Skip to main content
Log in

Determination of plasma and brain concentrations of SCH 39166 and their correlation to conditioned avoidance behavior in rats

  • Original Investigations
  • Published:
Psychopharmacology Aims and scope Submit manuscript

Abstract

Plasma and brain concentrations of the dopamine D1 receptor antagonist, SCH 39166, were measured and compared to behavioral activity in the conditioned avoidance response paradigm (CAR). SCH 39166 was administered at two behaviorally active doses (1 mg/kg, SC and 10 mg/kg, PO) and the time course for CAR activity was compared with the plasma and brain concentrations of unconjugated SCH 39166. Conjugation andN-demethylation of SCH 39166 after oral administration were also determined and first pass metabolism examined. Results from these studies demonstrated a similar time-dependent disappearance of unconjugated SCH 39166 from both the plasma and brain, independent of route of administration. Brain concentrations of SCH 39166 were approximately 5-fold higher than corresponding plasma concentrations, regardless of route. However, plasma and brain concentrations of unconjugated SCH 39166 were higher after SC administration of 1.0 mg/kg, than after PO administration of 10 mg/kg, suggesting a substantial first pass metabolism of SCH 39166. In addition, total (conjugated and unconjugated) plasma concentrations of SCH 39166 were at least 10-fold higher than unconjugated concentrations of SCH 39166 after PO administration of 10 mg/kg, demonstrating that a high proportion of drug was conjugated. Metabolism to theN-desmethyl analog, SCH 40853, was observed after PO administration of 10 mg/kg SCH 39166 and a high proportion of conjugation of the desmethyl analog was also seen. Finally, plasma concentrations of unconjugated SCH 39166 exhibited a high positive correlation (r=0.934,P<0.001) with brain concentrations of unconjugated SCH 39166. Behavioral activity in the CAR was also positively correlated with plasma concentrations (r=0.95,P<0.001) and brain concentrations (r=0.88,P<0.001) of unconjugated SCH 39166.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Barnett A, lorio LC, McQuade RM, Chipkin RE (1988) Pharmacological and behavioral effects of D1 dopamine antagonists. In: Goldstein, Fuxe, Tabachnick (eds) Central D1 dopamine receptors. Plenum, New York, pp. 137–144

    Google Scholar 

  • Chipkin RE (1990) D1 antagonist in clinical trial. TIPS 11:185

    Google Scholar 

  • Chipkin RE, lorio LC, Coffin VL, McQuade RD, Berger JG, Barnett A (1988) Pharmacological profile of SCH 39166: a dopamine D1 selective benzonaphthazepine with potential antipsychotic activity. J Pharmacol Exp Ther 247:1093–1102

    Google Scholar 

  • Coffin VL, Latranyi MB, Chipkin RE (1989) Acute extrapyramidal syndrome in cebus monkeys: development mediated by dopamine D2 but not D1 receptors. J Pharmacol Exp Ther 249:769–774

    Google Scholar 

  • Coffin VL, McHugh D, Chipkin RE, Barnett A (1992) SCH 39166, a potential antipsychotic drug, does not evoke movement disorders in cebus monkeys. Neurochem Int 20 [Suppl]: 141S-145S

    Google Scholar 

  • Cook L, Davidson AB (1978) Behavioral pharmacology: animal models involving aversive control of behavior. In: Lipton, M.A., Dimascio, A., Killam K. (eds) Psychopharmacology: a generation of progress. Raven, New York, p. 563

    Google Scholar 

  • Davidson AB, Weidley E (1976) Differential effects of neuroleptics and other psychotropic agents on acquisition of avoidance in rats. Life Sci 18:1279–1285.

    Google Scholar 

  • Hietala J, Seppälä T, Lappalainen J, Syvälahti E (1992) Quantification of SCH 39166, a novel selective D1 dopamine receptor antagonist, in rat brain and blood. Psychopharmacology 106:455–458

    Google Scholar 

  • lorio LC, Barnett A, Leitz FH, Houser VP, Korduba CA (1983) SCH 23390, a potential benzazepine antipsychotic with unique interactions on dopaminergic systems. J Pharmacol Exp Ther 226:462–468

    Google Scholar 

  • McQuade RD, Duffy RA, Coffin VL, Chipkin RE, Barnett A (1991) In vivo binding of SCH 39166: a selective D1 antagonist. J Pharmacol Exp Ther 257:42–49.

    Google Scholar 

  • McQuade RD, Duffy RA, Coffin VL, Barnett A (1992) In vivo binding to dopamine receptors: a correlate of potential antipsychotic activity. Eur J Pharmacol 215:29–34.

    Google Scholar 

  • Tedford CE, Ruperto VB, Barnett A (1991) Characterization of rat liver glucuronosyltransferase that glucuronidates the selective D1 antagonist, SCH 23390 and other benzazepines. Drug Metab Dispos 19:1152–1159

    Google Scholar 

  • Tedford CE, Ruperto V, Coffin VL, Winston-Cohen M, Libonati M, Barnett A (1992a) Glucuronidation of a novel D1 receptor antagonist, SCH 39166: characterization and species differences. Drug Dev Res 26:389–404

    Google Scholar 

  • Tedford CE, Crosby GJr, lorio LC, Chipkin RE (1992b) Effect of SCH 39166, a novel dopamine D1 receptor antagonist, on [3H] acetylcholine release in rat striatal slices. Eur J Pharmacol 211:169–176

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tedford, C.E., Coffin, V.L., Ruperto, V. et al. Determination of plasma and brain concentrations of SCH 39166 and their correlation to conditioned avoidance behavior in rats. Psychopharmacology 113, 199–204 (1993). https://doi.org/10.1007/BF02245697

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02245697

Key words

Navigation