Neuroscience is at a historic turning point. Today, a full decade after the “Decade of the Brain,” a continuous stream of advances is shattering long-held notions about how the human brain works and what happens when it doesn’t. These advances are also reshaping the landscapes of other fields, from psychology to economics, education and the law.
Until the Decade of the Brain, scientists believed that, once development was over, the adult brain underwent very few changes. This perception contributed to polarizing perspectives on whether genetics or environment determines a person’s temperament and personality, aptitudes, and vulnerability to mental disorders. But during the past two decades, neuroscientists have steadily built the case that the human brain, even when fully mature, is far more plastic—changing and malleable—than we originally thought.1 It turns out that the brain (at all ages) is highly responsive to environmental stimuli and that connections between neurons are dynamic and can rapidly change within minutes of stimulation.
It also has become increasingly clear that the human brain is particularly sensitive to social stimuli, which likely has accelerated the rate of human brain evolution. Humans have evolved a complex neuronal circuitry in large areas in the brain to process complex social information (such as predicting others’ reactions and emotions) and to respond appropriately. New research has revealed that social stimuli (such as parenting style and early-life stress) can epigenetically modify the expression of genes that influence brain morphology and function including the sensitivity of an individual to stressful stimuli.2 In the future, this knowledge will enable us to tailor personalized prevention interventions that are based on information on how genetics and epigenetics affect brain function and behavior. For example, a recent study showed that a prevention intervention based on improving parenting style reduced the risk for substance use disorders only in adolescents with a particular variant of a gene that recycles the chemical serotonin back into the neurons, which is a variant that results in greater sensitivity to social adversity.3
In the coming decade, insights about what underlies neuroplasticity, combined with technological advances that allow us to “see” with greater precision the human brain in action, are bound to revolutionize the way we view learning and the methods we use to educate young people. New research will also show us how to help people overcome or compensate for many of the deficits associated with drug abuse, addiction and other mental disorders.4
For example, scientists are using imaging technologies in neurofeedback programs that train people to voluntarily recalibrate their neural activity in specific areas of the brain, allowing them to gain unprecedented control over, for example, pain perception5 or emotional processing.6 During drug addiction treatment, this approach could greatly reduce the risk of relapse by enabling a patient to control the powerful cravings triggered by a host of cues (e.g., people, things, places) that have become tightly linked, in the brain of the user, to the drug experience.
Other promising advances stem from ongoing research and development of direct communication pathways between a brain and external computer devices, the so called brain-computer interfaces (BCI). In a recent study, one version of BCI appeared to help paralyzed stroke victims regain some movement control.7 In the next decade, forms of BCI might help people with a variety of neuropsychiatric conditions that have proved resistant to traditional treatments. For example, early evidence suggests that BCI training could benefit patients with epilepsy or attention-deficit/hyperactivity disorder (ADHD) that is unresponsive to drugs.8
As we build on these rapid advances in neuroscience research, we must keep a watchful eye on their vast social and political implications. For example, neurologists have started to uncover the molecular components and neural circuitry that underlie the learning process.9 We also are learning how to use transcranial magnetic stimulation (TMS), a noninvasive method to modulate the activity within a neural circuit, more effectively.10 Should we use this knowledge to better educate young people and teach new skills to seniors, or should we use these tools only to treat people with neuropsychiatric disorders? As we begin to understand how parenting styles affect the development and function of the brain, how far should we go to protect children from the long-term and deleterious effects of bad parenting?
Recent progress in brain research and associated fields has been impressive, and we are sure to witness further acceleration in the pace of neuroscientific discovery in the next couple of decades. Indeed, we are entering a new era in which our technologies are beginning to affect our lives in profound ways. We are bound to recast our relationship with our brains and, in the process, to redraw the boundaries of human evolution.
Blakemore: Plasticity Made Us Human
Moheb Costandi, Dana Foundation News and Features
August 5, 2010
Teasing Out the Effects of the Environment on the Brain
Moheb Costandi, Dana Foundation News and Features
June 4, 2010
Epigenetic changes and parenting:
DNA Is Not Destiny
Ethan Watters, Discover Magazine November 2006
Genetic Risk for Substance Use Can Be Neutralized by Good Parenting
ScienceDaily February 26, 2009
Overcoming drug abuse damage:
Brain Shows Ability to Recover from Some Methamphetamine Damage
Brookhaven National Laboratory News Release
December 1, 2001
Neurofeedback for pain:
Brain Can Be Trained To Reduce Pain
Miranda Hill, Fox News.com December 13, 2005
BCI for stroke victims:
Tapping Brain Waves
Innovation: The Magazine of Research and Technology
By Linda Lim
Transcranial Magnetic stimulation:
Study Supports Transcranial Magnetic Stimulation to Treat Depression
Dana Foundation Feature
Maria Schamis Turner, August 9, 2010
1. A. Holtmaat and K. Svoboda, “Experience-Dependent Structural Synaptic Plasticity in the Mammalian Brain,” Nature Reviews Neuroscience 10, no. 9 (2009): 647–658; M. Butz, F. Worgotter, and A. van Ooyen, “Activity-Dependent Structural Plasticity,” Brain Research Reviews 60, no. 2 (2009): 287–305.
2. I. C. Weaver, N. Cervoni, F. A. Champagne, A. C. D’Alessio, S. Sharma, J. R. Seckl, S. Dymov, M. Szyf, and M. J. Meaney, “Epigenetic Programming by Maternal Behavior,” Nature Neuroscience 7, no. 8 (2004): 847–854.
3. G. H. Brody, S. R. Beach, R. A. Philibert, Y. F. Chen, M. K. Lei, V. M. Murry, and A. C. Brown, “Parenting Moderates a Genetic Vulnerability Factor in Longitudinal Increases in Youths’ Substance Use,” Journal of Consulting and Clinical Psychology 77, no. 1 (2009): 1–11.
4. N. D. Volkow, L. Chang, G. J. Wang, J. S. Fowler, D. Franceschi, M. Sedler, S. J. Gatley, E. Miller, R. Hitzemann, Y. S. Ding, and J. Logan, “Loss of Dopamine Transporters in Methamphetamine Abusers Recovers with Protracted Abstinence,” Journal of Neuroscience 21, no. 23 (2001): 9414–9418.
5. R. C. deCharms, F. Maeda, G. H. Glover, D. Ludlow, J. M. Pauly, D. Soneji, J. D. Gabrieli, and S. C. Mackey, “Control over Brain Activation and Pain Learned by Using Real-time Functional MRI,” Proceedings of the National Academy of Sciences USA 102, no. 51 (2005): 18626–18631; S. J. Johnston, S. G. Boehm, D. Healy, R. Goebel, and D. E. Linden, “Neurofeedback: A Promising Tool for the Self-regulation of Emotion Networks,” Neuroimage 49, no. 1 (2009): 1066–1072.
6. S. Johnston, S. Boehm, D. Healy, R. Goebel, and D. Linden, “Neurofeedback: A promising tool for the self-regulation of emotion networks,” Neuroimage 49 (2009):1066-1072.
7. E. Buch, C. Weber, L. G. Cohen, C. Braun, M. A. Dimyan, T. Ard, J. Mellinger, A. Caria, S. Soekadar, A. Fourkas, and N. Birbaumer, “Think to Move: a Neuromagnetic Brain-Computer Interface (BCI) System for Chronic Stroke,” Stroke 39, no. 3 (2008): 910–917.
8. N. Birbaumer, A. Ramos Murguialday, C. Weber, and P. Montoya, “Neurofeedback and Brain-Computer Interface Clinical Applications,” International Review of Neurobiology 86 (2009): 107–117.
9. C. A. Miller, S. L. Campbell, and J. D. Sweatt, “DNA Methylation and Histone Acetylation Work in Concert to Regulate Memory Formation and Synaptic Plasticity,” Neurobiology of Learning and Memory 89, no. 4 (2008): 599–603.
10. C. A. Dockery, R. Hueckel-Weng, N. Birbaumer, and C. Plewnia, “Enhancement of Planning Ability by Transcranial Direct Current Stimulation,” Journal of Neuroscience 29, no. 22 (2009): 7271–7277.
* This article was previously published in Cerebrum, 2010