Coker, R H4; Simonsen, L1; Bülow, J2; Wasserman, D H4; Kjaer, M3
1 Anæstesiologisk Afdeling Z, Bispebjerg and Frederiksberg Hospital, The Capital Region of Denmark2 Klinisk Fysiologisk/Nuklearmedicinsk Afdeling, Bispebjerg and Frederiksberg Hospital, The Capital Region of Denmark3 Ortopædkirurgisk Afdeling M, Bispebjerg and Frederiksberg Hospital, The Capital Region of Denmark4 unknown
To determine the importance of basal glucagon to the stimulation of net splanchnic glucose output (NSGO) during exercise, seven healthy males performed cycle exercise during a pancreatic islet cell clamp. In one group (BG), glucagon was replaced at basal levels and insulin was adjusted to achieve euglycemia. In another group (GD), only insulin was replaced at the identical rate used in BG, and basal glucagon was not replaced. Exogenous glucose infusion was necessary to maintain euglycemia during exercise in BG and during rest and exercise in GD. Arterial glucagon was at least twofold greater in BG than in GD throughout the pancreatic islet cell clamp. Although basal NSGO remained stable in BG (2.5 +/- 0.5 mg x kg(-1) x min(-1)), basal NSGO dropped by 70% in GD (0.7 +/- 0.3 mg. kg(-1) x min(-1)). NSGO was also greater in BG than in GD at 10 min of moderate exercise, most likely due to the residual effect of basal glucagon replacement. However, NSGO increased slightly and remained similar throughout the remainder of moderate and heavy exercise in BG and GD. Therefore, a mechanism independent of changes in pancreatic hormones and/or the level of glycemia contributes toward modest stimulation of NSGO during moderate and heavy exercise.
American Journal of Physiology: Endocrinology and Metabolism, 2001, Vol 280, Issue 6