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Rats self-administer carbachol directly into the nucleus accumbens
S Ikemoto1, B S Glazier, J M Murphy
1Department of Psychiatry, Indiana University School of Medicine, Indiana University-Purdue University at Indianapolis, 46202, USA.
Physiology & Behavior
|June 9, 1998
Summary
Carbachol, a muscarinic agonist, was self-administered by rats into the nucleus accumbens (ACB), indicating its reinforcing effects. Scopolamine blocked this effect, suggesting muscarinic receptor involvement in reinforcement.
Area of Science:
- Neuroscience
- Pharmacology
- Behavioral Science
Background:
- The nucleus accumbens (ACB) is a key brain region involved in reward and motivation.
- Cholinergic systems, particularly muscarinic receptors, play a role in modulating these behaviors.
Purpose of the Study:
- To investigate the potential reinforcing effects of the muscarinic cholinergic agonist carbachol within the nucleus accumbens.
- To determine if direct activation of muscarinic receptors in the ACB supports self-administration behavior.
Main Methods:
- Intracranial self-administration technique in female Wistar rats.
- Dose-dependent administration of carbachol (0.0-6.6 mM) directly into the ACB.
- Assessment of lever-press preference for drug infusions versus no consequence.
- Inhibition studies using muscarinic antagonist scopolamine and nicotinic antagonist mecamylamine.
Main Results:
- Rats dose-dependently self-administered carbachol into the ACB, with significant preference for 3.3 and 6.6 mM doses over vehicle.
- The caudate putamen did not support reliable self-administration of carbachol.
- Preference was shown for the lever delivering carbachol infusions into the ACB.
- Scopolamine, but not mecamylamine, inhibited the self-infusion of carbachol into the ACB.
Conclusions:
- Direct activation of muscarinic receptors within the nucleus accumbens supports self-administration behavior in rats.
- This effect may be mediated by reinforcement or the elicitation of a novel stimulus.
- The findings highlight the role of central muscarinic pathways in reward and motivated behaviors.