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Psychopharmacology (Berl). 2006 Jun;186(2):177-84. Epub 2006 Mar 30.

Development of tolerance and sensitization to different opioid agonists in rats.

Author information

1
Institute of Pharmacology and Toxicology, Faculty of Medicine, Otto-von-Guericke-University Magdeburg, Leipziger Str. 44, 39120 Magdeburg, Germany. gisela.grecksch@medizin.uni-magdeburg.de

Abstract

RATIONALE:

Despite numerous investigations, the mechanisms underlying the development of opioid tolerance are far from clear. However, several in vitro studies implicated a protective role of agonist-induced micro-opioid receptor endocytosis in the development of opioid tolerance. Moreover, we have recently demonstrated that the high-efficacy agonist etonitazene promotes rapid endocytosis of micro-opioid receptors, whereas the agonist morphine and the low-efficacy agonist buprenorphine fail to promote detectable receptor endocytosis in micro-opioid receptor expressing HEK293 cells.

OBJECTIVES:

The present study explored the effects of these opioids on the development of tolerance and sensitization in rats in vivo.

METHODS:

The opioid effects were quantified using the hot plate, electric tail root stimulation, and the locomotor activity chamber in male Wistar rats. Dose-response curves were generated for each test drug. To induce tolerance, equieffective doses of etonitazene, morphine, and buprenorphine were administered daily for 29 days.

RESULTS:

We found that chronic treatment with the non-internalizing drugs buprenorphine and morphine resulted in a greater development of tolerance than etonitazene. In addition, the sensitization to the locomotor stimulant effect was high after buprenorphine and morphine, but was lacking after chronic etonitazene application.

CONCLUSION:

The results support a role for the endocytotic potency of agonists in the development of tolerance and addiction during long-term opioid treatment.

PMID:
16572262
DOI:
10.1007/s00213-006-0365-8
[Indexed for MEDLINE]

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