Literature DB >> 11224409

Procedural examination of behavioural sensitisation to morphine: lack of blockade by MK-801, occurrence of sensitised sniffing, and evidence for cross-sensitisation between morphine and MK-801.

T.M. Tzschentke1, W.J. Schmidt.   

Abstract

Rats were tested in an open field, a "sniffing box" and an eight-arm maze, to examine in detail the behavioural changes induced by morphine (10mg/kg, i.p.) and MK-801 (0.1mg/kg, i.p.), either alone or in combination, during a 10 day treatment and subsequent drug challenges. In addition to locomotion, a number of other behaviours such as sniffing, rearing and exploration were examined. After morphine challenge, sensitised locomotion and rearing were found in the open field, and sensitised sniffing and turning were observed in the sniffing box. In addition, in the sniffing box, saline challenge produced significant conditioned sniffing and turning, and after a challenge with MK-801, sensitised sniffing and turning were seen in the group pretreated with morphine, suggesting a cross-sensitisation between morphine and MK-801 (but not vice versa). In the eight-arm maze, sensitised locomotion was found after morphine challenge. Morphine and MK-801 changed the preference for particular angles run during trials in a characteristic manner. In none of the behavioural measures was MK-801 able to block the development (and expression) of sensitisation to morphine. In several cases, rather, MK-801 enhanced the acute morphine effects. Sensitisation of sniffing suggests that sensitisation has also developed within the nigrostriatal dopamine system and not only within the mesolimbic dopamine system, as is generally discussed in the context of the most commonly assessed behaviour, locomotion. This finding argues for the additional use of the sniffing box in sensitisation experiments.

Entities:  

Year:  1996        PMID: 11224409

Source DB:  PubMed          Journal:  Behav Pharmacol        ISSN: 0955-8810            Impact factor:   2.293


  5 in total

1.  Effects of blockade of glutamate NMDA receptors or of NO synthase on the development or the expression of associative or non-associative sensitization to locomotor activation by morphine.

Authors:  A Atalla; K Kuschinsky
Journal:  J Neural Transm (Vienna)       Date:  2005-04-22       Impact factor: 3.575

2.  NMDA receptor antagonists inhibit opiate antinociceptive tolerance and locomotor sensitization in rats.

Authors:  Ian A Mendez; Keith A Trujillo
Journal:  Psychopharmacology (Berl)       Date:  2007-11-10       Impact factor: 4.530

3.  The neurobiology of opiate tolerance, dependence and sensitization: mechanisms of NMDA receptor-dependent synaptic plasticity.

Authors:  Keith A Trujillo
Journal:  Neurotox Res       Date:  2002-06       Impact factor: 3.911

4.  A GABA(B) agonist reverses the behavioral sensitization to morphine in rats.

Authors:  Maria Bartoletti; Francesca Ricci; Margherita Gaiardi
Journal:  Psychopharmacology (Berl)       Date:  2007-01-23       Impact factor: 4.415

5.  Dissociable roles of mGlu5 and dopamine receptors in the rewarding and sensitizing properties of morphine and cocaine.

Authors:  M M J Veeneman; H Boleij; M H Broekhoven; E M S Snoeren; M Guitart Masip; J Cousijn; W Spooren; L J M J Vanderschuren
Journal:  Psychopharmacology (Berl)       Date:  2010-12-01       Impact factor: 4.530

  5 in total

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