So, if this modification of the Aggleton learn more and Brown view is correct, the thalamic material-specific memory hypothesis should predict that left-sided lesions of the medial/magnocellular MDT should disrupt familiarity memory for verbal materials and right-sided lesions should disrupt familiarity memory for visual materials with the effects of parvicellular lesions remaining currently unspecified. Caution should be exercised because it is extremely

difficult to be sure about the precise localization and extent of small thalamic lesions in humans. In an attempt to reconcile the sometime discordant clinical and animal lesion evidence of the contribution if different medial thalamic nuclei

to recognition memory, Aggleton, Dumont, and Warburton (2011) have proposed the ‘multi-effect multi nuclei’ model that proposes that anteromedial thalamic nuclei can have both direct and indirect effects on recognition. Building on the earlier Aggleton and Brown (1999) model, direct effects on recollection are mediated via the mammillary body, MTT, and anterior thalamus, and on familiarity via the MDT. AZD4547 solubility dmso However, the major addition introduced by the multi-effect multi-nuclei model are the indirect influences that can act on both recollection and familiarity in a non-specific manner. The mechanisms by which these effects are mediated is by the modulation of arousal and attention by connections between the intralaminar and midline thalamic nuclei, the MDT, and prefrontal areas (Portas et al., 1998). The aim of our study was to investigate material-specific

lateralization of long-term memory in two patients with thalamic pathology (SM and OG). These patients were particularly well suited to the purpose, as high-resolution structural magnetic resonance imaging has shown that the SM’s lesion is clearly limited to the left thalamus and OG’s lesion is limited to the right thalamus. In both patients, the lesion involves the midline nuclei (central medial and paraventricular nuclei), the medial/magnocellular and part of the parviceullar subdivisions of the MDT, the intramedullary lamina, and encroached on the MTT, thereby partially disconnecting the mammillary bodies from the anterior ioxilan thalamus. It should be noted that our patients’ unilateral lesions are not exact mirror images of each other. OG’s lesion is centred on the medial division of the MDT whereas SM’s lesion is more anterior and ventral. Importantly, in both cases, there is no evidence of pathology in structures that have been related to memory functions in the contralateral diencephalon and medial temporal lobes. However, volume measures of these structures were performed to determine if retrograde or anterograde degeneration had occurred and, therefore, may also contribute to the memory loss.