Brunnlieb Claudia, Nave Gideon, Camerer Colin F, Schosser Stephan, Vogt Bodo, Münte Thomas F, Heldmann Marcus
Department of Neurology, University Lübeck, 23562 Lübeck, Germany; Center for Behavioral Brain Sciences, 39120 Magdeburg, Germany; Department of Empirical Economics, Otto-von-Guericke-University Magdeburg, 39106 Magdeburg, Germany; Department of Social Medicine and Health Economics, Otto-von-Guericke-University Magdeburg, 39120 Magdeburg, Germany;
Computation and Neural Systems, California Institute of Technology, Pasadena, CA 91125;
Proc Natl Acad Sci U S A. 2016 Feb 23;113(8):2051-6. doi: 10.1073/pnas.1518825113. Epub 2016 Feb 8.
The history of humankind is an epic of cooperation, which is ubiquitous across societies and increasing in scale. Much human cooperation occurs where it is risky to cooperate for mutual benefit because successful cooperation depends on a sufficient level of cooperation by others. Here we show that arginine vasopressin (AVP), a neuropeptide that mediates complex mammalian social behaviors such as pair bonding, social recognition and aggression causally increases humans' willingness to engage in risky, mutually beneficial cooperation. In two double-blind experiments, male participants received either AVP or placebo intranasally and made decisions with financial consequences in the "Stag hunt" cooperation game. AVP increases humans' willingness to cooperate. That increase is not due to an increase in the general willingness to bear risks or to altruistically help others. Using functional brain imaging, we show that, when subjects make the risky Stag choice, AVP down-regulates the BOLD signal in the left dorsolateral prefrontal cortex (dlPFC), a risk-integration region, and increases the left dlPFC functional connectivity with the ventral pallidum, an AVP receptor-rich region previously associated with AVP-mediated social reward processing in mammals. These findings show a previously unidentified causal role for AVP in social approach behavior in humans, as established by animal research.
人类历史是一部合作的史诗,这种合作在各个社会中普遍存在且规模不断扩大。许多人类合作发生在为了互利而合作存在风险的情况下,因为成功的合作取决于他人有足够的合作水平。在此我们表明,精氨酸加压素(AVP),一种介导诸如配偶关系、社会识别和攻击等复杂哺乳动物社会行为的神经肽,能因果性地增加人类参与有风险的互利合作的意愿。在两项双盲实验中,男性参与者经鼻接受AVP或安慰剂,并在“猎鹿”合作博弈中做出会产生财务后果的决策。AVP增加了人类的合作意愿。这种增加并非由于承担风险的总体意愿增加或利他地帮助他人的意愿增加。使用功能性脑成像,我们表明,当受试者做出有风险的猎鹿选择时,AVP会下调左侧背外侧前额叶皮层(dlPFC)(一个风险整合区域)的血氧水平依赖(BOLD)信号,并增加左侧dlPFC与腹侧苍白球之间的功能连接,腹侧苍白球是一个富含AVP受体的区域,先前在哺乳动物中与AVP介导的社会奖赏处理相关。这些发现表明,如动物研究所示,AVP在人类社会趋近行为中具有先前未被识别的因果作用。