Faculty Opinions recommendation of Presynaptic opioid and nicotinic receptor modulation of dopamine overflow in the nucleus accumbens.

Abstract

Behaviorally relevant stimuli prompt midbrain dopamine (DA) neurons to switch from tonic to burst firing patterns. Similar shifts to burst activity are thought to contribute to the addictive effects of opiates and nicotine. The nucleus accumbens DA overflow produced by these drugs is a key element in their pathological effects. Using electrochemical techniques in brain slices, we explored the effects of opioids on single-spike and burst stimuli-evoked DA overflow in the dorsal and ventral striatum. In specific subregions of the nucleus accumbens, mu-opioids inhibit DA overflow elicited with single-spike stimuli while leaving that produced by burst stimuli unaffected. This is similar to published effects of nicotinic receptor blockade or desensitization, and is mediated by opioid receptor-induced inhibition of cholinergic interneurons. Whereas delta-opioids have similar effects, kappa-opioids inhibit evoked DA overflow throughout the striatum in a manner that is not overcome with high-frequency stimuli. These observations reveal remarkable mechanistic overlap between the effects of nicotine and opiates within the dopamine reward pathway. PMID: 18272687 Funding information This work was supported by: NIDA NIH HHS, United States Grant ID: F31 DA023340 NIDA NIH HHS, United States Grant ID: P01 DA019695 NIDA NIH HHS, United States Grant ID: DA019695 NIGMS NIH HHS, United States Grant ID: T32GM07839 NIDA NIH HHS, United States Grant ID: DA015918 NIGMS NIH HHS, United States Grant ID: T32 GM007839 NIDA NIH HHS, United States Grant ID: R01 DA015918 NIDA NIH HHS, United States Grant ID: F31DA023340 More Less keyboard_arrow_down