A set-point model with oscillatory behavior predicts the time course of 8-OH-DPAT-induced hypothermia

被引:43
作者
Zuideveld, KP
Maas, HJ
Treijtel, N
Hulshof, J
Van der Graaf, PH
Peletier, LA
Danhof, M
机构
[1] Leiden Amsterdam Ctr Drug Res, Div Pharmacol, Sylvius Lab, NL-2300 RA Leiden, Netherlands
[2] Free Univ Amsterdam, Dept Math, NL-1081 HV Amsterdam, Netherlands
[3] Leiden Univ, Inst Math, NL-2300 RA Leiden, Netherlands
关键词
pharmacokinetic-pharmacodynamic modeling; 5-hydroxytryptamine(1A) receptor; R-8-hydroxy-2-(di-n-propylamino)tetralin; S-8-hydroxy-2-(di-n-propylamino)tetralin;
D O I
10.1152/ajpregu.2001.281.6.R2059
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Agonists for the 5-hydroxytryptamine (HT)(1A) receptor induce a hypothermic response that is believed to occur by lowering of the body's set-point temperature. We have developed a physiological model that can be used to predict the complex time course of the hypothermic response after administration of 5-HT1A agonists to rats. In the model, 5-HT1A agonists exert their effect by changing heat loss through a control mechanism with a thermostat signal that is proportional to the difference between measured and set-point temperature. Agonists exert their effect in a direct concentration-dependent manner, with saturation occurring at higher concentrations. On the basis of simulations, it is shown that, depending on the concentration and the intrinsic efficacy of a 5-HT1A agonist, the model shows oscillatory behavior. The model was successfully applied to characterize the complex hypothermic response profiles after administration of the reference 5-HT1A agonists R-8-hydroxy-2-(di-n-propylamino)tetralin (R-8-OH-DPAT) and S-8-OH-DPAT. This analysis revealed that the observed difference in effect vs. time profile for these two reference agonists could be explained by a difference in in vivo intrinsic efficacy.
引用
收藏
页码:R2059 / R2071
页数:13
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