National Brain Research Program of the Hungarian Academy of Sciences(NAP 3.0)
(K146086)
(K141934) Támogató: Hungarian National Research, Development and Innovation Office
(K138763) Támogató: NKFIH
(K134221)
(K120311) Támogató: NKFIH
(TKP2021-EGA-16)
(TKP2021-EGA-25)
According to previous studies, the median raphe region (MRR) is known to contribute
significantly to social behavior. Besides serotonin, there have also been reports
of a small population of dopaminergic neurons in this region. Dopamine is linked to
reward and locomotion, but very little is known about its role in the MRR. To address
that, we first confirmed the presence of dopaminergic cells in the MRR of mice (immunohistochemistry,
RT-PCR), and then also in humans (RT-PCR) using healthy donor samples to prove translational
relevance. Next, we used chemogenetic technology in mice containing the Cre enzyme
under the promoter of the dopamine transporter. With the help of an adeno-associated
virus, designer receptors exclusively activated by designer drugs (DREADDs) were expressed
in the dopaminergic cells of the MRR to manipulate their activity. Four weeks later,
we performed an extensive behavioral characterization 30 min after the injection of
the artificial ligand (Clozapine-N-Oxide). Stimulation of the dopaminergic cells in
the MRR decreased social interest without influencing aggression and with an increase
in social discrimination. Additionally, inhibition of the same cells increased the
friendly social behavior during social interaction test. No behavioral changes were
detected in anxiety, memory or locomotion. All in all, dopaminergic cells were present
in both the mouse and human samples from the MRR, and the manipulation of the dopaminergic
neurons in the MRR elicited a specific social response.