Peer-Reviewed Journal Details
Mandatory Fields
Fendt, M;Schmid, S;Thakker, DR;Jacobson, LH;Yamamoto, R;Mitsukawa, K;Maier, R;Natt, F;Husken, D;Kelly, PH;McAllister, KH;Hoyer, D;van der Putten, H;Cryan, JF;Flor, PJ
2008
October
Molecular Psychiatry
mGluR7 facilitates extinction of aversive memories and controls amygdala plasticity
Validated
WOS: 100 ()
Optional Fields
METABOTROPIC GLUTAMATE-RECEPTOR CONDITIONED TASTE-AVERSION FEAR-POTENTIATED STARTLE LONG-TERM POTENTIATION ADULT-MOUSE BRAIN INSULAR CORTEX D-CYCLOSERINE PREFRONTAL CORTEX MOLECULAR-CLONING RNA INTERFERENCE
13
970
979
Formation and extinction of aversive memories in the mammalian brain are insufficiently understood at the cellular and molecular levels. Using the novel metabotropic glutamate receptor 7 (mGluR7) agonist AMN082, we demonstrate that mGluR7 activation facilitates the extinction of aversive memories in two different amygdala-dependent tasks. Conversely, mGluR7 knockdown using short interfering RNA attenuated the extinction of learned aversion. mGluR7 activation also blocked the acquisition of Pavlovian fear learning and its electrophysiological correlate long-term potentiation in the amygdala. The finding that mGluR7 critically regulates extinction, in addition to acquisition of aversive memories, demonstrates.
LONDON
1359-4184
10.1038/sj.mp.4002073
Grant Details