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DOI: 10.1055/s-0030-1269880
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York
Effect of Hyperthyroidism on Clearance and Secretion of Glucagon in Man
Publikationsverlauf
received 08.09.2010
first decision 26.10.2010
accepted 23.11.2010
Publikationsdatum:
24. Januar 2011 (online)

Abstract
Objective: Glucagon has been proposed to contribute to the increased glucose production found in hyperthyroidism. However, fasting plasma glucagon levels are not increased in hyperthyroidism suggesting that the activity of the α-cell is normal. Nevertheless, an increase in the clearance rate of glucagon may mask increased glucagon secretion. This study was designed to examine the effects of hyperthyroidism on the kinetics of glucagon.
Design and methods: A primed-continuous infusion of glucagon was administered to 9 euthyroid and 9 hyperthyroid subjects at 3 sequential rates (1 200, 3 000 and 6 000 pg/kg/min, each given for 2 h). Arterialized blood was drawn at 15–30 min intervals for determination of glucagon.
Results: Fasting plasma glucagon levels were comparable in euthyroids (195±8 pg/ml) and hyperthyroids (231±16 pg/ml). During infusions (1 200, 3 000 and 6 000 pg/kg/min), plasma glucagon increased to 387±19, 624±44 and 977±51 pg/ml in euthyroids and to 348±23, 597±42 and 938±56 pg/ml in hyperthyroids respectively. At these infusion rates, metabolic clearance of glucagon (ml/kg/min) was 6.6±0.5, 7.4±0.6 and 7.9±0.5 in euthyroids and 12.6±2, 8.9±1 and 8.8±0.6 in hyperthyroids, respectively. Metabolic clearance of glucagon differed between hyperthyroids and euthyroids at 1 200 pg/kg/min infusion rate (p=0.001). The basal delivery rate of glucagon (ng/kg/min) was 1.3±0.1 in euthyroids and 2.9±0.6 in hyperthyroids (p=0.0005).
Conclusions: In hyperthyroidism, the secretion and metabolic clearance rates of glucagon are increased. These effects may explain the changes in plasma glucagon levels observed in hyperthyroidism and support the important role of glucagon in increasing endogenous glucose production in this condition.
Key words
endogenous glucose production - insulin resistance - thyroid hormones
References
- 1
Bratusch-Mairain P, Gasic S, Waldhausl W.
Triiodothyronine increases splachnic release and peripheral uptake of glucose in healthy
human.
Am J Physiol.
1984;
257
E681-E687
MissingFormLabel
- 2
Casla A, Rovira A, Wells J. et al .
Increased glucose transporter (GLUT4) protein expression in hyperthyroidism.
Biochem and Biophys Res Commun.
1990;
171
182-188
MissingFormLabel
- 3
Dimitriadis G, Baker B, Marsh H. et al .
Effect of thyroid hormone excess on action, secretion and metabolism of insulin in
humans.
Am J Physiol.
1985;
248
E593-E601
MissingFormLabel
- 4
Dimitriadis G, Mitrou P, Lambadiari V. et al .
Insulin-stimulated rates of glucose uptake in muscle in hyperthyroidism: the importance
of blood flow.
J Clin Endocrinol Metab.
2008;
93
2413-2415
MissingFormLabel
- 5
Dimitriadis G, Mitrou P, Lambadiari V. et al .
Glucose and lipid fluxes in the adipose tissue after meal ingestion in hyperthyroidism.
J Clin Endocrinol Metab.
2006;
91
1112-1118
MissingFormLabel
- 6 Dimitriadis G, Newsholme EA. Integration of some biochemical and physiologic effects of insulin that may play a
role in the control of blood glucose concentration. In: LeRoith D, Taylor S, Olefsky J (eds)Diabetes Mellitus, a fundamental and clinical
text Philadelphia, Baltimore, New York, London, Buenos Aires, Hong Kong, Sydney, Tokyo: Lippincott Williams and Wilkins; 2004: 183-197
MissingFormLabel
- 7
Dimitriadis G, Parry-Billings M, Bevan S. et al .
The effects of insulin on transport and metabolism of glucose in skeletal muscle from
hyperthyroid and hypothyroid rats.
Eur J Clin Invest.
1997;
27
475-483
MissingFormLabel
- 8
Dimitriadis G, Raptis SA.
Thyroid hormones and glucose intolerance.
Exp and Clin Endocrinol Diabetes.
2001;
109
(S 02)
S225-S239
MissingFormLabel
- 9 Falloona G, Unger R. Glucagon. In: Jaffe B and Behrman H (eds)Methods of Hormone Radioimmunoassay New York: Academic; 1974: 317-323
MissingFormLabel
- 10
Fisher M, Sherwin R, Hendler R. et al .
Kinetics of glucagon in man: effects of starvation.
Proc Natl Acad Sci (USA).
1976;
73
1735-1739
MissingFormLabel
- 11
Hales C, Hyams D.
Plasma concentrations of glucose nonesterified fatty acids and insulin during oral
glucose tolerance tests in thyrotoxicosis.
Lancet.
1964;
2
69-71
MissingFormLabel
- 12 Ingbar S, Woeber K. The Thyroid Gland. In: Williams R (ed) Textbook of Endocrinology Philadelphia, Toronto, London, Tokyo: WB Saunders; 1981: 117-147
MissingFormLabel
- 13
Kabadi U, Eisenstein A.
Glucose intolerance in hyperthyroidism: Role of glucagon.
J Clin Endocrinol Metab.
1980a;
50
392-396
MissingFormLabel
- 14
Kabadi U, Eisenstein A.
Impaired pancreatic a-cell response in hyperthyroidism.
J Clin Endocrinol Metab.
1980b;
51
478-482
MissingFormLabel
- 15
Klieverik LP, Janssen SF, van Riel A. et al .
Thyroid hormone modulates glucose production via a sympathetic pathway from the hypothalamic
paraventicular nucleous to the liver.
Proc Natl Acad Sci (USA).
2009;
106
5966-5971
MissingFormLabel
- 16
McCulloch A, Nosadini R, Pernet A. et al .
Glucose turnover and indices of recycling in thyrotoxicosis and primary thyroid failure.
Clin Sci.
1983;
64
41-47
MissingFormLabel
- 17
Mitrou P, Raptis SA, Dimitriadis G.
Insulin action in hyperthyroidism: a focus on muscle and adipose tissue.
Endocr rev.
2010;
31
663-679
MissingFormLabel
- 18
Mokuno T, Uchimura K, Hayashi R. et al .
Glucose transporter concentrations in hyper- and hypothyroid rat livers.
J Endocrinol.
1999;
160
285-289
MissingFormLabel
- 19
Okajima F, Ui M.
Metabolism of glucose in hyper- and hypothyroid rats in-vivo.
Biochem J.
1979a;
182
565-575
MissingFormLabel
- 20
Okajima F, Ui M.
Metabolism of glucose in hyper- and hypothyroid rats in-vivo: relation of catecholamine
actions to thyroid activity in controlling glucose turnover.
Biochem J.
1979b;
182
585-592
MissingFormLabel
- 21
Riis ALD, Jorgensen JO, Ivarsen P. et al .
Increased protein turnover and proteolysis is an early and primary feature of short-term
experimental hyperthyroidism in healthy women.
J Clin Endocrinol Metab.
2008;
93
3999-4005
MissingFormLabel
- 22
Roti E, Braverman LE, Robuschi G. et al .
Basal and glucose- and arginine-stimulated serum concentrations of insulin, c-peptide,
and glucagon in hyperthyroid patients.
Metabolism.
1986;
35
337-342
MissingFormLabel
- 23
Sandler M, Robinson R, Rabin D. et al .
The effect of thyroid hormones on gluconeogenesis and forearm metabolism in man.
J Clin Endocrinol Metab.
1983;
56
479-485
MissingFormLabel
- 24
Tosi F, Moghetti P, Castello R. et al .
Early changes in plasma glucagon and growth hormone response to oral glucose in experimental
hyperthyroidism.
Metabolism.
1996;
45
1029-1033
MissingFormLabel
- 25
Weinstein S, O’Boyle E, Fisher M. et al .
Regulation of GLUT 2 glucose transporter expression in liver by thyroid hormone: Evidence
for hormonal regulation of hepatic glucose transport system.
Endocrinology.
1994;
135
649-654
MissingFormLabel
- 26
Wennlund A, Felig P, Hagenfeldt L. et al .
Hepatic glucose production and splachnic glucose exchange in hyperthyroidism.
J Clin Endocrinol Metab.
1986;
65
174-180
MissingFormLabel
- 27
Wolf E, Eisenstein A.
Portal vein blood insulin and glucagon are increased in experimental hyperthyroidism.
Endocrinology.
1981;
108
2109-2113
MissingFormLabel
Correspondence
Prof. G. DimitriadisMD, DPhil
2 nd Department of Internal
Medicine, Research Institute
and Diabetes Center
Athens University Medical
School,“Attikon” University
Hospital
1 Rimini Street
GR-12462 Haidari
Greece
Telefon: +30/210/583 2547
Fax: +30/210/583 2561
eMail: gdimi@ath.forthnet.gr
eMail: gdimitr@med.uoa.gr