The  neuroanatomical linkage that emerges from a normal part of business  experience—the reaction to success and also to failure (especially if  that failure happens to someone else)—is the focus of this post. I am often asked to speak to groups of business executives, mostly to  discuss a possible connection between neuroscience and business  practices. These meetings are always challenging for me, because I don’t  think brain science has much to do with the world of business. My own  opinion is that the field of neuroscience is simply not mature enough to  tell business executives how to manage their subordinates or how to  lure customers into buying their products. “I have nothing real to say  to you,” I usually start, “We don’t even understand how humans know how  to put their socks on in the morning.” There are usually some  murmurs in the crowd at this point, but since I still have 45 to 60  minutes to burn, I continue, “My perspective isn’t hopeless, though. In  fact, almost all of the brain’s neural circuitry can be easily  explained—especially if you are looking at people’s interior  motivations.” Then I continue with what turns into a Darwinian lecture:  “People will do whatever they think will ultimately benefit them. And  people will do whatever they can to avoid pain. Almost everything we  know about how the brain generates behavior can be couched as  combinatorial activations of these 2 broad sets of purpose-driven  circuits—seeking pleasure, avoiding pain.” The human brain as a mass of biological  tissue is most clearly understood as a survival organ—the world’s most  sophisticated. Given this performance envelope, a great deal of  theoretical common ground exists between what we know about the brain  and the needs of business. Even though not much of the brain has been  mapped, my corporate audiences and I usually end up with lots to say to  each other. This post is all about mapping a specific  parcel of this common ground between pleasure and pain and gives a  suggestion for a specific investigative direction. We will explore how a  subset of these circuits supports the social experience of pleasure and  pain. There is a powerful bridge between pleasure and pain and  their social equivalents; indeed, to the brain, they are nearly  identical. Recent findings confirm that the same reward circuits are  activated during sex and also while delighting in someone else’s  misfortune (schadenfreude).1 Similarly, both physical pain and envy over another person’s success activate these circuits. The biology of pleasure and pain We  start with a basic review of canonical circuits normally associated  with pleasure and pain, and then discuss interesting data from a  collaboration of scientists in Japan and the United Kingdom. Much of the  brain’s pleasure circuitry has been studied through the lens of reward  reception and the establishment of addictive behavior. Invariably, this  involves the neurotransmitter dopamine and a number of neural circuits  that have been isolated and characterized in surprising detail. Three  networks are briefly reviewed. The first circuit involves the  interaction of dopamine in neurons within the ventral tegmental area,  especially in response to external rewards (eg, sexual activity, drugs,  food). Associated with  these circuits, the second network comprises neurons embedded in the  nucleus accumbens, within the ventral striatum. The nucleus accumbens  has been shown to play a vital role in the learning of reward and the  regulation of pleasurable states. The third circuit involves the  ventromedial prefrontal cortex in association with the amygdala. These 3  networks are also vital parts of the dopaminergic system and are  thought to mediate reward processing and the emotional responses  involved in the experience of pleasure. Association  never means causation. If you could somehow temporarily  deactivate the  ventral striatum, would schadenfreude suddenly disappear? The various circuits associated with mediating the experience of pain are collectively termed the “cortical pain network” (see Figure).  This network consists of specific regions, mostly ventral to the  pleasure centers; in turn, these are coupled with 2 subcortical  structures. The specific regions are the somatosensory cortex, the  dorsal anterior cingulate cortex (dACC), and the insula. The connecting  subcortical regions are the periaqueductal gray and the thalamus. These circuits undergird the twin Darwinian “motivations.” But can I really  say that? After all, they have been mostly characterized as physical  reactions to rewarding stimuli (such as drugs) or as physical reactions  to aversive stimuli (such as an electrical shock). These networks have  deep evolutionary roots, which means we share many of these same  circuits with other mammals. However, none of this history involves a  businessperson’s reaction to marketing strategies or mitigating highbrow  office politics that are associated with management. Does the  creation and perception of social rewards and punishments activate the  same regions as nucleus accumbens and the dACC? In the past few years,  the surprising answer from research is a clear “yes.” Social rewards and  punishments appear to hijack the same systems we use to mediate  laboratory-based measurements of pleasure and pain. If you are being  treated fairly, are feeling cooperative, or have been blessed with a  good reputation, you feel so in part because of circuits activating the  ventral striatum. This reward network is activated whenever you make a  charitable contribution—even more than if you suddenly inherited a lot  of money! Similarly, specific circuits of the cortical pain  network become activated whenever you experience social pain, such as  grief over the loss of a loved one. The same circuits are activated if  you feel you are being treated unfairly. The dACC and insula are  recruited whenever you feel socially excluded. The more social pain you  feel, the more activity is generated within the dACC. The bottom  line is that the brain appears to treat material physical stimuli and  amorphous social perceptions in a manner more similar than previously  thought. The data Researchers from Japan  and the United Kingdom explored 2 specific types of social interactions  in a 2-part study1 involving the above data. What they found has  potentially high relevance to business practices. While it is beyond the  scope of this column to go into specifics, we will say that in general,  19 volunteer participants were supplied with information concerning  imaginary target persons. These persons were characterized by levels of  possession and self-relevance. The participants underwent functional  MRI, more social information was supplied, and the experiments  commenced. When the participants were told that the targets had  superior possessions and self-relevance, they reported strong feelings  of envy. Surprisingly, the areas of the brain associated with physical  pain—particularly the dACC—showed a very strong signal in the people  experiencing envy, even though no physical pain was being experienced.  The effect appeared to be linear and cumulative. The more envy evinced,  the stronger the dACC signal was observed. For the second part of the study, researchers tested for schadenfreude,  or delight in someone else’s misfortune. The participants were told  that the “superior” targets had experienced something awful. What did  their brains do? The areas associated with pleasure, particularly the  ventral striatum, showed an immediate and powerful activation. This  effect was also linear and cumulative. The more envy evoked in the first  part of study, the greater the pleasure signals were observed in the  second. For the first time, research demonstrated a lively and dramatic  integration between the experiences of social pleasure and social pain. Conclusions There  is a lot more work to be done before a clear picture emerges. For one  thing, areas of the brain—such as the dACC and the ventral  striatum—include a broad range of activities, not all of which fall  under the rubric of pleasure and pain mitigation. Experiments will need  to rely on the power of future technologies to identify the boundaries  of actual neural networks involved. And, of course, association never  means causation. If you could somehow temporarily deactivate the ventral  striatum, would schadenfreude suddenly disappear? This research has yet to be done. Still,  the data in context with previous research undergird critical insight  into the incredible evolutionary importance of social relationships to  the human brain. Many researchers believe it was our dependence on  relational activities that created the need for this big, unique brain  of ours in the first place. As weak as our bodies are, it was more  convenient for us to double our biomass by creating a cooperative ally  than by creating a bigger body. This meant putting pressure on a  relatively small number of neurons in the brain, rather than a large  number of cells throughout the body. Moreover, the brain is an  efficient and evolutionary manager of its bioenergetic needs. It is not  surprising that regions associated with the physical needs of pleasure  and pain might be recruited for the more abstract social versions of the  same thing. The gift this gives people interested in the biological  roots of behavior is enormous: certain previously considered subjective  experiences—such as envy—may not be as subjective as we once thought.  If that’s the case, I will eventually owe my business audiences a big  apology. Perhaps in a few years, brain scientists will have something to  say to business people interested in improving their “bottom lines.”Each  region makes unique contributions in the perception of pain. For  example, the somatosensory cortex is associated with the localization of  the stimulus within the body. The dACC and, to a lesser extent, the  insula are associated with the processing of more distressing aspects of  pain.
Reference
1. Takahashi H, Kato M, Matsuura, et al. When your  gain is my pain and your pain is my gain: neural correlates of envy and  schadenfreude.Science.2009;323:937-939.
This post originally appeared in the November 2010 issue of the Psychiatric Times.
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