# How helping others helps us: neural mechanisms linking prosocial behavior to psychological and physical wellbeing

**Authors:** M. Justin Kim, Sunhae Sul

PMC · DOI: 10.3389/fnhum.2026.1686801 · Frontiers in Human Neuroscience · 2026-02-23

## TL;DR

Helping others can improve our mental and physical health through specific brain mechanisms that support empathy and reward.

## Contribution

This review integrates current evidence on how prosocial behavior affects wellbeing and the underlying neural mechanisms.

## Key findings

- Prosocial behavior reduces depression, anxiety, and loneliness while enhancing positive emotions and life satisfaction.
- Key brain regions involved in reward, empathy, and mentalizing support prosocial actions and their health benefits.
- Prosocial behavior may create self-reinforcing cycles that buffer stress and enhance social connectedness.

## Abstract

Prosocial behavior—voluntary actions intended to benefit others—not only holds moral and social value but also promotes psychological and physical wellbeing through complex neural mechanisms. This Mini Review summarizes current evidence on the health benefits of helping others, including reductions in depression, anxiety, and loneliness, as well as enhancements in positive affect, life satisfaction, and physiological health markers. Then, we provide an overview of the neural systems that support prosociality, highlighting key regions involved in reward processing, empathy, and mentalizing, and how their integration supports flexible, context-sensitive helping behavior. Furthermore, we discuss possible neural pathways linking prosocial actions to stress buffering, mood enhancement, and social connectedness, forming self-reinforcing cycles that sustain wellbeing. We also discuss individual difference factors—including personality traits and early life experiences—that may act to modulate these neural mechanisms and impact prosocial engagement. Understanding how helping others benefits the helper holds promise for advancing population health and fostering resilience across diverse contexts.

## Full-text entities

- **Genes:** OXTR (oxytocin receptor) [NCBI Gene 5021] {aka OT-R, OTR}, OXT (oxytocin/neurophysin I prepropeptide) [NCBI Gene 5020] {aka OT, OT-NPI, OXT-NPI}
- **Diseases:** hyperactivity (MESH:D006948), fatigue (MESH:D005221), anxiety (MESH:D001007), inflammation (MESH:D007249), pain (MESH:D010146), impairments in social functioning (OMIM:300082), depression (MESH:D003866), burnout (MESH:D002055)
- **Chemicals:** cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970011/full.md

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Source: https://tomesphere.com/paper/PMC12970011