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. Author manuscript; available in PMC: 2014 Sep 30.
Published in final edited form as: Pharm Res. 2006 Feb 2;23(4):670–679. doi: 10.1007/s11095-005-9608-3

Table II.

Estimated and Fixed Pharmacodynamic Parameters for GS Modeling

Parameter Definition Value CV (%)
α Intracellular/plasma ratio 0.0175 67
Bmax_normal (fmol mg protein−1) Cytosolic GR density in normal rats 44.0 90
τ (h) Mean transit time 1.13 65
kdgr_GSm (h−1) GS mRNA degradation rate 0.203 41
S [(fmol/mg protein)−1] Stimulatory coefficient 0.142 28
kdgr_GS (h−1) GS Degradation Rate 0.0512 19
ksyn_GSm_normal (fmol g tissue−1 h−1) GS mRNA synthesis rate in normal rats 0.267 109
ksyn_GS_normal (µmol min−1 g protein−1 h−1) GS synthesis rate in normal rats 0.210 20
ksyn_GSm_ADX (fmol g tissue−1 h−1) GS mRNA synthesis rate in ADX rats 0.487 a
ksyn_GS_ADX (µmol min−1 g protein−1 h−1) GS synthesis rate in ADX rats 0.370 a
Kd_CS (nM) Corticosterone dissociation constant 5.13 Fixed
Kd_HYD (nM) Hydrocortisone dissociation constant 13.5 Fixed
Kd_DEX (nM) Dexamethasone dissociation constant 1.32 Fixed
Bmax_ADX (fmol mg protein−1) Cytosolic GR density in ADX rats 66.3 Fixed
GSm_ADX0 (fmol g tissue−1) GS mRNA baseline in ADX rats 2.43 Fixed
GSADX0 (µmol min−1 g protein−1) GS activity baseline in ADX rats 17.6 Fixed
a

Secondary parameter calculated from degradation rate and baseline.