- Papez circuit
- James Papez's 1937 proposed circuit for emotion: hypothalamus → anterior thalamic nuclei → cingulate cortex → hippocampus → fornix → mammillary bodies → hypothalamus. Papez proposed that the cingulate cortex was the substrate of emotional experience (the "stream of feeling") while the hypothalamus controlled emotional expression (the "stream of movement"). Though the hippocampus is now understood as primarily a memory structure rather than an emotional one, the Papez circuit identified many components that remain central to understanding emotion and memory, and established that emotion has a distributed neural substrate, not a single location.
- MacLean's triune brain (and its critique)
- Paul MacLean's model (1952–1990) proposed three hierarchically organised brain components: the reptilian complex (brainstem, basal ganglia — instinctive behaviours), the paleomammalian limbic system (emotion, memory, social bonding), and the neomammalian neocortex (rational thought, language). Hugely influential in popular science and some clinical traditions, the model is now rejected by comparative neurobiologists: (1) no brain structures are uniquely reptilian; (2) brain evolution does not work by adding new layers; (3) limbic structures are involved in far more than emotion; (4) the cortex-as-reason vs limbic-system-as-emotion dualism misrepresents how emotion and cognition interact.
- Fornix
- The principal white matter output tract of the hippocampus, carrying fibres from the hippocampal subiculum and CA1 to the mammillary bodies, septal nuclei, and anterior thalamic nuclei — completing the Papez circuit. Damage to the fornix (from tumours, trauma, or ischaemia) produces diencephalic amnesia: the hippocampus can no longer send its memory output to thalamic and hypothalamic targets. The fornix also carries cholinergic input to the hippocampus from the septal nuclei, which modulate hippocampal theta rhythms during navigation and memory encoding.
- Cingulate cortex
- A cortical strip wrapping over the corpus callosum, typically divided into anterior and posterior portions. The dorsal anterior cingulate cortex (dACC) is activated by conflict between competing responses, error signals, and the unpleasant (affective) dimension of pain. The subgenual anterior cingulate (Area 25) regulates mood and autonomic function; its hyperactivity in depression has made it a target for deep brain stimulation. The posterior cingulate cortex (PCC) is a major hub of the default mode network, active during rest and self-referential processing.
- Mammillary bodies
- Small paired structures at the base of the hypothalamus, receiving the major hippocampal output via the fornix and projecting to the anterior thalamic nuclei. Part of the Papez circuit for memory and emotion. Disproportionately damaged in Wernicke-Korsakoff syndrome (thiamine deficiency): their haemorrhagic lesions contribute to the severe anterograde amnesia and confabulation of that condition. The mammillary bodies are also involved in spatial memory and head direction cell activity.
- Entorhinal cortex
- A parahippocampal cortex that serves as the primary input and output gateway to the hippocampus, mediating communication between the hippocampus and the rest of the neocortex. Grid cells — the spatially periodic neurons discovered by May-Britt and Edvard Moser (Nobel Prize 2014) — are found in the entorhinal cortex, forming a coordinate system for navigation. The entorhinal cortex is among the first areas affected by Alzheimer's disease pathology, which explains why spatial disorientation and memory difficulties are early symptoms.
- Klüver-Bucy syndrome
- A syndrome produced by bilateral removal of the temporal lobes in primates (Klüver & Bucy, 1939), causing: placidity (loss of fear and aggression), hypersexuality, hyperorality (oral examination of all objects), and psychic blindness (inability to recognise the emotional significance of stimuli). Partial Klüver-Bucy syndrome occurs in humans following bilateral temporal lobe damage (herpes simplex encephalitis, severe traumatic brain injury). The syndrome implicates the amygdala (fear/emotional recognition), hippocampus (memory), and temporal association cortex (object recognition).