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º¸»ó½Ã½ºÅÛ : like vs want

º¸»ó½Ã½ºÅÛ
- Like vs Want
- ½Ä¿å : ½Ä¿å ±âÀÛ
- Áßµ¶ : ºñ¸¸Àº º¸»ó Áßµ¶ÀÌ´Ù
- ¿£µµ¸ð¸£ÇÉ : Food morphine



Neurophysiologist Kent Berridge suggests (with strong scientific support) that our desire for food (and drugs) must be distinguished into two separate phenomena: liking, or pleasure induced during eating, and wanting, the (non-hedonic) desire to choose that food. Berridge¡¯s work is tough reading and difficult to understand because it is not biologically intuitive. (But the good doctor is always quick to answer my e-mails when I need further clarification.) In an article on liking vs. wanting, scientist David Mela (2006) explains that the key to understanding food behavior involves physiological cues, anticipated pleasure, and external cues (conscious and unconscious). He says that oral pleasure is not the only food-purchase criteria; the other dimension is a desire for ¡°wanting¡± that food based on a non-hedonic choice. He suggests that wanting may be related to the experience of food boredom—we simply want food with differing sensory properties. Low calorie foods, he hypothesizes, must be optimized for both wanting and liking. Why is this important? Well, it is fairly easy to measure and to manipulate how much you like something, but measuring how much you want something, especially when you are not aware of it, is quite another matter! Mela believes that this new dimension of wanting is a major factor in purchase intent and deserves much more serious study. In the future, manipulation of food ¡°wanting¡± may be a major product development endeavor.

Berridge and his colleagues disclose that the intense liking of sweetness is due to mu-opioid stimulation localized in the rostrodorsal region of the nucleus accumbens shell (a pleasure circuit in the limbic brain) and the ventral pallidum. Dopamine was widely believed to be the major pleasure neurotransmitter in the brain, but this may not be the case at all. Mice that are bred to have no brain dopamine still experience pleasant taste, however, they lack the will to work for it. Shimura et al. (2006) also found that GABA, opioid, and D1 receptors in the ventral pallidum (brain pleasure structure) are involved in the consumption of hedonically positive taste stimuli. The authors suggest that many common motivated behaviors activate the ventral pallidum such as consuming food, mating behavior, sexual activity, and in the liking for number of drugs such as alcohol, heroin, and cocaine. The brain pleasure response, it appears, likes to share a final common pathway.

 
 

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