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Updated: Aug 15, 2026

Glucose-Stimulated Insulin Secretion via Perfusion through the Mice Vasculature with an Intact Pancreas
Published on: July 25, 2025
Pulsatile insulin secretion in isolated rat islets
Insights
Isolated islets exhibit pulsatile insulin secretion, indicating islets themselves may act as pacemakers for this crucial endocrine function. This finding advances understanding of glucose regulation and insulin dynamics.
Area of Science:
- Endocrinology
- Metabolic Research
- Cellular Physiology
Background:
- Pancreatic insulin secretion occurs in an oscillatory pattern.
- The specific pacemaker for pulsatile insulin release remains unidentified.
Purpose of the Study:
- To investigate if isolated islets secrete insulin in a pulsatile manner.
- To determine if islets possess intrinsic pacemaking capabilities for insulin secretion.
Main Methods:
- Isolated rat islets were perifused for 8 hours.
- Insulin secretion was collected at 3.3-minute intervals.
- Pulsatility was analyzed using the Clifton Cycle Detection Program.
Main Results:
- Perifused islets demonstrated spontaneous, regular pulsatile insulin secretion under all tested conditions.
- Higher glucose concentrations (16.7 mM) significantly increased insulin secretion periodicity and amplitude compared to 5.5 mM glucose.
- Theophylline enhanced insulin secretion amplitude and overall concentration, also increasing cycle period.
Conclusions:
- Isolated islets exhibit intrinsic pulsatile insulin secretion.
- These findings suggest that islets may contain the pacemaker for pulsatile insulin release.
- Islet pulsatility is modulated by glucose concentration and pharmacological agents like theophylline.
Abstract:
The pancreas secretes insulin in an oscillatory fashion, but the precise site of the pacemaker for pulsatile insulin secretion has not been identified. These studies were designed to determine whether islets also secrete insulin in a pulsatile fashion if they are isolated from their pancreatic milieu. Isolated rat islets (80-100) were perifused 8 h in culture medium after overnight incubation, and samples were collected at 3.3-min intervals. Insulin secretion was evaluated for pulsatility with the Clifton Cycle Detection Program. Perifusion of islets was associated with a spontaneous, persistent, and regular pulsatility of insulin secretion, which was observed in all conditions tested. Perifusion with medium containing 5.5 mM glucose (n = 11) demonstrated oscillations with a mean periodicity of 17.6 +/- 1.1 min and a mean amplitude of 4.8 +/- 0.4 microU/ml when overall mean insulin concentration was 16.7 +/- 2.4 microU/ml. When the glucose concentration was 16.7 mM (n = 9), overall mean insulin concentration was 54.4 +/- 2.6 microU/ml, with increases in periodicity (22.0 +/- 1.3 min) and amplitude (10.7 +/- 0.5 microU/ml). All measurements were significantly different from those observed during perifusion with 5.5 mM glucose (P less than 0.02-0.001). Theophylline (1 mM) also enhanced the overall mean insulin concentration and amplitude (69.4 +/- 10.4 and 14.2 +/- 1.2 microU/ml, respectively) compared with control studies without theophylline (16.7 +/- 5.3 and 4.3 +/- 0.5 microU/ml) (P less than 0.01). The period of the cycle was also increased from 17.5 +/- 1.1 to 26.4 +/- 6.3 min, but this was not significantly different from the control group.(ABSTRACT TRUNCATED AT 250 WORDS)
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