have not been clearly established. We recruited 17 healthy volunteers to receive two sequential OGTTs, at time 0-min and 180-min (Study I). The protocol was repeated on a separate day (Study II) except that plasma glucose was clamped at 8.3 mmol/l between 60-180min. beta-cell function was analyzed by mathematical modeling of C-peptide concentrations. In a subgroup, glucose kinetics were measured by a triple-tracer technique (infusion of [6,6-(2)H2]-glucose and labeling of the 2 glucose loads with [1-(2)H]-glucose and U-(13)C-glucose). In both Study I and II, the plasma glucose response to the second OGTT equaled 84+/-2% (p=0.003) of the response to the first OGTT. Absolute insulin secretion was lower (37.8+/-4.3 vs 42.8+/-5.1 nmol.m(-2), p=0.02), but glucose potentiation (ie, higher secretion at the same glycemia) was stronger (1.08+/-0.02 fold vs 0.92+/-0.02 fold, p=0.006), the increment being higher in Study II (+36+/-5%) than Study I (+19+/-6 %, p<0.05). In pooled data, a higher glucose area during the first OGTT was associated with a higher potentiation during the second OGTT (rho=0.60, p=0.002). Neither insulin clearance nor glucose clearance differed between loads, and appearance of glucose over 3 hours totalled 60+/-6 g for the first load and 52+/-5 g for the second load (p=ns). Fasting endogenous glucose production (13.3+/-0.6 micromol.min(-1).kgFFM(-1)) averaged 6.0+/-3.8 micromol.min(-1).kgFFM(-1) between 0-180min and 1.7+/-2.6 between 180-360min (p<0.03). Glucose potentiation and stronger suppression of endogenous glucose release are the main mechanisms underlying the Staub-Traugott effect. Key words: Staub-Traugott effect, glucose potentiation, glucose tolerance, ss-cell function. (literal)
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