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Dopaminergic dominance in the ventral medial hypothalamus: A pivotal regulator for methamphetamine-induced pathological aggression.
- Source :
-
Progress in Neuro-Psychopharmacology & Biological Psychiatry . Jun2024, Vol. 132, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Methamphetamine (METH) abuse is associated with a spectrum of behavioral consequences, among which heightened aggression presents a significant challenge. However, the causal role of METH's impact in aggression and its target circuit mechanisms remains largely unknown. We established an acute METH exposure-aggression mouse model to investigate the role of ventral tegmental area (VTA) dopaminergic neurons and ventral medial hypothalamus VMH glutamatergic neuron. Our findings revealed that METH-induced VTA dopamine excitability activates the ventromedial hypothalamus (VMH) glutamatergic neurons, contributing to pathological aggression. Notably, we uncovered a dopaminergic transmission within the VTA-VMH circuit that exclusively functioned under METH influence. This dopaminergic pathway emerged as a potential key player in enabling dopamine-related pathological aggression, with heightened dopaminergic excitability implicated in various psychiatric symptoms. Also, the modulatory function of this pathway opens new possibilities for targeted therapeutic strategies for intervention to improve treatment in METH abuse and may have broader implications for addressing pathological aggression syndromes. • Elevated VTA dopaminergic excitability emerges as a key contributor to METH-induced aggression. • Dopamine presence in the VMH is exclusive to METH influence. • The VTA-VMH circuit is engaged, playing a dual role in both the development and modulation of METH-induced aggression. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02785846
- Volume :
- 132
- Database :
- Academic Search Index
- Journal :
- Progress in Neuro-Psychopharmacology & Biological Psychiatry
- Publication Type :
- Academic Journal
- Accession number :
- 176541948
- Full Text :
- https://doi.org/10.1016/j.pnpbp.2024.110971