Hypocretin (orexin) and dynorphin are neuropeptides with opposing actions on motivated behavior.
First-pass extracted concept
Hypocretin (orexin)
Aliases
hypocretin, orexin
Evidence Snippets
Supporting Sources
Linked Claims
Disruption of orexin function blunts the rewarding effects of lateral hypothalamic stimulation, eliminates cocaine-induced impulsivity, and reduces cocaine self-administration.
Disruption of orexin function blunts the rewarding effects of lateral hypothalamic (LH) stimulation, eliminates cocaine-induced impulsivity, and reduces cocaine self-administration.
Concomitant disruption of dynorphin function reverses the behavioral changes caused by disruption of orexin function.
Concomitant disruption of dynorphin function reverses these behavioral changes.
Orexin and dynorphin are packaged in the same synaptic vesicles within the hypothalamus.
We show that, despite their opposing actions, these peptides are packaged in the same synaptic vesicles within the hypothalamus.
Orexin and dynorphin have opposing actions on the excitability of VTA dopamine neurons.
We also show that orexin and dynorphin have opposing actions on excitability of ventral tegmental area (VTA) dopamine neurons.
Orexin facilitates reward by occluding the reward-threshold-elevating effects of coreleased dynorphin and thereby acts permissively to facilitate reward.
Our findings identify a unique cellular process by which orexin can occlude the reward threshold-elevating effects of coreleased dynorphin and thereby act in a permissive fashion to facilitate reward.
Intra-VTA orexin antagonism decreases cocaine self-administration and lateral hypothalamic self-stimulation, and these decreases are reversed by dynorphin antagonism.
intra-VTA orexin antagonism causes decreases in cocaine self-administration and LH self-stimulation that are reversed by dynorphin antagonism