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Who Needs Emotions? The Brain Meets the Robot

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46 brains<br />

voluntary control of actions is fur<strong>the</strong>r enabled by superimposition of cortical<br />

systems on <strong>the</strong> basic sensory-reflexive network. Moreover, <strong>the</strong>re is extensive<br />

reciprocal communication between <strong>the</strong> cerebral hemispheres and motor effector<br />

networks. An additional major principle for organization of <strong>the</strong> behavioral<br />

control columns is that <strong>the</strong>y project massively back to <strong>the</strong> cerebral cortex/<br />

voluntary control system directly or indirectly via <strong>the</strong> dorsal thalamus (Risold,<br />

Thompson, & Swanson, 1997; Swanson, 2000). For example, nearly <strong>the</strong> entire<br />

hypothalamus projects to <strong>the</strong> dorsal thalamus, which in turn projects to<br />

widespread regions of <strong>the</strong> neocortex. Moreover, recently characterized<br />

neuropeptide-coded systems have revealed that orexin/hypocretin- and melanin<br />

concentrating hormone–containing cells within <strong>the</strong> lateral hypothalamus<br />

project directly to widespread regions within <strong>the</strong> neocortex, amygdala, hippocampus,<br />

and ventral striatum and may be very important for behavioral<br />

state regulation and arousal (Espana, Baldo, Kelley, & Berridge, 2001;<br />

Peyron et al., 1998). This feed-forward hypothalamic projection to <strong>the</strong><br />

cerebral hemispheres is an extremely important anatomical fact for grasping<br />

<strong>the</strong> notions elaborated above, that intimate access of associative and<br />

cognitive cortical areas to basic motivational networks enables <strong>the</strong> generation<br />

of emotions or <strong>the</strong> manifestation of “motivational potential.” Thus, in <strong>the</strong><br />

primate brain, this substantial reciprocal interaction between phylogenetically<br />

old behavioral control columns and <strong>the</strong> more recently developed cortex<br />

subserving higher-order processes such as language and cognition has enabled<br />

a two-way street for emotion. Not only can circuits controlling voluntary motor<br />

actions, decision making, and executive control influence and modulate our<br />

basic drives, but activity within <strong>the</strong> core motivational networks can impart<br />

emotional coloring to conscious processes. A flat map anatomical diagram from<br />

<strong>the</strong> work of Swanson (2000), showing some of <strong>the</strong> pathways described here,<br />

is provided in Figure 3.5.<br />

EVOLUTIONARY DEVELOPMENT OF<br />

NEUROTRANSMITTER SYSTEMS<br />

Neurochemical signaling pathways involved in emotional processing in <strong>the</strong><br />

mammalian brain have evolved over <strong>the</strong> billions of years since <strong>the</strong> origins<br />

of life. Within <strong>the</strong> constraints of genetic evolution, nervous systems became<br />

more complex and enabled progressively greater possibilities for <strong>the</strong><br />

animal in its relationship with its environment. Chemical signaling played<br />

a critical role in this connectivity and adaptation. Neurotransmitter signaling<br />

networks and <strong>the</strong>ir corresponding receptor molecules, particularly <strong>the</strong> biogenic<br />

amines, small neuropeptides, and neuropeptide hormones, became<br />

specialized for particular behaviors or motivational states (Niall, 1982;

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