Participation of adenosine system in the ketamine-induced motor activity in mice.
Marcin Mandryk, Sylwia Fidecka, Ewa Poleszak, Danuta Malec
Abstract
Marcin Mandryk, Sylwia Fidecka, Ewa Poleszak, Danuta Malec
Abstract
The influence of adenosine receptor ligands on ketamine-induced locomotor activity was studied in mice. Ketamine-induced hyperactivity (10 mg/kg) was significantly and dose-dependently attenuated by CGS 21680 (selective A(2A) receptor agonist), and NECA (A1/A2 adenosine receptor agonist), but not by CPA (cyclopentyladenosine, selective A1 adenosine receptor agonist). Motor activity produced by subthreshold dose (2.5 mg/kg) of ketamine was significantly increased by DMPX (selective A1 receptor antagonist) and caffeine (A1/A2 adenosine receptor antagonist), but not by DPCPX (selective A1 adenosine receptor antagonist). These results suggest that adenosinergic system is involved in ketamine-induced motor activity and seem to indicate a predominant role of A(2A) adenosine receptor in this effect.
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The influence of adenosine receptor ligands on ketamine-induced locomotor activity was studied in mice. Ketamine-induced hyperactivity (10 mg/kg) was significantly and dose-dependently attenuated by CGS 21680 (selective A(2A) receptor agonist), and NECA (A1/A2 adenosine receptor agonist), but not by CPA (cyclopentyladenosine, selective A1 adenosine receptor agonist). Motor activity produced by subthreshold dose (2.5 mg/kg) of ketamine was significantly increased by DMPX (selective A1 receptor antagonist) and caffeine (A1/A2 adenosine receptor antagonist), but not by DPCPX (selective A1 adenosine receptor antagonist). These results suggest that adenosinergic system is involved in ketamine-induced motor activity and seem to indicate a predominant role of A(2A) adenosine receptor in this effect.
Key concepts: Adenosinergic, CGS-21680, Adenosine, Adenosine receptor antagonist, Agonist, Adenosine A1 receptor, Adenosine receptor, Chemistry