scholarly journals Learning-Induced Changes in mPFC–BLA Connections After Fear Conditioning, Extinction, and Reinstatement of Fear

2011 ◽  
Vol 36 (11) ◽  
pp. 2276-2285 ◽  
Author(s):  
Rose-Marie Vouimba ◽  
Mouna Maroun
2010 ◽  
Vol 203 (2) ◽  
pp. 285-297 ◽  
Author(s):  
Erin L. Zelinski ◽  
Nancy S. Hong ◽  
Amanda V. Tyndall ◽  
Brett Halsall ◽  
Robert J. McDonald

2015 ◽  
Vol 57 (7) ◽  
pp. 818-832 ◽  
Author(s):  
Miriam Liora Den ◽  
Bronwyn M. Graham ◽  
Carol Newall ◽  
Rick Richardson

2018 ◽  
Vol 194 ◽  
pp. 268-276 ◽  
Author(s):  
Takuya Yoshiike ◽  
Motoyasu Honma ◽  
Naoto Yamada ◽  
Yoshiharu Kim ◽  
Kenichi Kuriyama

2013 ◽  
Vol 14 (6) ◽  
pp. 417-428 ◽  
Author(s):  
Stephen Maren ◽  
K. Luan Phan ◽  
Israel Liberzon

2015 ◽  
Vol 112 (28) ◽  
pp. E3729-E3737 ◽  
Author(s):  
Paul J. Fitzgerald ◽  
Thomas F. Giustino ◽  
Jocelyn R. Seemann ◽  
Stephen Maren

Stress-induced impairments in extinction learning are believed to sustain posttraumatic stress disorder (PTSD). Noradrenergic signaling may contribute to extinction impairments by modulating medial prefrontal cortex (mPFC) circuits involved in fear regulation. Here we demonstrate that aversive fear conditioning rapidly and persistently alters spontaneous single-unit activity in the prelimbic and infralimbic subdivisions of the mPFC in behaving rats. These conditioning-induced changes in mPFC firing were mitigated by systemic administration of propranolol (10 mg/kg, i.p.), a β-noradrenergic receptor antagonist. Moreover, propranolol administration dampened the stress-induced impairment in extinction observed when extinction training is delivered shortly after fear conditioning. These findings suggest that β-adrenoceptors mediate stress-induced changes in mPFC spike firing that contribute to extinction impairments. Propranolol may be a helpful adjunct to behavioral therapy for PTSD, particularly in patients who have recently experienced trauma.


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