Appetitive Instrumental Learning Is Impaired by Inhibition of cAMP-Dependent Protein Kinase within the Nucleus Accumbens

• Published in: Neurobiology of learning and memory 2002-01, Vol.77 (1), p.44-62
• Main Authors: Baldwin, Anne E., Sadeghian, Kenneth, Holahan, Matthew R., Kelley, Ann E.
• Format: Article
• Language: English
• Subjects: Animals; Appetitive Behavior - drug effects; appetitive learning; Biological and medical sciences; cAMP-dependent protein kinase; Corpus Striatum - drug effects; Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors; Discrimination Learning - drug effects; dopamine; Feeding Behavior - drug effects; Locomotion - drug effects; Male; Neuronal Plasticity - drug effects; nucleus accumbens; Nucleus Accumbens - drug effects; Nucleus Accumbens - enzymology; PKA, striatum; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D1 - drug effects; spiny neurons
• ISSN: 1074-7427; 1095-9564
• DOI: 10.1006/nlme.2000.4002

The medium spiny neurons of the nucleus accumbens receive a unique convergence of dopaminergic and glutamatergic inputs from regions associated with motivational, cognitive, and sensory processes. Long-term forms of plasticity in the nucleus accumbens associated with such processes as appetitive learning and drug addiction may require coactivation of both dopamine D1 and glutamate N-methyl-d-aspartate (NMDA) receptors. This notion implies that an intracellular mechanism is likely to be involved in these long-term neuroadaptive processes. The present series of experiments examined the effects of intra-accumbens microinfusion of protein kinase inhibitors on acquisition of an instrumental task, lever-pressing for food. Male Sprague-Dawley rats were bilaterally implanted with chronic indwelling cannulae aimed at the nucleus accumbens core. Following recovery, animals were food-restricted and subsequently trained for operant responding. The broad-based serine/threonine kinase inhibitor H-7 (5 or 27 nmol per side) dose-dependently impaired learning when infused immediately after testing on days 1–4. Rp-cAMPS, a cAMP-dependent protein kinase (PKA) inhibitor, also impaired learning regardless of whether it was infused immediately before (5 or 20 nmol) or immediately after (10 nmol) testing on days 1–4. Rp-cAMPS (10 nmol) also inhibited learning when infused 1 h after testing, though to a lesser extent than when administered before or immediately after testing. The PKA stimulator Sp-cAMPS (5 or 20 nmol) also impaired learning when infused before testing, suggesting that there is an optimal level of PKA activity required for learning. None of the drugs used produced nonspecific motor or feeding effects. These results provide evidence supporting the involvement of nucleus accumbens PKA in appetitive learning and suggest that this kinase may be involved in long-term changes associated with this and other motivationally based neuroadaptive processes.