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- 2008
Mechanism-based pharmacodynamic modeling of S(-)-atenolol: estimation of in vivo affinity for the beta1-adrenoceptor with an agonist-antagonist interaction model,
J Pharmacol Exp Ther, vol. 324, no. 3, pp. 1234-42.
- 2007
Pharmacokinetic-pharmacodynamic modelling of S(-)-atenolol in rats: reduction of isoprenaline-induced tachycardia as a continuous pharmacodynamic endpoint,
Br J Pharmacol, vol. 151, no. 3, pp. 356-66.
Reproducible and time-dependent modification of serum protein binding in Wistar Kyoto rats,
J Pharmacol Toxicol Methods, vol. 56, no. 1, pp. 72-8.
- 1997
On the reliability of affinity and efficacy estimates obtained by direct operational model fitting of agonist concentration-effect curves following irreversible receptor inactivation,
J Pharmacol Toxicol Methods, vol. 38, no. 2, pp. 81-5.
Determination of dexmedetomidine in rat plasma by a sensitive [3H]clonidine radioreceptor assay,
J Pharm Sci, vol. 86, no. 7, pp. 822-6.
Pharmacokinetic-pharmacodynamic characterization of the cardiovascular, hypnotic, EEG and ventilatory responses to dexmedetomidine in the rat,
J Pharmacol Exp Ther, vol. 283, no. 3, pp. 1051-8.
- 1995
Application of intracerebral microdialysis to study regional distribution kinetics of drugs in rat brain,
Br J Pharmacol, vol. 116, no. 5, pp. 2538-44.



