μ-Opioid modulation in the rostral solitary nucleus and reticular formation alters taste reactivity: evidence for a suppressive effect on consummatory behavior
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Published on: June 10, 2013
Nicole R Kinzeler1, Susan P Travers
1Department of Psychology, The Ohio State University, Columbus, Ohio, USA. kinzeler.2@osu.edu
Abstract:
The neural control of feeding involves many neuromodulators, including the endogenous opioids that bind μ-opioid receptors (MORs). Injections of the MOR agonist, Damgo, into limbic and hypothalamic forebrain sites increase intake, particularly of palatable foods. Indeed, forebrain Damgo injections increase sucrose-elicited licking but reduce aversive responding (gaping) to quinine, suggesting that MOR activation may enhance taste palatability. A μ-opioid influence on taste reactivity has not been assessed in the brain stem. However, MORs are present in the first-order taste relay, the rostral nucleus of the solitary tract (rNST), and in the immediately subjacent reticular formation (RF), a region known to be essential for consummatory responses. Thus, to evaluate the consequences of rNST/dorsal RF Damgo in this region, we implanted rats with intraoral cannulas, electromyographic electrodes, and brain cannulas aimed at the ventral border of the rNST. Licking and gaping elicited with sucrose, water, and quinine were assessed before and after intramedullary Damgo and saline infusions. Damgo slowed the rate, increased the amplitude, and decreased the size of fluid-induced lick and gape bouts. In addition, the neutral stimulus water, which typically elicits licks, began to evoke gapes. Thus, the current results demonstrate that μ-opioid activation in the rNST/dorsal RF exerts complex effects on oromotor responding that contrast with forebrain effects and are more indicative of a suppressive, rather than a facilitatory effect on ingestion.
Insights
Activation of μ-opioid receptors (MORs) in the brainstem
Area of Science:
- Neuroscience
- Neurobiology
- Feeding Behavior Research
Background:
- Endogenous opioids and μ-opioid receptors (MORs) modulate feeding behavior.
- Forebrain MOR activation enhances intake of palatable foods and taste palatability.
- The role of MORs in brainstem taste processing remains unclear.
Purpose of the Study:
- To investigate the effects of MOR activation in the rostral nucleus of the solitary tract (rNST) and dorsal reticular formation (RF) on oromotor responses.
- To determine if MOR activation in the brainstem influences taste reactivity and consummatory behaviors.
Main Methods:
- Rats were implanted with intraoral cannulas, electromyographic electrodes, and brain cannulas targeting the ventral rNST.
- Licking and gaping responses to sucrose, water, and quinine were measured before and after infusions of a MOR agonist (Damgo) or saline.
- Oromotor responses were analyzed for rate, amplitude, and bout size.
Main Results:
- Damgo infusions into the rNST/dorsal RF altered lick and gape bout characteristics, slowing the rate, increasing amplitude, and decreasing bout size.
- Neutral stimuli like water, typically eliciting licking, evoked gaping responses after Damgo administration.
- These effects contrast with the facilitatory effects of MOR activation in the forebrain.
Conclusions:
- μ-opioid receptor activation in the rNST/dorsal RF has complex, suppressive effects on oromotor responding.
- Brainstem MOR signaling appears to inhibit, rather than facilitate, ingestion, contrasting with forebrain mechanisms.
- This study reveals a differential role of MORs in taste processing within the central nervous system.
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