The effect of repeated administration of morphine, cocaine and ethanol on mu and delta opioid receptor density in the nucleus accumbens and striatum of the rat

Author(s): Turchan J, Przewlocka B, Toth G, LasonW, Borsodi A, et al.

Abstract

The present study was carried out to evaluate the effect of morphine, cocaine and ethanol on the density of opioid receptors in the nucleus accumbens and striatum of rat brain. The animals were injected i.p. with morphine in a single dose 20 mg/kg, or twice daily for 10 days in increasing doses of 20-100 mg/kg. Cocaine was administered in a dose of 60 mg/kg/day following the "binge" paradigm, every hour for 3 h, one day (single treatment) or five days (chronic treatment). Ethanol was administered in drinking water at increasing concentrations of 1-6% v/v, for one month. As shown by receptor autoradiography, single morphine and cocaine administration did not influence the binding density of the selective ligand of delta2 receptors [3H]Ile5,6deltorphin b, but single administration of cocaine decreased binding density of a highly selective antagonist of delta receptors, [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH. Repeated morphine administration decreased the receptor density after both ligands of the delta receptor in the nucleus accumbens after 3, 24 and 48 h, and in the striatum after 24 and 48 h. The density of [3H]Ile5,6deltorphin b binding remained unchanged in both structures following repeated cocaine administration. After repeated cocaine administration either no changes (3 h) or a decrease in the binding of [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH in the nucleus accumbens and striatum were observed after 24 and 48 h. Ethanol did not influence the binding density of [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH and [3H]Ile5,6deltorphin b in the nucleus accumbens and striatum at any time-point studied. In the nucleus accumbens and striatum, no changes were found in the binding density of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol following single or repeated morphine administration. At 3 h after single or repeated "binge" cocaine administration, the binding of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol was not changed in either structure, but after 24 h the density of mu opioid receptors was decreased in both structures. Ethanol given to rats in drinking water decreased the binding of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol at the time of exposure to ethanol, yet in the nucleus accumbens only. Ethanol withdrawal decreased the density of the mu receptor in both structures after 24, 48 and 96 h. The above data indicate that repeated administration of morphine evokes a long-lasting down-regulation of the density of delta1 and delta2 opioid receptors, whereas cocaine affects in a similar way only the delta1 subtype in the nucleus accumbens, and to a lesser extent in the striatum. A long-term intake of ethanol solution down-regulates mu opioid receptors in both structures, but has no effect on any type of delta receptors. Thus changes in the particular opioid receptor depend on the type of drug used. Furthermore, the most profound changes are observed after late withdrawal, which may play some role in maintaining the state of dependence.

Similar Articles

Enhanced morphine analgesia in mice lacking beta-arrestin 2

Author(s): Bohn LM, Lefkowitz RJ, Gainetdinov RR, Peppel K, Caron MG, et al.

Mu-opioid receptor desensitization by beta-arrestin-2 determines morphine tolerance but not dependence

Author(s): Bohn LM, Gainetdinov RR, Lin FT, Lefkowitz RJ, Caron MG, et al.

Ligand-directed signalling within the opioid receptor family

Author(s): Pradhan AA, Smith ML, Kieffer BL, Evans CJ

μ-opioid receptors: correlation of agonist efficacy for signalling with ability to activate internalization

Author(s): McPherson J, Rivero G, Baptist M, Llorente J, Al-Sabah S, et al.

Morphine-like opiates selectively antagonize receptor-arrestin interactions

Author(s): Molinari P, Vezzi V, Sbraccia M, Grò C, Riitano D, et al.

Pharmacological characterization of AR-M1000390 at human delta opioid receptors

Author(s): Marie N, Landemore G, Debout C, Jauzac P, Allouche S

SK-N-BE: a human neuroblastoma cell line containing two subtypes of delta-opioid receptors

Author(s): Polastron J, Mur M, Mazarguil H, Puget A, Meunier JC, et al.

ßarrestin1-biased agonism at human δ-opioid receptor by peptidic and alkaloid ligands

Author(s): Aguila B, Coulbault L, Davis A, Marie N, Hasbi A, et al.

Molecular control of δ-opioid receptor signalling

Author(s): Fenalti G, Giguere PM, Katritch V, Huang XP, Thompson AA, et al.

Development and validation of a genetic algorithm for flexible docking

Author(s): Jones G, Willett P, Glen RC, Leach AR, Taylor R, et al.

Agonist-selective mechanisms of GPCR desensitization

Author(s): Kelly E, Bailey CP, Henderson G

Recovery from mu-opioid receptor desensitization after chronic treatment with morphine and methadone

Author(s): Quillinan N, Lau EK, Virk M, von Zastrow M, Williams JT

Beta-arrestin-dependent formation of beta2 adrenergic receptor-Src protein kinase complexes

Author(s): Luttrell LM, Ferguson SS, Daaka Y, Miller WE, Maudsley S, et al.