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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Biotechnol Bioeng. 2017 Sep 19;115(1):232–245. doi: 10.1002/bit.26442

Table 2.

Summary of Hill function parameters used in the present model (Figure 1 and eq. 2; for detailed equations see (Buchwald, 2011)).

Rate Var. CHf n Rmax Property and comments
Roxy coxy 1 μM 1 −0.034 mol/m3/s Oxygen consumption, basic part.
Cut to 0 below critical value, coxy < Ccr,oxy.
Roxy cgluc 7 mM 2.5 N/A Oxygen consumption, φo,g metabolic part. Follows increase in metabolic demand; parallels second-phase insulin secretion rate.
Rgluc cgluc 10 μM 1 −0.028 mol/m3/s Glucose consumption. Under most conditions, it has no significant influence on insulin secretion.
Rins,ph2 cgluc 7 mM 2.5 H: 1.8×10−5 mol/m3/s
M: 3×10−5 mol/m3/s
Insulin secretion rate (second-phase). Total secretion rate is modulated by local oxygen availability (last row). H and M denote values used for human and murine islets, respectively.
Rins,ph1 ct (∂cgluc/∂t) 0.03 mM/s 2 H: 10×10−5 mol/m3/s
M: 21×10−5 mol/m3/s
Insulin secretion rate (first-phase). Modulated to have maximum sensibility around cgluc = 5 mM and be limited at very large or low cgluc. Hill slope of modulating function, σi1,g, changed to 2.5 (previously 4) for a wider range response in phase 1. Release rates kinsL are H: 0.003, M: 0.006 s−1.
Rins, φo,g coxy 3 μM 3 N/A Oxygen modulation of insulin secretion rate, φo,g.
Limits insulin secretion if coxy becomes critically low.