Isseroff et al., 1982
|
Bilateral MD – ablations |
Spatial delayed alternation |
Impaired |
|
|
Spatial delayed response |
Impaired |
Aggleton and Mishkin, 1983
|
Bilateral MD – ablations |
Object recognition memory |
Impaired |
|
|
Object-reward associations |
Impaired |
Zola-Morgan and Squire, 1985
|
Bilateral MD – ablations |
Delayed non-match to sample |
Impaired |
|
|
Pattern discriminations |
Not Impaired |
Parker et al., 1997
|
Bilateral MDmc – ablations |
Object recognition memory |
Impaired, if large numbers of objects used |
Gaffan and Parker, 2000
|
Bilateral MDmc – ablations |
Learnt 20 novel object-in-place scene discriminations within a session |
Impaired |
Gaffan and Parker, 2000
|
Bilateral MDmc – ablations |
Learnt object-reward associations within a session |
Impaired |
Mitchell et al., 2007a
|
Bilateral MDmc – neurotoxins |
Learnt 20 novel object-in-place scene discriminations within a session |
Impaired–increased switching not perseverative responding |
Mitchell et al., 2007a
|
Bilateral MDmc – neurotoxins |
Implementation of preoperatively acquired strategy |
Not Impaired |
Mitchell et al., 2007b
|
Bilateral MDmc – neurotoxins |
Learnt 60 object-reward associations across sessions to criterion |
Not Impaired |
Mitchell et al., 2007b
|
Bilateral MDmc – neurotoxins |
Food devaluation |
Impaired |
Mitchell and Gaffan, 2008
|
Bilateral MDmc – neurotoxins |
Retention of 300 preoperative acquired object-in-place scene discriminations |
Not Impaired |
Mitchell and Gaffan, 2008
|
Bilateral MDmc – neurotoxins |
Postoperative learning of 100 novel object-in-place scene discriminations across sessions |
Impaired |
Mitchell et al., 2008
|
Bilateral MDmc – neurotoxins + fornix transection |
Retention of 300 preoperative acquired object-in-place scene discriminations |
Impaired, combined damage to two interdependent neural circuits caused retention deficits |
Mitchell et al., 2008
|
Bilateral MDmc – neurotoxins + fornix transection |
Postoperative learning of 100 novel object-in-place scene discriminations across sessions |
Impaired, greater deficit compared to bilateral MDmc lesions alone–Mitchell and Gaffan, 2008
|
Izquierdo and Murray, 2010
|
Unilateral MDmc – neurotoxic + contralateral amygdala + orbitofrontal cortex |
Food devaluation |
Impaired |
Browning et al., 2015
|
Unilateral MDmc – neurotoxins |
Learning 20 novel object-in-place scene discriminations within a session |
Impaired |
Browning et al., 2015
|
Unilateral ventrolateral PFC and orbitofrontal cortex ablation |
Learning 20 novel object-in-place scene discriminations within a session |
Not impaired |
Browning et al., 2015
|
Contralateral ventrolateral PFC and orbitofrontal cortex X MDmc – neurotoxins |
Learning 20 novel object-in-place scene discriminations within a session |
Impaired |
Browning et al., 2015
|
Contralateral ventrolateral PFC and orbitofrontal cortex X MDmc – neurotoxins |
Food devaluation |
Impaired |
Browning et al., 2015
|
Ipsilateral ventrolateral PFC and orbitofrontal cortex + MDmc – neurotoxins |
Learning 20 novel object-in-place scene discriminations within a session |
Not impaired |
Browning et al., 2015
|
Ipsilateral ventrolateral PFC and orbitofrontal cortex + MDmc – neurotoxins |
Food devaluation |
Impaired |
Chakraborty et al., 2016
|
Bilateral MDmc – neurotoxins |
Learning novel 3-choice probabilistic object-reward associations within a session and reversals |
Impaired–increased switching. Disrupted rapid updating of next choice response based on recent choice history |