Direct effects of glucagon on glucose uptake and lipolysis in human adipocytes

Pereira, Maria J, 1981- (author): Uppsala universitet,Klinisk diabetologi och metabolism

Thombare, Ketan (author): Uppsala universitet,Klinisk diabetologi och metabolism

Sarsenbayeva, Assel (author): Uppsala universitet,Klinisk diabetologi och metabolism

Kamble, Prasad G. (author): Uppsala universitet,Klinisk diabetologi och metabolism

Almby, Kristina (author): Uppsala universitet,Klinisk diabetologi och metabolism

Lundqvist, Martin (author): Uppsala universitet,Klinisk diabetologi och metabolism

Eriksson, Jan W. (author): Uppsala universitet,Klinisk diabetologi och metabolism,Uppsala Univ, Dept Med Sci, Clin Diabet & Metab, Uppsala, Sweden

(creator_code:org_t)

ELSEVIER IRELAND LTD, 2020
2020
English.
In: Molecular and Cellular Endocrinology. - : ELSEVIER IRELAND LTD. - 0303-7207 .- 1872-8057. ; 503

Related links:: https://urn.kb.se/re...; show more...; https://doi.org/10.1...; show less...

Abstract Subject headings

We aim to investigate the expression of the glucagon receptor (GCGR) in human adipose tissue, and the impact of glucagon in glucose uptake and lipolysis in human adipocytes. GCGR gene expression in human subcutaneous and visceral adipose tissue was demonstrated, albeit at low levels and with an inter-individual variation. Furthermore, GCGR expression was not significantly different between subjects with T2D and matched controls, and we found no significant association with BMI. Glucagon only at a supra-physiological concentration (10-100 nM) significantly increased basal and insulin-stimulated glucose uptake by up to 1.5-fold. Also, glucagon (0.01 and 1 nM) dose-dependently increased basal and isoproterenol-stimulated lipolysis up to 3.7- and 1.7-fold, respectively, compared to control. In addition, glucagon did not change insulin sensitivity to stimulate glucose uptake or inhibit lipolysis. In conclusion, we show that the GCGR gene is expressed at low levels in human adipose tissue, and glucagon at high concentrations can increase both glucose uptake and lipolysis in human adipocytes. Taken together, our data suggest that glucagon at physiological levels has minor direct effects on the regulation of adipocyte metabolism, but does not antagonize the insulin effect to stimulate glucose uptake and inhibit lipolysis in human adipocytes.

By the author/editor: Pereira, Maria J ...; Thombare, Ketan; Sarsenbayeva, As ...; Kamble, Prasad G ...; Almby, Kristina; Lundqvist, Marti ...; show more...; Eriksson, Jan W.; show less...

About the subject

MEDICAL AND HEALTH SCIENCES: MEDICAL AND HEAL ...; and Clinical Medicin ...; and Endocrinology an ...

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