Measurement of Pulsatile Insulin Secretion: Rationale and Methodology.
C-peptide kinetics
hormone deconvolution
insulin pulses
pulsatile insulin secretion
Journal
Metabolites
ISSN: 2218-1989
Titre abrégé: Metabolites
Pays: Switzerland
ID NLM: 101578790
Informations de publication
Date de publication:
22 Jun 2021
22 Jun 2021
Historique:
received:
31
05
2021
revised:
17
06
2021
accepted:
18
06
2021
entrez:
2
7
2021
pubmed:
3
7
2021
medline:
3
7
2021
Statut:
epublish
Résumé
Pancreatic β-cells are responsible for the synthesis and exocytosis of insulin in response to an increase in circulating glucose. Insulin secretion occurs in a pulsatile manner, with oscillatory pulses superimposed on a basal secretion rate. Insulin pulses are a marker of β-cell health, and secretory parameters, such as pulse amplitude, time interval and frequency distribution, are impaired in obesity, aging and type 2 diabetes. In this review, we detail the mechanisms of insulin production and β-cell synchronization that regulate pulsatile insulin secretion, and we discuss the challenges to consider when measuring fast oscillatory secretion in vivo. These include the anatomical difficulties of measuring portal vein insulin noninvasively in humans before the hormone is extracted by the liver and quickly removed from the circulation. Peripheral concentrations of insulin or C-peptide, a peptide cosecreted with insulin, can be used to estimate their secretion profile, but mathematical deconvolution is required. Parametric and nonparametric approaches to the deconvolution problem are evaluated, alongside the assumptions and trade-offs required for their application in the quantification of unknown insulin secretory rates from known peripheral concentrations. Finally, we discuss the therapeutical implication of targeting impaired pulsatile secretion and its diagnostic value as an early indicator of β-cell stress.
Identifiants
pubmed: 34206296
pii: metabo11070409
doi: 10.3390/metabo11070409
pmc: PMC8305896
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : NIH HHS
ID : DK126206
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR000137
Pays : United States
Organisme : Mayo Clinic General Clinical Research Center
ID : DK TR000135
Organisme : NIDDK NIH HHS
ID : R01 DK126206
Pays : United States
Organisme : NIH HHS
ID : DK116231
Pays : United States
Organisme : NIH HHS
ID : DK78646
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK116231
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK078646
Pays : United States
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