Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes

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Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. / Fehse, Frauke; Trautmann, Michael; Holst, Jens Juul; Halseth, Amy E; Nanayakkara, Nuwan; Nielsen, Loretta L; Fineman, Mark S; Kim, Dennis D; Nauck, Michael A.

In: The Journal of clinical endocrinology and metabolism, Vol. 90, No. 11, 11.2005, p. 5991-7.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fehse, F, Trautmann, M, Holst, JJ, Halseth, AE, Nanayakkara, N, Nielsen, LL, Fineman, MS, Kim, DD & Nauck, MA 2005, 'Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes', The Journal of clinical endocrinology and metabolism, vol. 90, no. 11, pp. 5991-7. https://doi.org/10.1210/jc.2005-1093

APA

Fehse, F., Trautmann, M., Holst, J. J., Halseth, A. E., Nanayakkara, N., Nielsen, L. L., Fineman, M. S., Kim, D. D., & Nauck, M. A. (2005). Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. The Journal of clinical endocrinology and metabolism, 90(11), 5991-7. https://doi.org/10.1210/jc.2005-1093

Vancouver

Fehse F, Trautmann M, Holst JJ, Halseth AE, Nanayakkara N, Nielsen LL et al. Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. The Journal of clinical endocrinology and metabolism. 2005 Nov;90(11):5991-7. https://doi.org/10.1210/jc.2005-1093

Author

Fehse, Frauke ; Trautmann, Michael ; Holst, Jens Juul ; Halseth, Amy E ; Nanayakkara, Nuwan ; Nielsen, Loretta L ; Fineman, Mark S ; Kim, Dennis D ; Nauck, Michael A. / Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. In: The Journal of clinical endocrinology and metabolism. 2005 ; Vol. 90, No. 11. pp. 5991-7.

Bibtex

@article{8ed4e5d2792646d486a252c0175d2e5d,
title = "Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes",
abstract = "CONTEXT: First-phase insulin secretion (within 10 min after a sudden rise in plasma glucose) is reduced in type 2 diabetes mellitus (DM2). The incretin mimetic exenatide has glucoregulatory activities in DM2, including glucose-dependent enhancement of insulin secretion.OBJECTIVE: The objective of the study was to determine whether exenatide can restore a more normal pattern of insulin secretion in subjects with DM2.DESIGN: Fasted subjects received iv insulin infusion to reach plasma glucose 4.4-5.6 mmol/liter. Subjects received iv exenatide (DM2) or saline (DM2 and healthy volunteers), followed by iv glucose challenge.PATIENTS: Thirteen evaluable DM2 subjects were included in the study: 11 males, two females; age, 56 +/- 7 yr; body mass index, 31.7 +/- 2.4 kg/m2; hemoglobin A1c, 6.6 +/- 0.7% (mean +/- sd) treated with diet/exercise (n = 1), metformin (n = 10), or acarbose (n = 2). Controls included 12 healthy, weight-matched subjects with normal glucose tolerance: nine males, three females; age, 57 +/- 9 yr; and body mass index, 32.0 +/- 3.0 kg/m2.SETTING: The study was conducted at an academic hospital.MAIN OUTCOME MEASURES: Plasma insulin, plasma C-peptide, insulin secretion rate (derived by deconvolution), and plasma glucagon were the main outcome measures.RESULTS: DM2 subjects administered saline had diminished first-phase insulin secretion, compared with healthy control subjects. Exenatide-treated DM2 subjects had an insulin secretory pattern similar to healthy subjects in both first (0-10 min) and second (10-180 min) phases after glucose challenge, in contrast to saline-treated DM2 subjects. In exenatide-treated DM2 subjects, the most common adverse event was moderate nausea (two of 13 subjects).CONCLUSIONS: Short-term exposure to exenatide can restore the insulin secretory pattern in response to acute rises in glucose concentrations in DM2 patients who, in the absence of exenatide, do not display a first phase of insulin secretion. Loss of first-phase insulin secretion in DM2 patients may be restored by treatment with exenatide.",
keywords = "Adult, Diabetes Mellitus, Type 2, Female, Glucagon-Like Peptide 1, Glucose, Humans, Insulin, Male, Middle Aged, Peptides, Venoms",
author = "Frauke Fehse and Michael Trautmann and Holst, {Jens Juul} and Halseth, {Amy E} and Nuwan Nanayakkara and Nielsen, {Loretta L} and Fineman, {Mark S} and Kim, {Dennis D} and Nauck, {Michael A}",
year = "2005",
month = nov,
doi = "10.1210/jc.2005-1093",
language = "English",
volume = "90",
pages = "5991--7",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "11",

}

RIS

TY - JOUR

T1 - Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes

AU - Fehse, Frauke

AU - Trautmann, Michael

AU - Holst, Jens Juul

AU - Halseth, Amy E

AU - Nanayakkara, Nuwan

AU - Nielsen, Loretta L

AU - Fineman, Mark S

AU - Kim, Dennis D

AU - Nauck, Michael A

PY - 2005/11

Y1 - 2005/11

N2 - CONTEXT: First-phase insulin secretion (within 10 min after a sudden rise in plasma glucose) is reduced in type 2 diabetes mellitus (DM2). The incretin mimetic exenatide has glucoregulatory activities in DM2, including glucose-dependent enhancement of insulin secretion.OBJECTIVE: The objective of the study was to determine whether exenatide can restore a more normal pattern of insulin secretion in subjects with DM2.DESIGN: Fasted subjects received iv insulin infusion to reach plasma glucose 4.4-5.6 mmol/liter. Subjects received iv exenatide (DM2) or saline (DM2 and healthy volunteers), followed by iv glucose challenge.PATIENTS: Thirteen evaluable DM2 subjects were included in the study: 11 males, two females; age, 56 +/- 7 yr; body mass index, 31.7 +/- 2.4 kg/m2; hemoglobin A1c, 6.6 +/- 0.7% (mean +/- sd) treated with diet/exercise (n = 1), metformin (n = 10), or acarbose (n = 2). Controls included 12 healthy, weight-matched subjects with normal glucose tolerance: nine males, three females; age, 57 +/- 9 yr; and body mass index, 32.0 +/- 3.0 kg/m2.SETTING: The study was conducted at an academic hospital.MAIN OUTCOME MEASURES: Plasma insulin, plasma C-peptide, insulin secretion rate (derived by deconvolution), and plasma glucagon were the main outcome measures.RESULTS: DM2 subjects administered saline had diminished first-phase insulin secretion, compared with healthy control subjects. Exenatide-treated DM2 subjects had an insulin secretory pattern similar to healthy subjects in both first (0-10 min) and second (10-180 min) phases after glucose challenge, in contrast to saline-treated DM2 subjects. In exenatide-treated DM2 subjects, the most common adverse event was moderate nausea (two of 13 subjects).CONCLUSIONS: Short-term exposure to exenatide can restore the insulin secretory pattern in response to acute rises in glucose concentrations in DM2 patients who, in the absence of exenatide, do not display a first phase of insulin secretion. Loss of first-phase insulin secretion in DM2 patients may be restored by treatment with exenatide.

AB - CONTEXT: First-phase insulin secretion (within 10 min after a sudden rise in plasma glucose) is reduced in type 2 diabetes mellitus (DM2). The incretin mimetic exenatide has glucoregulatory activities in DM2, including glucose-dependent enhancement of insulin secretion.OBJECTIVE: The objective of the study was to determine whether exenatide can restore a more normal pattern of insulin secretion in subjects with DM2.DESIGN: Fasted subjects received iv insulin infusion to reach plasma glucose 4.4-5.6 mmol/liter. Subjects received iv exenatide (DM2) or saline (DM2 and healthy volunteers), followed by iv glucose challenge.PATIENTS: Thirteen evaluable DM2 subjects were included in the study: 11 males, two females; age, 56 +/- 7 yr; body mass index, 31.7 +/- 2.4 kg/m2; hemoglobin A1c, 6.6 +/- 0.7% (mean +/- sd) treated with diet/exercise (n = 1), metformin (n = 10), or acarbose (n = 2). Controls included 12 healthy, weight-matched subjects with normal glucose tolerance: nine males, three females; age, 57 +/- 9 yr; and body mass index, 32.0 +/- 3.0 kg/m2.SETTING: The study was conducted at an academic hospital.MAIN OUTCOME MEASURES: Plasma insulin, plasma C-peptide, insulin secretion rate (derived by deconvolution), and plasma glucagon were the main outcome measures.RESULTS: DM2 subjects administered saline had diminished first-phase insulin secretion, compared with healthy control subjects. Exenatide-treated DM2 subjects had an insulin secretory pattern similar to healthy subjects in both first (0-10 min) and second (10-180 min) phases after glucose challenge, in contrast to saline-treated DM2 subjects. In exenatide-treated DM2 subjects, the most common adverse event was moderate nausea (two of 13 subjects).CONCLUSIONS: Short-term exposure to exenatide can restore the insulin secretory pattern in response to acute rises in glucose concentrations in DM2 patients who, in the absence of exenatide, do not display a first phase of insulin secretion. Loss of first-phase insulin secretion in DM2 patients may be restored by treatment with exenatide.

KW - Adult

KW - Diabetes Mellitus, Type 2

KW - Female

KW - Glucagon-Like Peptide 1

KW - Glucose

KW - Humans

KW - Insulin

KW - Male

KW - Middle Aged

KW - Peptides

KW - Venoms

U2 - 10.1210/jc.2005-1093

DO - 10.1210/jc.2005-1093

M3 - Journal article

C2 - 16144950

VL - 90

SP - 5991

EP - 5997

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 11

ER -

ID: 132053549