The Role of the Left Dorsolateral Prefrontal Cortex in Altruistic Behavior Under Inequity Situations: A tDCS Study

Zhang Hanqi, Wu Shijing

Journal of Psychological Science ›› 2026, Vol. 49 ›› Issue (1) : 45-55.

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Journal of Psychological Science ›› 2026, Vol. 49 ›› Issue (1) : 45-55. DOI: 10.16719/j.cnki.1671-6981.20260106
General Psychology,Experimental Psychology & Ergonomics

The Role of the Left Dorsolateral Prefrontal Cortex in Altruistic Behavior Under Inequity Situations: A tDCS Study

  • Zhang Hanqi1,2, Wu Shijing2
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Abstract

Altruism, which is defined as behavior in which individuals deplete their own resources to benefit others, has played a pivotal role in human evolution and is deeply embedded in social and political life. Although highly valued, altruistic behavior is susceptible to influence by inequity situations. Specifically, individuals are more willing to act altruistically when they possess a higher initial endowment than their partners (an advantageous inequity situation) compared to when they have a lower initial endowment (a disadvantageous inequity situation). Neuroimaging studies suggest that advantageous and disadvantageous inequity engage distinct neurocognitive mechanisms. The left dorsolateral prefrontal cortex (lDLPFC), a brain region critical for executive function and impulse control, is hypothesized to play a role in altruistic decision-making. However, whether the lDLPFC differentially modulates altruism in advantageous versus disadvantageous inequity contexts remains unclear.
To address this question, we employed transcranial direct current stimulation (tDCS) to modulate the activity of lDLPFC and examined its effects on altruistic behavior under both advantageous and disadvantageous inequity conditions. Using a 2 × 2 mixed design, we manipulated stimulation condition (between-subjects factor: anodal vs. sham tDCS) and the inequity condition (within-subjects factor: advantageous vs. disadvantageous). A total of 70 healthy participants were recruited in the experiment (35 female, Mage = 20.79 ± 1.84 years). Participants were randomly assigned to receive either anodal tDCS (1.5 mA applied to the lDLPFC for 20 minutes) or sham tDCS (stimulation terminated after 30 seconds). Following the stimulation, participants completed a modified Dictator Game task to assess altruistic propensities. In this task, participants allocated monetary payoffs between themselves and anonymous partners across multiple trials, with no time constraints imposed.
In advantageous inequity trials, participants' payoffs exceeded those of their partners (e.g., $50 vs. $20), while in disadvantageous inequity trials, participants' payoffs were lower (e.g., $20 vs. $50). Altruistic choices involved participants sacrificing a portion of their own payoff (e.g.,$4) to increase their partner's payoff (e.g.,$13). Trials were presented in separate, counterbalanced blocks. Using mixed-effects logistic regression (lme4 package in R), we analyzed the impact of lDLPFC stimulation on altruistic behavior.
The results demonstrated that anodal tDCS over the lDLPFC significantly enhanced altruistic tendencies in advantageous inequity conditions, reducing participants' focus on personal losses. In advantageous inequity conditions, participants' altruistic behavior decreased as the cost of altruism increased (β = -1.630, p < .001, Bonferroni-corrected) and increased as the benefit of altruism increased (β = .991, p < .001, Bonferroni-corrected). The interaction between tDCS stimulation and the cost of altruism was significant (β = .564, p < .01, Bonferroni-corrected). Anodal tDCS over the left DLPFC attenuated the impact of altruistic costs on altruism in advantageous inequity conditions, indicating that anodal stimulation of the left DLPFC reduced participants' focus on self-interest in such contexts. In contrast, no significant effect was observed in disadvantageous inequity conditions. In disadvantageous inequity conditions, participants' altruistic behavior also decreased as the cost of altruism increased (β = -2.403, p < .001, Bonferroni-corrected) and increased as the benefit of altruism increased (β = .871, p < .001, Bonferroni-corrected). However, the interaction between tDCS stimulation and the cost of altruism was not significant (β = .279, p > .05), nor was the interaction between tDCS stimulation and the benefit of altruism (β = -.218, p > .05). These findings highlight the critical role of the lDLPFC in promoting altruism under advantageous inequity, enabling individuals to transcend self-interest and prioritize the welfare of others.
In summary, this study investigated the impact of tDCS applied to the dorsolateral prefrontal cortex (DLPFC) on altruistic behavior under conditions of inequality. Anodal tDCS stimulation of the left DLPFC was found to reduce participants' sensitivity to altruistic costs in situations of advantageous inequality. However, it did not influence their sensitivity to altruistic costs in disadvantageous inequity condition. These findings suggest that the left DLPFC plays a specific role in promoting altruistic behavior in contexts of advantageous inequality, while its involvement in altruism appears to differ in situation of disadvantageous inequity.

Key words

inequity / altruism / left dorsolateral prefrontal cortex / transcranial direct current stimulation

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Zhang Hanqi, Wu Shijing. The Role of the Left Dorsolateral Prefrontal Cortex in Altruistic Behavior Under Inequity Situations: A tDCS Study[J]. Journal of Psychological Science. 2026, 49(1): 45-55 https://doi.org/10.16719/j.cnki.1671-6981.20260106

References

[1] Barbey A. K., Koenigs M., & Grafman J. (2013). Dorsolateral prefrontal contributions to human working memory. Cortex, 49(5), 1195-1205.
[2] Baron-Cohen S., Ring H. A., Wheelwright S., Bullmore E. T., Brammer M. J., Simmons A., & Williams, S. C. R. (1999). Social intelligence in the normal and autistic brain: An fMRI study. European Journal of Neuroscience, 11(6), 1891-1898.
[3] Batson C. D., O'Quin K., Fultz J., Vanderplas M., & Isen A. M. (1983). Influence of self-reported distress and empathy on egoistic versus altruistic motivation to help. Journal of Personality and Social Psychology, 45(3), 706.
[4] Bekkers, R. (2006). Traditional and health-related philanthropy: The role of resources and personality. Social Psychology Quarterly, 69(4), 349-366.
[5] Bode N. W. F., Miller J., O'Gorman R., & Codling E. A. (2015). Increased costs reduce reciprocal helping behaviour of humans in a virtual evacuation experiment. Scientific Reports, 5(1), 15896.
[6] Brosnan, S. F., & De Waal, F. B. M. (2014). Evolution of responses to (un)fairness. Science, 346(6207).
[7] Carrington, S. J., & Bailey, A. J. (2009). Are there theory of mind regions in the brain? A review of the neuroimaging literature. Human Brain Mapping, 30(8), 2313-2335.
[8] Cutler, J., & Campbell-Meiklejohn, D. (2019). A comparative fMRI meta-analysis of altruistic and strategic decisions to give. NeuroImage, 184, 227-241.
[9] Fehr, E., & Fischbacher, U. (2003). The nature of human altruism. Nature, 425(6960), 785-791.
[10] FeldmanHall O., Dalgleish T., Evans D., & Mobbs D. (2015). Empathic concern drives costly altruism. NeuroImage, 105, 347-356.
[11] Figner B., Knoch D., Johnson E. J., Krosch A. R., Lisanby S. H., Fehr E., & Weber E. U. (2010). Lateral prefrontal cortex and self-control in intertemporal choice. Nature Neuroscience, 13(5), 538-539.
[12] Gao X., Yu H., Sáez I., Blue P. R., Zhu L., Hsu M., & Zhou X. (2018). Distinguishing neural correlates of context-dependent advantageous- and disadvantageous-inequity aversion. Proceedings of the National Academy of Sciences of the United States of America, 115(33), E7680-E7689.
[13] Glass L., Moody L., Grafman J., & Krueger F. (2015). Neural signatures of third-party punishment: Evidence from penetrating traumatic brain injury. Social Cognitive and Affective Neuroscience, 11(2), 253-262.
[14] Guo X., Zheng L., Zhu L., Li J., Wang Q., Dienes Z., & Yang Z. (2013). Increased neural responses to unfairness in a loss context. NeuroImage, 77, 246-253.
[15] Güroğlu B., van den Bos W., Rombouts S. A. R. B., & Crone E. A. (2010). Unfair? It depends: Neural correlates of fairness in social context. Social Cognitive and Affective Neuroscience, 5(4), 414-423.
[16] Hamilton, W. D. (1964). The genetical evolution of social behaviour. II. Journal of Theoretical Biology, 7(1), 17-52.
[17] Hofmann W., Schmeichel B. J., & Baddeley A. D. (2012). Executive functions and self-regulation. Trends in Cognitive Sciences, 16(3), 174-180.
[18] Hu J., Hu Y., Li Y., & Zhou X. (2021). Computational and neurobiological substrates of cost-benefit integration in altruistic helping decision. Journal of Neuroscience, 41(15), 3545-3561.
[19] Karim A. A., Schneider M., Lotze M., Veit R., Sauseng P., Braun C., & Birbaumer N. (2010). The truth about lying: Inhibition of the anterior prefrontal cortex improves deceptive behavior. Cerebral Cortex, 20(1), 205-213.
[20] Knoch D., Pascual-Leone A., Meyer K., Treyer V., & Fehr E. (2006). Diminishing reciprocal fairness by disrupting the right prefrontal cortex. Science, 314(5800), 829-832.
[21] Li F., Ball S., Zhang X., & Smith A. (2020). Focal stimulation of the temporoparietal junction improves rationality in prosocial decision-making. Scientific Reports, 10(1), 1-10.
[22] Li S., Cai Y., Liu J., Li D., Feng Z., Chen C., & Xue G. (2017). Dissociated roles of the parietal and frontal cortices in the scope and control of attention during visual working memory. NeuroImage, 149, 210-219.
[23] Maréchal M. A., Cohn A., Ugazio G., & Ruff C. C. (2017). Increasing honesty in humans with noninvasive brain stimulation. Proceedings of the National Academy of Sciences, 114(17), 4360-4364.
[24] Martin A. K., Huang J., Hunold A., & Meinzer M. (2017). Sex mediates the effects of high-definition transcranial direct current stimulation on "mind-reading." Neuroscience, 366, 84-94.
[25] Martin A. K., Huang J., Hunold A., & Meinzer M. (2019). Dissociable roles within the social brain for self-other processing: A HD-tDCS study. Cerebral Cortex, 29(8), 3642-3654.
[26] McAuliffe K., Blake P. R., Steinbeis N., & Warneken F. (2017). The developmental foundations of human fairness. Nature Human Behaviour, 1(2), 410-433.
[27] Meyer B., Mann C., Götz M., Gerlicher A., Saase V., Yuen K. S. L., Aedo-Jury F., Gonzalez-Escamilla G., Stroh A., & Kalisch R. (2019). Increased neural activity in mesostriatal regions after prefrontal transcranial direct current stimulation and L-DOPA administration. Journal of Neuroscience, 39(27), 5326-5335.
[28] Moll J., Krueger F., Zahn R., Pardini M., de Oliveira-Souza R., & Grafman J. (2006). Human fronto-mesolimbic networks guide decisions about charitable donation. Proceedings of the National Academy of Sciences, 103(42), 15623-15628.
[29] Moll J., Zahn R., de Oliveira-Souza R., Krueger F., & Grafman J. (2005). The neural basis of human moral cognition. Nature Reviews Neuroscience, 6(10), 799-809.
[30] Morishima Y., Schunk D., Bruhin A., Ruff C. C., & Fehr E. (2012). Linking brain structure and activation in temporoparietal junction to explain the neurobiology of human altruism. Neuron, 75(1), 73-79.
[31] Nagel B. J., Herting M. M., Maxwell E. C., Bruno R., & Fair D. (2013). Hemispheric lateralization of verbal and spatial working memory during adolescence. Brain and Cognition, 82(1), 58-68.
[32] Obeso I., Moisa M., Ruff C. C., & Dreher J. C. (2018). A causal role for right temporo-parietal junction in signaling moral conflict. eLife, 7, 1-16.
[33] Penner L. A., Dovidio J. F., Piliavin J. A., & Schroeder D. A. (2005). Prosocial behavior: Multilevel perspectives. Annual Review of Psychology, 56, 365-392.
[34] Ruff C. C., Ugazio G., & Fehr E. (2013). Changing social norm compliance with noninvasive brain stimulation. Science, 342(6157), 482-484.
[35] Sanfey A. G., Hastie R., Colvin M. K., & Grafman J. (2003). Phineas gauged: Decision-making and the human prefrontal cortex. Neuropsychologia, 41(9), 1218-1229.
[36] Smith M. J., Schroeder M. P., Abram, S. V, Goldman, M. B., Parrish T. B., Wang X., Derntl B., Habel U., Decety J., Reilly J. L., Csernansky J. G., & Breiter H. C. (2015). Alterations in brain activation during cognitive empathy are related to social functioning in schizophrenia. Schizophrenia Bulletin, 41(1), 211-222.
[37] Speitel C., Traut-Mattausch E., & Jonas E. (2019). Functions of the right DLPFC and right TPJ in proposers and responders in the ultimatum game. Social Cognitive and Affective Neuroscience, 14(3), 263-270.
[38] Stagg C. J., Antal A., & Nitsche M. A. (2018). Physiology of transcranial direct current stimulation. The Journal of ECT, 34(3), 144-152.
[39] Steinbeis N., Bernhardt B. C., & Singer T. (2012). Impulse control and underlying functions of the left DLPFC mediate age-related and age-independent individual differences in strategic social behavior. Neuron, 73(5), 1040-1051.
[40] Tabibnia G., Satpute A. B., & Lieberman M. D. (2008). The sunny side of fairness: preference for fairness activates reward circuitry (and disregarding unfairness activates self-control circuitry). Psychological Science, 19(4), 339-347.
[41] Tomasello, M. (2009). Why we cooperate. MIT Press..
[42] Tricomi E., Rangel A., Camerer C. F., & Odoherty J. P. (2010). Neural evidence for inequality-averse social preferences. Nature, 463(7284), 1089-1091.
[43] van den Bos K., Peters S. L., Bobocel D. R., & Ybema J. F. (2006). On preferences and doing the right thing: Satisfaction with advantageous inequity when cognitive processing is limited. Journal of Experimental Social Psychology, 42(3), 273-289.
[44] Wang G., Li J., Yin X., Li S., & Wei M. (2016). Modulating activity in the orbitofrontal cortex changes trustees' cooperation: A transcranial direct current stimulation study. Behavioural Brain Research, 303, 71-75.
[45] Wang, H., & Zhang, H. (2021). High-definition transcranial direct current stimulation over the right lateral prefrontal cortex increases maximization tendencies. Frontiers in Behavioral Neuroscience, 15, 653987-653987.
[46] Wang Y., Ge J., Zhang H., Wang H., & Xie X. (2020). Altruistic behaviors relieve physical pain. Proceedings of the National Academy of Sciences of the United States of America, 117(2), 950-958.
[47] Warneken, F., & Tomasello, M. (2009). Varieties of altruism in children and chimpanzees. Trends in Cognitive Sciences, 13(9), 397-402.
[48] Xiong G., She Z., Zhao J., & Zhang H. (2021). Transcranial direct current stimulation over the right dorsolateral prefrontal cortex has distinct effects on choices involving risk and ambiguity. Behavioural Brain Research, 400, 113044.
[49] Yang C. C., Khalifa N., Lankappa S., & Völlm B. (2018). Effects of intermittent theta burst stimulation applied to the left dorsolateral prefrontal cortex on empathy and impulsivity in healthy adult males. Brain and Cognition, 128, 37-45.
[50] Zhang H., Dong Z., Cai S., Wu S., & Zhao J. (2023). Modulating the activity of the right dorsolateral prefrontal cortex alters altruism in situations of advantageous inequity. Neuroscience, 509, 36-42.
[51] Zhang H., Dong Z., Cai S., & Zhao J. (2022). Distinguishing the roles of the dorsomedial prefrontal cortex and right temporoparietal junction in altruism in situations of inequality: A transcranial direct current stimulation study. Frontiers in Human Neuroscience, 16, 1-7.
[52] Zheng W., Li Y., Ye H., & Luo J. (2021). Effect of modulating DLPFC activity on antisocial and prosocial behavior: Evidence from a tDCS study. Frontiers in Psychology, 11, 579792.
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