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Ghrelin secretion is inhibited by glucose load and insulin-induced hypoglycaemia but unaffected by glucagon and arginine in humans
被引:65
作者:

Broglio, F
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Gottero, C
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

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Destefanis, S
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Gauna, C
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h-index: 0
机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Me, E
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Riganti, F
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Vivenza, D
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Rapa, A
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Martina, V
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机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

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Bona, G
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h-index: 0
机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

van der Lely, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands

Ghigo, E
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h-index: 0
机构: Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands
机构:
[1] Erasmus Univ, Dept Internal Med, Div Endocrinol, NL-3000 DR Rotterdam, Netherlands
[2] Univ Turin, Dept Internal Med, Div Endocrinol & Metab, I-10124 Turin, Italy
[3] Piemonte Orientale Univ, Dept Med Sci, Unit Paediat, Novara, Italy
关键词:
D O I:
10.1111/j.1365-2265.2004.02121.x
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
OBJECTIVE Circulating ghrelin levels are increased by fasting and decreased by feeding, glucose load, insulin and somatostatin. Whether hyperglycaemia and insulin directly inhibit ghrelin secretion still remains matter of debate. The aim of the present study was therefore to investigate further the regulatory effects of glucose and insulin on ghrelin secretion. DESIGN AND SUBJECTS We studied the effects of glucose [oral glucose tolerance test (OGTT) 100 g orally], insulin-induced hypoglycaemia [ITT, 0.1 IU/kg insulin intravenously (i.v.)], glucagon (1 mg i.v.), arginine (0.5 mg/kg i.v.) and saline on ghrelin, GH, insulin, glucose and glucagon levels in six normal subjects. MEASUREMENTS In all the sessions, blood samples were collected every 15 min from 0 up to + 120 min. Ghrelin, GH, insulin, glucagon and glucose levels were assayed at each time point. RESULTS OGTT increased (P < 0.01) glucose and insulin while decreasing (P < 0.01) GH and ghrelin levels. ITT increased (P < 0.01) GH but decreased (P < 0.01) ghrelin levels. Glucagon increased (P < 0.01) glucose and insulin without modifying GH and ghrelin. Arginine increased (P < 0.01) GH, insulin, glucagon and glucose (P < 0.05) but did not affect ghrelin secretion. CONCLUSIONS Ghrelin secretion in humans is inhibited by OGTT-induced hyperglycaemia and ITT but not by glucagon and arginine, two substances able to increase insulin and glucose levels. These findings question the assumption that glucose and insulin directly regulate ghrelin secretion. On the other hand, ghrelin secretion is not associated with the GH response to ITT or arginine, indicating that the somatotroph response to these stimuli is unlikely to be mediated by ghrelin.
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页码:503 / 509
页数:7
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h-index: 0
机构:
Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Obes Res Ctr, New York, NY 10025 USA Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Obes Res Ctr, New York, NY 10025 USA
[10]
Orexigenic action of peripheral ghrelin is mediated by neuropeptide Y and agouti-related protein
[J].
Chen, HY
;
Trumbauer, ME
;
Chen, AS
;
Weingarth, DT
;
Adams, JR
;
Frazier, EG
;
Shen, Z
;
Marsh, DJ
;
Feighner, SD
;
Guan, XM
;
Ye, Z
;
Nargund, RP
;
Smith, RG
;
Van Der Ploeg, LHT
;
Howard, AD
;
Macneil, DJ
;
Qian, S
.
ENDOCRINOLOGY,
2004, 145 (06)
:2607-2612

Chen, HY
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Trumbauer, ME
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Chen, AS
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Weingarth, DT
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Adams, JR
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Frazier, EG
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Shen, Z
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Marsh, DJ
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Feighner, SD
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Guan, XM
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Ye, Z
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Nargund, RP
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Smith, RG
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Van Der Ploeg, LHT
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Howard, AD
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Macneil, DJ
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA

Qian, S
论文数: 0 引用数: 0
h-index: 0
机构: Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA