Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1978 Mar;27(3):341-51.
doi: 10.1016/0026-0495(78)90114-2.

Plasma insulin patterns in the unanesthetized rat during intracardial infusion and spontaneous ingestion of graded loads of glucose

Free article

Plasma insulin patterns in the unanesthetized rat during intracardial infusion and spontaneous ingestion of graded loads of glucose

J H Strubbe et al. Metabolism. 1978 Mar.
Free article

Abstract

Rats were provided with double permanent heart catheters, allowing simultaneous infusion and rapid blood sampling in the freely moving animals. Intracardial glucose infusion (75, 150, and 300 mg) over 15-min periods induced biphasic plasma insulin responses, their onset and magnitude being correlated with the blood glucose increments. The insulin-ogenic index decreased at increasing infused loads. After spontaneous oral ingestion of 75, 150, 300, and 750 mg glucose over 2 min or less, plasma insulin increased rapidly during the initial 4 to 8 min. At the highest leads this was followed by a gradual further increase until 15 min. The rapid insulin response increased with the ingested load. About half of this response had occurred already at 2 min, i.e., prior to the first rise of blood glucose at 3 min. Maximum blood glucose levels (125-135 mg/dl) occurred between 8 and 15 min and did not correlate with the ingested loads. The insulinogenic index increased at higher oral loads. It is suggested that the plasma insulin response to glucose ingestion results from successive and cumulative operation of anticipatory nervously triggered insulin secretion, anticipatory loaded-dependent potentiation of secretory stimulation by rising blood glucose, and further adjustment of the secretion rate until blood glucose declines. The possible mechanisms are discussed.

PubMed Disclaimer

LinkOut - more resources