American Journal of Physiology-Endocrinology and MetabolismPhysiologyPeer-reviewed journal article
Assessing the Rate-Dependence of the First Phase of Glucose-Stimulated Insulin Secretion: Dynamic Perifusion Studies with Isolated Human Pancreatic Islets
Péter BuchwaldiD, Sung-Ting ChuangiD, Brandon Watts, Oscar Alcazar
Abstract
Insulin released in response to a stepwise increase in glucose (square wave) is biphasic with a transient first-phase peak of 5-10 min and a more sustained second phase. While it is usually assumed that the first phase is rate- and the second is concentration-dependent, there are no detailed investigations into the rate-sensitivity of the first phase. We performed dynamic perifusion studies with isolated human pancreatic islets in a system that allowed fully customizable glucose ramps and established the corresponding insulin secretion time-profiles with high (once-a-minute) time-resolution. We considered the first-phase release to be the excess amount of insulin in addition to what would be expected from the glucose concentration-dependent second-phase release and examined its dependence on the glucose gradient (rate of increase). The average first-phase insulin release rate calculated this way increased with the gradient and could be fitted well with a Hill-type sigmoid function having a half-maximal value around 1.25 mM/min (nHill=1.8, r2=0.96). This agrees well with our previously introduced glucose-insulin control system built on a general framework of a sigmoid proportional-integral-derivative ({sigma}PID) controller, a generalized PID controller more suitable for biological systems than classic linear ones as biological responses are always limited between zero and a possible maximum. Experimental results obtained here were used to slightly readjust the parameters of this local glucose concentration-based computational model resulting in predictions in good agreement with measured first- and second-phase insulin secretions (r2>0.90). Thus, glucose-stimulated insulin secretion (GSIS) of perifused human islets can be described well as the sum of a rate-sensitive first phase, which is a sigmoid function of the glucose gradient with half-maximal value around 1.25 mM/min, and a concentration-sensitive second phase, which is a sigmoid function of the glucose concentration with half-maximal value around 8 mM.
- Citations
- 2
- FWCI
- 1.87
- Field percentile
- top 13%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Insulin secretion chip (InS-chip) reveals two peaks within first-phase that temporally coincide with a transition in glucose metabolism.
Y. Wang, R. Regeenes, … J. V. Rocheleau·bioRxiv·Mar 7, 2023
- A Consensus Model of Glucose-Stimulated Insulin Secretion in the Pancreatic beta-Cell
M. Deepa Maheshvare, Soumyendu Raha, … Debnath Pal·bioRxiv·Mar 10, 2023
- Evaluating the Importance of Glucagon in the Insulin-Glucose Regulatory System: A Mechanistic Modeling Approach
Mackenzie Dalton, Emmanuel Asante-Asamani, James M. Greene·Evaluating the Importance of Glucagon in the Insulin-Glucose Regulatory System: A Mechanistic Modeling ApproachPeer-reviewed·Jan 1, 2024
- An INS-1 beta-cell proteome highlights the role of fatty acid biosynthesis in glucose-stimulated insulin secretion
Nina Stremmel, Oliver Lemke, … Markus Ralser·PROTEOMICSPeer-reviewed·Jul 20, 2025
- Effect of Immunosuppressive Drugs on Glucose-Stimulated Insulin Secretion: Concentration-Response Studies in Dynamic Perifusion Assays
Sung-Ting Chuang, Brandon Watts, … Péter Buchwald·Frontiers in ImmunologyPeer-reviewed·Oct 5, 2026
- Continuous variable response, kinetic gating and connectivity that determine topology of insulin signaling are perturbed in hyper-insulinemic states
Namrata Shukla, Shantanu Kadam, … Ullas Kolthur‐Seetharam·bioRxiv·Jul 27, 2020