Impaired Feedback Inhibition of Insulin Secretion by Hyperinsulinemia in Patients with Insulinoma

By means of the euglycemic three step hyperinsulinemic clamp technique, suppression of endogenous C-peptide secretion by exogenous insulin infusion was evaluated in patients with insulinoma (n=8) and healthy controls (n=20). Euglycemic hyperinsulinemic clamp studies were performed with an artificial...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Endocrine Journal 1995, Vol.42(1), pp.39-42
Hauptverfasser: HIRAMATSU, SHINSUKE, SAKO, YASUHIRO, MIMURA, KAZUO, ONO, YASUHIRO, IWASHIGE, KENICHI, TANIGUCHI, SUSUMU, UMEDA, FUMIO, NAWATA, HAJIME
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:By means of the euglycemic three step hyperinsulinemic clamp technique, suppression of endogenous C-peptide secretion by exogenous insulin infusion was evaluated in patients with insulinoma (n=8) and healthy controls (n=20). Euglycemic hyperinsulinemic clamp studies were performed with an artificial pancreas (STG-22 NIKKISO, Tokyo, Japan). Insulin (Actrapid human insulin) was infused at the rate of 1.12, 3, and 10mU/kg/min. Plasma glucose levels were clamped at 80mg/dl, and high insulin levels were maintained in all subjects (833±78μU/ml at the rate of 10mU/kg/min insulin infusion). During the clamp studies, plasma C-peptide levels in normal subjects declined from 2.0±0.2 to 0.9±0.2ng/ml, indicating suppression of endogenous insulin secretion by exogenous insulin infusion. In patients with insulinoma, plasma C-peptide levels were 3.1±1.6ng/ml in the basal state, and were not suppressed even during exogenous hyperinsulinemia. We concluded that the feedback inhibition of insulin secretion by exogenous insulin infusion is attenuated in patients with insulinoma, and that the hyperinsulinemic clamp technique may be a useful method for the diagnosis of insulinoma.
ISSN:0918-8959
1348-4540
DOI:10.1507/endocrj.42.39