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Arias-Montano, J.-A.

Publications and source records attributed to Arias-Montano, J.-A..

2 recordsLinked to original sources

Nucleus accumbens D2-expressing neurons: Balancing reward and licking disruption through rhythmic optogenetic stimulation

Dopamine D1 receptor-expressing neurons in the nucleus accumbens (NAc) are known to be critical for processing reward and regulating food intake. However, the role of D2-expressing neurons in this region remains less understood. This study employed optogenetic manipulations to investigate the role of NAc D2-expressing neurons in reward processing and sucrose consumption. Optogenetic activation of these neurons decreased sucrose preference (at 20 Hz), disrupted licking patterns (particularly at 8 and 20 Hz), and increased self-stimulation. Conversely, synchronizing stimulation with the animals licking rhythm mitigated licking disruption and even increased sucrose intake, suggesting a rewarding effect. Furthermore, 20 Hz stimulation (but not 8 Hz) induced place preference in a real-time place preference (RTPP) test. In contrast, inhibiting D2 neurons produced a negative hedonic state, although not reaching a complete aversion, influencing food choices in specific contexts. For instance, while the RTPP test per se was not sensitive enough to observe place aversion when mice could choose between consuming a high-fat diet (HFD) pellet in a context associated with or without inhibition of D2 neurons, they preferred to consume HFD on the non-inhibited side. This suggests that the palatability of HFD can unmask (but also overshadow) the negative hedonic state associated with D2 neuron inhibition. A negative reinforcement paradigm further confirmed the active avoidance behavior induced by D2 neuron inhibition. In conclusion, NAc D2 neuron inhibition induces a negative hedonic state, while activation has a dual effect--it is rewarding yet disrupts licking behavior--highlighting its complex role in reward and consummatory behavior. Importantly, self-paced stimulation, where the animal controls the timing of the stimulation by its licking behavior, offers a more efficient and natural approach for stimulating NAc activity.

neuroscience↗

Functional histamine H3 and adenosine A2A receptor heteromers in recombinant cells and rat striatum

In the striatum, histamine H3 receptors (H3Rs) are co-expressed with adenosine A2A receptors (A2ARs) in the cortico-striatal glutamatergic afferents and the GABAergic medium-sized spiny neurons that originate the indirect pathway of the basal ganglia. This location allows H3Rs and A2ARs to regulate the striatal GABAergic and glutamatergic transmission. However, whether these receptors interact to modulate the intra-striatal synaptic transmission has not yet been assessed. To test this hypothesis a heteromer-selective in vitro assay was used to detect functional complementation between a chimeric A2AR302-Gqi4 and wild-type H3Rs in transfected HEK-293 cells. H3R activation with the agonist RAMH resulted in Ca2+ mobilization (pEC50 7.31 {+/-} 0.23; maximal stimulation, Emax 449 {+/-} 25 % of basal) indicative of receptor heterodimerization. This response was not observed with histamine, suggesting a RAMH bias for heteromers. Functional A2AR-H3R heteromers were confirmed by co-immunoprecipitation and observations of differential cAMP signaling when both receptors were co-expressed in the same cell. In membranes from rat striatal synaptosomes, H3R activation decreased A2AR affinity for the agonist CGS-21680 (pKi values 8.10 {+/-} 0.04 and 7.70 {+/-} 0.04). Moreover, H3Rs and A2ARs co-immunoprecipitated in protein extracts from striatal synaptosomes. These results support the existence of a H3R/A2AR heteromer, and reveal a new mechanism by which these receptors may modulate the unction of the striatum and the basal ganglia.

neuroscience↗