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Who Needs Emotions? The Brain Meets the Robot

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64 brains<br />

benefits that also presented vulnerabilities. For example, genes related to <strong>the</strong><br />

DA system that may have enhanced novelty seeking may have provided<br />

advantages in seeking and finding new habitats and resources. In ancestral<br />

environments, such genetic quirks would be beneficial or at <strong>the</strong> very least<br />

not deleterious; however, in modern environments, with availability of pure<br />

drugs such as cocaine, disproportionate susceptibility among individuals may<br />

occur. Gerald and Higley (2002) have proposed a fascinating model for genetic<br />

susceptibility to alcohol dependence in relation to variations in serotonin<br />

function. <strong>The</strong>ir research shows that monkeys with lower levels of brain<br />

5-HT tend to be less affiliative and social, to be more aggressive and impulsive,<br />

and to have a higher mortality in <strong>the</strong> wild. <strong>The</strong>se monkeys drink excessive<br />

amounts of alcohol compared to monkeys with high 5-HT levels. Thus,<br />

heritable traits that may have been advantageous in certain contexts could<br />

contribute to susceptibility to alcoholism and excessive alcohol intake.<br />

Ultimately, it is critical to address <strong>the</strong> remarkable similarities between<br />

plant alkaloids and nervous system chemicals and receptors in animals. Figure<br />

3.8 shows examples of cannabinoid and opiate receptors in <strong>the</strong> mammalian<br />

brain. Sullivan and Hagen (2002) ponder this question and propose<br />

that psychotropic substance seeking is an adaptation reflective of a coevolutionary<br />

relationship between psychotropic plant substances and humans that<br />

is millions of years old. Plants containing allelochemicals (toxic metabolites<br />

used by plants to discourage herbivores and pathogens) were widespread in<br />

<strong>the</strong> ancestral environment, and <strong>the</strong>se alkaloids were often chemical analogues<br />

of vertebrate and invertebrate neurotransmitters.<br />

this “deep time” relationship is self-evident both in <strong>the</strong> extant<br />

chemical–ecological adaptations that have evolved in mammals to<br />

metabolize psychotropic plant substances and in <strong>the</strong> structure of<br />

plant defensive chemicals that have evolved to mimic <strong>the</strong> structure,<br />

and interfere with <strong>the</strong> function, of mammalian neurotransmitters.<br />

(Sullivan & Hagen, 2002)<br />

Taking an anthropological point of view, <strong>the</strong>se authors suggest that extensive<br />

evidence of substance use in antiquity may have been a mundane,<br />

ubiquitous activity similar to how we use caffeine in <strong>the</strong> present. <strong>The</strong>se authors<br />

propose that <strong>the</strong>re may have been selective and relatively specific benefits<br />

of plant use, particularly before <strong>the</strong> advent of agriculture. <strong>The</strong> use of <strong>the</strong><br />

coca plant can be traced at least as far back as 7000 years ago, and Sullivan and<br />

Hagen (2002) cite archeological evidence that <strong>the</strong> betel nut (containing<br />

arecoline, a muscarinic agonist) was chewed 13,000 years ago in Timor and<br />

10,700 years ago in Thailand. <strong>The</strong>se authors suggest that in a foraging environment<br />

humans may have exploited <strong>the</strong>se neurotransmitter analogue chemicals<br />

to enhance energy and fitness, particularly for nutritionally constrained

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