The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP).

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP). / Meier, Juris J; Gallwitz, Baptist; Siepmann, Nina; Holst, Jens J; Deacon, Carolyn F; Schmidt, Wolfgang E; Nauck, Michael A.

In: Regulatory Peptides, Vol. 113, No. 1-3, 2003, p. 95-100.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Meier, JJ, Gallwitz, B, Siepmann, N, Holst, JJ, Deacon, CF, Schmidt, WE & Nauck, MA 2003, 'The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP).', Regulatory Peptides, vol. 113, no. 1-3, pp. 95-100.

APA

Meier, J. J., Gallwitz, B., Siepmann, N., Holst, J. J., Deacon, C. F., Schmidt, W. E., & Nauck, M. A. (2003). The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP). Regulatory Peptides, 113(1-3), 95-100.

Vancouver

Meier JJ, Gallwitz B, Siepmann N, Holst JJ, Deacon CF, Schmidt WE et al. The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP). Regulatory Peptides. 2003;113(1-3):95-100.

Author

Meier, Juris J ; Gallwitz, Baptist ; Siepmann, Nina ; Holst, Jens J ; Deacon, Carolyn F ; Schmidt, Wolfgang E ; Nauck, Michael A. / The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP). In: Regulatory Peptides. 2003 ; Vol. 113, No. 1-3. pp. 95-100.

Bibtex

@article{63135b20ab4c11ddb5e9000ea68e967b,
title = "The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP).",
abstract = "Since the C-peptide/insulin ratio is reduced after oral glucose ingestion, the incretin hormone gastric inhibitory polypeptide (GIP) has been assumed to decrease hepatic insulin extraction. It was the aim of the present study to evaluate the effects of GIP on insulin extraction. Seventy-eight healthy subjects (27 male, 51 female, 43+/-11 years) were subjected to (a). an oral glucose tolerance test and (b). an intravenous injection of 20 pmol GIP/kg body weight, with capillary and venous blood samples collected over 30 min for insulin, C-peptide and GIP (specific immunoassays). Following GIP administration, plasma concentrations of total and intact GIP reached to peak levels of 80+/-7 and 54+/-5 pmol/l, respectively (p<0.0001). The rise in insulin after oral glucose and after intravenous GIP administration significantly exceeded the rise in C-peptide (p<0.0001). Estimating insulin extraction from the total integrated insulin and C-peptide concentrations (AUCs), only the oral glucose load (p<0.0001), but not the intravenous GIP administration (p=0.18) significantly reduced insulin clearance. Therefore, insulin clearance is reduced after an oral glucose load. This effect does not appear to be mediated by GIP.",
author = "Meier, {Juris J} and Baptist Gallwitz and Nina Siepmann and Holst, {Jens J} and Deacon, {Carolyn F} and Schmidt, {Wolfgang E} and Nauck, {Michael A}",
note = "Keywords: Administration, Oral; Adolescent; Adult; Aged; Blood Glucose; C-Peptide; Female; Gastric Inhibitory Polypeptide; Glucose; Glucose Tolerance Test; Humans; Insulin; Liver; Male; Metabolic Clearance Rate; Middle Aged; Time Factors",
year = "2003",
language = "English",
volume = "113",
pages = "95--100",
journal = "Regulatory Peptides",
issn = "0167-0115",
publisher = "Elsevier",
number = "1-3",

}

RIS

TY - JOUR

T1 - The reduction in hepatic insulin clearance after oral glucose is not mediated by gastric inhibitory polypeptide (GIP).

AU - Meier, Juris J

AU - Gallwitz, Baptist

AU - Siepmann, Nina

AU - Holst, Jens J

AU - Deacon, Carolyn F

AU - Schmidt, Wolfgang E

AU - Nauck, Michael A

N1 - Keywords: Administration, Oral; Adolescent; Adult; Aged; Blood Glucose; C-Peptide; Female; Gastric Inhibitory Polypeptide; Glucose; Glucose Tolerance Test; Humans; Insulin; Liver; Male; Metabolic Clearance Rate; Middle Aged; Time Factors

PY - 2003

Y1 - 2003

N2 - Since the C-peptide/insulin ratio is reduced after oral glucose ingestion, the incretin hormone gastric inhibitory polypeptide (GIP) has been assumed to decrease hepatic insulin extraction. It was the aim of the present study to evaluate the effects of GIP on insulin extraction. Seventy-eight healthy subjects (27 male, 51 female, 43+/-11 years) were subjected to (a). an oral glucose tolerance test and (b). an intravenous injection of 20 pmol GIP/kg body weight, with capillary and venous blood samples collected over 30 min for insulin, C-peptide and GIP (specific immunoassays). Following GIP administration, plasma concentrations of total and intact GIP reached to peak levels of 80+/-7 and 54+/-5 pmol/l, respectively (p<0.0001). The rise in insulin after oral glucose and after intravenous GIP administration significantly exceeded the rise in C-peptide (p<0.0001). Estimating insulin extraction from the total integrated insulin and C-peptide concentrations (AUCs), only the oral glucose load (p<0.0001), but not the intravenous GIP administration (p=0.18) significantly reduced insulin clearance. Therefore, insulin clearance is reduced after an oral glucose load. This effect does not appear to be mediated by GIP.

AB - Since the C-peptide/insulin ratio is reduced after oral glucose ingestion, the incretin hormone gastric inhibitory polypeptide (GIP) has been assumed to decrease hepatic insulin extraction. It was the aim of the present study to evaluate the effects of GIP on insulin extraction. Seventy-eight healthy subjects (27 male, 51 female, 43+/-11 years) were subjected to (a). an oral glucose tolerance test and (b). an intravenous injection of 20 pmol GIP/kg body weight, with capillary and venous blood samples collected over 30 min for insulin, C-peptide and GIP (specific immunoassays). Following GIP administration, plasma concentrations of total and intact GIP reached to peak levels of 80+/-7 and 54+/-5 pmol/l, respectively (p<0.0001). The rise in insulin after oral glucose and after intravenous GIP administration significantly exceeded the rise in C-peptide (p<0.0001). Estimating insulin extraction from the total integrated insulin and C-peptide concentrations (AUCs), only the oral glucose load (p<0.0001), but not the intravenous GIP administration (p=0.18) significantly reduced insulin clearance. Therefore, insulin clearance is reduced after an oral glucose load. This effect does not appear to be mediated by GIP.

M3 - Journal article

VL - 113

SP - 95

EP - 100

JO - Regulatory Peptides

JF - Regulatory Peptides

SN - 0167-0115

IS - 1-3

ER -

ID: 8417500