Bed Nucleus of the Stria Terminalis–Derived Corticotropin-Releasing Factor Controls Binge Alcohol Drinking Via Interacting With Corticotropin-Releasing Factor Receptors 1 and 2 in the Ventral Tegmental Area

2017 ◽  
Vol 81 (11) ◽  
pp. 905-906 ◽  
Author(s):  
Leszek Kaczmarek
2011 ◽  
Vol 71 ◽  
pp. e322
Author(s):  
Takehiro Kudo ◽  
Motokazu Uchigashima ◽  
Taisuke Miyazaki ◽  
Miwako Yamasaki ◽  
Masabumi Minami ◽  
...  

2014 ◽  
Vol 39 (11) ◽  
pp. 1796-1809 ◽  
Author(s):  
Takehiro Kudo ◽  
Kohtarou Konno ◽  
Motokazu Uchigashima ◽  
Yuchio Yanagawa ◽  
Ichiro Sora ◽  
...  

2009 ◽  
Vol 33 (8) ◽  
pp. 1336-1346 ◽  
Author(s):  
Marion Jalabert ◽  
Gary Aston-Jones ◽  
Etienne Herzog ◽  
Olivier Manzoni ◽  
François Georges

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Olivia B. Levine ◽  
Mary Jane Skelly ◽  
John D. Miller ◽  
Jean K. Rivera-Irizarry ◽  
Sydney A. Rowson ◽  
...  

AbstractBed nucleus of the stria terminalis (BNST) neurons that synthesize corticotropin-releasing factor (CRF) drive binge alcohol drinking and anxiety. Here, we found that female C57BL/6J mice binge drink more than males and have greater basal BNSTCRF neuron excitability and synaptic excitation. We identified a dense VGLUT2 + synaptic input from the paraventricular thalamus (PVT) that releases glutamate directly onto BNSTCRF neurons but also engages a large BNST interneuron population to ultimately inhibit BNSTCRF neurons, and this polysynaptic PVTVGLUT2-BNSTCRF circuit is more robust in females than males. Chemogenetic inhibition of the PVTBNST projection promoted binge alcohol drinking only in female mice, while activation reduced avoidance behavior in both sexes. Lastly, repeated binge drinking produced a female-like phenotype in the male PVT-BNSTCRF excitatory synapse without altering the function of PVTBNST neurons per se. Our data describe a complex, feedforward inhibitory PVTVGLUT2-BNSTCRF circuit that is sex-dependent in its function, behavioral roles, and alcohol-induced plasticity.


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