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  lüll kappa-Opioid receptor signaling and brain reward function Bruijnzeel AWBrain Res Rev  2009[Dec]; 62 (1): 127-46The dynorphin-like peptides have profound effects on the state of the brain  reward system and human and animal behavior. The dynorphin-like peptides affect  locomotor activity, food intake, sexual behavior, anxiety-like behavior, and drug  intake. Stimulation of kappa-opioid receptors, the endogenous receptor for the  dynorphin-like peptides, inhibits dopamine release in the striatum (nucleus  accumbens and caudate putamen) and induces a negative mood state in humans and  animals. The administration of drugs of abuse increases the release of dopamine  in the striatum and mediates the concomitant release of dynorphin-like peptides  in this brain region. The reviewed studies suggest that chronic drug intake leads  to an upregulation of the brain dynorphin system in the striatum and in  particular in the dorsal part of the striatum/caudate putamen. This might inhibit  drug-induced dopamine release and provide protection against the neurotoxic  effects of high dopamine levels. After the discontinuation of chronic drug intake  these neuroadaptations remain unopposed which has been suggested to contribute to  the negative emotional state associated with drug withdrawal and increased drug  intake. kappa-Opioid receptor agonists have also been shown to inhibit calcium  channels. Calcium channel inhibitors have antidepressant-like effects and inhibit  the release of norepinephrine. This might explain that in some studies  kappa-opioid receptor agonists attenuate nicotine and opioid withdrawal  symptomatology. A better understanding of the role of dynorphins in the  regulation of brain reward function might contribute to the development of novel  treatments for mood disorders and other disorders that stem from a dysregulation  of the brain reward system.|*Reward[MESH]|Animals[MESH]|Brain/*metabolism[MESH]|Dynorphins/metabolism[MESH]|Humans[MESH]|Receptors, Opioid, kappa/*metabolism[MESH]|Substance Withdrawal Syndrome/metabolism[MESH]|Substance-Related Disorders/metabolism[MESH] |