Molecular Neurobiology

, Volume 11, Issue 1–3, pp 31–46 | Cite as

Behavioral sensitization and tolerance to cocaine and the occupation of dopamine receptors by dopamine

  • Mathew Thomas Martin-Iverson
  • Lynn Yvonne Burger
Proceedings of the Symposium Cellular and Molecular Mechanisms of Drugs of Abuse Cocaine and Methamphetamine held in Nice, France, August 19–20, 1993

Abstract

Data from the authors’ laboratory on the neural substrates of Pavlovian conditioning and behavioral sensitization to psychomotor stimulants are reviewed. The findings of a recent experiment on the role of occupation of dopamine receptors by dopamine and its association to behavioral sensitization are reported. Daily intermittent injections of cocaine produced behavioral sensitization to the locomotor response in rats, whereas continuous cocaine infusions produced behavioral tolerance. Behavioral sensitization to cocaine was blocked by coadministration of nimodipine, anL-type calcium channel blocker. The increases in locomotion produced by cocaine was associated with an increase in the occupation of striatal dopamine D1 and D2 receptors, measured as the density of receptors protected from denaturation byN-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ). This association was not observed when rats were given a challenge injection of cocaine 10 d after withdrawal from similar treatment regimens. Rats given a cocaine challenge after withdrawal from either intermittent or continuous cocaine treatment regimens exhibited increased occupations of striatal D1 and D2 receptors. This increase was similar in magnitude to that observed in rats without a history of cocaine treatments after a challenge injection of cocaine. This suggests tnat the differences in occupancy of striatal dopamine receptors by dopamine observed in the prewithdrawal condition are likely the result of differences in brain levels of cocaine achieved by the two treatment regimens. Occupancy of striatals dopamine D1 and D2 receptors does not appear to be related to the development of sensitization to the motor-stimulating effects of cocaine.

Index Entries

Cocaine sensitization tolerance dopamine receptor occupation treatment regimen nimodipine D1 D2 dopamine release 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Akimoto K., Hamamura T., and Otsuki S. (1989) Subchronic cocaine treatment enhances cocaine-induced dopamine efflux: studies byin vivo intracerebral dialysis.Brain Res. 490, 339–344.PubMedCrossRefGoogle Scholar
  2. Akimoto K., Hamamura T., Kazahaya Y., Akiyama K., and Otsuki S. (1990) Enhanced extracellular dopamine levels may be the fundamental neuropharmacological basis of cross-behavioral sensitization between methamphetamine and cocaine —anin vivo dialysis study in freely moving rats.Brain Res. 507, 344–346.PubMedCrossRefGoogle Scholar
  3. Angrist B. (1983) Psychoses induced by central nervous system stimulants and related drugs, inStimulants: Neurochemical, Behavioral, and Clinical Perspectives (Creese I., ed.), Raven, New York, pp. 1–30.Google Scholar
  4. Arbuthnott G. W., Fairbrother I. S., and Butcher S. P. (1990) Dopamine release and metabolism in the rat striatum: an analysis by “in vivo” brain microdialysis.Pharmacol. Ther. 48, 281–293.PubMedCrossRefGoogle Scholar
  5. Arnold E. B., Molinoff P. B., and Rutledge C. O. (1977) The release of endogeneous norepinephrine and DA from cerebral cortex by amphetamine.J. Pharmacol. Exp. Ther. 202, 544–557.PubMedGoogle Scholar
  6. Barr G. A., Sharpless N. S., Cooper S., Schiff S. R., Paredes W., and Bridger, W. H. (1983) Classical conditioning, decay and extinction of cocaine-induced hyperactivity and stereotypy.Life Sci. 33, 1341–1351.PubMedCrossRefGoogle Scholar
  7. Beninger R. J. and Hahn B. (1983) Pimozide blocks establishment but not expression of amphetamine-produced environment-specific conditioning.Science 220, 1304–1306.PubMedCrossRefGoogle Scholar
  8. Beninger R. J. and Herz R. S. (1986) Pimozide blocks establishment but not expression of cocaine-produced environment-specific conditioning.Life Sci. 38, 1425–1431.PubMedCrossRefGoogle Scholar
  9. Brown E. E. and Fibiger H. C. (1992) Cocaine-induced conditioned locomotion: absence of increases in dopamine release.Neurosci. 48, 621–629.CrossRefGoogle Scholar
  10. Brown E. E., Robertson G. S., and Fibiger H. C. (1992) Evidence for conditional neuronal activation following exposure to a cocaine-paired environment: role of forebrain limbic structures.J. Neurosci. 12, 4112–4121.PubMedGoogle Scholar
  11. Burger L. Y. and Martin-Iverson M. T. (1993) Day/night differences in D1 but not D2 DA receptor protection from EEDQ denaturation in rats treated with continuous cocaine.Synapse 13, 20–29.PubMedCrossRefGoogle Scholar
  12. Burger L. Y. and Martin-Iverson M. T. (1994) Increased occupation of D1 and D2 dopamine receptors accompanies cocaine-induced behavioural sensitization.Brain Res. 639, 228–232.PubMedCrossRefGoogle Scholar
  13. Castenada E., Becker J. B., and Robinson T. W. (1988) The long-term effects of repeated amphetamine treatment in vivo on amphetamine, KCl and electrical stimulation evoked striatal dopamine release in vitro.Life Sci. 42, 2447–2456.CrossRefGoogle Scholar
  14. Damianopoulos E. N. and Carey R. J. (1992) Conditioning, habituation and behavioral reorganization factors in chronic cocaine effects.Behav. Brain Res. 49, 149–157.PubMedCrossRefGoogle Scholar
  15. DiLullo S. L. and Martin-Iverson M. T. (1991) Presynaptic dopaminergic neurotransmission mediates amphetamine-induced unconditioned but not amphetamine-conditioned locomotion and defecation in the rat.Brain Res. 568, 45–54.CrossRefGoogle Scholar
  16. DiLullo S. L. and Martin-Iverson M. T. (1992a) Evidence for presynaptic dopamine mechanisms underlying amphetamine-conditioned locomotion.Brain Res. 578, 161–167.PubMedCrossRefGoogle Scholar
  17. DiLullo S. L. and Martin-Iverson M. T. (1992b) Calcium channel blockade interacts with a neuroleptic to attenuate the conditioning of amphetamine’s behavioral effects in the rat.Biol. Psychiat. 31, 1143–1150.PubMedCrossRefGoogle Scholar
  18. Drew K. L. and Glick S. D. (1988) Characterization of the associative nature of sensitization to amphetamine-induced circling behavior and of the environment dependent placebo-like response.Psychopharmacology 95, 482–487.PubMedCrossRefGoogle Scholar
  19. Eikelboom R. and Stewart J. (1982) Conditioning of drug-induced physiological responses.Psychol. Rev. 89, 507–528.PubMedCrossRefGoogle Scholar
  20. Ellison G. (1992) Continuous amphetamine and cocaine have similar neurotoxic effects in lateral habenular nucleus and fasciculus retroflexus.Brain Res. 598, 353–356.PubMedCrossRefGoogle Scholar
  21. Fischer J. F. and Cho A. K. (1979) Chemical release of DA from striatal homogenates: evidence for an exchange diffusion model.J. Pharmacol. Exp. Ther. 192, 642–653.Google Scholar
  22. Gold L. H., Swerdlow N. R., and Koob G. F. (1988) The role of mesolimbic dopamine in conditioned locomotion produced by amphetamine.Behav. Neurosci. 102, 544–552.PubMedCrossRefGoogle Scholar
  23. Hinson R. E. and Poulos C. X. (1981) Sensitization of the behavioral effects of cocaine: modification by Pavlovian conditioning.Pharmacol. Biochem. Behav. 15, 559–562.PubMedCrossRefGoogle Scholar
  24. Hurd Y. L., Weiss F., Koob G. F., and Ungerstedt N. (1989) Cocaine reinforcement and extracellular dopamine overflow in rat nucleus accumbens: anin vivo microdialysis study.Brain Res. 498, 199–203.PubMedCrossRefGoogle Scholar
  25. Johanson C.-E. and Fischman M. W. (1989) The pharmacology of cocaine related to its abuse.Pharmacol. Rev. 41, 3–52.PubMedGoogle Scholar
  26. Kalivas P. W. and Duffy P. (1990) The effect of acute and daily cocaine treatment on extracellular dopamine in the nucleus accumbens.Synapse 5, 48–58.PubMedCrossRefGoogle Scholar
  27. Kalivas P. W. and Duffy P. (1993) Time course of extracellular dopamine and behavioral sensitization to cocaine. I. dopamine axon terminals.J. Neurosci. 13, 266–275.PubMedGoogle Scholar
  28. Kazahaya Y., Akimoto K., and Saburo O. (1989) Subchronic methamphetamine treatment enhances methamphetamine- or cocaine-induced dopamine effluxin vivo.Biol. Psychiat. 25, 903–912.PubMedCrossRefGoogle Scholar
  29. Kiess H. O. (1989)Statistical Concepts for the Behavioral Sciences. Allyn and Bacon, Boston, pp. 326–331.Google Scholar
  30. King G. R., Joyner C., Lee T., and Ellinwood E. H. (1992) Intermittent and continuous cocaine administration: residual behavioral states during withdrawal.Pharmacol. Biochem. Behav. 43, 243–248.PubMedCrossRefGoogle Scholar
  31. King G. R., Kuhn C., and Ellinwood E. (1993) Dopamine efflux during withdrawal from continuous or intermittent cocaine.Psychopharmacology 111, 179–184.PubMedCrossRefGoogle Scholar
  32. Kleven M. S., Woolverton W., and Seiden L. (1988) Lack of long-term monoamine depletions following repeated or continuous exposure to cocaine.Brain Res. Bull. 21, 233–237.PubMedCrossRefGoogle Scholar
  33. Kuczenski R. (1978) Biochemical actions of amphetamine and other stimulants, inStimulants: Neurochemical, Behavioral, and Clinical Perspectives (Creese I., ed.), Raven, New York, pp. 31–61.Google Scholar
  34. Kuczenski R. and Segal D. S. (1990)In vivo measures of monoamines during amphetamine-induced behavior in rat.Prog. Neuropsychopharmacol. Biol. Psychiat. 14, S37-S50.CrossRefGoogle Scholar
  35. Martin-Iverson M. T. (1991a) An animal model of stimulant-induced psychoses, inNeuromethods, vol. 19. Animal Models in Psychiatry I (Boulton A. A., Baker G. B., and Martin-Iverson M. T., eds.), Humana, Clifton, NJ, pp. 103–149.CrossRefGoogle Scholar
  36. Martin-Iverson M. T. (1991b) Chronic treatment with D1 and D2 dopamine receptor agonists: combined treatments interact to differentially affect brain levels of monoamines.Naunyn-Schmiedebergs Arch. Pharmacol. 344, 281–285.PubMedGoogle Scholar
  37. Martin-Iverson M. T. and McManus D. (1990) Stimulant-conditioned locomotion is not affected by blockade of D1 and/or D2 receptors during conditioning,Brain Res. 521, 175–184.PubMedCrossRefGoogle Scholar
  38. Martin-Iverson M. T. and Reimer A. R. (1994) Effects of nimodipine and/or haloperidol on the expression of conditioned locomotion and sensitization to cocaine in rats.Psychopharmacology 114, 315–320.PubMedCrossRefGoogle Scholar
  39. Martin-Iverson M. T. and Yamada N. (1992) Synergistic behavioral effects of dopamine D1 and D2 agonists are determined by circadian rhythms.Eur. J. Pharmacol. 215, 119–125.PubMedCrossRefGoogle Scholar
  40. Martin-Iverson M. T., Stahl S. M., and Iversen S. D. (1988a) Chronic administration of a selective dopamine D2 agonist: factors determining behavioral tolerance and sensitization.Psychopharmacology 95, 534–539.PubMedCrossRefGoogle Scholar
  41. Martin-Iverson M. T., Iversen S. D., and Stahl S. M. (1988b) Long-term motor stimulant effects of (+)-4-propyl-9-hydroxynaphthoxazine (PHNO), a dopamine D2 receptor agonist: interactions with a dopamine D1 receptor antagonist and agonist.Eur. J. Pharmacol. 149, 25–31.PubMedCrossRefGoogle Scholar
  42. Martin-Iverson M. T., DiLullo S. L., and Reimer A. R. (1993) Nimodipine and haloperidol interactions in amphetamine and cocaine conditioned behaviors, inDrugs in Development: Ca2 + Antagonists in CNS, vol. 2 (Scriabine A., ed.), Niva, Branford, CT, pp. 417–433.Google Scholar
  43. Mattingly B. A. and Gotsick J. E. (1989) Conditioning and experiential factors affecting the development of sensitization to apomorphine.Behav. Neurosci. 103, 1311–1317.PubMedCrossRefGoogle Scholar
  44. Miller H. H. and Shore P. A. (1982) Effects of amphetamine and amfoelic acid on the disposition of striatal newly synthesized DA.Eur. J. Pharmacol. 78, 33–44.PubMedCrossRefGoogle Scholar
  45. Muntaner C., Cascella N. G., Kumor K. M., Nagoshi C., Herning R., and Jaffe J. (1989) Placebo responses to cocaine administration in humans: effects of prior administrations and verbal instructions,Psychopharmacology 99, 282–286.PubMedCrossRefGoogle Scholar
  46. O’Brien C. P., Childress A. R., Arndt I. O., McLennan A. T., Woody G. E., and Maany I. (1988) Pharmacological and behavioral treatments of cocaine dependence: controlled studies.J. Clin. Psychiat. 49, 17–22.Google Scholar
  47. Pani L., Carboni S., Kusmin A., Gessa G. L., and Rossetti Z. L. (1990) Nimodipine inhibits cocaine-induced dopamine release and motor stimulation.Eur. J. Pharmacol. 176, 245–246.PubMedCrossRefGoogle Scholar
  48. Patrick S. L., Thompson T. L., Walker J. M., and Patrick R. L. (1991) Concomitant sensitization of amphetamine-induced behavioral stimulation and in vivo dopamine release from rat caudate nucleus.Brain Res. 538, 343–346.PubMedCrossRefGoogle Scholar
  49. Pettit H. O., Pan H.-T., Parson L. H., and Justice J. B. Jr. (1990) Extracellular concentrations of cocaine and dopamine are enhanced during chronic cocaine administration.J. Neurochem. 55, 798–804.PubMedCrossRefGoogle Scholar
  50. Post R. M. (1980) Intermittent versus continuous stimulation: effect of time interval on the development of sensitization or tolerance.Life Sci. 26, 1275–1282.PubMedCrossRefGoogle Scholar
  51. Post R. M., Lockfield A., Squillace K. M., and Contel N. R. (1981) Drug-environment interaction: context dependency of cocaine-induced sensitization.Life Sci. 28, 755–760.PubMedCrossRefGoogle Scholar
  52. Poulos C. X. and Cappel H. (1991) Homeostatic theory of drug tolerance: general model of physiological adaptation.Psychol. Rev. 98, 390–408.PubMedCrossRefGoogle Scholar
  53. Raiteri M., Cerrito F., Cervoni A., and Levi G. (1979) DA can be released by two mechanisms differentially affected by the DA transport inhibitor nomifensine.J. Pharmacol. Exp. Ther. 208, 195–202.PubMedGoogle Scholar
  54. Reimer A. R. and Martin-Iverson M. T. (1994) Nimodipine and haloperidol attenuate behavioural sensitization to cocaine but only nimodipine blocks the establishment of conditioned locomotion induced by cocaine.Psychopharmacology 113, 404–410.PubMedCrossRefGoogle Scholar
  55. Robinson T. E. and Becker J. B. (1986) Enduring changes in brain and behavior produced by chronic amphetamine administration: a review and evaluation of animal models of amphetamine psychosis.Brain Res. Rev. 11, 157–198.CrossRefGoogle Scholar
  56. Robinson T. E., Jurson P. A., Bennett J. A., and Bentgen K. M. (1988) Persistent sensitization of dopamine neurotransmission in ventral striatum (nucleus accumbens) produced by prior experience with (+)-amphetamine: a micro-dialysis study in freely moving rats.Brain Res. 462, 211–222.PubMedCrossRefGoogle Scholar
  57. Robinson T. E., Yew J., Paulson P. E., and Camp D. M. (1990) The long-term effects of neurotoxic doses of methamphetamine on the extracellular concentration of dopamine measured with microdialysis in striatum.Neurosci. Lett. 110, 193–198.PubMedCrossRefGoogle Scholar
  58. Ross S. B. (1977) On the mode of action of central stimulatory agents.Acta Pharmacol. Toxicol. 41, 392–396.CrossRefGoogle Scholar
  59. Ryan L., Martone M., Linder J., and Groves P. M. (1988) Cocaine, in contrast tod-amphetamine, does not cause axonal terminal degeneration in neostriatum and agranular frontal cortex of Long-Evans rats.Life Sci. 43, 1403–1409.PubMedCrossRefGoogle Scholar
  60. Scheel-Kruger J. (1971) Comparative studies of various amphetamine analogues demonstrating different interactions with the metabolism of the catecholamines in the brain.Eur. J. Pharmacol. 14, 47–59.PubMedCrossRefGoogle Scholar
  61. Segal D. S. and Kuczenski R. (1992a)In vivo microdialysis reveals a diminished ampheta-mine-induced dopamine response corresponding to behavioral sensitization produced by repeated amphetamine pretreatments.Brain Res. 571, 330–337.PubMedCrossRefGoogle Scholar
  62. Segal D. S. and Kuczenski R. (1992b) Repeated cocaine administration induces behavioral sensitization and corresponding decreased extracellular dopamine responses in caudate and accumbens.Brain Res. 577, 351–355.PubMedCrossRefGoogle Scholar
  63. Stewart J. and Druhan J. P. (1993) Development of both conditioning and sensitization of the behavioral activating effects of amphetamine is blocked by the non-competitive NMDA receptor antagonist, MK-801.Psychopharmacology 110, 125–132.PubMedCrossRefGoogle Scholar
  64. Stewart J. and Vezina P. (1989) Microinjections of SCH-23390 into the ventral tegmental area and substantia nigra pars reticulata attenuate the development of sensitization to the locomotor activating effects of systemic amphetamine.Brain Res. 495, 401–406.PubMedCrossRefGoogle Scholar
  65. Stewart J. and Vezina P. (1991) Extinction procedures abolish conditioned stimulus control but spare sensitized responding to amphetamine.Behav. Pharmacol. 2, 65–71.PubMedCrossRefGoogle Scholar
  66. Tilson H. A. and Rech R. H. (1973) Conditioned drug effects and absence of tolerance to d-amphetamine induced motor activity.Pharmacol. Biochem. Behav. 1, 149–153.CrossRefGoogle Scholar
  67. Vezina P. (1993) Amphetamine injected into the ventral tegmental area sensitizes the nucleus accumbens dopaminergic response to systemic amphetamine: an in vivo microdialysis study in the rat.Brain Res. 605, 332–337.PubMedCrossRefGoogle Scholar
  68. Vezina P. and Stewart J. (1990) Amphetamine administered to the ventral tegemental area but not to the nucleus accumbens sensitizes rats to systemic morphine: lack of conditioned effects.Brain Res. 516, 99–106.PubMedCrossRefGoogle Scholar
  69. Westerink B. H. C., Hofsteede R. M., Damsma G., Rollema H., and de Vries J. B. (1989) Use of calcium antagonism for the characterization of drugevoked DA release from the brain of conscious rats determined by microdialysis.J. Neurochem. 52, 722–729.PubMedCrossRefGoogle Scholar

Copyright information

© Humana Press Inc 1995

Authors and Affiliations

  • Mathew Thomas Martin-Iverson
    • 1
  • Lynn Yvonne Burger
    • 1
  1. 1.Neurochemical Research Unit, Department of PsychiatryUniversity of AlbertaEdmontonCanada

Personalised recommendations