pain |
human |
stereotactic implantation technique |
posterior IC is involved in the processing of both painful and innocuous somaesthetic inputs |
(Ostrowsky et al., 2002) |
|
mice |
electrophysiology |
NMDARs contributes to neuropathic pain |
(Qiu et al., 2013) |
|
mice |
electrophysiology |
AMPARs is enhanced after nerve injury |
(Qiu et al., 2014) |
Emotion |
human |
fMRI |
functional connectivity between the amygdala and anterior IC relates to fear |
(Yoshihara et al., 2016) |
|
human |
PET |
relation to sadness |
(Damasio et al., 2000) |
|
human |
fMRI, PET |
PTSD, social anxiety disorder and specific phobia show great activities |
(Etkin and Wager, 2007) |
Memory |
mice |
electrophysiology, CTA |
LTD attenuates taste aversive memory |
(Li et al., 2016) |
|
rats |
electrophysiology (in vivo), CTA |
CTA induces LTP |
(Rodriguez-Duran et al., 2011) |
|
rats |
CTA |
long-term memory is inhibited by an inhibition of PKMζ |
(Shema et al., 2007) |
|
rats |
electrophysiology (in vivo), CTA |
NMDAR dependent LTP is required for taste learning |
(Escobar et al., 1998) |
|
rats |
CTA |
PSD-5 induction is necessary for learning novel tastes |
(Elkobi et al., 2008) |
|
rats |
CTA |
only the early robust trace is maintained by a NMDA-dependent CaMKII-AMPAR pathway |
(Adaikkan and Rosenblum, 2015) |
|
rats |
electrophysiology (in vivo) |
LTP contributes to taste learning |
(Jones et al., 1999) |
|
rats |
CTA |
NMDARs is involved in taste learning |
(Rosenblum et al., 1997) |