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Shamseddin Ahmadi

Shamseddin Ahmadi

Academic rank: Associate Professor
ORCID: 0000-0003-0300-3226
Education: PhD.
ScopusId: 12141695900
Faculty: Faculty of Science
Address: Department of Biological Science, Faculty of Science, University of Kurdistan, Sanandaj, Iran
Phone: 08733664600 (2510)

Research

Title
GABAA receptors in the basolateral amygdala are involved in mediating morphine reward
Type
JournalPaper
Keywords
Morphine- Muscimol- Bicuculine- Conditioned place preference
Year
2004
Journal Brain Research
DOI
Researchers Mohammad Reza Zarrindast ، Shamseddin Ahmadi ، Ali Haeri-Rohani ، Ameneh Rezayof ، mohammad reza Jafari ، Majid Ja'fari-sabet

Abstract

In the present study, the effects of intra-basolateral amygdala (BLA) injection of GABAA receptor agonist and antagonist on morphine induced conditioned place preference (CPP) in male Wistar rats have been investigated. Subcutaneous (s.c.) administration of different doses of morphine sulfate (1–9 mg/kg) produced a dose-dependent CPP. Using a 3-day schedule of conditioning, it was found that the GABAA receptor agonist, muscimol (0.125, 0.25 and 0.5 Ag/rat) or the GABAA receptor antagonist, bicuculline (0.125, 0.25 and 0.5 Ag/rat), did not produce a significant place preference or place aversion. Intra-BLA administration of muscimol (0.25 and 0.5 Ag/rat) decreased the acquisition of CPP induced by morphine (6 mg/kg). On the other hand, intra-BLA injection of bicuculline (0.25 and 0.5 Ag/rat) in combination with an ineffective dose of morphine (1 mg/kg) elicited a significant CPP. The response of different doses of muscimol was attenuated by bicuculline (0.125 and 0.25 Ag/rat). Furthermore, intra-BLA administration of bicuculline but not muscimol before testing significantly decreased the expression of morphine (6 mg/kg)-induced place preference. The administration of the higher doses of bicuculline (0.25 and 0.5 Ag/rat) during acquisition and the higher dose of muscimol (2 Ag/rat) on the test day decreased the locomotor activity of the animals on the testing phase. It can be concluded that GABAA receptors in the amygdala are involved in morphine reward.